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    <title>Recent plantpath_ucd items</title>
    <link>https://escholarship.org/uc/plantpath_ucd/rss</link>
    <description>Recent eScholarship items from Department of Plant Pathology</description>
    <pubDate>Fri, 26 Jun 2026 13:01:25 +0000</pubDate>
    <item>
      <title>KitBase Expanded: An Integrated Genomic and Phenotypic Resource for 3,268 Fast-Neutron-Irradiated Rice Mutants.</title>
      <link>https://escholarship.org/uc/item/2zw8d4kq</link>
      <description>Fast-neutron mutagenesis creates diverse genome-wide mutations, providing a powerful tool for crop functional genomics. Here, we present an expanded genomic and phenotypic analysis of 3268 fast-neutron (FN)-induced mutant rice lines (Oryza sativa L. cv. Kitaake). All FN lines were whole-genome sequenced, and mutations were identified by alignment in the Nipponbare and KitaakeX reference genomes. We cataloged over 428,000 mutations affecting 78.49% of Nipponbare genes and 70.38% of KitaakeX genes. In silico expression analysis indicates that 575 non-mutated Nipponbare genes are highly expressed and likely essential for viability. Each mutant carries, on average, 68.5 mutations in the Nipponbare alignments or 63.2 mutations for KitaakeX alignments, distributed randomly across all 12 chromosomes with no evident hotspots. FN lines have approximately 8.5% fewer mutations when using the KitaakeX alignment, underscoring the unique contributions of each reference genome and the importance...</description>
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      <pubDate>Wed, 17 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>de Araujo, Artur</name>
      </author>
      <author>
        <name>Jain, Rashmi</name>
      </author>
      <author>
        <name>Ruan, Deling</name>
      </author>
      <author>
        <name>Chern, Mawsheng</name>
      </author>
      <author>
        <name>Ho, Nguyen</name>
      </author>
      <author>
        <name>Jhingan, Rohan</name>
      </author>
      <author>
        <name>Li, Guotian</name>
      </author>
      <author>
        <name>Duong, Phat</name>
      </author>
      <author>
        <name>Ercoli, Maria</name>
      </author>
      <author>
        <name>Ronald, Pamela</name>
      </author>
    </item>
    <item>
      <title>Temporal dynamics of Grapevine red blotch virus accumulation in grapevine leaves is influenced by fruit maturity stages.</title>
      <link>https://escholarship.org/uc/item/1rp7p8dm</link>
      <description>Grapevine red blotch disease (GRBD) poses a serious threat to viticulture in the United States. Grapevine red blotch virus (GRBV), a member species of Grablovirus vitis (family Geminiviridae), the causal agent of GRBD, disrupts grapevine physiology and metabolism, thereby interfering with the natural processes of fruit ripening. To date, there is limited knowledge about how grape maturity stages influence the timing of changes in viral load and disease progression. This study elucidates the effect of fruit maturity stages on GRBV accumulation in Vitis vinifera L. cv. Merlot grapevines in a Central Coast vineyard in California. Petioles from six basal leaves at random from previously GRBV-infected vines were collected at pre-véraison, véraison, post-véraison, and harvest stages, across two years (2021 and 2022). The viral copy number was quantified using digital PCR. The study identified significant differences (p &amp;lt; 0.05) in GRBV copy number across different maturity stages...</description>
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      <pubDate>Tue, 26 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Singh, Prem</name>
      </author>
      <author>
        <name>Reddy, Kishorekumar</name>
      </author>
      <author>
        <name>Scully, Hazel</name>
      </author>
      <author>
        <name>Boghozian, Arpa</name>
      </author>
      <author>
        <name>Medina-Plaza, Cristina</name>
      </author>
      <author>
        <name>Oberholster, Anita</name>
      </author>
      <author>
        <name>Sudarshana, Mysore</name>
      </author>
    </item>
    <item>
      <title>Laboratory Protocols for Candidatus Liberibacter asiaticus Transmission Biology and Management Research</title>
      <link>https://escholarship.org/uc/item/1sb63017</link>
      <description>Candidatus Liberibacter asiaticus (CLas), the causal agent of Huanglongbing, is transmitted by the Asian citrus psyllid (Diaphorina citri) in a persistent, propagative manner. Reproducible transmission studies require not only controlled inoculation assays but also standardized propagation of citrus host plants, maintenance of D. citri colonies, and reliable pathogen detection. This study presents a comprehensive set of coordinated protocols that collectively support controlled CLas transmission experimentation. The workflow includes propagation of Citrus macrophylla for colony and assay use; generation and maintenance of CLas-infected citrus and D. citri colonies; synchronization of D. citri populations to enable CLas acquisition; and a controlled single-D. citri transmission assay with defined inoculation access periods, and a Dellaporta-based nucleic acid extraction method compatible with citrus and psyllid tissues. Quantitative PCR detection is integrated throughout to verify...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1sb63017</guid>
      <pubDate>Fri, 8 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Galdeano, Diogo M</name>
      </author>
      <author>
        <name>Ingram, William</name>
      </author>
      <author>
        <name>Erickson, Anna</name>
      </author>
      <author>
        <name>Carlson, Curtis R</name>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
      <author>
        <name>Kuo, Yen‐Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
    </item>
    <item>
      <title>STREAMS guidelines: standards for technical reporting in environmental and host-associated microbiome studies</title>
      <link>https://escholarship.org/uc/item/0nt0t4k2</link>
      <description>The interdisciplinary nature of microbiome research, coupled with the generation of complex multi-omics data, makes knowledge sharing challenging. The Strengthening the Organization and Reporting of Microbiome Studies (STORMS) guidelines provide a checklist for the reporting of study information, experimental design and analytical methods within a scientific manuscript on human microbiome research. Here, in this Consensus Statement, we present the standards for technical reporting in environmental and host-associated microbiome studies (STREAMS) guidelines. The guidelines expand on STORMS and include 67 items to support the reporting and review of environmental (for example, terrestrial, aquatic, atmospheric and engineered), synthetic and non-human host-associated microbiome studies in a standardized and machine-actionable manner. Based on input from 248 researchers spanning 28 countries, we provide detailed guidance, including comparisons with STORMS, and case studies that demonstrate...</description>
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      <pubDate>Wed, 6 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kelliher, Julia M</name>
      </author>
      <author>
        <name>Mirzayi, Chloe</name>
      </author>
      <author>
        <name>Bordenstein, Sarah R</name>
      </author>
      <author>
        <name>Oliver, Aaron</name>
        <uri>https://orcid.org/0000-0002-0410-8284</uri>
      </author>
      <author>
        <name>Kellogg, Christina A</name>
      </author>
      <author>
        <name>Hatcher, Eneida L</name>
      </author>
      <author>
        <name>Berg, Maureen</name>
      </author>
      <author>
        <name>Baldrian, Petr</name>
      </author>
      <author>
        <name>Aljumaah, Mashael</name>
      </author>
      <author>
        <name>Miller, Cassandra Maria Luz</name>
      </author>
      <author>
        <name>Mungall, Christopher</name>
      </author>
      <author>
        <name>Novak, Vlastimil</name>
        <uri>https://orcid.org/0000-0001-7890-4593</uri>
      </author>
      <author>
        <name>Palucki, Alexis</name>
      </author>
      <author>
        <name>Smith, Ethan</name>
      </author>
      <author>
        <name>Tabassum, Nazifa</name>
      </author>
      <author>
        <name>Bonito, Gregory</name>
      </author>
      <author>
        <name>Brister, J Rodney</name>
      </author>
      <author>
        <name>Chain, Patrick SG</name>
      </author>
      <author>
        <name>Chen, Mingfei</name>
      </author>
      <author>
        <name>Degregori, Samuel</name>
      </author>
      <author>
        <name>Dundore-Arias, Jose Pablo</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
      <author>
        <name>Moreira C. Fernandes, Vanessa</name>
      </author>
      <author>
        <name>Flores, Roberto</name>
      </author>
      <author>
        <name>Gonzalez, Antonio</name>
      </author>
      <author>
        <name>Hansen, Zoe A</name>
      </author>
      <author>
        <name>Jackson, Scott A</name>
      </author>
      <author>
        <name>Moustafa, Ahmed M</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Pariente, Nonia</name>
      </author>
      <author>
        <name>Pett-Ridge, Jennifer</name>
      </author>
      <author>
        <name>Record, Sydne</name>
      </author>
      <author>
        <name>Reji, Linta</name>
      </author>
      <author>
        <name>Reysenbach, Anna-Louise</name>
      </author>
      <author>
        <name>Rich, Virginia I</name>
      </author>
      <author>
        <name>Richardson, Lorna</name>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
      <author>
        <name>Schriml, Lynn M</name>
      </author>
      <author>
        <name>Shabman, Reed S</name>
      </author>
      <author>
        <name>Sierra, Maria A</name>
      </author>
      <author>
        <name>Sullivan, Matthew B</name>
      </author>
      <author>
        <name>Sundaramurthy, Punithavathi</name>
      </author>
      <author>
        <name>Thibault, Katherine M</name>
      </author>
      <author>
        <name>Thompson, Luke R</name>
      </author>
      <author>
        <name>Tighe, Scott</name>
      </author>
      <author>
        <name>Vereen, Ethell</name>
      </author>
      <author>
        <name>Eloe-Fadrosh, Emiley A</name>
        <uri>https://orcid.org/0000-0002-8162-1276</uri>
      </author>
    </item>
    <item>
      <title>Reduced methane emissions in transgenic rice genotypes are associated with altered rhizosphere microbial hydrogen cycling</title>
      <link>https://escholarship.org/uc/item/7rr0p6zq</link>
      <description>Rice paddies significantly contribute to atmospheric methane (CH4). Here, we show that two independent rice genotypes overexpressing genes for PLANT PEPTIDES CONTAINING SULFATED TYROSINE (PSY) reduce cumulative CH4 emissions by 38% (PSY1) and 58% (PSY2) over 70 days of growth compared with controls. Genome-resolved metatranscriptomic data from PSY rhizosphere soils reveal lower ratios of gene activities for (mostly hydrogenotrophic) CH4 production versus consumption, decreased activity of H2-producing genes, and increased activity of bacterial H2 oxidation pathways. Metabolic modeling using metagenomic and metabolomic data predicts elevated H2 oxidation and suppressed H2 production in the PSY rhizosphere. Assembled genomes of rhizosphere H2-oxidizing bacteria are enriched in genes utilizing gluconeogenic acids compared with H2-producing counterparts, and their activities are likely stimulated by elevated levels of gluconeogenic acids, primarily amino acids, in PSY root exudates....</description>
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      <pubDate>Fri, 17 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shi, Ling-Dong</name>
      </author>
      <author>
        <name>Ercoli, Maria Florencia</name>
        <uri>https://orcid.org/0000-0001-5587-6227</uri>
      </author>
      <author>
        <name>Kim, Junhyeong</name>
      </author>
      <author>
        <name>de Araujo Junior, Artur Teixeira</name>
      </author>
      <author>
        <name>Estera-Molina, Katerina</name>
      </author>
      <author>
        <name>Soni, Subah</name>
      </author>
      <author>
        <name>Weitz, Tracy Satomi</name>
      </author>
      <author>
        <name>Shigenaga, Alexandra M</name>
      </author>
      <author>
        <name>Dukovski, Ilija</name>
      </author>
      <author>
        <name>Sachdeva, Rohan</name>
      </author>
      <author>
        <name>Turumtay, Halbay</name>
        <uri>https://orcid.org/0000-0003-4224-8103</uri>
      </author>
      <author>
        <name>Louie, Katherine B</name>
      </author>
      <author>
        <name>Bowen, Benjamin P</name>
        <uri>https://orcid.org/0000-0003-1368-3958</uri>
      </author>
      <author>
        <name>Kosina, Suzanne M</name>
        <uri>https://orcid.org/0000-0003-2885-1248</uri>
      </author>
      <author>
        <name>Scheller, Henrik V</name>
        <uri>https://orcid.org/0000-0002-6702-3560</uri>
      </author>
      <author>
        <name>Pett-Ridge, Jennifer</name>
      </author>
      <author>
        <name>Segrè, Daniel</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
      </author>
      <author>
        <name>Ronald, Pamela C</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
      <author>
        <name>Banfield, Jillian F</name>
      </author>
    </item>
    <item>
      <title>Lifestyle-associated variation in type IV secretion systems between phytopathogenic and environmental &lt;i&gt;Ralstonia&lt;/i&gt;.</title>
      <link>https://escholarship.org/uc/item/1g77f6n8</link>
      <description>Type IV secretion systems (T4SSs) are versatile machines with variable functions including DNA uptake and release, protein translocation, and DNA conjugation. However, the diversity, distribution, and functional roles of the T4SS in the &lt;i&gt;Ralstonia&lt;/i&gt; genus remain poorly understood. The &lt;i&gt;Ralstonia solanacearum&lt;/i&gt; species complex (RSSC) comprises three species of plant-pathogenic bacteria that cause bacterial wilt disease. The &lt;i&gt;Ralstonia&lt;/i&gt; genus also includes non-RSSC species that are primarily environmental bacteria and rare opportunistic human pathogens. This study compared the diversity and phylogenetic distribution of T4SSs in the RSSC phytopathogens vs. non-RSSC environmentals. Phylogenetic analysis of VirB4 sequences and synteny analysis revealed 16 distinct T4SS clusters in &lt;i&gt;Ralstonia&lt;/i&gt;, with 10 clusters found in RSSC phytopathogen genomes, 12 in non-RSSC environmental genomes, and 6 clusters in both groups. Collectively, these gene clusters were more prevalent...</description>
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      <pubDate>Fri, 17 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Cowell, Tabitha</name>
      </author>
      <author>
        <name>Cope-Arguello, Matthew</name>
      </author>
      <author>
        <name>Shin, Gi</name>
      </author>
      <author>
        <name>Bogdanove, Adam</name>
      </author>
      <author>
        <name>Carpenter, Sara</name>
      </author>
      <author>
        <name>Nahar, Kamrun</name>
      </author>
      <author>
        <name>Saha, Apurba</name>
      </author>
      <author>
        <name>Lowe-Power, Tiffany</name>
      </author>
    </item>
    <item>
      <title>A protocol for chemical competence in phytopathogenic Ralstonia.</title>
      <link>https://escholarship.org/uc/item/3630232x</link>
      <description>Here, we present a protocol for the transformation of &lt;i&gt;Ralstonia solanacearum&lt;/i&gt; species complex (RSSC) strains by calcium chloride-induced chemical competence. We include a step-by-step protocol with media and solution recipes, quantitative results of the protocols efficacy for four of five tested RSSC strains, and an explanation of the logic underlying the protocol development. The protocol involves sequentially treating overnight cultures with a cold calcium chloride solution and a cold calcium chloride/magnesium chloride/glycerol solution, transforming through alternating heat shocks and ice incubations, and recovering cells via an outgrowth in rich medium.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3630232x</guid>
      <pubDate>Fri, 3 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Cowell, Tabitha</name>
      </author>
      <author>
        <name>Guillome, Noah</name>
      </author>
      <author>
        <name>Cope-Arguello, Matthew</name>
      </author>
      <author>
        <name>Prasad, Neha</name>
      </author>
      <author>
        <name>Lowe-Power, Tiffany</name>
      </author>
    </item>
    <item>
      <title>Teaching in Emergencies: Building Resilient Practices as Language-Learning Teachers</title>
      <link>https://escholarship.org/uc/item/4622b47j</link>
      <description>Teaching in Emergencies: Building Resilient Practices as Language-Learning Teachers</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4622b47j</guid>
      <pubDate>Wed, 25 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sasaki, Mia</name>
        <uri>https://orcid.org/0000-0002-0372-3322</uri>
      </author>
      <author>
        <name>Levi, Sarah</name>
      </author>
    </item>
    <item>
      <title>Deep change in low-resource classrooms: Data-driven teacher professional development for educators from Burma using a choice-based approach</title>
      <link>https://escholarship.org/uc/item/89p211bx</link>
      <description>Deep change in low-resource classrooms: Data-driven teacher professional development for educators from Burma using a choice-based approach</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/89p211bx</guid>
      <pubDate>Wed, 11 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Tyrosvoutis, Greg</name>
      </author>
      <author>
        <name>Sasaki, Mia</name>
      </author>
      <author>
        <name>Chan, Lawi</name>
      </author>
      <author>
        <name>Win, Naing</name>
      </author>
      <author>
        <name>Zar, Tin</name>
      </author>
      <author>
        <name>Win, Nwet Nwet</name>
      </author>
      <author>
        <name>Moo, Naw Th'Blay</name>
      </author>
      <author>
        <name>Paw, Naw Nay Yu</name>
      </author>
    </item>
    <item>
      <title>Trapping Failure Leads to Discovery of Potent Semiochemical Repellent for the Walnut Twig Beetle</title>
      <link>https://escholarship.org/uc/item/78k8q56b</link>
      <description>The walnut twig beetle, Pityophthorus juglandis Blackman, and its associated fungal pathogen that causes thousand cankers disease, currently threaten the viability of walnut trees across much of North America. During a 2011 assessment of seasonal flight patterns of P. juglandis with yellow sticky traps baited with the male-produced aggregation pheromone component, 3-methyl-2-buten-1-ol, dramatically reduced catches were recorded when Tree Tanglefoot adhesive was used to coat the traps. In summer 2011, two trap adhesives were tested for potential repellency against P. juglandis in a field trapping bioassay. SuperQ extracts of volatiles from the most repellent adhesive were analyzed by gas chromatography-mass spectrometry, and limonene and α-pinene were identified as predominant components. In field-based, trapping experiments both enantiomers of limonene at a release rate of ~700 mg/d conferred 91-99% reduction in trap catches of P. juglandis to pheromone-baited traps. (+)- and...</description>
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      <pubDate>Wed, 11 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Audley, Jackson P</name>
      </author>
      <author>
        <name>Dallara, Paul L</name>
      </author>
      <author>
        <name>Nelson, Lori J</name>
      </author>
      <author>
        <name>Hamud, Shakeeb M</name>
      </author>
      <author>
        <name>Bostock, Richard M</name>
        <uri>https://orcid.org/0000-0001-9928-4610</uri>
      </author>
      <author>
        <name>Seybold, Steven J</name>
      </author>
    </item>
    <item>
      <title>Walnut twig beetle landing rates differ between host and nonhost hardwood trees under the influence of aggregation pheromone in a northern California riparian forest</title>
      <link>https://escholarship.org/uc/item/4s04c6mv</link>
      <description>Abstract    Host selection behaviour of the walnut twig beetle (WTB) among hardwood trees was investigated in a riparian forest in northern California by monitoring the landing rate of the beetle with sticky traps on branches baited with 3‐methyl‐2‐buten‐1‐ol, the male‐produced aggregation pheromone.    The assay was conducted over 7 days (22 May to 29 May 2017) and compared landing rates on branches of six nonhost species paired with northern California black walnut, Juglans hindsii (the host).     A total of 2242/1192 WTB were collected on branches of host/nonhost pairs, and more WTB landed on J. hindsii than on nonhosts in 42 of 58 instances. Female landing rate generally exceeded male landing rate, which underscores the influence of the male‐produced synthetic pheromone in this system.     Landing rates of WTB males, females, and the combined sexes on boxelder, Acer negundo , and valley oak, Quercus lobata , did not differ significantly from the landing rates on J. hindsii...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4s04c6mv</guid>
      <pubDate>Wed, 11 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Homicz, Crystal S</name>
      </author>
      <author>
        <name>Audley, Jackson P</name>
      </author>
      <author>
        <name>Chen, Yigen</name>
      </author>
      <author>
        <name>Bostock, Richard M</name>
        <uri>https://orcid.org/0000-0001-9928-4610</uri>
      </author>
      <author>
        <name>Tauber, Catherine A</name>
      </author>
      <author>
        <name>Seybold, Steven J</name>
      </author>
    </item>
    <item>
      <title>The EPS-I exopolysaccharide transforms &lt;i&gt;Ralstonia&lt;/i&gt; wilt pathogen biofilms into viscoelastic fluids for rapid dissemination in planta.</title>
      <link>https://escholarship.org/uc/item/55s112r4</link>
      <description>&lt;i&gt;Ralstonia solanacearum&lt;/i&gt; species complex (RSSC) pathogens cause destructive plant wilt diseases of a wide variety of crops, leading to significant agricultural losses worldwide. These bacteria rapidly spread through the water-transporting xylem where they grow prolifically and produce abundant biofilm that clogs xylem vessels. To understand RSSC biofilm behavior in planta, we examined their complex fluid mechanics. Rheological analyses revealed that unlike all previously analyzed microbial biofilms, RSSC biofilms are shear-thinning, viscoelastic fluids at physiologically relevant shear forces. To determine which factors confer these unique mechanics, we analyzed biofilms of bacterial mutants with altered biofilm components. Genetic analysis demonstrated that development of the viscous-dominant biofilms required production of EPS-I, an amphiphilic exopolysaccharide that is a major virulence factor for all RSSC pathogens. We show that EPS-I confers biofilm mobility, which allows...</description>
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      <pubDate>Sat, 31 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Cope-Arguello, Matthew</name>
      </author>
      <author>
        <name>Li, Jiayu</name>
      </author>
      <author>
        <name>Konkel, Zachary</name>
      </author>
      <author>
        <name>Aoun, Nathalie</name>
      </author>
      <author>
        <name>Cowell, Tabitha</name>
      </author>
      <author>
        <name>Wagner, Nicholas</name>
      </author>
      <author>
        <name>Han Chan, A</name>
      </author>
      <author>
        <name>Chu, Lan</name>
      </author>
      <author>
        <name>Wang, Samantha</name>
      </author>
      <author>
        <name>Carter, Mariama</name>
      </author>
      <author>
        <name>Allen, Caitilyn</name>
      </author>
      <author>
        <name>Caverly, Lindsay</name>
      </author>
      <author>
        <name>Bui, Loan</name>
      </author>
      <author>
        <name>DeAngelis, Kristen</name>
      </author>
      <author>
        <name>Wargo, Matthew</name>
      </author>
      <author>
        <name>Tran, Tuan</name>
      </author>
      <author>
        <name>Jacobs, Jonathan</name>
      </author>
      <author>
        <name>Manikantan, Harishankar</name>
      </author>
      <author>
        <name>Lowe-Power, Tiffany</name>
      </author>
    </item>
    <item>
      <title>Comparison of short-read and long-read metagenome assemblies in a natural soil community highlights systematic bias in recovery of high-diversity populations</title>
      <link>https://escholarship.org/uc/item/5qz8b72k</link>
      <description>Comparisons of long-read and short-read (meta)genome assemblies typically show that short-read sequence assemblies are less error-prone, but struggle to assemble complicated genome regions (e.g. repeats) compared to long-read sequence assemblies. Accurate metagenome assembly is especially challenging in diverse environments, such as soil, and long-read sequencing has been shown to improve assembly. Here, we use metagenomic data with paired long-read and short-read sequences to identify specific factors that impact genome assembly and assess their relative importance in a natural soil community. Our analysis suggests that low coverage and high sequence diversity are the two main factors leading to misassemblies in short-read data, and many of these "missed" regions tend to be variable parts of the genome, such as integrated viruses or defense system islands. Taken together, our results demonstrate that short-read metagenomes can possibly underestimate the diversity of these genome...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5qz8b72k</guid>
      <pubDate>Tue, 27 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Berg, Maureen</name>
      </author>
      <author>
        <name>Reiter, Taylor</name>
      </author>
      <author>
        <name>Emerson, Joanne</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
      <author>
        <name>Brown, C Titus</name>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
    </item>
    <item>
      <title>Unlocking expanded flagellin perception through rational receptor engineering</title>
      <link>https://escholarship.org/uc/item/81f8k8s0</link>
      <description>The surface-localized receptor kinase FLS2 detects the flg22 epitope from bacterial flagella. FLS2 is conserved across land plants, but bacterial pathogens exhibit polymorphic flg22 epitopes. Most FLS2 homologues possess narrow perception ranges, but four with expanded perception have been identified. Using diversity analyses, AlphaFold modelling and amino acid properties, key residues enabling expanded recognition were mapped to FLS2’s concave surface, interacting with the co-receptor and polymorphic flg22 residues. Synthetic biology enabled engineering of expanded recognition from QvFLS2 (Quercus variabilis) into a homologue with canonical perception. A similar approach enabled transfer of Agrobacterium perception from FLS2XL (Vitis riparia) into VrFLS2. Evolutionary analyses across three plant orders showed residues under positive selection aligning with those binding the co-receptor and flg22’s C terminus, suggesting more alleles with expanded perception exist. Our experimental...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/81f8k8s0</guid>
      <pubDate>Wed, 5 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Tianrun</name>
      </author>
      <author>
        <name>Jarquin Bolaños, Esteban</name>
      </author>
      <author>
        <name>Stevens, Danielle M</name>
      </author>
      <author>
        <name>Sha, Hanxu</name>
      </author>
      <author>
        <name>Prigozhin, Daniil M</name>
        <uri>https://orcid.org/0000-0003-2075-0231</uri>
      </author>
      <author>
        <name>Coaker, Gitta</name>
        <uri>https://orcid.org/0000-0003-0899-2449</uri>
      </author>
    </item>
    <item>
      <title>Direct evidence for the semipersistent transmission of Cucurbit chlorotic yellows virus by a whitefly vector</title>
      <link>https://escholarship.org/uc/item/6t12v7v2</link>
      <description>Cucurbit chlorotic yellows virus (CCYV) (genus Crinivirus, family Closteroviridae) is an emerging plant virus, and is now spreading and causing severe economic losses to cucurbit crops in many Asian countries. CCYV is believed to be transmitted specifically by the sweetpotato whitefly, Bemisia tabaci, in a semipersistent manner. In the present study, we provide direct evidence for the semipersistent transmission of CCYV by Mediterranean (MED) cryptic species of B. tabaci complex. We investigated CCYV transmission characteristics, and immunofluorescently labeled and localized the virus retention site within the vector by laser confocal microscopy. Whiteflies required ≥1 h of acquisition access period (AAP) to successfully acquire CCYV, and the proportion of RT-PCR positive whitefly individuals reached to 100% at 48 h of AAP. CCYV virons could be retained within vectors as long as 12 d, but the proportion of RT-PCR positive whiteflies dropped to 55% by 3 d. Groups of thirty whiteflies...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6t12v7v2</guid>
      <pubDate>Wed, 8 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Jingjing</name>
      </author>
      <author>
        <name>Liang, Xiangzhi</name>
      </author>
      <author>
        <name>Wang, Xueli</name>
      </author>
      <author>
        <name>Shi, Yan</name>
      </author>
      <author>
        <name>Gu, Qinsheng</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
      <author>
        <name>Yan, Fengming</name>
      </author>
    </item>
    <item>
      <title>Carrot mottle virus ORF4 movement protein targets plasmodesmata by interacting with the host cell SUMOylation system</title>
      <link>https://escholarship.org/uc/item/5rb5b0b0</link>
      <description>Plant virus movement proteins (MPs) facilitate virus spread in their plant hosts, and some of them are known to target plasmodesmata (PD). However, how the MPs target PD is still largely unknown. Carrot mottle virus (CMoV) encodes the ORF3 and ORF4 proteins, which are involved in CMoV movement. In this study, we used CMoV as a model to study the PD targeting of a plant virus MP. We showed that the CMoV ORF4 protein, but not the ORF3 protein, modified PD and led to the virus movement. We found that the CMoV ORF4 protein interacts with the host cell small ubiquitin-like modifier (SUMO) 1, 2 and the SUMO-conjugating enzyme SCE1, resulting in the ORF4 protein SUMOylation. Downregulation of mRNAs for NbSCE1 and NbSUMO impaired CMoV infection. The SUMO-interacting motifs (SIMs) LVIVF, VIWV, and a lysine residue at position 78 (K78) are required for the ORF4 protein SUMOylation. The mutation of these motifs prevented the protein to efficiently target PD, and further slowed or completely...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5rb5b0b0</guid>
      <pubDate>Wed, 8 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Jiang, Jun</name>
      </author>
      <author>
        <name>Kuo, Yen‐Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Salem, Nidà</name>
      </author>
      <author>
        <name>Erickson, Anna</name>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
    </item>
    <item>
      <title>RNA Interference Mechanisms and Applications in Plant Pathology</title>
      <link>https://escholarship.org/uc/item/3t86r22m</link>
      <description>The origin of RNA interference (RNAi), the cell sentinel system widely shared among eukaryotes that recognizes RNAs and specifically degrades or prevents their translation in cells, is suggested to predate the last eukaryote common ancestor ( 138 ). Of particular relevance to plant pathology is that in plants, but also in some fungi, insects, and lower eukaryotes, RNAi is a primary and effective antiviral defense, and recent studies have revealed that small RNAs (sRNAs) involved in RNAi play important roles in other plant diseases, including those caused by cellular plant pathogens. Because of this, and because RNAi can be manipulated to interfere with the expression of endogenous genes in an intra- or interspecific manner, RNAi has been used as a tool in studies of gene function but also for plant protection. Here, we review the discovery of RNAi, canonical mechanisms, experimental and translational applications, and new RNA-based technologies of importance to plant pathology.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3t86r22m</guid>
      <pubDate>Wed, 8 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Rosa, Cristina</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Wuriyanghan, Hada</name>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
    </item>
    <item>
      <title>Insect-specific viruses: from discovery to potential translational applications</title>
      <link>https://escholarship.org/uc/item/32t541rn</link>
      <description>Over the past decade the scientific community has experienced a new age of virus discovery in arthropods in general, and in insects in particular. Next generation sequencing and advanced bioinformatics tools have provided new insights about insect viromes and viral evolution. In this review, we discuss some high-throughput sequencing technologies used to discover viruses in insects and the challenges raised in data interpretations. Additionally, the discovery of these novel viruses that are considered as insect-specific viruses (ISVs) has gained increasing attention in their potential use as biological agents. As example, we show how the ISV Nhumirim virus was used to reduce West Nile virus transmission when co-infecting the mosquito vector. We also discuss new translational opportunities of using ISVs to limit insect vector competence by using them to interfere with pathogen acquisition, to directly target the insect vector or to confer pathogen resistance by the insect vector.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32t541rn</guid>
      <pubDate>Wed, 8 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Nouri, Shahideh</name>
      </author>
      <author>
        <name>Matsumura, Emilyn E</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
    </item>
    <item>
      <title>Characterization and Epidemiology of Outbreaks of Impatiens necrotic spot virus on Lettuce in Coastal California.</title>
      <link>https://escholarship.org/uc/item/2tm5p7q5</link>
      <description>California is the leading producer of lettuce (Lactuca sativa) for the United States and grows 77% of the country's supply. Prior to 2006, coastal California lettuce was only periodically and incidentally infected by a single tospoviruses species: Tomato spotted wilt virus (TSWV). However, beginning in 2006 and continuing through 2012, severe outbreaks of disease caused by Impatiens necrotic spot virus (INSV) have affected the coastal lettuce crop, though TSWV was also present. In contrast, TSWV was the only tospovirus associated with disease outbreaks in Central Valley lettuce during this period. Disease surveys conducted over two seasons (2008 and 2009) in 10 commercial fields (acreage of 6 to 20 ha) indicated that INSV was the only tospovirus associated with economically damaging disease outbreaks in lettuce in the coastal region, with incidences of 0.5 to 27% (mean = 5.7%). Molecular characterization of INSV isolates associated with these disease outbreaks revealed little...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2tm5p7q5</guid>
      <pubDate>Wed, 8 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Gilbertson, Robert L</name>
      </author>
      <author>
        <name>Turini, Tom</name>
      </author>
      <author>
        <name>Brennan, Eric B</name>
      </author>
      <author>
        <name>Smith, Richard F</name>
      </author>
      <author>
        <name>Koike, Steven T</name>
      </author>
    </item>
    <item>
      <title>Emerging strategies for RNA interference (RNAi) applications in insects</title>
      <link>https://escholarship.org/uc/item/2s21h0vj</link>
      <description>RNA interference (RNAi) in insects is a gene regulatory process that also plays a vital role in the maintenance and in the regulation of host defenses against invading viruses. Small RNAs determine the specificity of the RNAi through precise recognition of their targets. These small RNAs in insects comprise small interfering RNAs (siRNAs), micro RNAs (miRNAs) and Piwi interacting RNAs (piRNAs) of various lengths. In this review, we have explored different forms of the RNAi inducers that are presently in use, and their applications for an effective and efficient fundamental and practical RNAi research with insects. Further, we reviewed trends in next generation sequencing (NGS) technologies and their importance for insect RNAi, including the identification of novel insect targets as well as insect viruses. Here we also describe a rapidly emerging trend of using plant viruses to deliver the RNAi inducer molecules into insects for an efficient RNAi response.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2s21h0vj</guid>
      <pubDate>Wed, 8 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Nandety, Raja Sekhar</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Nouri, Shahideh</name>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
    </item>
    <item>
      <title>RNA interference approaches for plant disease control</title>
      <link>https://escholarship.org/uc/item/0np7g0ck</link>
      <description>Plant diseases caused by a variety of pathogens can have severe effects on crop plants and even plants in natural ecosystems. Despite many effective conventional approaches to control plant diseases, new, efficacious, environmentally sound and cost-effective approaches are needed, particularly with our increasing human population and the effects on crop production and plant health caused by climate change. RNA interference (RNAi) is a gene regulation and antiviral response mechanism in eukaryotes; transgenic and non transgenic plant-based RNAi approaches have shown great effectiveness and potential to target specific plant pathogens and help control plant diseases, especially when no alternatives are available. Here we discuss ways in which RNAi has been used against different plant pathogens, and some new potential applications for plant disease control.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0np7g0ck</guid>
      <pubDate>Wed, 8 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
    </item>
    <item>
      <title>Candidatus Liberibacter asiaticus exploits cytoskeletal system of psyllid vector for circulative propagative infection</title>
      <link>https://escholarship.org/uc/item/8j33x07q</link>
      <description>The citrus disease Huanglongbing (HLB) in Asia and the US is caused by Candidatus Liberibacter asiaticus (CLas), which is primarily transmitted by Diaphorina citri, also known as Asian citrus psyllid in a persistent and propagative manner. However, the exact mechanisms underlying CLas circulation within D. citri remain largely unclear. Here, immunofluorescence microscopy and electron microscopy were utilized to track the sequential infection of CLas in D. citri, from alimentary canal to salivary glands, and ultimately to the plant host. CLas was found to initially infect the epithelium of filter chamber, after which it rapidly spreads to visceral muscles for further infection throughout the alimentary canal. The rapid spread in D. citri adults causes the duration of CLas circulation to be as short as 9 days. The duration of latent period may be explained by the recruitment of cytoskeletal α-actinin by the outer membrane protein (OMP) of CLas. Inhibition of actin filament or knocking...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8j33x07q</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Zhiqiang</name>
      </author>
      <author>
        <name>Yang, Xiao</name>
      </author>
      <author>
        <name>Guo, Yuxin</name>
      </author>
      <author>
        <name>Zhang, Xiaofeng</name>
      </author>
      <author>
        <name>Li, You</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Wei, Taiyun</name>
      </author>
      <author>
        <name>Chen, Qian</name>
      </author>
    </item>
    <item>
      <title>Artificial microRNA guide strand selection from duplexes with no mismatches shows a purine‐rich preference for virus‐ and non‐virus‐based expression vectors in plants</title>
      <link>https://escholarship.org/uc/item/7hm7b23d</link>
      <description>Artificial microRNA (amiRNA) technology has allowed researchers to direct efficient silencing of specific transcripts using as few as 21 nucleotides (nt). However, not all the artificially designed amiRNA constructs result in selection of the intended ~21-nt guide strand amiRNA. Selection of the miRNA guide strand from the mature miRNA duplex has been studied in detail in human and insect systems, but not so much for plants. Here, we compared a nuclear-replicating DNA viral vector (tomato mottle virus, ToMoV, based), a cytoplasmic-replicating RNA viral vector (tobacco mosaic virus, TMV, based), and a non-viral binary vector to express amiRNAs in plants. We then used deep sequencing and mutational analysis and show that when the structural factors caused by base mismatches in the mature amiRNA duplex were excluded, the nucleotide composition of the mature amiRNA region determined the guide strand selection. We found that the strand with excess purines was preferentially selected...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7hm7b23d</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kuo, Yen‐Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
    </item>
    <item>
      <title>Identification of a novel recombinant polerovirus and other emergent viruses and tombusvirus-like associated RNA species associated with carrot motley dwarf disease in the United States</title>
      <link>https://escholarship.org/uc/item/5t0563st</link>
      <description>Carrot motley dwarf (CMD) is a viral disease complex caused by co-infection of the polerovirus carrot red leaf virus with the umbraviruses carrot mottle virus or carrot mottle mimic virus, and/or a tombusvirus like associated RNA (tlaRNA), which depend on co-infection with a helper polerovirus to gain aphid transmissibility. In 2020 and 2021 carrot samples from Washington, United States (U.S.), and parsley and cilantro samples from California, U.S., exhibiting typical symptoms of CMD were submitted for diagnosis. Initial RT-PCR diagnostic assays identified the typical CMD viruses in the carrot samples, however only the umbraviruses and tlaRNAs were detected in the parsley and cilantro samples; as such, these samples were retested with another RT-PCR assay for generic polerovirus detection. Unexpectedly, the poleroviruses Torilis crimson leaf virus (TorCLV) and fennel motley virus were identified. Subsequent RNA sequencing analysis was conducted to confirm these results and look...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5t0563st</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Erickson, Anna</name>
      </author>
      <author>
        <name>Horst, Anneliek M Ter</name>
      </author>
      <author>
        <name>Carlson, Curtis R</name>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
    </item>
    <item>
      <title>A conserved viral RNA fold enables nuclease resistance across kingdoms of life</title>
      <link>https://escholarship.org/uc/item/5hn7j26h</link>
      <description>Viral exoribonuclease-resistant RNA (xrRNA) structures block cellular nucleases to produce subgenomic viral RNAs during infection. High sequence variability among xrRNAs from distantly related viruses raises questions about the shared molecular features that enable these RNAs to withstand the strong unwinding forces of exoribonucleases. Here, we present the first structure of a plant-virus xrRNA in its active conformation and uncover universal principles of xrRNA folding. Comparison with the structure of a human-pathogenic flavivirus xrRNA reveals that both share a core structural motif-a protective ring encircling the RNA's 5' end-despite lacking sequence similarity. Disrupting this core motif through targeted mutagenesis eliminates exoribonuclease-resistance and attenuates viral infection. We identify hundreds of related structures across multiple virus families, supporting the conservation of this mechanism. Our study demonstrates how distantly related RNA viruses have converged...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5hn7j26h</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gezelle, Jeanine G</name>
      </author>
      <author>
        <name>Korn, Sophie M</name>
      </author>
      <author>
        <name>McDonald, Jayden T</name>
      </author>
      <author>
        <name>Gong, Zhen</name>
      </author>
      <author>
        <name>Erickson, Anna</name>
      </author>
      <author>
        <name>Huang, Chih-Hung</name>
      </author>
      <author>
        <name>Yang, Feiyue</name>
      </author>
      <author>
        <name>Cronin, Matt</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Wimberly, Brian T</name>
      </author>
      <author>
        <name>Steckelberg, Anna-Lena</name>
      </author>
    </item>
    <item>
      <title>The pseudoknot structure of a viral RNA reveals a conserved mechanism for programmed exoribonuclease resistance</title>
      <link>https://escholarship.org/uc/item/5183s9bx</link>
      <description>Exoribonuclease-resistant RNAs (xrRNAs) are viral RNA structures that block degradation by cellular 5'-3' exoribonucleases to produce subgenomic viral RNAs during infection. Initially discovered in flaviviruses, xrRNAs have since been identified in wide range of RNA viruses, including those that infect plants. High sequence variability among viral xrRNAs raises questions about the shared molecular features that characterize this functional RNA class. Here, we present the first structure of a plant-virus xrRNA in its active exoribonuclease-resistant conformation. The xrRNA forms a 9 base pair pseudoknot that creates a knot-like topology similar to that of flavivirus xrRNAs, despite lacking sequence similarity. Biophysical assays confirm a compact pseudoknot structure in solution, and functional studies validate its relevance both &lt;i&gt;in vitro&lt;/i&gt; and during infection. Our study reveals how viral RNAs achieve a common functional outcome through highly divergent sequences and identifies...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5183s9bx</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gezelle, Jeanine G</name>
      </author>
      <author>
        <name>Korn, Sophie M</name>
      </author>
      <author>
        <name>McDonald, Jayden T</name>
      </author>
      <author>
        <name>Gong, Zhen</name>
      </author>
      <author>
        <name>Erickson, Anna</name>
      </author>
      <author>
        <name>Huang, Chih-Hung</name>
      </author>
      <author>
        <name>Yang, Feiyue</name>
      </author>
      <author>
        <name>Cronin, Matt</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Wimberly, Brian T</name>
      </author>
      <author>
        <name>Steckelberg, Anna-Lena</name>
      </author>
    </item>
    <item>
      <title>Biological properties and vector competence of Diaphorina citri for Candidatus Liberibacter asiaticus modulated by an insect-specific virus</title>
      <link>https://escholarship.org/uc/item/4r21g70b</link>
      <description>Insect-specific viruses (ISVs) infect only insects and have been studied primarily in mosquitoes. Here, we extend the concept of ISVs to include those found in plant-feeding insect vectors, such as &lt;i&gt;Diaphorina citri&lt;/i&gt;, the vector of &lt;i&gt;Candidatus&lt;/i&gt; Liberibacter asiaticus (&lt;i&gt;C&lt;/i&gt;Las), the causal agent of citrus Huanglongbing. Using Diaphorina citri flavi-like virus (DcFLV) as a model, we examined its effects on host biology and &lt;i&gt;C&lt;/i&gt;Las transmission. DcFLV infection delayed development and preoviposition and reduced feeding activity, whereas overall survival, oviposition, and sex ratio were unaffected. DcFLV-infected &lt;i&gt;D. citri&lt;/i&gt; transmitted &lt;i&gt;C&lt;/i&gt;Las with ∼20% greater efficiency than uninfected controls, despite no significant difference in &lt;i&gt;C&lt;/i&gt;Las titers. These findings suggest that ISVs can modulate the transmission dynamics of plant pathogens by insect vectors, adding complexity to vector-pathogen interactions.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4r21g70b</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Galdeano, Diogo M</name>
      </author>
      <author>
        <name>Rawat, Tanvi</name>
      </author>
      <author>
        <name>Ingram, William</name>
      </author>
      <author>
        <name>Carlson, Curtis R</name>
      </author>
      <author>
        <name>Alves, Gustavo Rodrigues</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
    </item>
    <item>
      <title>Development of Agrobacterium tumefaciens Infiltration of Infectious Clones of Grapevine Geminivirus A Directly into Greenhouse-Grown Grapevine and Nicotiana benthamiana Plants.</title>
      <link>https://escholarship.org/uc/item/3646f1r2</link>
      <description>Grapevine virus infectious clones are important tools for fundamental studies, but also because of their potential for translational applications for grapevine improvement. Although several grapevine virus infectious clones have been developed, there has been difficulty in directly infecting mature grapevine plants, and many of the viruses used still cause disease symptoms in grapevine plants, making them less likely candidates for biotechnological applications in grapes. Here, we developed an improved &lt;i&gt;Agrobacterium tumefaciens&lt;/i&gt; infiltration method that can be used to deliver DNA plasmids and viral infectious clones directly into approximately 20-&amp;nbsp;to 40-cm-high (above soil) greenhouse-grown grapevine plants. We also developed infectious clones for two isolates of grapevine geminivirus A (GGVA): Longyan (China; GenBank accession KX570611; GGVA-76) and Super Hamburg (Japan; GenBank accession KX570610; GGVA-93). Neither virus caused any obvious symptoms when inoculated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3646f1r2</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Bednarska, Alicja</name>
      </author>
      <author>
        <name>Al Rwahnih, Maher</name>
        <uri>https://orcid.org/0000-0003-1589-9234</uri>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
    </item>
    <item>
      <title>Preventative Management of Trunk Diseases in Table Grape Vitis vinifera Autumn King</title>
      <link>https://escholarship.org/uc/item/81k9q8dr</link>
      <description>Background and goals In California’s southern San Joaquin Valley, applications of pruning-wound protectants may lower the incidence of grapevine trunk diseases. Rain is important for spore dispersal of the causal fungi, which infect pruning wounds. Despite low annual rainfall in this region, pruning wounds are at risk of infection, based on reports of symptoms and pathogen detection in vineyards, and from controlled inoculations demonstrating susceptibility of Vitis vinifera table grape cultivars. Therefore, our goal was to evaluate protectants for pruning wounds, testing two commercial fungicides, thiophanate-methyl (Topsin; UPL) and pyraclostrobin + boscalid (Pristine; BASF), for three years in an 8-yr-old Autumn King vineyard. Methods and key findings For three years, liquid formulations of fungicides were applied alone or with Pentra-bark (Quest Products Corp.), an adjuvant to enhance pesticide penetration of the bark of woody crops. After spray application, pruning wounds...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/81k9q8dr</guid>
      <pubDate>Wed, 10 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Baumgartner, Kendra</name>
      </author>
      <author>
        <name>Torres, Gabriel</name>
      </author>
      <author>
        <name>Rojas, Alejandro I Hernandez</name>
      </author>
      <author>
        <name>Travadon, Renaud</name>
        <uri>https://orcid.org/0000-0001-6062-1755</uri>
      </author>
    </item>
    <item>
      <title>Meeting report: International soil virus conference 2024</title>
      <link>https://escholarship.org/uc/item/2551z3gp</link>
      <description>The research field of soil viral ecology continues to advance rapidly as the roles of viruses in the functioning of soil ecosystems are increasingly recognized. To address recent developments in the field, the second International Soil Virus Conference was held in Livermore, California, USA, from June 25 to 27th, 2024, providing soil viral ecologists the opportunity to share new findings and suggest guidelines for future research, while encouraging international scientific discussion and collaboration. The meeting was held in person with sessions simultaneously streamed online. Fifty researchers attended from ten different countries and spanned a wide range of subfields and career stages. A total of 21 oral presentations were presented, followed by discussions covering key themes in soil viral research. This report summarizes the main takeaways and recommendations from the talks and discussions.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2551z3gp</guid>
      <pubDate>Sat, 30 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Touceda-Suárez, María</name>
      </author>
      <author>
        <name>Perry, Matthew A</name>
      </author>
      <author>
        <name>Frizzo, Riccardo</name>
      </author>
      <author>
        <name>Lotz-McMillen, John Henry</name>
      </author>
      <author>
        <name>Gilmore, Ruby Ann</name>
      </author>
      <author>
        <name>Bennett, Shauna M</name>
      </author>
      <author>
        <name>Basso, Jonelle TR</name>
      </author>
      <author>
        <name>Donovan, William</name>
      </author>
      <author>
        <name>Fudyma, Jane D</name>
      </author>
      <author>
        <name>Geonczy, Sara E</name>
      </author>
      <author>
        <name>Gittrich, Marissa</name>
      </author>
      <author>
        <name>Gogul, Grant</name>
      </author>
      <author>
        <name>Hazard, Christina</name>
      </author>
      <author>
        <name>Hillary, Luke S</name>
      </author>
      <author>
        <name>Jameson, Ellie</name>
      </author>
      <author>
        <name>Jiraska, Lucie</name>
      </author>
      <author>
        <name>Johnson, Sarah Stewart</name>
      </author>
      <author>
        <name>Kosmopoulos, James C</name>
      </author>
      <author>
        <name>Leleiwi, Ikaia</name>
      </author>
      <author>
        <name>Ma, Bin</name>
      </author>
      <author>
        <name>Mageeney, Catherine M</name>
      </author>
      <author>
        <name>Millard, Andrew</name>
      </author>
      <author>
        <name>Neri, Uri</name>
      </author>
      <author>
        <name>Rodríguez-Ramos, Josué</name>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
      <author>
        <name>Tong, Di</name>
      </author>
      <author>
        <name>Wang, Yiling</name>
      </author>
      <author>
        <name>Williamson, Kurt</name>
      </author>
      <author>
        <name>Wu, Ruonan</name>
      </author>
      <author>
        <name>Martins, Paula Dalcin</name>
      </author>
      <author>
        <name>Sapkota, Rumakanta</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
      <author>
        <name>Trubl, Gareth</name>
      </author>
    </item>
    <item>
      <title>A call for caution in the biological interpretation of viral auxiliary metabolic genes</title>
      <link>https://escholarship.org/uc/item/12v5v27c</link>
      <description>Virus-encoded auxiliary metabolic genes (AMGs) are non-essential genes that increase viral fitness by maintaining or manipulating host metabolism during infection. AMGs are intriguing from an evolutionary perspective, as most viral genomes are highly compact and have limited coding capacity for accessory genes. Advances in viral (meta)genomics have expanded the detection of putative AMGs from viruses in diverse environments. However, this has also led to many instances of misannotation due to the limitations of annotation tools, resulting in misinterpretations about the roles of some viral genes. Here, we highlight studies that support claims about AMGs with more than just function predictions for guidance on best practices. We then propose the adoption of an expanded, inclusive view of all genes auxiliary to core viral functions with the term ‘auxiliary viral genes’ (AVGs), alongside an associated eco-evolutionary framework for considering the types of analyses that can better...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/12v5v27c</guid>
      <pubDate>Sat, 30 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Martin, Cody</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
      <author>
        <name>Anantharaman, Karthik</name>
      </author>
    </item>
    <item>
      <title>Integration of crop modeling and sensing into molecular breeding for nutritional quality and stress tolerance</title>
      <link>https://escholarship.org/uc/item/1f36k0x1</link>
      <description>Integrating innovative technologies into plant breeding is critical to bolster food and nutritional security under biotic and abiotic stresses in changing climates. While breeding efforts have focused primarily on yield and stress tolerance, emerging evidence highlights the need to also prioritize nutritional quality. Advanced molecular breeding approaches have enhanced our ability to develop improved crop varieties and could be substantially informed by the routine integration of crop modeling and remote sensing technologies. This review article discusses the potential of combining crop modeling and sensing with molecular breeding to address the dual challenge of nutritional quality and stress tolerance. We provide overviews of stress response strategies, challenges in breeding for quality traits, and the use of environmental data in genomic prediction. We also describe the status of crop modeling and sensing technologies in grain legumes, rice, and leafy greens, alongside the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1f36k0x1</guid>
      <pubDate>Wed, 27 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Berlingeri, Jonathan</name>
      </author>
      <author>
        <name>Fuentes, Abelina</name>
      </author>
      <author>
        <name>Ranario, Earl</name>
      </author>
      <author>
        <name>Yun, Heesup</name>
      </author>
      <author>
        <name>Rim, Ellen Y</name>
      </author>
      <author>
        <name>Garrett, Oscar</name>
      </author>
      <author>
        <name>Howard, Alexander</name>
      </author>
      <author>
        <name>LaPorte, Mary-Francis</name>
      </author>
      <author>
        <name>Lo, Sassoum</name>
      </author>
      <author>
        <name>Pauli, Duke</name>
      </author>
      <author>
        <name>Hershberger, Jenna</name>
      </author>
      <author>
        <name>Earles, Mason</name>
      </author>
      <author>
        <name>Van Deynze, Allen</name>
      </author>
      <author>
        <name>Brummer, Edward Charles</name>
      </author>
      <author>
        <name>Michelmore, Richard</name>
      </author>
      <author>
        <name>Wong, Christopher YS</name>
      </author>
      <author>
        <name>Magney, Troy S</name>
        <uri>https://orcid.org/0000-0002-9033-0024</uri>
      </author>
      <author>
        <name>Ronald, Pamela C</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
      <author>
        <name>Runcie, Daniel E</name>
        <uri>https://orcid.org/0000-0002-3008-9312</uri>
      </author>
      <author>
        <name>Bailey, Brian N</name>
      </author>
      <author>
        <name>Diepenbrock, Christine H</name>
        <uri>https://orcid.org/0000-0001-8411-0343</uri>
      </author>
    </item>
    <item>
      <title>The Ralstonia Research Community Rejects the Proposal to Classify Phylotype I Ralstonia into the New Species Ralstonia nicotianae</title>
      <link>https://escholarship.org/uc/item/87h63638</link>
      <description>The Ralstonia solanacearum species complex is a group of globally important plant pathogens. Bacteria in this very large and genetically diverse group all colonize the xylem elements of angiosperm plants and cause high-impact wilting diseases of many crops. Because they threaten economic and food security, several R. solanacearum species complex subgroups are strictly regulated as quarantine pests. Biologically meaningful and consistent nomenclature is essential for organisms that have major economic and regulatory importance, such as plant-pathogenic Ralstonia. There are currently three species of Ralstonia wilt pathogens: R. pseudosolanacearum (corresponding to two phylogenetic groups that are described in the literature as phylotypes I and III), R. solanacearum (phylotypes IIA, IIB, and IIC), and R. syzygii (phylotype IV, containing three subspecies: subsp. syzygii, subsp. celebensis, and subsp. indonesiensis). A recent paper proposed reclassifying phylotype I as a new species...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/87h63638</guid>
      <pubDate>Wed, 30 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lowe-Power, Tiffany</name>
        <uri>https://orcid.org/0000-0003-2681-3563</uri>
      </author>
      <author>
        <name>Sharma, Parul</name>
      </author>
      <author>
        <name>Alfenas-Zerbini, Poliane</name>
      </author>
      <author>
        <name>Álvarez, Belén</name>
      </author>
      <author>
        <name>Arif, Mohammad</name>
      </author>
      <author>
        <name>Baroukh, Caroline</name>
      </author>
      <author>
        <name>Bocsanczy, Ana Maria</name>
      </author>
      <author>
        <name>Biosca, Elena G</name>
      </author>
      <author>
        <name>Castillo, José A</name>
      </author>
      <author>
        <name>Cellier, Gilles</name>
      </author>
      <author>
        <name>Coutinho, Teresa</name>
      </author>
      <author>
        <name>Drenth, André</name>
      </author>
      <author>
        <name>Friman, Ville-Petri</name>
      </author>
      <author>
        <name>Genin, Stephane</name>
      </author>
      <author>
        <name>Guidot, Alice</name>
      </author>
      <author>
        <name>Hikichi, Yasufumi</name>
      </author>
      <author>
        <name>Huang, Qi</name>
      </author>
      <author>
        <name>Iyer-Pascuzzi, Anjali</name>
      </author>
      <author>
        <name>Kai, Kenji</name>
      </author>
      <author>
        <name>Pecrix, Yann</name>
      </author>
      <author>
        <name>Poussier, Stephane</name>
      </author>
      <author>
        <name>Ray, Jane D</name>
      </author>
      <author>
        <name>Rossato, Maurício</name>
      </author>
      <author>
        <name>Schomer, Rebecca</name>
      </author>
      <author>
        <name>Siri, Maria Inés</name>
      </author>
      <author>
        <name>Vinatzer, Boris A</name>
      </author>
      <author>
        <name>Allen, Caitilyn</name>
      </author>
    </item>
    <item>
      <title>Characterization of Ralstonia pseudosolanacearum Diversity and Screening Tomato, Pepper, and Eggplant Resistance to Manage Bacterial Wilt in South Asia</title>
      <link>https://escholarship.org/uc/item/0xj6k661</link>
      <description>In South Asia, bacterial wilt pathogens in the Ralstonia solanacearum species complex (RSSC) impose major constraints on eggplant, tomato, and pepper production. To improve the efficacy of bacterial wilt management, the goals of this study were to (i) conduct a survey of RSSC pathogens in Bangladesh and Nepal, (ii) characterize the genetic diversity of these isolates, and (iii) screen 37 tomato, eggplant, and pepper accessions for resistance to six representative isolates from South Asia. We isolated 99 isolates from Bangladesh and 20 isolates from Nepal and determined that all are phylotype I isolates of the Ralstonia pseudosolanacearum species. We sequenced and assembled draft genomes for 25 isolates. Phylogenomic analyses suggest that there is a wide diversity of endemic phylotype I isolates in South Asia and possible introductions of two clonal phylotype I lineages into Bangladesh and Nepal. We contextualize our newly described isolates based on prior reports of RSSC diversity...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0xj6k661</guid>
      <pubDate>Wed, 30 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Subedi, Nagendra</name>
      </author>
      <author>
        <name>Cowell, Tabitha</name>
      </author>
      <author>
        <name>Cope-Arguello, Matthew</name>
      </author>
      <author>
        <name>Paul, Pierce</name>
      </author>
      <author>
        <name>Cellier, Gilles</name>
      </author>
      <author>
        <name>Bkayrat, Hashem</name>
      </author>
      <author>
        <name>Bonagura, Nicolas</name>
      </author>
      <author>
        <name>Cadatal, Angela</name>
      </author>
      <author>
        <name>Chen, Rachel</name>
      </author>
      <author>
        <name>Enriquez, Ariana</name>
      </author>
      <author>
        <name>Parasar, Rama</name>
      </author>
      <author>
        <name>Repetto, Lisa</name>
      </author>
      <author>
        <name>Rivas, Aracely Hernandez</name>
      </author>
      <author>
        <name>Shahbaz, Mahnoor</name>
      </author>
      <author>
        <name>White, Kaitlin</name>
      </author>
      <author>
        <name>Lowe-Power, Tiffany M</name>
        <uri>https://orcid.org/0000-0003-2681-3563</uri>
      </author>
      <author>
        <name>Miller, Sally A</name>
      </author>
    </item>
    <item>
      <title>Microbiome data management in action workshop: Atlanta, GA, USA, June 12–13, 2024</title>
      <link>https://escholarship.org/uc/item/5tz1m4qf</link>
      <description>Microbiome research is revolutionizing human and environmental health, but the value and reuse of microbiome data are significantly hampered by the limited development and adoption of data standards. While several ongoing efforts are aimed at improving microbiome data management, significant gaps still remain in terms of defining and promoting adoption of consensus standards for these datasets. The Strengthening the Organization and Reporting of Microbiome Studies (STORMS) guidelines for human microbiome research have been endorsed and successfully utilized by many research organizations, publishers, and funding agencies, and have been recognized as a consensus community standard. No equivalent effort has occurred for environmental, synthetic, and non-human host-associated microbiomes. To address this growing need within the microbiome research community, we convened the Microbiome Data Management in Action Workshop (June 12–13, 2024, in Atlanta, GA, USA), to bring together key...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5tz1m4qf</guid>
      <pubDate>Mon, 23 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kelliher, Julia M</name>
      </author>
      <author>
        <name>Aljumaah, Mashael</name>
      </author>
      <author>
        <name>Bordenstein, Sarah R</name>
      </author>
      <author>
        <name>Brister, J Rodney</name>
      </author>
      <author>
        <name>Chain, Patrick SG</name>
      </author>
      <author>
        <name>Dundore-Arias, Jose Pablo</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
      <author>
        <name>Fernandes, Vanessa Moreira C</name>
      </author>
      <author>
        <name>Flores, Roberto</name>
      </author>
      <author>
        <name>Gonzalez, Antonio</name>
      </author>
      <author>
        <name>Hansen, Zoe A</name>
      </author>
      <author>
        <name>Hatcher, Eneida L</name>
      </author>
      <author>
        <name>Jackson, Scott A</name>
      </author>
      <author>
        <name>Kellogg, Christina A</name>
      </author>
      <author>
        <name>Madupu, Ramana</name>
      </author>
      <author>
        <name>Miller, Cassandra Maria Luz</name>
      </author>
      <author>
        <name>Mirzayi, Chloe</name>
      </author>
      <author>
        <name>Moustafa, Ahmed M</name>
      </author>
      <author>
        <name>Mungall, Christopher</name>
      </author>
      <author>
        <name>Oliver, Aaron</name>
        <uri>https://orcid.org/0000-0002-0410-8284</uri>
      </author>
      <author>
        <name>Pariente, Nonia</name>
      </author>
      <author>
        <name>Pett-Ridge, Jennifer</name>
      </author>
      <author>
        <name>Record, Sydne</name>
      </author>
      <author>
        <name>Reji, Linta</name>
      </author>
      <author>
        <name>Reysenbach, Anna-Louise</name>
      </author>
      <author>
        <name>Rich, Virginia I</name>
      </author>
      <author>
        <name>Richardson, Lorna</name>
      </author>
      <author>
        <name>Schriml, Lynn M</name>
      </author>
      <author>
        <name>Shabman, Reed S</name>
      </author>
      <author>
        <name>Sierra, Maria A</name>
      </author>
      <author>
        <name>Sullivan, Matthew B</name>
      </author>
      <author>
        <name>Sundaramurthy, Punithavathi</name>
      </author>
      <author>
        <name>Thibault, Katherine M</name>
      </author>
      <author>
        <name>Thompson, Luke R</name>
      </author>
      <author>
        <name>Tighe, Scott</name>
      </author>
      <author>
        <name>Vereen, Ethell</name>
      </author>
      <author>
        <name>Eloe-Fadrosh, Emiley A</name>
        <uri>https://orcid.org/0000-0002-8162-1276</uri>
      </author>
    </item>
    <item>
      <title>Structural Analysis of an Avr4 Effector Ortholog Offers Insight into Chitin Binding and Recognition by the Cf-4 Receptor</title>
      <link>https://escholarship.org/uc/item/1zw0t3qw</link>
      <description>Chitin is a key component of fungal cell walls and a potent inducer of innate immune responses. Consequently, fungi may secrete chitin-binding lectins, such as the Cf-Avr4 effector protein from the tomato pathogen Cladosporium fulvum, to shield chitin from host-derived chitinases during infection. Homologs of Cf-Avr4 are found throughout Dothideomycetes, and despite their modest primary sequence identity, many are perceived by the cognate tomato immune receptor Cf-4. Here, we determined the x-ray crystal structure of Pf-Avr4 from the tomato pathogen Pseudocercospora fuligena, thus providing a three-dimensional model of an Avr4 effector protein. In addition, we explored structural, biochemical, and functional aspects of Pf-Avr4 and Cf-Avr4 to further define the biology of core effector proteins and outline a conceptual framework for their pleiotropic recognition by single immune receptors. We show that Cf-Avr4 and Pf-Avr4 share functional specificity in binding (GlcNAc)6 and in...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1zw0t3qw</guid>
      <pubDate>Mon, 23 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kohler, Amanda C</name>
      </author>
      <author>
        <name>Chen, Li-Hung</name>
      </author>
      <author>
        <name>Hurlburt, Nicholas</name>
      </author>
      <author>
        <name>Salvucci, Anthony</name>
      </author>
      <author>
        <name>Schwessinger, Benjamin</name>
      </author>
      <author>
        <name>Fisher, Andrew J</name>
        <uri>https://orcid.org/0000-0003-3488-6594</uri>
      </author>
      <author>
        <name>Stergiopoulos, Ioannis</name>
        <uri>https://orcid.org/0000-0002-2368-6119</uri>
      </author>
    </item>
    <item>
      <title>On Collaborative Governance: Building Consensus on Priorities to Manage Invasive Species Through Collective Action</title>
      <link>https://escholarship.org/uc/item/7qs5j84p</link>
      <description>Invasive forest pests can spread across large landscapes that include numerous land-use management jurisdictions. As such, forest pest invasions need to be addressed with collaborative efforts because a single entity is seldom able to respond to the full scope of the problem. A collaborative governance framework provides a collective decision-making process that allows diverse sets of actors who share an interest in a policy or management issue to work together towards mutually beneficial outcomes. Here, I apply a theoretical model of collaborative governance to understand the conditions in cooperative decision-making that led to a consensus on statewide priorities to control an important invasive pest in California, the Fusarium dieback invasive shothole borers (FD-ISHB) beetle-pathogen invasion. This provides (1) an empirical case study of collaborative governance in action throughout the stakeholder consensus building process and (2) interrogates that case study for theoretical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7qs5j84p</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lynch, Shannon Colleen</name>
      </author>
    </item>
    <item>
      <title>Wood Microbiome Variation and Interactions with Fungal Symbionts of Invasive Ambrosia Beetles</title>
      <link>https://escholarship.org/uc/item/3tw2j284</link>
      <description>The microbiomes of plants can modulate the impacts of pests, including through interactions with the microbiomes of pathogen vectors, such as ambrosia beetles. Although physical and chemical traits of plant hosts are known to affect beetle-carried microbes, how beetle and host microbiomes interact is seldom explored. We aimed to determine whether wood-inhabiting endophytes mediate host susceptibility to Fusarium dieback, an emergent tree disease complex that includes ambrosia beetle vectors. We studied three competent host tree species ( Persea americana, Salix spp., and Platanus racemosa) common in disease hot spots in agricultural and wildland habitats. Using culturing methods, we compared the wood microbiomes of 319 attacked and 133 nonattacked trees across a network of 47 beetle-infested and 41 noninfested plots in Southern California, United States. We conducted 1,148 in vitro assays to evaluate antagonism by wood-inhabiting endophytic fungi (60 species) and bacteria (40...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3tw2j284</guid>
      <pubDate>Wed, 18 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lynch, Shannon Colleen</name>
      </author>
      <author>
        <name>Na, Francis</name>
      </author>
      <author>
        <name>Reyes-Gonzalez, Edeli</name>
      </author>
      <author>
        <name>Bossard, Emily L</name>
      </author>
      <author>
        <name>Alarcon, Karen S</name>
      </author>
      <author>
        <name>Eskalen, Akif</name>
        <uri>https://orcid.org/0000-0002-8829-7413</uri>
      </author>
      <author>
        <name>Gilbert, Gregory S</name>
        <uri>https://orcid.org/0000-0002-5195-9903</uri>
      </author>
    </item>
    <item>
      <title>Differential physiological responses of resistant and susceptible grape cultivars to Eutypa dieback</title>
      <link>https://escholarship.org/uc/item/82h9h054</link>
      <description>Eutypa lata is a fungal pathogen of grapevine that causes widespread economic damage and threatens vineyard longevity worldwide. This study was initiated to further understanding of how grapevines resist E. lata infections, using an integrated approach combining inoculation assays in the greenhouse with physiological and biochemical measurements. Resistant 'Zinfandel' and susceptible 'Syrah' grapevines were subjected to control and inoculation treatments, and assessed for gas exchange, water status, photosynthetic biochemistry, hydraulic conductivity, wood chemistry, and fungal spread (lesion length). Infection reduced leaf photochemical function and gas exchange in Zinfandel and increased these variables in Syrah (P&amp;lt;0.05). Infection produced shorter lesions in Zinfandel (P&amp;lt;0.05), suggesting that down-regulating gas exchange limited pathogen spread by reducing the carbon supply to the pathogen or fungal movement in the transpiration stream. Neither cultivar up-regulated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/82h9h054</guid>
      <pubDate>Wed, 21 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sinclair, Gabriela C</name>
      </author>
      <author>
        <name>Travadon, Renaud</name>
        <uri>https://orcid.org/0000-0001-6062-1755</uri>
      </author>
      <author>
        <name>Eschen, Paula J</name>
      </author>
      <author>
        <name>Wallis, Christopher</name>
      </author>
      <author>
        <name>Baumgartner, Kendra</name>
      </author>
      <author>
        <name>Delmas, Chloé EL</name>
      </author>
      <author>
        <name>Hnizdor, Joshua F</name>
      </author>
      <author>
        <name>Bartlett, Megan K</name>
        <uri>https://orcid.org/0000-0003-0975-8777</uri>
      </author>
    </item>
    <item>
      <title>Beneath the surface: Unsolved questions in soil virus ecology</title>
      <link>https://escholarship.org/uc/item/5fp1m7mw</link>
      <description>Soil virus ecology is an exciting but still nascent field of research in soil microbiology. While there has been a recent surge in soil virus research studies, many fundamental questions remain unanswered, and a range of technical and bioinformatic challenges need to be overcome. In this perspective article, we present a series of key questions that highlight fruitful research areas for ongoing and future efforts. These include describing the challenges involved in understanding soil viral abundance and activity, spatiotemporal dynamics, life strategy prevalence, virus-mediated biogeochemical impacts, viral protein function, host prediction, and soil RNA virus discovery. In the near term, combining approaches (e.g., cultivation-based, meta-omics, biogeochemical, experimental, and bioinformatic) will be key to assessing the ecological and biogeochemical impacts of soil viruses from the microscopic to the field and global scales. Still, we stress that results must be tempered by...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5fp1m7mw</guid>
      <pubDate>Thu, 10 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hazard, Christina</name>
      </author>
      <author>
        <name>Anantharaman, Karthik</name>
      </author>
      <author>
        <name>Hillary, Luke S</name>
      </author>
      <author>
        <name>Neri, Uri</name>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
      <author>
        <name>Trubl, Gareth</name>
      </author>
      <author>
        <name>Williamson, Kurt</name>
      </author>
      <author>
        <name>Pett-Ridge, Jennifer</name>
      </author>
      <author>
        <name>Nicol, Graeme W</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
    </item>
    <item>
      <title>Bark beetle mycobiome: collaboratively defined research priorities on a widespread insect-fungus symbiosis</title>
      <link>https://escholarship.org/uc/item/0mk3v9nm</link>
      <description>One of the main threats to forests in the Anthropocene are novel or altered interactions among trees, insects and fungi. To critically assess the contemporary research on bark beetles, their associated fungi, and their relationships with trees, the international Bark Beetle Mycobiome research coordination network has been formed. The network comprises 22 researchers from 17 institutions. This forward-looking review summarizes the group’s assessment of the current status of the bark beetle mycobiome research field and priorities for its advancement. Priorities include data mobility and standards, the adoption of new technologies for the study of these symbioses, reconciliation of conflicting paradigms, and practices for robust inference of symbiosis and tree epidemiology. The Net work proposes contemporary communication strategies to interact with the global community of researchers studying symbioses and natural resource managers. We conclude with a call to the broader scientific...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0mk3v9nm</guid>
      <pubDate>Thu, 10 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hulcr, Jiri</name>
      </author>
      <author>
        <name>Barnes, Irene</name>
      </author>
      <author>
        <name>De Beer, Z Wilhelm</name>
      </author>
      <author>
        <name>Duong, Tuan A</name>
      </author>
      <author>
        <name>Gazis, Romina</name>
      </author>
      <author>
        <name>Johnson, Andrew J</name>
      </author>
      <author>
        <name>Jusino, Michelle A</name>
      </author>
      <author>
        <name>Kasson, Matthew T</name>
      </author>
      <author>
        <name>Li, You</name>
      </author>
      <author>
        <name>Lynch, Shannon</name>
      </author>
      <author>
        <name>Mayers, Chase</name>
      </author>
      <author>
        <name>Musvuugwa, Tendai</name>
      </author>
      <author>
        <name>Roets, Francois</name>
      </author>
      <author>
        <name>Seltmann, Katja C</name>
        <uri>https://orcid.org/0000-0001-5354-6048</uri>
      </author>
      <author>
        <name>Six, Diana</name>
      </author>
      <author>
        <name>Vanderpool, Dan</name>
      </author>
      <author>
        <name>Villari, Caterina</name>
      </author>
    </item>
    <item>
      <title>DNA-based detection of grapevine trunk-disease pathogens from environmental spore samples.</title>
      <link>https://escholarship.org/uc/item/84m686sd</link>
      <description>In California vineyards, spore dispersal of fungi that cause grapevine trunk diseases Botryosphaeria dieback and Eutypa dieback occurs with winter rains. Spores infect through pruning wounds made to the woody structure of the vine in winter. Better timing of preventative practices that minimize infection may benefit from routine spore-trapping, which could pinpoint site-specific time frames of spore dispersal. To speed pathogen detection from environmental spore samples, we identified species-specific PCR primers and protocols. Then we compared the traditional culture-based method versus our new DNA-based method.•PCR primers for Botryosphaeria-dieback pathogen Neofusicoccum parvum and Eutypa-dieback pathogen Eutypa lata were confirmed species-specific, through extensive testing of related species (in families Botryosphaeriaceae and Diatrypaceae, respectively), other trunk-disease pathogens, and saprophytic fungi that sporulate in vineyards.•Consistent detection of N. parvum was...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/84m686sd</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Fujiyoshi, Phillip</name>
      </author>
      <author>
        <name>Lawrence, Daniel</name>
      </author>
      <author>
        <name>Travadon, Renaud</name>
      </author>
      <author>
        <name>Baumgartner, Kendra</name>
      </author>
    </item>
    <item>
      <title>Two dominant loci determine resistance to Phomopsis cane lesions in F1 families of hybrid grapevines.</title>
      <link>https://escholarship.org/uc/item/324808x7</link>
      <description>Rapid characterization of novel NB-LRR-associated resistance to Phomopsis cane spot on grapevine using high-throughput sampling and low-coverage sequencing for genotyping, locus mapping and transcriptome analysis provides insights into genetic resistance to a hemibiotrophic fungus. Phomopsis cane and leaf spot, caused by the hemibiotrophic fungus Diaporthe ampelina (syn&amp;nbsp;=&amp;nbsp;Phomopsis viticola), reduces the productivity in grapevines. Host resistance was studied on three F1 families derived from crosses involving resistant genotypes Horizon, Illinois 547-1, Vitis cinerea B9 and V. vinifera Chardonnay. All families had progeny with extremely susceptible phenotypes, developing lesions on both dormant canes and maturing fruit clusters. Segregation of symptoms was observed under natural levels of inoculum in the field, while phenotypes on green shoots were confirmed under controlled inoculations in greenhouse. High-density genetic maps were used to localize novel qualitative...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/324808x7</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Barba, Paola</name>
      </author>
      <author>
        <name>Lillis, Jacquelyn</name>
      </author>
      <author>
        <name>Luce, R</name>
      </author>
      <author>
        <name>Travadon, Renaud</name>
      </author>
      <author>
        <name>Osier, Michael</name>
      </author>
      <author>
        <name>Baumgartner, Kendra</name>
      </author>
      <author>
        <name>Wilcox, Wayne</name>
      </author>
      <author>
        <name>Reisch, Bruce</name>
      </author>
      <author>
        <name>Cadle-Davidson, Lance</name>
      </author>
    </item>
    <item>
      <title>Fungal species associated with grapevine trunk diseases in Washington wine grapes and California table grapes, with novelties in the genera Cadophora, Cytospora, and Sporocadus.</title>
      <link>https://escholarship.org/uc/item/6dr8g4j7</link>
      <description>Grapevine trunk diseases cause serious economic losses to grape growers worldwide. The identification of the causal fungi is critical to implementing appropriate management strategies. Through a culture-based approach, we identified the fungal species composition associated with symptomatic grapevines from wine grapes in southeastern Washington and table grapes in the southern San Joaquin Valley of California, two regions with contrasting winter climates. Species were confirmed through molecular identification, sequencing two to six gene regions per isolate. Multilocus phylogenetic analyses were used to identify novel species. We identified 36 species from 112 isolates, with a combination of species that are new to science, are known causal fungi of grapevine trunk diseases, or are known causal fungi of diseases of other woody plants. The novel species Cadophora columbiana, Cytospora macropycnidia, Cytospora yakimana, and Sporocadus incarnatus are formally described and introduced,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6dr8g4j7</guid>
      <pubDate>Sat, 5 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Travadon, Renaud</name>
      </author>
      <author>
        <name>Lawrence, Daniel</name>
      </author>
      <author>
        <name>Moyer, Michelle</name>
      </author>
      <author>
        <name>Fujiyoshi, Phillip</name>
      </author>
      <author>
        <name>Baumgartner, Kendra</name>
      </author>
    </item>
    <item>
      <title>A WRKY transcription factor confers broad-spectrum resistance to biotic stresses and yield stability in rice</title>
      <link>https://escholarship.org/uc/item/9gr4p2w5</link>
      <description>Plants are subject to attack by diverse pests and pathogens. Few genes conferring broad-spectrum resistance to both insects and pathogens have been identified. Because of the growth-defense tradeoff, it is often challenging to balance biotic stress resistance and yield for crops. Here, we report that &lt;i&gt;OsWRKY36&lt;/i&gt; suppresses the resistance to insects and pathogens via transcriptional repression of &lt;i&gt;Phenylalanine Ammonia Lyases&lt;/i&gt; (&lt;i&gt;PALs&lt;/i&gt;), a key enzyme in phenylpropanoid pathway in rice. Knocking out &lt;i&gt;OsWRKY36&lt;/i&gt; causes elevated lignin biosynthesis and increased sclerenchyma thickness of leaf sheath, leading to enhanced resistance to multiple pests and pathogens. Additionally, loss of &lt;i&gt;OsWRKY36&lt;/i&gt; also derepresses the transcription of &lt;i&gt;Ideal Plant Architecture 1&lt;/i&gt; (&lt;i&gt;IPA1&lt;/i&gt;) and &lt;i&gt;MONOCULM2&lt;/i&gt; (&lt;i&gt;MOC2&lt;/i&gt;), resulting in increased spikelet number per panicle and tiller number. These findings provide mechanistic insights into biotic stress tolerance in...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9gr4p2w5</guid>
      <pubDate>Thu, 3 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Daoming</name>
      </author>
      <author>
        <name>He, Jun</name>
      </author>
      <author>
        <name>Li, Qi</name>
      </author>
      <author>
        <name>Zhang, Xiao</name>
      </author>
      <author>
        <name>Wang, Yongsheng</name>
      </author>
      <author>
        <name>Sun, Quanguang</name>
      </author>
      <author>
        <name>Wang, Wenhui</name>
      </author>
      <author>
        <name>Zhang, Menglong</name>
      </author>
      <author>
        <name>Wang, Yunlong</name>
      </author>
      <author>
        <name>Xu, Haosen</name>
      </author>
      <author>
        <name>Fang, Liang</name>
      </author>
      <author>
        <name>Jiang, Ling</name>
      </author>
      <author>
        <name>Liu, Shijia</name>
      </author>
      <author>
        <name>Chen, Liangming</name>
      </author>
      <author>
        <name>Tian, Yunlu</name>
      </author>
      <author>
        <name>Liu, Xi</name>
      </author>
      <author>
        <name>Wang, Ruyi</name>
      </author>
      <author>
        <name>Zhang, Zhengguang</name>
      </author>
      <author>
        <name>Chern, Mawsheng</name>
      </author>
      <author>
        <name>Dong, Xiaoou</name>
      </author>
      <author>
        <name>Wang, Haiyang</name>
      </author>
      <author>
        <name>Liu, Yuqiang</name>
      </author>
      <author>
        <name>Ronald, Pamela C</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
      <author>
        <name>Wan, Jianmin</name>
      </author>
    </item>
    <item>
      <title>Host Jumps and Pathogenicity of Botryosphaeriaceae Species on Grapevines (Vitis vinifera) in Chile</title>
      <link>https://escholarship.org/uc/item/3nv7v5n9</link>
      <description>Botryosphaeria dieback disease is a significant grapevine trunk disease (GTD) caused by species of Botryosphaeriaceae in Chile and worldwide. Moreover, Botryosphaeriaceae have been described attacking fruit and nut crops in Chile. However, it remains unknown whether fungal isolates from tree hosts have the potential to infect grapevines in Chile. The aggressiveness and potential cross infection of species of Botryosphaeriaceae collected from crops (grapevines, apples, blueberries, and walnuts), was assessed on grapevines. Plant materials, including nursery cuttings, lignified canes, and green shoots of grapevine cultivars (Cabernet Sauvignon, Syrah, Sauvignon Blanc, Malbec, Aspirant Bouschet, and Merlot), were inoculated with &lt;i&gt;Diplodia mutila&lt;/i&gt;, &lt;i&gt;D. seriata&lt;/i&gt;, &lt;i&gt;Dothiorella sarmentorum&lt;/i&gt;, &lt;i&gt;Lasiodiplodia theobromae&lt;/i&gt;, &lt;i&gt;Neofusicoccum arbuti&lt;/i&gt;, and &lt;i&gt;N. parvum&lt;/i&gt;, under greenhouse and vineyard conditions. Regardless of the origin of the isolates, most species...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3nv7v5n9</guid>
      <pubDate>Wed, 2 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hernández, Yadira</name>
      </author>
      <author>
        <name>Lolas, Mauricio</name>
      </author>
      <author>
        <name>Elfar, Karina</name>
      </author>
      <author>
        <name>Eskalen, Akif</name>
        <uri>https://orcid.org/0000-0002-8829-7413</uri>
      </author>
      <author>
        <name>Gainza-Cortés, Felipe</name>
      </author>
      <author>
        <name>Díaz, Gonzalo A</name>
      </author>
    </item>
    <item>
      <title>De novo transcriptome assembly, polymorphic SSR markers development and population genetics analyses for southern corn rust (Puccinia polysora)</title>
      <link>https://escholarship.org/uc/item/9kd080ds</link>
      <description>Southern corn rust is a destructive maize disease caused by Puccinia polysora Underw that can lead to severe yield losses. However, genomic information and microsatellite markers are currently unavailable for this disease. In this study, we generated a total of 27,295,216 high-quality cDNA sequence reads using Illumina sequencing technology. These reads were assembled into 17,496 unigenes with an average length of 1015&amp;nbsp;bp. The functional annotation indicated that 8113 (46.37%), 1933 (11.04%) and 5516 (31.52%) unigenes showed significant similarity to known proteins in the NCBI Nr, Nt and Swiss-Prot databases, respectively. In addition, 2921 (16.70%) unigenes were assigned to KEGG database categories; 4218 (24.11%), to KOG database categories; and 6,603 (37.74%), to GO database categories. Furthermore, we identified 8,798 potential SSRs among 6653 unigenes. A total of 9 polymorphic SSR markers were developed to evaluate the genetic diversity and population structure of 96...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9kd080ds</guid>
      <pubDate>Fri, 21 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sun, Qiuyu</name>
      </author>
      <author>
        <name>Liu, Jie</name>
      </author>
      <author>
        <name>Zhang, Keyu</name>
      </author>
      <author>
        <name>Huang, Chong</name>
      </author>
      <author>
        <name>Li, Leifu</name>
      </author>
      <author>
        <name>Dong, Jiayu</name>
      </author>
      <author>
        <name>Luo, Yong</name>
      </author>
      <author>
        <name>Ma, Zhanhong</name>
      </author>
    </item>
    <item>
      <title>Population Genetic Structures of Puccinia striiformis f. sp. tritici in the Gansu-Ningxia Region and Hubei Province, China</title>
      <link>https://escholarship.org/uc/item/9jx5z1kf</link>
      <description>Wheat stripe rust, caused by the fungal pathogen &lt;i&gt;Puccinia striiformis&lt;/i&gt; f. sp. &lt;i&gt;tritici&lt;/i&gt; (&lt;i&gt;Pst&lt;/i&gt;), is a destructive wheat disease in China. The Gansu-Ningxia region (GN) is a key area for pathogen over-summering in China, and northwestern Hubei (HB) is an important region for pathogen over-wintering, serving as a source of inoculum in spring epidemic regions. The spatiotemporal population genetic structure of &lt;i&gt;Pst&lt;/i&gt; in HB and the pathogen population exchanges between GN and HB are important for estimating the risk of interregional epidemics. Here, 567 isolates from GN and HB were sampled from fall 2016 to spring 2018 and were genotyped using simple sequence repeat markers. The genotypic and genetic diversity of &lt;i&gt;Pst&lt;/i&gt; subpopulations in HB varied among seasons and locations. Greater genetic diversification levels were found in the spring compared with fall populations using principal coordinate analysis and Bayesian assignments. In total, there were 17 common...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9jx5z1kf</guid>
      <pubDate>Fri, 21 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Cuicui</name>
      </author>
      <author>
        <name>Jiang, Bingbing</name>
      </author>
      <author>
        <name>Liang, Junmin</name>
      </author>
      <author>
        <name>Li, Leifu</name>
      </author>
      <author>
        <name>Gu, Yilin</name>
      </author>
      <author>
        <name>Li, Jintang</name>
      </author>
      <author>
        <name>Luo, Yong</name>
      </author>
      <author>
        <name>Ma, Zhanhong</name>
      </author>
    </item>
    <item>
      <title>Engineering sorghum for higher 4-hydroxybenzoic acid content</title>
      <link>https://escholarship.org/uc/item/3px9t89n</link>
      <description>Lignocellulosic biomass represents a renewable source of sugars for the manufacturing of bioproducts such as biofuels. The high cost associated with deconstruction of plant biomass to simple sugars remains one of the challenges preventing the deployment of economically sustainable advanced bioproducts. The accumulation in-planta of value-added coproducts such as platform chemicals can improve the economics of biofuels. Among other crops, sorghum is an ideal bioenergy feedstock due to its low input requirements, efficient nitrogen recycling, and high water use efficiency and biomass yields. In this work, we engineered sorghum to overproduce the valuable chemical 4-hydroxybenzoic acid (4-HBA) by co-expressing plastid-targeted versions of Escherichia coli chorismate pyruvate-lyase (UbiC) and feedback-resistant 3-deoxy-D-arabino-heptulonate-7-phosphate synthase (AroG*). Two independent lines containing the dual aroG* - ubiC construct were selected for characterization in the T2 generation....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3px9t89n</guid>
      <pubDate>Tue, 11 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lin, Chien-Yuan</name>
      </author>
      <author>
        <name>Tian, Yang</name>
      </author>
      <author>
        <name>Nelson-Vasilchik, Kimberly</name>
      </author>
      <author>
        <name>Hague, Joel</name>
      </author>
      <author>
        <name>Kakumanu, Ramu</name>
      </author>
      <author>
        <name>Lee, Mi Yeon</name>
      </author>
      <author>
        <name>Trinh, Jessica</name>
        <uri>https://orcid.org/0000-0002-5044-0720</uri>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Baidoo, Edward EK</name>
        <uri>https://orcid.org/0000-0001-5787-1219</uri>
      </author>
      <author>
        <name>Kausch, Albert P</name>
      </author>
      <author>
        <name>Scheller, Henrik V</name>
        <uri>https://orcid.org/0000-0002-6702-3560</uri>
      </author>
      <author>
        <name>Eudes, Aymerick</name>
        <uri>https://orcid.org/0000-0002-1387-6111</uri>
      </author>
    </item>
    <item>
      <title>A phylogenetic epidemiology approach to predicting the establishment of multi-host plant pests</title>
      <link>https://escholarship.org/uc/item/0ph7d18z</link>
      <description>Forecasting emergent pest spread is paramount to mitigating their impacts. For host-specialized pests, epidemiological models of spread through a single host population are well developed. However, most pests attack multiple host species; the challenge is predicting which communities are most vulnerable to infestation. Here, we develop a phylogenetically-informed approach to predict establishment of emergent multi-host pests across heterogeneous landscapes. We model a beetle-pathogen symbiotic complex on trees, introduced from Southeast Asia to California. The phyloEpi model for likelihood of establishment was predicted from the phylogenetic composition of woody species in the invaded community and the influence of temperature on beetle reproduction. Plant communities dominated by close relatives of known epidemiologically critical hosts were four times more likely to become infested than communities with more distantly related species. Where microclimate favored beetle reproduction,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0ph7d18z</guid>
      <pubDate>Mon, 3 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lynch, Shannon Colleen</name>
      </author>
      <author>
        <name>Reyes-Gonzalez, Edeli</name>
      </author>
      <author>
        <name>Bossard, Emily L</name>
      </author>
      <author>
        <name>Alarcon, Karen S</name>
      </author>
      <author>
        <name>Love, Natalie LR</name>
      </author>
      <author>
        <name>Hollander, Allan D</name>
      </author>
      <author>
        <name>Nobua-Behrmann, Beatriz E</name>
      </author>
      <author>
        <name>Gilbert, Gregory S</name>
        <uri>https://orcid.org/0000-0002-5195-9903</uri>
      </author>
    </item>
    <item>
      <title>Robust increase of leaf size by Arabidopsis thaliana GRF3-like transcription factors under different growth conditions</title>
      <link>https://escholarship.org/uc/item/405710wn</link>
      <description>An increase in crop yield is essential to reassure food security to meet the accelerating global demand. Several genetic modifications can increase organ size, which in turn might boost crop yield. Still, only in a few cases their performance has been evaluated under stress conditions. MicroRNA miR396 repress the expression of GROWTH-REGULATING FACTOR (GRF) genes that codes for transcription factors that promote organ growth. Here, we show that both Arabidopsis thaliana At-GRF2 and At-GRF3 genes resistant to miR396 activity (rGRF2 and rGRF3) increased organ size, but only rGRF3 can produce this effect without causing morphological defects. Furthermore, introduction of At-rGRF3 in Brassica oleracea can increase organ size, and when At-rGRF3 homologs from soybean and rice are introduced in Arabidopsis, leaf size is also increased. This suggests that regulation of GRF3 activity by miR396 is important for organ growth in a broad range of species. Plants harboring rGRF3 have larger...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/405710wn</guid>
      <pubDate>Wed, 29 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Beltramino, Matías</name>
      </author>
      <author>
        <name>Ercoli, María Florencia</name>
        <uri>https://orcid.org/0000-0001-5587-6227</uri>
      </author>
      <author>
        <name>Debernardi, Juan Manuel</name>
      </author>
      <author>
        <name>Goldy, Camila</name>
      </author>
      <author>
        <name>Rojas, Arantxa ML</name>
      </author>
      <author>
        <name>Nota, Florencia</name>
      </author>
      <author>
        <name>Alvarez, María Elena</name>
      </author>
      <author>
        <name>Vercruyssen, Liesbeth</name>
      </author>
      <author>
        <name>Inzé, Dirk</name>
      </author>
      <author>
        <name>Palatnik, Javier F</name>
      </author>
      <author>
        <name>Rodriguez, Ramiro E</name>
      </author>
    </item>
    <item>
      <title>Control of cell proliferation and elongation by miR396</title>
      <link>https://escholarship.org/uc/item/2w29072w</link>
      <description>The combinatory effects of cell proliferation and cell elongation determines the rate at which organs growth. In the root meristematic zone cells both divide and expand, while post-mitotic cells in the elongation zone only expands until they reach their final size. The transcription factors of the GROWTH-REGULATING FACTOR (GRF) class promote cell proliferation in various plant organs. Their expression is restricted to cells with a high proliferative capacity, yet strong downregulation of the GRF activity compromise the plant survival. Part of expression pattern of the GRFs is ensured by the post-transcriptional repression mediated by the conserved microRNA miR396. Here we show the quantitative effects in root growth caused by GRF depletion in a series of transgenic lines with different miR396 levels. We show that high miRNA levels affect cell elongation and proliferation in roots. Detailed analysis suggests that cell proliferation is restricted due to a reduction in cell cycle...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2w29072w</guid>
      <pubDate>Wed, 29 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ercoli, María Florencia</name>
        <uri>https://orcid.org/0000-0001-5587-6227</uri>
      </author>
      <author>
        <name>Rojas, Arantxa ML</name>
      </author>
      <author>
        <name>Debernardi, Juan Manuel</name>
      </author>
      <author>
        <name>Palatnik, Javier F</name>
      </author>
      <author>
        <name>Rodriguez, Ramiro E</name>
      </author>
    </item>
    <item>
      <title>Draft genome sequences for Neonectria magnoliae and Neonectria punicea, canker pathogens of Liriodendron tulipifera and Acer saccharum in West Virginia</title>
      <link>https://escholarship.org/uc/item/0f82g52x</link>
      <description>The fungal genus &lt;i&gt;Neonectria&lt;/i&gt; contains many phytopathogenic species currently impacting forests and fruit trees worldwide. Despite their importance, a majority of &lt;i&gt;Neonectria&lt;/i&gt; spp. lack sufficient genomic resources to resolve suspected cryptic species. Here, we report draft genomes and assemblies for &lt;i&gt;Neonectria magnoliae&lt;/i&gt; NRRL 64651 and &lt;i&gt;Neonectria punicea&lt;/i&gt; NRRL 64653.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0f82g52x</guid>
      <pubDate>Tue, 28 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Petronek, Hannah M</name>
      </author>
      <author>
        <name>Kasson, Matt T</name>
      </author>
      <author>
        <name>Metheny, Amy M</name>
      </author>
      <author>
        <name>Stauder, Cameron M</name>
      </author>
      <author>
        <name>Lovett, Brian</name>
      </author>
      <author>
        <name>Lynch, Shannon C</name>
      </author>
      <author>
        <name>Garnas, Jeff R</name>
      </author>
      <author>
        <name>Kasson, Lindsay R</name>
      </author>
      <author>
        <name>Stajich, Jason E</name>
        <uri>https://orcid.org/0000-0002-7591-0020</uri>
      </author>
    </item>
    <item>
      <title>High-Throughput Sequencing for the Detection of Viruses in Grapevine: Performance Analysis and Best Practices</title>
      <link>https://escholarship.org/uc/item/0rw2s1w3</link>
      <description>Among the cultivated crop species, the economically and culturally important grapevine plays host to the greatest number of distinctly characterized viruses. A critical component of the management and containment of these viral diseases in grapevine is both the identification of infected vines and the characterization of new pathogens. Next-generation high-throughput sequencing technologies, i.e., HTS technologies, have been widely adopted for their ability to quickly, broadly and directly characterize molecular sequences associated with potential pathogens. We empirically analyze the performance of HTS as a diagnostic tool in a phytosanitary context and make recommendations on its deployment for detecting known and novel viruses in grapevine. Three popular and widely used modalities for analyzing HTS data are characterized and compared using the standard diagnostic performance criteria of sensitivity (the true positive rate), specificity (the true negative rate) and analytical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0rw2s1w3</guid>
      <pubDate>Fri, 17 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Stevens, Kristian A</name>
      </author>
      <author>
        <name>Al Rwahnih, Maher</name>
        <uri>https://orcid.org/0000-0003-1589-9234</uri>
      </author>
    </item>
    <item>
      <title>Transcriptome analysis of two isolates of the tomato pathogen Cladosporium fulvum, uncovers genome-wide patterns of alternative splicing during a host infection cycle.</title>
      <link>https://escholarship.org/uc/item/8124n7x8</link>
      <description>Alternative splicing (AS) is a key element of eukaryotic gene expression that increases transcript and proteome diversity in cells, thereby altering their responses to external stimuli and stresses. While AS has been intensively researched in plants and animals, its frequency, conservation, and putative impact on virulence, are relatively still understudied in plant pathogenic fungi. Here, we profiled the AS events occurring in genes of Cladosporium fulvum isolates Race 5 and Race 4, during nearly a complete compatible infection cycle on their tomato host. Our studies revealed extensive heterogeneity in the transcript isoforms assembled from different isolates, infections, and infection timepoints, as over 80% of the transcript isoforms were singletons that were detected in only a single sample. Despite that, nearly 40% of the protein-coding genes in each isolate were predicted to be recurrently AS across the disparate infection timepoints, infections, and the two isolates. Of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8124n7x8</guid>
      <pubDate>Thu, 16 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zaccaron, Alex</name>
      </author>
      <author>
        <name>Chen, Li-Hung</name>
      </author>
      <author>
        <name>Stergiopoulos, Ioannis</name>
      </author>
    </item>
    <item>
      <title>MIBiG 4.0: advancing biosynthetic gene cluster curation through global collaboration</title>
      <link>https://escholarship.org/uc/item/33w736t3</link>
      <description>Specialized or secondary metabolites are small molecules of biological origin, often showing potent biological activities with applications in agriculture, engineering and medicine. Usually, the biosynthesis of these natural products is governed by sets of co-regulated and physically clustered genes known as biosynthetic gene clusters (BGCs). To share information about BGCs in a standardized and machine-readable way, the Minimum Information about a Biosynthetic Gene cluster (MIBiG) data standard and repository was initiated in 2015. Since its conception, MIBiG has been regularly updated to expand data coverage and remain up to date with innovations in natural product research. Here, we describe MIBiG version 4.0, an extensive update to the data repository and the underlying data standard. In a massive community annotation effort, 267 contributors performed 8304 edits, creating 557 new entries and modifying 590 existing entries, resulting in a new total of 3059 curated entries...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/33w736t3</guid>
      <pubDate>Wed, 15 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zdouc, Mitja M</name>
      </author>
      <author>
        <name>Blin, Kai</name>
      </author>
      <author>
        <name>Louwen, Nico LL</name>
      </author>
      <author>
        <name>Navarro, Jorge</name>
      </author>
      <author>
        <name>Loureiro, Catarina</name>
      </author>
      <author>
        <name>Bader, Chantal D</name>
      </author>
      <author>
        <name>Bailey, Constance B</name>
      </author>
      <author>
        <name>Barra, Lena</name>
      </author>
      <author>
        <name>Booth, Thomas J</name>
      </author>
      <author>
        <name>Bozhüyük, Kenan AJ</name>
      </author>
      <author>
        <name>Cediel-Becerra, José DD</name>
      </author>
      <author>
        <name>Charlop-Powers, Zachary</name>
      </author>
      <author>
        <name>Chevrette, Marc G</name>
      </author>
      <author>
        <name>Chooi, Yit Heng</name>
      </author>
      <author>
        <name>D’Agostino, Paul M</name>
      </author>
      <author>
        <name>de Rond, Tristan</name>
      </author>
      <author>
        <name>Del Pup, Elena</name>
      </author>
      <author>
        <name>Duncan, Katherine R</name>
      </author>
      <author>
        <name>Gu, Wenjia</name>
      </author>
      <author>
        <name>Hanif, Novriyandi</name>
      </author>
      <author>
        <name>Helfrich, Eric JN</name>
      </author>
      <author>
        <name>Jenner, Matthew</name>
      </author>
      <author>
        <name>Katsuyama, Yohei</name>
      </author>
      <author>
        <name>Korenskaia, Aleksandra</name>
      </author>
      <author>
        <name>Krug, Daniel</name>
      </author>
      <author>
        <name>Libis, Vincent</name>
      </author>
      <author>
        <name>Lund, George A</name>
      </author>
      <author>
        <name>Mantri, Shrikant</name>
      </author>
      <author>
        <name>Morgan, Kalindi D</name>
      </author>
      <author>
        <name>Owen, Charlotte</name>
      </author>
      <author>
        <name>Phan, Chin-Soon</name>
      </author>
      <author>
        <name>Philmus, Benjamin</name>
      </author>
      <author>
        <name>Reitz, Zachary L</name>
      </author>
      <author>
        <name>Robinson, Serina L</name>
      </author>
      <author>
        <name>Singh, Kumar Saurabh</name>
      </author>
      <author>
        <name>Teufel, Robin</name>
      </author>
      <author>
        <name>Tong, Yaojun</name>
      </author>
      <author>
        <name>Tugizimana, Fidele</name>
      </author>
      <author>
        <name>Ulanova, Dana</name>
      </author>
      <author>
        <name>Winter, Jaclyn M</name>
      </author>
      <author>
        <name>Aguilar, César</name>
      </author>
      <author>
        <name>Akiyama, Daniel Y</name>
      </author>
      <author>
        <name>Al-Salihi, Suhad AA</name>
      </author>
      <author>
        <name>Alanjary, Mohammad</name>
      </author>
      <author>
        <name>Alberti, Fabrizio</name>
      </author>
      <author>
        <name>Aleti, Gajender</name>
      </author>
      <author>
        <name>Alharthi, Shumukh A</name>
      </author>
      <author>
        <name>Rojo, Mariela Y Arias</name>
      </author>
      <author>
        <name>Arishi, Amr A</name>
      </author>
      <author>
        <name>Augustijn, Hannah E</name>
      </author>
      <author>
        <name>Avalon, Nicole E</name>
      </author>
      <author>
        <name>Avelar-Rivas, J Abraham</name>
      </author>
      <author>
        <name>Axt, Kyle K</name>
      </author>
      <author>
        <name>Barbieri, Hellen B</name>
      </author>
      <author>
        <name>Barbosa, Julio Cesar J</name>
      </author>
      <author>
        <name>Segato, Lucas Gabriel Barboza</name>
      </author>
      <author>
        <name>Barrett, Susanna E</name>
      </author>
      <author>
        <name>Baunach, Martin</name>
      </author>
      <author>
        <name>Beemelmanns, Christine</name>
      </author>
      <author>
        <name>Beqaj, Dardan</name>
      </author>
      <author>
        <name>Berger, Tim</name>
      </author>
      <author>
        <name>Bernaldo-Agüero, Jordan</name>
      </author>
      <author>
        <name>Bettenbühl, Sandra M</name>
      </author>
      <author>
        <name>Bielinski, Vincent A</name>
      </author>
      <author>
        <name>Biermann, Friederike</name>
      </author>
      <author>
        <name>Borges, Ricardo M</name>
      </author>
      <author>
        <name>Borriss, Rainer</name>
      </author>
      <author>
        <name>Breitenbach, Milena</name>
      </author>
      <author>
        <name>Bretscher, Kevin M</name>
      </author>
      <author>
        <name>Brigham, Michael W</name>
      </author>
      <author>
        <name>Buedenbender, Larissa</name>
      </author>
      <author>
        <name>Bulcock, Brodie W</name>
      </author>
      <author>
        <name>Cano-Prieto, Carolina</name>
      </author>
      <author>
        <name>Capela, João</name>
      </author>
      <author>
        <name>Carrion, Victor J</name>
      </author>
      <author>
        <name>Carter, Riley S</name>
      </author>
      <author>
        <name>Castelo-Branco, Raquel</name>
      </author>
      <author>
        <name>Castro-Falcón, Gabriel</name>
      </author>
      <author>
        <name>Chagas, Fernanda O</name>
      </author>
      <author>
        <name>Charria-Girón, Esteban</name>
      </author>
      <author>
        <name>Chaudhri, Ayesha Ahmed</name>
      </author>
      <author>
        <name>Chaudhry, Vasvi</name>
      </author>
      <author>
        <name>Choi, Hyukjae</name>
      </author>
      <author>
        <name>Choi, Yukyung</name>
      </author>
      <author>
        <name>Choupannejad, Roya</name>
      </author>
      <author>
        <name>Chromy, Jakub</name>
      </author>
      <author>
        <name>Donahey, Melinda S Chue</name>
      </author>
      <author>
        <name>Collemare, Jérôme</name>
      </author>
      <author>
        <name>Connolly, Jack A</name>
      </author>
      <author>
        <name>Creamer, Kaitlin E</name>
        <uri>https://orcid.org/0000-0002-0666-2107</uri>
      </author>
      <author>
        <name>Crüsemann, Max</name>
      </author>
      <author>
        <name>Cruz, Andres Arredondo</name>
      </author>
      <author>
        <name>Cumsille, Andres</name>
      </author>
      <author>
        <name>Dallery, Jean-Felix</name>
      </author>
      <author>
        <name>Damas-Ramos, Luis Caleb</name>
      </author>
      <author>
        <name>Damiani, Tito</name>
      </author>
      <author>
        <name>de Kruijff, Martinus</name>
      </author>
      <author>
        <name>Martín, Belén Delgado</name>
      </author>
      <author>
        <name>Della Sala, Gerardo</name>
      </author>
      <author>
        <name>Dillen, Jelle</name>
      </author>
    </item>
    <item>
      <title>The 24-kDa subunit of mitochondrial complex I regulates growth, microsclerotia development, stress tolerance, and virulence in Verticillium dahliae.</title>
      <link>https://escholarship.org/uc/item/8rm7c8wm</link>
      <description>BACKGROUND: The complete mitochondrial respiratory chain is a precondition for maintaining cellular energy supply, development, and metabolic balance. Due to the evolutionary differentiation of complexes and the semi-autonomy of mitochondria, respiratory chain subunits have become critical targets for crop improvement and fungal control. In fungi, mitochondrial complex I mediates growth and metabolism. However, the role of this complex in the pathogenesis of phytopathogenic fungi is largely unknown. RESULTS: In this study, we identified the NADH: ubiquinone oxidoreductase 24-kDa subunit (VdNuo1) of complex in vascular wilt pathogen, Verticillium dahliae, and examined its functional conservation in phytopathogenic fungi. Based on the treatments with respiratory chain inhibitors, the mitochondria-localized VdNuo1 was confirmed to regulate mitochondrial morphogenesis and homeostasis. VdNuo1 was induced during the different developmental stages in V. dahliae, including hyphal growth,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8rm7c8wm</guid>
      <pubDate>Fri, 3 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Huan</name>
      </author>
      <author>
        <name>Liu, Ying</name>
      </author>
      <author>
        <name>Wang, Dan</name>
      </author>
      <author>
        <name>Wang, Ya-Hong</name>
      </author>
      <author>
        <name>Sheng, Ruo-Cheng</name>
      </author>
      <author>
        <name>Kong, Zhi-Qiang</name>
      </author>
      <author>
        <name>Klosterman, Steven</name>
      </author>
      <author>
        <name>Chen, Jie-Yin</name>
      </author>
      <author>
        <name>Subbarao, Krishna</name>
      </author>
      <author>
        <name>Chen, Feng-Mao</name>
      </author>
      <author>
        <name>Zhang, Dan-Dan</name>
      </author>
    </item>
    <item>
      <title>The acyl-CoA-binding protein VdAcb1 is essential for carbon starvation response and contributes to virulence in Verticillium dahliae</title>
      <link>https://escholarship.org/uc/item/60v192zt</link>
      <description>In the face of carbon, nitrogen, and phosphorus starvation, microorganisms have evolved adaptive mechanisms to maintain growth. In a previous study, we identified a protein predicted to contain acyl-CoA-binding domains in the plant pathogenic fungus Verticillium dahliae. The predicted protein, designated VdAcb1, possesses an atypical signal peptide. However, the functions of this acyl-CoA-binding protein in V. dahliae are not clear. In this research, in vivo or in vitro assays confirmed that VdAcb1 is secreted extracellularly from V. dahliae, although it does not have the typical signal peptide. Furthermore, the unconventional secretion of VdAcb1 was dependent on VdGRASP, a member of the compartment for unconventional protein secretion (CUPS). The deletion mutant strain of VdAcb1 (ΔVdAcb1) exhibited significant sensitivity to carbon starvation. RNA-seq revealed that the expression of genes related to filamentous growth (MSB2 pathway) and sugar transport were regulated by VdAcb1...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/60v192zt</guid>
      <pubDate>Mon, 16 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zhuang, Jing</name>
      </author>
      <author>
        <name>Zhang, Ya-Duo</name>
      </author>
      <author>
        <name>Sun, Wei-Xia</name>
      </author>
      <author>
        <name>Zong, Juan</name>
      </author>
      <author>
        <name>Li, Jun-Jiao</name>
      </author>
      <author>
        <name>Dai, Xiao-Feng</name>
      </author>
      <author>
        <name>Klosterman, Steven J</name>
      </author>
      <author>
        <name>Chen, Jie-Yin</name>
      </author>
      <author>
        <name>Tian, Li</name>
      </author>
      <author>
        <name>Subbarao, Krishna V</name>
        <uri>https://orcid.org/0000-0002-2075-1835</uri>
      </author>
      <author>
        <name>Zhang, Dan-Dan</name>
      </author>
    </item>
    <item>
      <title>Genome editing of a rice CDP-DAG synthase confers multipathogen resistance</title>
      <link>https://escholarship.org/uc/item/2321j386</link>
      <description>The discovery and application of genome editing introduced a new era of plant breeding by giving researchers efficient tools for the precise engineering of crop genomes1. Here we demonstrate the power of genome editing for engineering broad-spectrum disease resistance in rice (Oryza sativa). We first isolated a lesion mimic mutant (LMM) from a mutagenized rice population. We then demonstrated that a 29-base-pair deletion in a gene we named RESISTANCE TO BLAST1 (RBL1) caused broad-spectrum disease resistance and showed that this mutation caused an approximately 20-fold reduction in yield. RBL1 encodes a cytidine diphosphate diacylglycerol synthase that is required for phospholipid biosynthesis2. Mutation of RBL1 results in reduced levels of phosphatidylinositol and its derivative phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2). In rice, PtdIns(4,5)P2 is enriched in cellular structures that are specifically associated with effector secretion and fungal infection, suggesting...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2321j386</guid>
      <pubDate>Tue, 3 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sha, Gan</name>
      </author>
      <author>
        <name>Sun, Peng</name>
      </author>
      <author>
        <name>Kong, Xiaojing</name>
      </author>
      <author>
        <name>Han, Xinyu</name>
      </author>
      <author>
        <name>Sun, Qiping</name>
      </author>
      <author>
        <name>Fouillen, Laetitia</name>
      </author>
      <author>
        <name>Zhao, Juan</name>
      </author>
      <author>
        <name>Li, Yun</name>
      </author>
      <author>
        <name>Yang, Lei</name>
      </author>
      <author>
        <name>Wang, Yin</name>
      </author>
      <author>
        <name>Gong, Qiuwen</name>
      </author>
      <author>
        <name>Zhou, Yaru</name>
      </author>
      <author>
        <name>Zhou, Wenqing</name>
      </author>
      <author>
        <name>Jain, Rashmi</name>
      </author>
      <author>
        <name>Gao, Jie</name>
      </author>
      <author>
        <name>Huang, Renliang</name>
      </author>
      <author>
        <name>Chen, Xiaoyang</name>
      </author>
      <author>
        <name>Zheng, Lu</name>
      </author>
      <author>
        <name>Zhang, Wanying</name>
      </author>
      <author>
        <name>Qin, Ziting</name>
      </author>
      <author>
        <name>Zhou, Qi</name>
      </author>
      <author>
        <name>Zeng, Qingdong</name>
      </author>
      <author>
        <name>Xie, Kabin</name>
      </author>
      <author>
        <name>Xu, Jiandi</name>
      </author>
      <author>
        <name>Chiu, Tsan-Yu</name>
      </author>
      <author>
        <name>Guo, Liang</name>
      </author>
      <author>
        <name>Mortimer, Jenny C</name>
      </author>
      <author>
        <name>Boutté, Yohann</name>
      </author>
      <author>
        <name>Li, Qiang</name>
      </author>
      <author>
        <name>Kang, Zhensheng</name>
      </author>
      <author>
        <name>Ronald, Pamela C</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
      <author>
        <name>Li, Guotian</name>
      </author>
    </item>
    <item>
      <title>Genetic modification can improve crop yields — but stop overselling it</title>
      <link>https://escholarship.org/uc/item/46v4f9r7</link>
      <description>With a changing climate and a growing population, the world increasingly needs more-productive and resilient crops. But improving them requires a knowledge of what actually works in the field.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/46v4f9r7</guid>
      <pubDate>Tue, 26 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Khaipho-Burch, Merritt</name>
      </author>
      <author>
        <name>Cooper, Mark</name>
      </author>
      <author>
        <name>Crossa, Jose</name>
      </author>
      <author>
        <name>de Leon, Natalia</name>
      </author>
      <author>
        <name>Holland, James</name>
      </author>
      <author>
        <name>Lewis, Ramsey</name>
      </author>
      <author>
        <name>McCouch, Susan</name>
      </author>
      <author>
        <name>Murray, Seth C</name>
      </author>
      <author>
        <name>Rabbi, Ismail</name>
      </author>
      <author>
        <name>Ronald, Pamela</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
      <author>
        <name>Ross-Ibarra, Jeffrey</name>
      </author>
      <author>
        <name>Weigel, Detlef</name>
      </author>
      <author>
        <name>Buckler, Edward S</name>
      </author>
    </item>
    <item>
      <title>Enhancing sustainable development through plant genetics</title>
      <link>https://escholarship.org/uc/item/29g6q12t</link>
      <description>In April 2023, scholars and experts met members of the US Congress for the Aspen Institute Congressional Program conference in Bellagio, Italy, to discuss strategies to ensure global food security. Building on her perspective from this meeting, Pamela Ronald highlights the role that plant genetics can have in achieving these goals.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/29g6q12t</guid>
      <pubDate>Mon, 18 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ronald, Pamela C</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
    </item>
    <item>
      <title>Dispersal, habitat filtering, and eco-evolutionary dynamics as drivers of local and global wetland viral biogeography</title>
      <link>https://escholarship.org/uc/item/94q856n4</link>
      <description>Wetlands store 20-30% of the world's soil carbon, and identifying the microbial controls on these carbon reserves is essential to predicting feedbacks to climate change. Although viral infections likely play important roles in wetland ecosystem dynamics, we lack a basic understanding of wetland viral ecology. Here 63 viral size-fraction metagenomes (viromes) and paired total metagenomes were generated from three time points in 2021 at seven fresh- and saltwater wetlands in the California Bodega Marine Reserve. We recovered 12,826 viral population genomic sequences (vOTUs), only 4.4% of which were detected at the same field site two years prior, indicating a small degree of population stability or recurrence. Viral communities differed most significantly among the seven wetland sites and were also structured by habitat (plant community composition and salinity). Read mapping to a new version of our reference database, PIGEONv2.0 (515,763 vOTUs), revealed 196 vOTUs present over...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/94q856n4</guid>
      <pubDate>Thu, 14 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Horst, Anneliek M ter</name>
      </author>
      <author>
        <name>Fudyma, Jane D</name>
      </author>
      <author>
        <name>Sones, Jacqueline L</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
    </item>
    <item>
      <title>Lectins and polysaccharide EPS I have flow-responsive roles in the attachment and biofilm mechanics of plant pathogenic Ralstonia</title>
      <link>https://escholarship.org/uc/item/34f5z2jp</link>
      <description>Bacterial biofilm formation and attachment to hosts are mediated by carbohydrate-binding lectins, exopolysaccharides, and their interactions in the extracellular matrix (ECM). During tomato infection Ralstonia pseudosolanacearum (Rps) GMI1000 highly expresses three lectins: LecM, LecF, and LecX. The latter two are uncharacterized. We evaluated the roles in bacterial wilt disease of LecF, a fucose-binding lectin, LecX, a xylose-binding lectin, and the Rps exopolysaccharide EPS I. Interestingly, single and double lectin mutants attached to tomato roots better and formed more biofilm under static conditions in vitro. Consistent with this finding, static bacterial aggregation was suppressed by heterologous expression of lecFGMI1000 and lecXGMI1000 in other Ralstonia strains that naturally lack these lectins. Crude ECM from a ΔlecF/X double mutant was more adhesive than the wild-type ECM, and LecF and LecX increased Rps attachment to ECM. The enhanced adhesiveness of the ΔlecF/X ECM...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/34f5z2jp</guid>
      <pubDate>Tue, 12 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Carter, Mariama D</name>
      </author>
      <author>
        <name>Tran, Tuan M</name>
      </author>
      <author>
        <name>Cope-Arguello, Matthew L</name>
      </author>
      <author>
        <name>Weinstein, Sofia</name>
      </author>
      <author>
        <name>Li, Hanlei</name>
      </author>
      <author>
        <name>Hendrich, Connor G</name>
      </author>
      <author>
        <name>Prom, Jessica L</name>
      </author>
      <author>
        <name>Li, Jiayu</name>
      </author>
      <author>
        <name>Chu, Lan Thanh</name>
      </author>
      <author>
        <name>Bui, Loan</name>
      </author>
      <author>
        <name>Manikantan, Harishankar</name>
        <uri>https://orcid.org/0000-0002-4270-3527</uri>
      </author>
      <author>
        <name>Lowe-Power, Tiffany M</name>
        <uri>https://orcid.org/0000-0003-2681-3563</uri>
      </author>
      <author>
        <name>Allen, Caitilyn</name>
      </author>
    </item>
    <item>
      <title>Pathogenicity, phylogenomic, and comparative genomic study of Pseudomonas syringae sensu lato affecting sweet cherry in California</title>
      <link>https://escholarship.org/uc/item/7g32r2wh</link>
      <description>To gain insights into the diversity of &lt;i&gt;Pseudomonas syringae&lt;/i&gt; sensu lato affecting sweet cherry in California, we sequenced and analyzed the phylogenomic and genomic architecture of 86 fluorescent pseudomonads isolated from symptomatic and asymptomatic cherry tissues. Fifty-eight isolates were phylogenetically placed within the &lt;i&gt;P. syringae&lt;/i&gt; species complex and taxonomically classified into five genomospecies: &lt;i&gt;P. syringae&lt;/i&gt; pv. &lt;i&gt;syringae&lt;/i&gt;, &lt;i&gt;P. syringae&lt;/i&gt;, &lt;i&gt;Pseudomonas cerasi&lt;/i&gt;, &lt;i&gt;Pseudomonas viridiflava&lt;/i&gt;, and &lt;i&gt;A&lt;/i&gt;. We annotated components of the type III secretion system and phytotoxin-encoding genes and correlated the data with pathogenicity phenotypes. Intact probable regulatory protein HrpR was annotated in the genomic sequences of all isolates of &lt;i&gt;P. syringae&lt;/i&gt; pv. &lt;i&gt;syringae&lt;/i&gt;, &lt;i&gt;P. syringae&lt;/i&gt;, &lt;i&gt;P. cerasi&lt;/i&gt;, and &lt;i&gt;A&lt;/i&gt;. Isolates of &lt;i&gt;P. viridiflava&lt;/i&gt; had atypical probable regulatory protein HrpR. Syringomycin and syringopeptin-encoding...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7g32r2wh</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Maguvu, Tawanda E</name>
      </author>
      <author>
        <name>Frias, Rosa J</name>
      </author>
      <author>
        <name>Hernandez-Rosas, Alejandro I</name>
      </author>
      <author>
        <name>Shipley, Erin</name>
      </author>
      <author>
        <name>Dardani, Greta</name>
      </author>
      <author>
        <name>Nouri, Mohamed T</name>
      </author>
      <author>
        <name>Yaghmour, Mohammad A</name>
      </author>
      <author>
        <name>Trouillas, Florent P</name>
      </author>
    </item>
    <item>
      <title>Genome sequence of Colletotrichum karsti isolated from rose leaves exhibiting anthracnose symptoms in Potchefstroom, South Africa</title>
      <link>https://escholarship.org/uc/item/5sb9x5zj</link>
      <description>We present the genome sequence of &lt;i&gt;Colletotrichum karsti&lt;/i&gt; isolated from rose leaves exhibiting anthracnose symptoms. The genome was assembled to 53.2 Mbp organized into 753 scaffolds having an N50 of 582,313 kbp and a GC content of 52.5%. The genome had an estimated 99.4% of the core Ascomycota genes.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5sb9x5zj</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Maguvu, Tawanda E</name>
      </author>
      <author>
        <name>Raimi, Adekunle</name>
      </author>
      <author>
        <name>Trouillas, Florent P</name>
      </author>
      <author>
        <name>Adeleke, Rasheed</name>
      </author>
      <author>
        <name>Bezuidenhout, Cornelius C</name>
      </author>
    </item>
    <item>
      <title>Characterization of Genetic Diversity in the Capsid Protein Gene of Grapevine Fleck Virus and Development of a New Real-Time RT-PCR Assay</title>
      <link>https://escholarship.org/uc/item/1k1153nr</link>
      <description>The grapevine fleck virus (GFkV) is a ubiquitous grapevine-infecting virus found worldwide, is associated with the grapevine fleck complex, and is often found in mixed infections with viruses of the grapevine leafroll complex and/or vitiviruses. Although GFkV has been studied for a long time, limited sequence information is available in the public databases. In this study, the GFkV sequence data available in GenBank and data generated at the Foundation Plant Services, University of California, Davis, were used to perform nucleotide sequence comparisons, construct a phylogenetic tree, and develop a new RT-qPCR assay. Sequence comparisons showed high genetic diversity among the GFkV isolates, and the phylogenetic analyses revealed a new group comprised of GFkV isolates identified in the present study. A new assay, referred to as GFkV-CP, was designed and validated using an existing GFkV positive control together with 11 samples known to be infected with combinations of different...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1k1153nr</guid>
      <pubDate>Tue, 5 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>de Souza, Juliana Osse</name>
      </author>
      <author>
        <name>Klaassen, Vicki</name>
      </author>
      <author>
        <name>Stevens, Kristian</name>
      </author>
      <author>
        <name>Erickson, Teresa M</name>
      </author>
      <author>
        <name>Heinitz, Claire</name>
      </author>
      <author>
        <name>Al Rwahnih, Maher</name>
        <uri>https://orcid.org/0000-0003-1589-9234</uri>
      </author>
    </item>
    <item>
      <title>The perception and evolution of flagellin, cold shock protein and elongation factor Tu from vector‐borne bacterial plant pathogens</title>
      <link>https://escholarship.org/uc/item/0wm1h55c</link>
      <description>Vector-borne bacterial pathogens cause devastating plant diseases that cost billions of dollars in crop losses worldwide. These pathogens have evolved to be host- and vector-dependent, resulting in a reduced genome size compared to their free-living relatives. All known vector-borne bacterial plant pathogens belong to four different genera: 'Candidatus Liberibacter', 'Candidatus Phytoplasma', Spiroplasma and Xylella. To protect themselves against pathogens, plants have evolved pattern recognition receptors that can detect conserved pathogen features as non-self and mount an immune response. To gain an understanding of how vector-borne pathogen features are perceived in plants, we investigated three proteinaceous features derived from cold shock protein (csp22), flagellin (flg22) and elongation factor Tu (elf18) from vector-borne bacterial pathogens as well as their closest free-living relatives. In general, vector-borne pathogens have fewer copies of genes encoding flagellin and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0wm1h55c</guid>
      <pubDate>Sat, 2 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Trinh, Jessica</name>
      </author>
      <author>
        <name>Tran, Megann</name>
      </author>
      <author>
        <name>Coaker, Gitta</name>
        <uri>https://orcid.org/0000-0003-0899-2449</uri>
      </author>
    </item>
    <item>
      <title>A pangenomic atlas reveals eco-evolutionary dynamics that shape type VI secretion systems in plant-pathogenic Ralstonia</title>
      <link>https://escholarship.org/uc/item/6rs075vk</link>
      <description>Soilborne &lt;i&gt;Ralstonia solanacearum&lt;/i&gt; species complex (RSSC) pathogens disrupt microbial communities as they invade roots and fatally wilt plants. RSSC pathogens secrete antimicrobial toxins using a type VI secretion system (T6SS). To investigate how evolution and ecology have shaped the T6SS of these bacterial pathogens, we analyzed the T6SS gene content and architecture across the RSSC and their evolutionary relatives. Our analysis reveals that two ecologically similar Burkholderiaceae taxa, xylem-pathogenic RSSC and &lt;i&gt;Paracidovorax&lt;/i&gt;, have convergently evolved to wield large arsenals of T6SS toxins. To understand the mechanisms underlying genomic enrichment of T6SS toxins, we compiled an atlas of 1,066 auxiliary T6SS toxin clusters ("&lt;i&gt;aux&lt;/i&gt;" clusters) across 99 high-quality RSSC genomes. We classified 25 types of &lt;i&gt;aux&lt;/i&gt; clusters with toxins that predominantly target lipids, nucleic acids, or unknown cellular substrates. The &lt;i&gt;aux&lt;/i&gt; clusters were located in diverse...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6rs075vk</guid>
      <pubDate>Fri, 1 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Aoun, Nathalie</name>
      </author>
      <author>
        <name>Georgoulis, Stratton J</name>
      </author>
      <author>
        <name>Avalos, Jason K</name>
      </author>
      <author>
        <name>Grulla, Kimberly J</name>
      </author>
      <author>
        <name>Miqueo, Kasey</name>
      </author>
      <author>
        <name>Tom, Cloe</name>
      </author>
      <author>
        <name>Lowe-Power, Tiffany M</name>
        <uri>https://orcid.org/0000-0003-2681-3563</uri>
      </author>
    </item>
    <item>
      <title>Combining physicochemical properties and microbiome data to evaluate the water quality of South African drinking water production plants</title>
      <link>https://escholarship.org/uc/item/6h4184q8</link>
      <description>Anthropogenic activities in catchments used for drinking water production largely contaminates source waters, and this may impact the quality of the final drinking water product. These contaminants may also affect taxonomic and functional profiles of the bacterial communities in the drinking water. Here, we report an integrated insight into the microbiome and water quality of four water treatment plants (NWC, NWE, WCA and NWG) that supply portable water to communities in South Africa. A new scoring system based on combined significant changes of physicochemical parameters and microbial abundance from raw to treated water was used to evaluate the effectiveness of the treatment plants at water purification. Physicochemical parameters which include total soluble solids, turbidity, pH, nitrites and phosphorus among others, were measured in source, treated, and distributed water. There were general statistically significant (P ≤ 0.05) differences between raw and treated water, demonstrating...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6h4184q8</guid>
      <pubDate>Thu, 19 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Maguvu, Tawanda E</name>
      </author>
      <author>
        <name>Bezuidenhout, Cornelius C</name>
      </author>
      <author>
        <name>Kritzinger, Rinaldo</name>
      </author>
      <author>
        <name>Tsholo, Karabo</name>
      </author>
      <author>
        <name>Plaatjie, Moitshepi</name>
      </author>
      <author>
        <name>Molale-Tom, Lesego G</name>
      </author>
      <author>
        <name>Mienie, Charlotte M</name>
      </author>
      <author>
        <name>Coertze, Roelof D</name>
      </author>
    </item>
    <item>
      <title>Whole Genome Sequencing Based Taxonomic Classification, and Comparative Genomic Analysis of Potentially Human Pathogenic Enterobacter spp. Isolated from Chlorinated Wastewater in the North West Province, South Africa</title>
      <link>https://escholarship.org/uc/item/5xn5n0f9</link>
      <description>Comparative genomics, in particular, pan-genome analysis, provides an in-depth understanding of the genetic variability and dynamics of a bacterial species. Coupled with whole-genome-based taxonomic analysis, these approaches can help to provide comprehensive, detailed insights into a bacterial species. Here, we report whole-genome-based taxonomic classification and comparative genomic analysis of potential human pathogenic &lt;i&gt;Enterobacter hormaechei&lt;/i&gt; subsp. &lt;i&gt;hoffmannii&lt;/i&gt; isolated from chlorinated wastewater. Genome Blast Distance Phylogeny (GBDP), digital DNA-DNA hybridization (dDDH), and average nucleotide identity (ANI) confirmed the identity of the isolates. The algorithm PathogenFinder predicted the isolates to be human pathogens with a probability of greater than 0.78. The potential pathogenic nature of the isolates was supported by the presence of biosynthetic gene clusters (BGCs), aerobactin, and aryl polyenes (APEs), which are known to be associated with pathogenic/virulent...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5xn5n0f9</guid>
      <pubDate>Thu, 19 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Maguvu, Tawanda E</name>
      </author>
      <author>
        <name>Bezuidenhout, Cornelius C</name>
      </author>
    </item>
    <item>
      <title>Whole genome sequence of Serratia marcescens 39_H1, a potential hydrolytic and acidogenic strain</title>
      <link>https://escholarship.org/uc/item/49n3d1vf</link>
      <description>Here, we report a high quality annotated draft genome of &lt;i&gt;Serratia marcescens&lt;/i&gt; 39_H1, a Gram-negative facultative anaerobe that was isolated from an anaerobic digester. The strain exhibited hydrolytic/acidogenic properties by significantly improving methane production when used as a single isolate inoculum during anaerobic digestion of water hyacinth and cow dung. The total genome size of the isolate was 5,106,712 bp which corresponds to an N50 of 267,528 and G + C content of 59.7 %. Genome annotation with the NCBI Prokaryotic Genome Annotation Pipeline (PGAP) predicted a total of 4,908 genes of which 4,755 were protein coding genes; there were no plasmids detected. A number of genes associated with hydrolytic/acidogenic activities as well as other metabolic activities were identified and discussed.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/49n3d1vf</guid>
      <pubDate>Thu, 19 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>U., Linda</name>
      </author>
      <author>
        <name>Tekere, Memory</name>
      </author>
      <author>
        <name>Roopnarain, Ashira</name>
      </author>
      <author>
        <name>Sanko, Tomasz</name>
      </author>
      <author>
        <name>Maguvu, Tawanda E</name>
      </author>
      <author>
        <name>Bezuidenhout, Cornelius C</name>
      </author>
      <author>
        <name>Adeleke, Rasheed A</name>
      </author>
    </item>
    <item>
      <title>Analysis of Genome Sequences of Coagulase-Negative Staphylococci Isolates from South Africa and Nigeria Highlighted Environmentally Driven Heterogeneity</title>
      <link>https://escholarship.org/uc/item/0zp7n4k8</link>
      <description>Here, we report high-quality annotated draft genomes of eight coagulase-negative staphylococci (CoNS) isolates obtained from South Africa and Nigeria. We explored the prevalence of antibiotic resistance and virulence genes, their association with mobile genetic elements. The pan-genomic analysis highlighted the environmentally driven heterogeneity of the isolates. Isolates from Nigeria had at least one gene for cadmium resistance/tolerance, these genes were not detected in isolates from South Africa. In contrast, isolates from South Africa had a &lt;i&gt;tetM&lt;/i&gt; gene, which was not detected among the isolates from Nigeria. The observed genomic heterogeneity correlates with anthropogenic activities in the area where the isolates were collected. Moreover, the isolates used in this study possess an open pan-genome, which could easily explain the environmentally driven heterogeneity.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0zp7n4k8</guid>
      <pubDate>Thu, 19 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Maguvu, Tawanda Elias</name>
      </author>
      <author>
        <name>Oladipo, Adegboyega Oyedele</name>
      </author>
      <author>
        <name>Bezuidenhout, Cornelius Carlos</name>
      </author>
    </item>
    <item>
      <title>Genetic diversity and population structure of Botryosphaeria dothidea and Neofusicoccum parvum on English walnut (Juglans regia L.) in France</title>
      <link>https://escholarship.org/uc/item/3126969v</link>
      <description>Botryosphaeriaceae species are the major causal agents of walnut dieback worldwide, along with Diaporthe species. Botryosphaeria dothidea and Neofusicoccum parvum are the only two Botryosphaeriaceae species associated with this recently emergent disease in France, and little is known about their diversity, structure, origin and dispersion in French walnut orchards. A total of 381 isolates of both species were genetically typed using a sequence-based microsatellite genotyping (SSR-seq) method. This analysis revealed a low genetic diversity and a high clonality of these populations, in agreement with their clonal mode of reproduction. The genetic similarity among populations, regardless of the tissue type and the presence of symptoms, supports the hypothesis that these pathogens can move between fruits and twigs and display latent pathogen lifestyles. Contrasting genetic patterns between N. parvum populations from Californian and Spanish walnut orchards and the French ones suggested...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3126969v</guid>
      <pubDate>Thu, 5 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Belair, Marie</name>
      </author>
      <author>
        <name>Picot, Adeline</name>
      </author>
      <author>
        <name>Lepais, Olivier</name>
      </author>
      <author>
        <name>Masson, Cyrielle</name>
      </author>
      <author>
        <name>Hébrard, Marie-Neige</name>
      </author>
      <author>
        <name>Moronvalle, Aude</name>
      </author>
      <author>
        <name>Comont, Gwénaëlle</name>
      </author>
      <author>
        <name>Gabri Martin, Victor M</name>
      </author>
      <author>
        <name>Tréguer, Sylvie</name>
      </author>
      <author>
        <name>Laloum, Yohana</name>
      </author>
      <author>
        <name>Corio-Costet, Marie-France</name>
      </author>
      <author>
        <name>Michailides, Themis J</name>
        <uri>https://orcid.org/0000-0002-0205-9861</uri>
      </author>
      <author>
        <name>Moral, Juan</name>
      </author>
      <author>
        <name>Le Floch, Gaétan</name>
      </author>
      <author>
        <name>Pensec, Flora</name>
      </author>
    </item>
    <item>
      <title>Draft genome sequence of Collimonas sp. strain H4R21, an effective mineral-weathering bacterial strain isolated from the beech rhizosphere</title>
      <link>https://escholarship.org/uc/item/28d2d62x</link>
      <description>We present the draft genome sequence of &lt;i&gt;Collimonas&lt;/i&gt; sp. strain H4R21, isolated from the rhizosphere of &lt;i&gt;Fagus sylvatica&lt;/i&gt; in the forest experimental site of Montiers (France). This genome features coding capacity for plant growth promotion, such as the ability to solubilize minerals, to produce siderophores and antifungal secondary metabolites.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/28d2d62x</guid>
      <pubDate>Wed, 4 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>E, Morin</name>
      </author>
      <author>
        <name>S, Uroz</name>
      </author>
      <author>
        <name>R, Kumar</name>
      </author>
      <author>
        <name>M W, Rey</name>
      </author>
      <author>
        <name>J, Pham</name>
      </author>
      <author>
        <name>F, Akum</name>
      </author>
      <author>
        <name>J H J, Leveau</name>
      </author>
    </item>
    <item>
      <title>The mobilization and transport of newly fixed carbon are driven by plant water use in an experimental rainforest under drought</title>
      <link>https://escholarship.org/uc/item/28q170rg</link>
      <description>Non-structural carbohydrates (NSCs) are building blocks for biomass and fuel metabolic processes. However, it remains unclear how tropical forests mobilize, export, and transport NSCs to cope with extreme droughts. We combined drought manipulation and ecosystem 13CO2 pulse-labeling in an enclosed rainforest at Biosphere 2, assessed changes in NSCs, and traced newly assimilated carbohydrates in plant species with diverse hydraulic traits and canopy positions. We show that drought caused a depletion of leaf starch reserves and slowed export and transport of newly assimilated carbohydrates below ground. Drought effects were more pronounced in conservative canopy trees with limited supply of new photosynthates and relatively constant water status than in those with continual photosynthetic supply and deteriorated water status. We provide experimental evidence that local utilization, export, and transport of newly assimilated carbon are closely coupled with plant water use in canopy...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/28q170rg</guid>
      <pubDate>Tue, 3 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Huang, Jianbei</name>
      </author>
      <author>
        <name>Ladd, S Nemiah</name>
      </author>
      <author>
        <name>Ingrisch, Johannes</name>
      </author>
      <author>
        <name>Kübert, Angelika</name>
      </author>
      <author>
        <name>Meredith, Laura K</name>
      </author>
      <author>
        <name>van Haren, Joost</name>
      </author>
      <author>
        <name>Bamberger, Ines</name>
      </author>
      <author>
        <name>Daber, L Erik</name>
      </author>
      <author>
        <name>Kühnhammer, Kathrin</name>
      </author>
      <author>
        <name>Bailey, Kinzie</name>
      </author>
      <author>
        <name>Hu, Jia</name>
      </author>
      <author>
        <name>Fudyma, Jane</name>
      </author>
      <author>
        <name>Shi, Lingling</name>
      </author>
      <author>
        <name>Dippold, Michaela A</name>
      </author>
      <author>
        <name>Meeran, Kathiravan</name>
      </author>
      <author>
        <name>Miller, Luke</name>
      </author>
      <author>
        <name>O’Brien, Michael J</name>
      </author>
      <author>
        <name>Yang, Hui</name>
      </author>
      <author>
        <name>Herrera-Ramírez, David</name>
      </author>
      <author>
        <name>Hartmann, Henrik</name>
      </author>
      <author>
        <name>Trumbore, Susan</name>
        <uri>https://orcid.org/0000-0003-3885-6202</uri>
      </author>
      <author>
        <name>Bahn, Michael</name>
      </author>
      <author>
        <name>Werner, Christiane</name>
      </author>
      <author>
        <name>Lehmann, Marco M</name>
      </author>
    </item>
    <item>
      <title>The genetics of resistance to lettuce drop (Sclerotinia spp.) in lettuce in a recombinant inbred line population from Reine des Glaces × Eruption</title>
      <link>https://escholarship.org/uc/item/9xt43390</link>
      <description>Key messageTwo QTLs for resistance to lettuce drop, qLDR1.1 and qLDR5.1, were identified. Associated SNPs will be useful in breeding for lettuce drop and provide the foundation for future molecular analysis.AbstractLettuce drop, caused by Sclerotinia minor and S. sclerotiorum, is an economically important disease of lettuce. The association of resistance to lettuce drop with the commercially undesirable trait of fast bolting has hindered the integration of host resistance in control of this disease. Eruption is a slow-bolting cultivar that exhibits a high level of resistance to lettuce drop. Eruption also is completely resistant to Verticillium wilt caused by race 1 of Verticillium dahliae. A recombinant inbred line population from the cross Reine des Glaces × Eruption was genotyped by sequencing and evaluated for lettuce drop and bolting in separate fields infested with either S. minor or V. dahliae. Two quantitative trait loci (QTLs) for lettuce drop resistance were consistently...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9xt43390</guid>
      <pubDate>Thu, 29 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Mamo, Bullo Erena</name>
        <uri>https://orcid.org/0000-0003-4778-9902</uri>
      </author>
      <author>
        <name>Hayes, Ryan J</name>
      </author>
      <author>
        <name>Truco, Maria José</name>
      </author>
      <author>
        <name>Puri, Krishna D</name>
      </author>
      <author>
        <name>Michelmore, Richard W</name>
      </author>
      <author>
        <name>Subbarao, Krishna V</name>
        <uri>https://orcid.org/0000-0002-2075-1835</uri>
      </author>
      <author>
        <name>Simko, Ivan</name>
      </author>
    </item>
    <item>
      <title>Measurements of Aerial Spore Load by qPCR Facilitates Lettuce Downy Mildew Risk Advisement.</title>
      <link>https://escholarship.org/uc/item/7fk0d13m</link>
      <description>The lettuce downy mildew pathogen, &lt;i&gt;Bremia lactucae&lt;/i&gt;, is an obligate oomycete that causes extensive produce losses. Initial chlorotic symptoms that severely reduce the market value of the produce are followed by the appearance of white, downy sporulation on the abaxial side of the leaves. These spores become airborne and disseminate the pathogen. Controlling lettuce downy mildew has relied on repeated fungicide applications to prevent outbreaks. However, in addition to direct economic costs, heterogeneity and rapid adaptation of this pathogen to repeatedly applied fungicides has led to the development of fungicide-insensitivity in the pathogen. We deployed a quantitative PCR assay-based detection method using a species-specific DNA target for &lt;i&gt;B. lactucae&lt;/i&gt; coupled with a spore trap system to measure airborne &lt;i&gt;B. lactucae&lt;/i&gt; spore loads within three commercial fields that each contained experimental plots, designated EXP1 to EXP3. Based upon these measurements, when...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7fk0d13m</guid>
      <pubDate>Thu, 29 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dhar, Nikhilesh</name>
      </author>
      <author>
        <name>Mamo, Bullo Erena</name>
        <uri>https://orcid.org/0000-0003-4778-9902</uri>
      </author>
      <author>
        <name>Subbarao, Krishna V</name>
        <uri>https://orcid.org/0000-0002-2075-1835</uri>
      </author>
      <author>
        <name>Koike, Steven T</name>
      </author>
      <author>
        <name>Fox, Alan</name>
      </author>
      <author>
        <name>Anchieta, Amy</name>
      </author>
      <author>
        <name>Klosterman, Steven J</name>
      </author>
    </item>
    <item>
      <title>Arabidopsis defense mutant ndr1-1 displays accelerated development and early flowering mediated by the hormone gibberellic acid</title>
      <link>https://escholarship.org/uc/item/30q7j26d</link>
      <description>NONRACE-SPECIFIC DISEASE RESISTANCE (NDR1) is a widely characterized gene that plays a key role in defense against multiple bacterial, fungal, oomycete and nematode plant pathogens. NDR1 is required for activation of resistance by multiple NB and LRR-containing (NLR) protein immune sensors and contributes to basal defense. The role of NDR1 in positively regulating salicylic acid (SA)-mediated plant defense responses is well documented. However, ndr1-1 plants flower earlier and show accelerated development in comparison to wild type (WT) Arabidopsis plants, indicating that NDR1 is a negative regulator of flowering and growth. Exogenous application of gibberellic acid (GA) further accelerates the early flowering phenotype in ndr1-1 plants, while the GA biosynthesis inhibitor paclobutrazol attenuated the early flowering phenotype of ndr1-1, but not to WT levels, suggesting partial resistance to paclobutrazol and enhanced GA response in ndr1-1 plants. Mass spectroscopy analyses confirmed...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/30q7j26d</guid>
      <pubDate>Thu, 29 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dhar, Nikhilesh</name>
      </author>
      <author>
        <name>Short, Dylan PG</name>
      </author>
      <author>
        <name>Mamo, Bullo Erena</name>
        <uri>https://orcid.org/0000-0003-4778-9902</uri>
      </author>
      <author>
        <name>Corrion, Alex J</name>
      </author>
      <author>
        <name>Wai, Ching Man</name>
      </author>
      <author>
        <name>Anchieta, Amy</name>
      </author>
      <author>
        <name>VanBuren, Robert</name>
      </author>
      <author>
        <name>Day, Brad</name>
      </author>
      <author>
        <name>Ajwa, Husein</name>
      </author>
      <author>
        <name>Subbarao, Krishna V</name>
        <uri>https://orcid.org/0000-0002-2075-1835</uri>
      </author>
      <author>
        <name>Klosterman, Steven J</name>
      </author>
    </item>
    <item>
      <title>Marker-free carotenoid-enriched rice generated through targeted gene insertion using CRISPR-Cas9</title>
      <link>https://escholarship.org/uc/item/5jk4024m</link>
      <description>Targeted insertion of transgenes at pre-determined plant&amp;nbsp;genomic safe harbors provides a desirable alternative to insertions at random sites&amp;nbsp;achieved through conventional methods. Most existing cases of targeted gene insertion in plants have&amp;nbsp;either relied on the presence of a selectable marker gene in the insertion cassette or occurred at low frequency with relatively small DNA fragments (&amp;lt;1.8 kb). Here, we report the use of an optimized CRISPR-Cas9-based method to achieve the targeted insertion of a 5.2 kb carotenoid biosynthesis cassette at two genomic safe harbors in rice. We obtain marker-free rice plants with high carotenoid content in the seeds and no detectable penalty in morphology or yield. Whole-genome sequencing reveals the absence of off-target mutations by Cas9 in the engineered plants. These results demonstrate targeted gene insertion of marker-free DNA in rice using CRISPR-Cas9 genome editing, and offer a promising strategy for genetic improvement...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5jk4024m</guid>
      <pubDate>Sun, 18 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dong, Oliver Xiaoou</name>
      </author>
      <author>
        <name>Yu, Shu</name>
      </author>
      <author>
        <name>Jain, Rashmi</name>
      </author>
      <author>
        <name>Zhang, Nan</name>
      </author>
      <author>
        <name>Duong, Phat Q</name>
      </author>
      <author>
        <name>Butler, Corinne</name>
      </author>
      <author>
        <name>Li, Yan</name>
      </author>
      <author>
        <name>Lipzen, Anna</name>
        <uri>https://orcid.org/0000-0003-2293-9329</uri>
      </author>
      <author>
        <name>Martin, Joel A</name>
        <uri>https://orcid.org/0000-0001-9511-6441</uri>
      </author>
      <author>
        <name>Barry, Kerrie W</name>
        <uri>https://orcid.org/0000-0002-8999-6785</uri>
      </author>
      <author>
        <name>Schmutz, Jeremy</name>
      </author>
      <author>
        <name>Tian, Li</name>
        <uri>https://orcid.org/0000-0001-6461-6072</uri>
      </author>
      <author>
        <name>Ronald, Pamela C</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
    </item>
    <item>
      <title>Botrytis cinerea combines four molecular strategies to tolerate membrane-permeating plant compounds and to increase virulence</title>
      <link>https://escholarship.org/uc/item/5mh171j7</link>
      <description>Saponins are plant secondary metabolites comprising glycosylated triterpenoids, steroids or steroidal alkaloids with a broad spectrum of toxicity to microbial pathogens and pest organisms that contribute to basal plant defense to biotic attack. Secretion of glycosyl hydrolases that enzymatically convert saponins into less toxic products was thus far the only mechanism reported to enable fungal pathogens to colonize their saponin-containing host plant(s). We studied the mechanisms that the fungus Botrytis cinerea utilizes to be tolerant to well-characterized, structurally related saponins from tomato and Digitalis purpurea. By gene expression studies, comparative genomics, enzyme assays and testing a large panel of fungal (knockout and complemented) mutants, we unraveled four distinct cellular mechanisms that participate in the mitigation of the toxic activity of these saponins and in virulence on saponin-producing host plants. The enzymatic deglycosylation that we identified is...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5mh171j7</guid>
      <pubDate>Thu, 15 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>You, Yaohua</name>
      </author>
      <author>
        <name>Suraj, HM</name>
      </author>
      <author>
        <name>Matz, Linda</name>
      </author>
      <author>
        <name>Herrera Valderrama, A Lorena</name>
      </author>
      <author>
        <name>Ruigrok, Paul</name>
      </author>
      <author>
        <name>Shi-Kunne, Xiaoqian</name>
      </author>
      <author>
        <name>Pieterse, Frank PJ</name>
      </author>
      <author>
        <name>Oostlander, Anne</name>
      </author>
      <author>
        <name>Beenen, Henriek G</name>
      </author>
      <author>
        <name>Chavarro-Carrero, Edgar A</name>
      </author>
      <author>
        <name>Qin, Si</name>
      </author>
      <author>
        <name>Verstappen, Francel WA</name>
      </author>
      <author>
        <name>Kappers, Iris F</name>
      </author>
      <author>
        <name>Fleißner, André</name>
      </author>
      <author>
        <name>van Kan, Jan AL</name>
      </author>
    </item>
    <item>
      <title>Allelic variations in the chpG effector gene within Clavibacter michiganensis populations determine pathogen host range.</title>
      <link>https://escholarship.org/uc/item/73t4r95r</link>
      <description>Plant pathogenic bacteria often have a narrow host range, which can vary among different isolates within a population. Here, we investigated the host range of the tomato pathogen Clavibacter michiganensis (Cm). We determined the genome sequences of 40 tomato Cm isolates and screened them for pathogenicity on tomato and eggplant. Our screen revealed that out of the tested isolates, five were unable to cause disease on any of the hosts, 33 were exclusively pathogenic on tomato, and two were capable of infecting both tomato and eggplant. Through comparative genomic analyses, we identified that the five non-pathogenic isolates lacked the chp/tomA pathogenicity island, which has previously been associated with virulence in tomato. In addition, we found that the two eggplant-pathogenic isolates encode a unique allelic variant of the putative serine hydrolase chpG (chpGC), an effector that is recognized in eggplant. Introduction of chpGC into a chpG inactivation mutant in the eggplant-non-pathogenic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/73t4r95r</guid>
      <pubDate>Sat, 10 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Verma, Raj</name>
      </author>
      <author>
        <name>Roman-Reyna, Veronica</name>
      </author>
      <author>
        <name>Raanan, Hagai</name>
      </author>
      <author>
        <name>Coaker, Gitta</name>
      </author>
      <author>
        <name>Jacobs, Jonathan</name>
      </author>
      <author>
        <name>Teper, Doron</name>
      </author>
    </item>
    <item>
      <title>Host cell wall composition and localized microenvironment implicated in resistance to basal stem degradation by lettuce drop (Sclerotinia minor)</title>
      <link>https://escholarship.org/uc/item/6k72x6dt</link>
      <description>BackgroundSclerotinia spp. are generalist fungal pathogens, infecting over 700 plant hosts worldwide, including major crops. While host resistance is the most sustainable and cost-effective method for disease management, complete resistance to Sclerotinia diseases is rare. We recently identified soft basal stem as a potential susceptibility factor to Sclerotinia minor infection in lettuce (Lactuca sativa) under greenhouse conditions.ResultsAnalysis of stem and root cell wall composition in five L. sativa and one L. serriola accessions with varying growth habits and S. minor&amp;nbsp;resistance levels revealed strong association between hemicellulose constituents, lignin polymers, disease phenotypes, and basal stem mechanical strength. Accessions resistant to basal stem degradation consistently exhibited higher levels of syringyl, guaiacyl, and xylose, but lower levels of fucose in stems. These findings suggest that stem cell wall polymers recalcitrant to breakdown by lignocellulolytic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6k72x6dt</guid>
      <pubDate>Thu, 8 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Simko, Ivan</name>
      </author>
      <author>
        <name>Mamo, Bullo Erena</name>
        <uri>https://orcid.org/0000-0003-4778-9902</uri>
      </author>
      <author>
        <name>Foster, Clifton E</name>
      </author>
      <author>
        <name>Adhikari, Neil D</name>
      </author>
      <author>
        <name>Subbarao, Krishna V</name>
        <uri>https://orcid.org/0000-0002-2075-1835</uri>
      </author>
    </item>
    <item>
      <title>The elite haplotype OsGATA8-H coordinates nitrogen uptake and productive tiller formation in rice</title>
      <link>https://escholarship.org/uc/item/6553895p</link>
      <description>Excessive nitrogen promotes the formation of nonproductive tillers in rice, which decreases nitrogen use efficiency (NUE). Developing high-NUE rice cultivars through balancing nitrogen uptake and the formation of productive tillers remains a long-standing challenge, yet how these two processes are coordinated in rice remains elusive. Here we identify the transcription factor OsGATA8 as a key coordinator of nitrogen uptake and tiller formation in rice. OsGATA8 negatively regulates nitrogen uptake by repressing transcription of the ammonium transporter gene OsAMT3.2. Meanwhile, it promotes tiller formation by repressing the transcription of OsTCP19, a negative modulator of tillering. We identify OsGATA8-H as a high-NUE haplotype with enhanced nitrogen uptake and a higher proportion of productive tillers. The geographical distribution of OsGATA8-H and its frequency change in historical accessions suggest its adaption to the fertile soil. Overall, this study provides molecular and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6553895p</guid>
      <pubDate>Sat, 27 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wu, Wei</name>
      </author>
      <author>
        <name>Dong, Xiaoou</name>
      </author>
      <author>
        <name>Chen, Gaoming</name>
      </author>
      <author>
        <name>Lin, Zhixi</name>
      </author>
      <author>
        <name>Chi, Wenchao</name>
      </author>
      <author>
        <name>Tang, Weijie</name>
      </author>
      <author>
        <name>Yu, Jun</name>
      </author>
      <author>
        <name>Wang, Saisai</name>
      </author>
      <author>
        <name>Jiang, Xingzhou</name>
      </author>
      <author>
        <name>Liu, Xiaolan</name>
      </author>
      <author>
        <name>Wu, Yujun</name>
      </author>
      <author>
        <name>Wang, Chunyuan</name>
      </author>
      <author>
        <name>Cheng, Xinran</name>
      </author>
      <author>
        <name>Zhang, Wei</name>
      </author>
      <author>
        <name>Xuan, Wei</name>
      </author>
      <author>
        <name>Terzaghi, William</name>
      </author>
      <author>
        <name>Ronald, Pamela C</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
      <author>
        <name>Wang, Haiyang</name>
      </author>
      <author>
        <name>Wang, Chunming</name>
      </author>
      <author>
        <name>Wan, Jianmin</name>
      </author>
    </item>
    <item>
      <title>An all-out assault on a dominant resistance gene: Local emergence, establishment, and spread of strains of tomato spotted wilt orthotospovirus (TSWV) that overcome Sw-5b-mediated resistance in fresh market and processing tomatoes in California</title>
      <link>https://escholarship.org/uc/item/33w153gj</link>
      <description>Tomato spotted wilt orthotospovirus (TSWV) causes substantial economic loss to tomato production, and the Sw-5b resistance gene is widely deployed for management. Here, we show (i) the emergence of resistance-breaking (RB) TSWV strains in processing and fresh market tomato production in California over the past ten years, and (ii) evolutionary relationships with RB strains from other areas. A specific RT-PCR test was used to show the C118Y RB strain that emerged in Fresno County in 2016 quickly became predominant in the central production area and remained so through this study. In 2021, the C118Y strain was detected in the Northern production area, and was predominant in 2022. However, in 2023, the C118Y strain was unexpectedly detected in fewer spotted wilt samples from resistant varieties. This was due to emergence of the T120N RB strain, previously known to occur in Spain. A specific RT-PCR test was developed and used to show that the T120N RB strain was predominant in Colusa...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/33w153gj</guid>
      <pubDate>Wed, 24 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Macedo, Mônica A</name>
      </author>
      <author>
        <name>Melgarejo, Tomas</name>
      </author>
      <author>
        <name>Cespedes, Margaret</name>
      </author>
      <author>
        <name>Rojas, Maria</name>
      </author>
      <author>
        <name>Lazicki, Patrícia</name>
      </author>
      <author>
        <name>Turini, Thomas</name>
      </author>
      <author>
        <name>Batuman, Ozgur</name>
      </author>
      <author>
        <name>Gilbertson, Robert</name>
      </author>
    </item>
    <item>
      <title>McrD binds asymmetrically to methyl-coenzyme M reductase improving active-site accessibility during assembly</title>
      <link>https://escholarship.org/uc/item/2zc7z5t0</link>
      <description>Methyl-coenzyme M reductase (MCR) catalyzes the formation of methane, and its activity accounts for nearly all biologically produced methane released into the atmosphere. The assembly of MCR is an intricate process involving the installation of a complex set of posttranslational modifications and the unique Ni-containing tetrapyrrole called coenzyme F&lt;sub&gt;430&lt;/sub&gt;. Despite decades of research, details of MCR assembly remain largely unresolved. Here, we report the structural characterization of MCR in two intermediate states of assembly. These intermediate states lack one or both F&lt;sub&gt;430&lt;/sub&gt; cofactors and form complexes with the previously uncharacterized McrD protein. McrD is found to bind asymmetrically to MCR, displacing large regions of the alpha subunit and increasing active-site accessibility for the installation of F&lt;sub&gt;430&lt;/sub&gt;-shedding light on the assembly of MCR and the role of McrD therein. This work offers crucial information for the expression of MCR in a heterologous...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2zc7z5t0</guid>
      <pubDate>Wed, 17 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Chadwick, Grayson L</name>
      </author>
      <author>
        <name>Joiner, Aaron MN</name>
      </author>
      <author>
        <name>Ramesh, Sangeetha</name>
        <uri>https://orcid.org/0000-0002-9229-2009</uri>
      </author>
      <author>
        <name>Mitchell, Douglas A</name>
      </author>
      <author>
        <name>Nayak, Dipti D</name>
        <uri>https://orcid.org/0000-0002-8390-7251</uri>
      </author>
    </item>
    <item>
      <title>Plant Assays for Quantifying Ralstonia solanacearum Virulence.</title>
      <link>https://escholarship.org/uc/item/68f08821</link>
      <description>Virulence assays are powerful tools to study microbial pathogenesis &lt;i&gt;in vivo&lt;/i&gt;. Good assays track disease development and, coupled with targeted mutagenesis, can identify pathogen virulence factors. Disease development in plants is extremely sensitive to environmental factors such as temperature, atmospheric humidity, and soil water level, so it can be challenging to standardize conditions to achieve consistent results. Here, we present optimized and validated experimental conditions and analysis methods for nine assays that measure specific aspects of virulence in the phytopathogenic bacterium &lt;i&gt;Ralstonia solanacearum&lt;/i&gt;, using tomato as the model host plant.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/68f08821</guid>
      <pubDate>Thu, 20 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Khokhani, Devanshi</name>
      </author>
      <author>
        <name>Tran, Tuan Minh</name>
      </author>
      <author>
        <name>Lowe-Power, Tiffany M</name>
        <uri>https://orcid.org/0000-0003-2681-3563</uri>
      </author>
      <author>
        <name>Allen, Caitilyn</name>
      </author>
    </item>
    <item>
      <title>Pathogen perception and deception in plant immunity by kinase fusion proteins</title>
      <link>https://escholarship.org/uc/item/3kk1z9cw</link>
      <description>Two studies describe kinase fusion proteins (KFPs) that regulate the perception and deception of wheat pathogens. These highlight the emergence of KFPs as plant immune regulators and emphasize the importance of crop wild relatives as a reservoir for resistance breeding and global food security.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3kk1z9cw</guid>
      <pubDate>Sat, 15 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Fahima, Tzion</name>
      </author>
      <author>
        <name>Coaker, Gitta</name>
        <uri>https://orcid.org/0000-0003-0899-2449</uri>
      </author>
    </item>
    <item>
      <title>Non-wounding contact-based Inoculation of fruits with fungal pathogens in postharvest</title>
      <link>https://escholarship.org/uc/item/2ws4486k</link>
      <description>BackgroundFungal pathogens significantly impact the quality of fruits and vegetables at different stages of the supply chain, leading to substantial food losses. Understanding how these persistent fungal infections occur and progress in postharvest conditions is essential to developing effective control strategies.ResultsIn this study, we developed a reliable and consistent inoculation protocol to simulate disease spread from infected fruits to adjacent healthy fruits during postharvest storage. We tested different combinations of relevant fruit commodities, including oranges, tomatoes, and apples, against impactful postharvest pathogens such as Penicillium digitatum, Penicillium italicum, Botrytis cinerea, and Penicillium expansum. We assessed the efficacy of this protocol using fruits treated with various postharvest methods and multiple isolates for each pathogen. We optimized the source of infected tissue and incubation conditions for each fruit-pathogen combination. Disease...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2ws4486k</guid>
      <pubDate>Mon, 10 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Sbodio, Adrian O</name>
        <uri>https://orcid.org/0000-0001-5099-8460</uri>
      </author>
      <author>
        <name>Mesquida-Pesci, Saskia D</name>
      </author>
      <author>
        <name>Yip, Nancy</name>
      </author>
      <author>
        <name>Alvarez-Rojo, Isabela</name>
      </author>
      <author>
        <name>Gutierrez-Baeza, Elia</name>
      </author>
      <author>
        <name>Tay, Samantha</name>
      </author>
      <author>
        <name>Bello, Pedro</name>
      </author>
      <author>
        <name>Wang, Luxin</name>
      </author>
      <author>
        <name>Blanco-Ulate, Barbara</name>
        <uri>https://orcid.org/0000-0002-8819-9207</uri>
      </author>
    </item>
    <item>
      <title>Indirect effects of plasma-activated water irrigation on Tetranychus urticae populations</title>
      <link>https://escholarship.org/uc/item/6pk9s3rn</link>
      <description>Plasma-activated water (PAW) is receiving increased attention as a booster of seed germination and seedling vigor, and some studies have described use of PAW to manage crop pathogens. Here, we examined physicochemical properties of two PAWs (referred to as PAW 6.0 and 9.4&amp;nbsp;min with atmospheric plasma jet) and assessed “their indirect effects” (applied as supplementary irrigation) on host suitability of tomato plants (Solanum lycopersicum L.) to two-spotted spider mites (Tetranychus urticae Koch). Exposure of water to cold plasma significantly lowered pH and increased concentrations of H2O2, NO2−, and NO3−. Supplementary PAW irrigations elicited significant increases in leaf composition of several elements (N, P, K S, Ca, and Mg), leaf reflectance, plant size, and trichome densities (except non-glandular trichomes on the adaxial surface). Preference bioassays revealed significant avoidance of settling and reduced oviposition by two-spotted spider mites on leaf discs from PAW-irrigated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6pk9s3rn</guid>
      <pubDate>Wed, 5 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Savi, Patrice Jacob</name>
      </author>
      <author>
        <name>Mantri, Anil</name>
      </author>
      <author>
        <name>Khodaverdi, Haleh</name>
      </author>
      <author>
        <name>Zou, Yugeng</name>
      </author>
      <author>
        <name>de Moraes, Gilberto José</name>
      </author>
      <author>
        <name>Nansen, Christian</name>
        <uri>https://orcid.org/0000-0003-1324-1949</uri>
      </author>
    </item>
    <item>
      <title>XA21-mediated resistance to Xanthomonas oryzae pv. oryzae is dose dependent</title>
      <link>https://escholarship.org/uc/item/81w457th</link>
      <description>The rice receptor kinase XA21 confers broad-spectrum resistance to &lt;i&gt;Xanthomonas oryzae&lt;/i&gt; pv. &lt;i&gt;oryzae&lt;/i&gt; (&lt;i&gt;Xoo&lt;/i&gt;), the causal agent of rice bacterial blight disease. To investigate the relationship between the expression level of &lt;i&gt;XA21&lt;/i&gt; and resulting resistance, we generated independent &lt;i&gt;HA-XA21&lt;/i&gt; transgenic rice lines accumulating the XA21 immune receptor fused with an HA epitope tag. Whole-genome sequence analysis identified the T-DNA insertion sites in sixteen independent T0 events. Through quantification of the HA-XA21 protein and assessment of the resistance to &lt;i&gt;Xoo&lt;/i&gt; strain PXO99 in six independent transgenic lines, we observed that XA21-mediated resistance is dose dependent. In contrast, based on the four agronomic traits quantified in these experiments, yield is unlikely to be affected by the expression level of &lt;i&gt;HA-XA21&lt;/i&gt;. These findings extend our knowledge of XA21-mediated defense and contribute to the growing number of well-defined genomic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/81w457th</guid>
      <pubDate>Tue, 28 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Nan</name>
      </author>
      <author>
        <name>Dong, Xiaoou</name>
      </author>
      <author>
        <name>Jain, Rashmi</name>
      </author>
      <author>
        <name>Ruan, Deling</name>
      </author>
      <author>
        <name>de Araujo, Artur Teixeira</name>
      </author>
      <author>
        <name>Li, Yan</name>
      </author>
      <author>
        <name>Lipzen, Anna</name>
        <uri>https://orcid.org/0000-0003-2293-9329</uri>
      </author>
      <author>
        <name>Martin, Joel</name>
      </author>
      <author>
        <name>Barry, Kerrie</name>
        <uri>https://orcid.org/0000-0002-8999-6785</uri>
      </author>
      <author>
        <name>Ronald, Pamela C</name>
        <uri>https://orcid.org/0000-0002-4107-1345</uri>
      </author>
    </item>
    <item>
      <title>Functional analysis of the mating type genes in Verticillium dahliae</title>
      <link>https://escholarship.org/uc/item/9rt4s9bp</link>
      <description>BackgroundPopulations of the plant pathogenic fungus Verticillium dahliae display a complex and rich genetic diversity, yet the existence of sexual reproduction in the fungus remains contested. As pivotal genes, MAT genes play a crucial role in regulating cell differentiation, morphological development, and mating of compatible cells. However, the functions of the two mating type genes in V. dahliae, VdMAT1-1-1, and VdMAT1-2-1, remain poorly understood.ResultsIn this study, we confirmed that the MAT loci in V. dahliae are highly conserved, including both VdMAT1-1-1 and VdMAT1-2-1 which share high collinearity. The conserved core transcription factor encoded by the two MAT loci may facilitate the regulation of pheromone precursor and pheromone receptor genes by directly binding to their promoter regions. Additionally, peptide activity assays demonstrated that the signal peptide of the pheromone VdPpg1 possessed secretory activity, while VdPpg2, lacked a predicted signal peptide....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9rt4s9bp</guid>
      <pubDate>Thu, 16 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Ya-Duo</name>
      </author>
      <author>
        <name>Ji, Xiao-Bin</name>
      </author>
      <author>
        <name>Zong, Juan</name>
      </author>
      <author>
        <name>Dai, Xiao-Feng</name>
      </author>
      <author>
        <name>Klosterman, Steven J</name>
      </author>
      <author>
        <name>Subbarao, Krishna V</name>
        <uri>https://orcid.org/0000-0002-2075-1835</uri>
      </author>
      <author>
        <name>Zhang, Dan-Dan</name>
      </author>
      <author>
        <name>Chen, Jie-Yin</name>
      </author>
    </item>
    <item>
      <title>Phylogenomic analyses and comparative genomics of Pseudomonas syringae associated with almond (Prunus dulcis) in California</title>
      <link>https://escholarship.org/uc/item/0zp8x2qw</link>
      <description>We sequenced and comprehensively analysed the genomic architecture of 98 fluorescent pseudomonads isolated from different symptomatic and asymptomatic tissues of almond and a few other Prunus spp. Phylogenomic analyses, genome mining, field pathogenicity tests, and in vitro ice nucleation and antibiotic sensitivity tests were integrated to improve knowledge of the biology and management of bacterial blast and bacterial canker of almond. We identified Pseudomonas syringae pv. syringae, P. cerasi, and P. viridiflava as almond canker pathogens. P. syringae pv. syringae caused both canker and foliar (blast) symptoms. In contrast, P. cerasi and P. viridiflava only caused cankers, and P. viridiflava appeared to be a weak pathogen of almond. Isolates belonging to P. syringae pv. syringae were the most frequently isolated among the pathogenic species/pathovars, composing 75% of all pathogenic isolates. P. cerasi and P. viridiflava isolates composed 8.3 and 16.7% of the pathogenic isolates,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0zp8x2qw</guid>
      <pubDate>Wed, 1 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Maguvu, Tawanda E</name>
      </author>
      <author>
        <name>Frias, Rosa J</name>
      </author>
      <author>
        <name>Hernandez-Rosas, Alejandro I</name>
      </author>
      <author>
        <name>Holtz, Brent A</name>
      </author>
      <author>
        <name>Niederholzer, Franz JA</name>
      </author>
      <author>
        <name>Duncan, Roger A</name>
      </author>
      <author>
        <name>Yaghmour, Mohammad A</name>
      </author>
      <author>
        <name>Culumber, Catherine M</name>
      </author>
      <author>
        <name>Gordon, Phoebe E</name>
      </author>
      <author>
        <name>Vieira, Flavia CF</name>
      </author>
      <author>
        <name>Rolshausen, Philippe E</name>
      </author>
      <author>
        <name>Adaskaveg, James E</name>
        <uri>https://orcid.org/0000-0003-0076-6164</uri>
      </author>
      <author>
        <name>Burbank, Lindsey P</name>
      </author>
      <author>
        <name>Lindow, Steven E</name>
      </author>
      <author>
        <name>Trouillas, Florent P</name>
      </author>
    </item>
    <item>
      <title>Attenuation of phytofungal pathogenicity of Ascomycota by autophagy modulators</title>
      <link>https://escholarship.org/uc/item/6j7979jz</link>
      <description>Autophagy in eukaryotes functions to maintain homeostasis by degradation and recycling of long-lived and unwanted cellular materials. Autophagy plays important roles in pathogenicity of various fungal pathogens, suggesting that autophagy is a novel target for development of antifungal compounds. Here, we describe bioluminescence resonance energy transfer (BRET)-based high-throughput screening (HTS) strategy to identify compounds that inhibit fungal ATG4 cysteine protease-mediated cleavage of ATG8 that is critical for autophagosome formation. We identified ebselen (EB) and its analogs ebselen oxide (EO) and 2-(4-methylphenyl)−1,2-benzisothiazol-3(2H)-one (PT) as inhibitors of fungal pathogens Botrytis cinerea and Magnaporthe oryzae ATG4-mediated ATG8 processing. The EB and its analogs inhibit spore germination, hyphal development, and appressorium formation in Ascomycota pathogens, B. cinerea, M. oryzae, Sclerotinia sclerotiorum and Monilinia fructicola. Treatment with EB and its...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6j7979jz</guid>
      <pubDate>Mon, 15 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Woo, Jongchan</name>
      </author>
      <author>
        <name>Jung, Seungmee</name>
      </author>
      <author>
        <name>Kim, Seongbeom</name>
      </author>
      <author>
        <name>Li, Yurong</name>
      </author>
      <author>
        <name>Chung, Hyunjung</name>
      </author>
      <author>
        <name>Roubtsova, Tatiana V</name>
      </author>
      <author>
        <name>Zhang, Honghong</name>
      </author>
      <author>
        <name>Caseys, Celine</name>
        <uri>https://orcid.org/0000-0003-4187-9018</uri>
      </author>
      <author>
        <name>Kliebenstein, Dan</name>
        <uri>https://orcid.org/0000-0001-5759-3175</uri>
      </author>
      <author>
        <name>Kim, Kyung-Nam</name>
      </author>
      <author>
        <name>Bostock, Richard M</name>
        <uri>https://orcid.org/0000-0001-9928-4610</uri>
      </author>
      <author>
        <name>Lee, Yong-Hwan</name>
      </author>
      <author>
        <name>Dickman, Martin B</name>
      </author>
      <author>
        <name>Choi, Doil</name>
      </author>
      <author>
        <name>Park, Eunsook</name>
      </author>
      <author>
        <name>Dinesh-Kumar, Savithramma P</name>
      </author>
    </item>
    <item>
      <title>Epidemiology and management of Fusarium wilt of Eucalyptus camaldulensis through systemic acquired resistance</title>
      <link>https://escholarship.org/uc/item/76d3g12t</link>
      <description>&lt;i&gt;Eucalyptus camaldulensis&lt;/i&gt; is a multifunctional tree and is globally used for the reclamation of problematic lands. &lt;i&gt;Eucalyptus camaldulensis&lt;/i&gt; is prone to attack by a number of pathogens, but the most important threat is the Fusarium wilt (&lt;i&gt;Fusarium oxysporum&lt;/i&gt;). Keeping in view the importance of &lt;i&gt;E. camaldulensis&lt;/i&gt; and to manage this disease, five plant activators, &lt;i&gt;i.e&lt;/i&gt;., salicylic acid (C&lt;sub&gt;7&lt;/sub&gt;H&lt;sub&gt;6&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt;), benzoic acid (C&lt;sub&gt;7&lt;/sub&gt;H&lt;sub&gt;6&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;), citric acid (C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;8&lt;/sub&gt;O&lt;sub&gt;7&lt;/sub&gt;), dipotassium phosphate (K&lt;sub&gt;2&lt;/sub&gt;HPO&lt;sub&gt;4&lt;/sub&gt;), monopotassium phosphate (KH&lt;sub&gt;2&lt;/sub&gt;PO&lt;sub&gt;4&lt;/sub&gt;) and nutritional mixture namely Compound (NPK) and nutriotop (Fe, Zn, Cu, B, Mn) were evaluated in the Fusarium infested field under RCBD in the Research Area, Department of Forestry and Range Management, University of Agriculture, Faisalabad (UAF). Among plant activators, salicylic acid and a combination of compound...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/76d3g12t</guid>
      <pubDate>Thu, 11 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ahmad, Irfan</name>
      </author>
      <author>
        <name>Mazhar, Komal</name>
      </author>
      <author>
        <name>Atiq, Muhammad</name>
      </author>
      <author>
        <name>Khalaf, Amna Kahtan</name>
      </author>
      <author>
        <name>Rashid, Muhammad Haroon U</name>
      </author>
      <author>
        <name>Asif, Muhammad</name>
      </author>
      <author>
        <name>Ahmed, Salman</name>
      </author>
      <author>
        <name>Adil, Zoha</name>
      </author>
      <author>
        <name>Fayyaz, Amna</name>
        <uri>https://orcid.org/0000-0002-4801-2540</uri>
      </author>
      <author>
        <name>Al-Sadoon, Mohammad Khalid</name>
      </author>
      <author>
        <name>Al-Otaibi, Hamad S</name>
      </author>
    </item>
    <item>
      <title>Modeling time-varying phytoplankton subsidy reveals at-risk species in a Chilean intertidal ecosystem</title>
      <link>https://escholarship.org/uc/item/7hg208q7</link>
      <description>The allometric trophic network (ATN) framework for modeling population dynamics has provided numerous insights into ecosystem functioning in recent years. Herein we extend ATN modeling of the intertidal ecosystem off central Chile to include empirical data on pelagic chlorophyll-a concentration. This intertidal community requires subsidy of primary productivity to support its rich ecosystem. Previous work models this subsidy using a constant rate of phytoplankton input to the system. However, data shows pelagic subsidies exhibit highly variable, pulse-like behavior. The primary contribution of our work is incorporating this variable input into ATN modeling to simulate how this ecosystem may respond to pulses of pelagic phytoplankton. Our model results show that: (1) closely related sea snails respond differently to phytoplankton variability, which is explained by the underlying network structure of the food web; (2) increasing the rate of pelagic-intertidal mixing increases fluctuations...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7hg208q7</guid>
      <pubDate>Mon, 1 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Duckwall, Casey</name>
      </author>
      <author>
        <name>Largier, John L</name>
        <uri>https://orcid.org/0000-0003-4273-4443</uri>
      </author>
      <author>
        <name>Wieters, Evie A</name>
      </author>
      <author>
        <name>Valdovinos, Fernanda S</name>
      </author>
    </item>
    <item>
      <title>Candidatus Kirkpatrickella diaphorinae gen. nov., sp. nov., an uncultured endosymbiont identified in a population of Diaphorina citri from Hawaii.</title>
      <link>https://escholarship.org/uc/item/9xq6z7j8</link>
      <description>&lt;i&gt;Diaphorina citri&lt;/i&gt; is the hemipteran pest and vector of a devastating bacterial pathogen of citrus worldwide. In addition to the two core bacterial endosymbionts of &lt;i&gt;D. citri&lt;/i&gt;, &lt;i&gt;Candidatus&lt;/i&gt; Carsonella ruddii and &lt;i&gt;Candidatus&lt;/i&gt; Profftella armatura, the genome of a novel endosymbiont and as of yet undescribed microbe was discovered in a Hawaiian &lt;i&gt;D. citri&lt;/i&gt; population through deep sequencing of multiple &lt;i&gt;D. citri&lt;/i&gt; populations. Found to be closely related to the genus &lt;i&gt;Asaia&lt;/i&gt; in the family &lt;i&gt;Acetobacteraceae&lt;/i&gt; by 16S rRNA gene sequence analysis, it forms a sister clade along with other insect-associated 16S rRNA gene sequences from uncultured bacterium found associated with &lt;i&gt;Aedes koreicus&lt;/i&gt; and &lt;i&gt;Sogatella furcifera&lt;/i&gt;. Multilocus sequence analysis confirmed the phylogenetic placement sister to the &lt;i&gt;Asaia&lt;/i&gt; clade. Despite the culturable &lt;i&gt;Asaia&lt;/i&gt; clade being the closest phylogenetic neighbour, attempts to culture this newly identified...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9xq6z7j8</guid>
      <pubDate>Wed, 27 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Henry, Elizabeth</name>
      </author>
      <author>
        <name>Carlson, Curtis R</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
    </item>
    <item>
      <title>High-quality, chromosome-scale genome assemblies: comparisons of three Diaphorina citri (Asian citrus psyllid) geographic populations</title>
      <link>https://escholarship.org/uc/item/7p11g1wh</link>
      <description>The Asian citrus psyllid, Diaphorina citri, is the insect vector of the causal agent of huanglongbing (HLB), a devastating bacterial disease of commercial citrus. Presently, few genomic resources exist for D. citri. In this study, we utilized PacBio HiFi and chromatin confirmation contact (Hi-C) sequencing to sequence, assemble, and compare three high-quality, chromosome-scale genome assemblies of D. citri collected from California, Taiwan, and Uruguay. Our assemblies had final sizes of 282.67 Mb (California), 282.89 Mb (Taiwan), and 266.67 Mb (Uruguay) assembled into 13 pseudomolecules-a reduction in assembly size of 41-45% compared with previous assemblies which we validated using flow cytometry. We identified the X chromosome in D. citri and annotated each assembly for repetitive elements, protein-coding genes, transfer RNAs, ribosomal RNAs, piwi-interacting RNA clusters, and endogenous viral elements. Between 19,083 and 20,357 protein-coding genes were predicted. Repetitive...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7p11g1wh</guid>
      <pubDate>Wed, 27 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Carlson, Curtis R</name>
      </author>
      <author>
        <name>Horst, Anneliek M ter</name>
      </author>
      <author>
        <name>Johnston, J Spencer</name>
      </author>
      <author>
        <name>Henry, Elizabeth</name>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
    </item>
    <item>
      <title>Construction and use of an infectious cDNA clone to identify aphid vectors and susceptible monocot hosts of the polerovirus barley virus G</title>
      <link>https://escholarship.org/uc/item/0zc26668</link>
      <description>Since its discovery in 2016, the Polerovirus Barley virus G has been reported in at least nine countries and multiple species of monocot plants. All of these reports have used PCR and/or sequencing based assays to identify BVG, however none have investigated the biology of BVG. In this study we detail the generation of the first infectious cDNA clone of BVG from archived RNA, thereby producing a valuable experimental tool and system for studying BVG biology. Using this system we identified two compatible aphid vectors and confirmed the susceptibility of several monocot plants, and the dicotyledonous plant host Nicotiana benthamiana, to BVG.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0zc26668</guid>
      <pubDate>Wed, 27 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Erickson, Anna</name>
      </author>
      <author>
        <name>Jiang, Jun</name>
      </author>
      <author>
        <name>Kuo, Yen-Wen</name>
        <uri>https://orcid.org/0000-0003-2746-2953</uri>
      </author>
      <author>
        <name>Falk, Bryce W</name>
      </author>
    </item>
    <item>
      <title>Correction: Haegeman et al. Looking beyond Virus Detection in RNA Sequencing Data: Lessons Learned from a Community-Based Effort to Detect Cellular Plant Pathogens and Pests. Plants 2023, 12, 2139</title>
      <link>https://escholarship.org/uc/item/7s47993s</link>
      <description>In the original publication [...].</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7s47993s</guid>
      <pubDate>Sat, 23 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Haegeman, Annelies</name>
      </author>
      <author>
        <name>Foucart, Yoika</name>
      </author>
      <author>
        <name>De Jonghe, Kris</name>
      </author>
      <author>
        <name>Goedefroit, Thomas</name>
      </author>
      <author>
        <name>Al Rwahnih, Maher</name>
        <uri>https://orcid.org/0000-0003-1589-9234</uri>
      </author>
      <author>
        <name>Boonham, Neil</name>
      </author>
      <author>
        <name>Candresse, Thierry</name>
      </author>
      <author>
        <name>Gaafar, Yahya ZA</name>
      </author>
      <author>
        <name>Hurtado-Gonzales, Oscar P</name>
      </author>
      <author>
        <name>Zwitter, Zala Kogej</name>
      </author>
      <author>
        <name>Kutnjak, Denis</name>
      </author>
      <author>
        <name>Lamovšek, Janja</name>
      </author>
      <author>
        <name>Lefebvre, Marie</name>
      </author>
      <author>
        <name>Malapi, Martha</name>
      </author>
      <author>
        <name>Pleško, Irena Mavrič</name>
      </author>
      <author>
        <name>Önder, Serkan</name>
      </author>
      <author>
        <name>Reynard, Jean-Sébastien</name>
      </author>
      <author>
        <name>Pamblanco, Ferran Salavert</name>
      </author>
      <author>
        <name>Schumpp, Olivier</name>
      </author>
      <author>
        <name>Stevens, Kristian</name>
      </author>
      <author>
        <name>Pal, Chandan</name>
      </author>
      <author>
        <name>Tamisier, Lucie</name>
      </author>
      <author>
        <name>Serçe, Çiğdem Ulubaş</name>
      </author>
      <author>
        <name>van Duivenbode, Inge</name>
      </author>
      <author>
        <name>Waite, David W</name>
      </author>
      <author>
        <name>Hu, Xiaojun</name>
      </author>
      <author>
        <name>Ziebell, Heiko</name>
      </author>
      <author>
        <name>Massart, Sébastien</name>
      </author>
    </item>
    <item>
      <title>Inhibition of a conserved bacterial dual-specificity phosphatase confers plant tolerance to Candidatus Liberibacter spp</title>
      <link>https://escholarship.org/uc/item/9pj4j7cw</link>
      <description>"Candidatus Liberibacter spp." are insect-vectored, fastidious, and vascular-limited phytopathogens. They are the presumptive causal agents of potato zebra chip, tomato vein clearing, and the devastating citrus greening disease worldwide. There is an urgent need to develop new strategies to control them. In this study, we characterized a dual-specificity serine/tyrosine phosphatase (STP) that is well conserved among thirty-three geographically diverse "&lt;i&gt;Candidatus&lt;/i&gt; Liberibacter spp." and strains that infect multiple Solanaceaea and citrus spp. The STP is expressed in infected plant tissues, localized at the plant cytosol and plasma membrane, and interferes with plant cell death responses. We employed an &lt;i&gt;in silico&lt;/i&gt; target-based molecular modeling and ligand screen to identify two small molecules with high binding affinity to STP. Efficacy studies demonstrated that the two molecules can inhibit "&lt;i&gt;Candidatus&lt;/i&gt; Liberibacter spp." but not unrelated pathogens and confer...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9pj4j7cw</guid>
      <pubDate>Wed, 20 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Haoqi</name>
      </author>
      <author>
        <name>Irigoyen, Sonia</name>
      </author>
      <author>
        <name>Liu, Jiaxing</name>
      </author>
      <author>
        <name>Ramasamy, Manikandan</name>
      </author>
      <author>
        <name>Padilla, Carmen</name>
      </author>
      <author>
        <name>Bedre, Renesh</name>
      </author>
      <author>
        <name>Yang, Chuanyu</name>
      </author>
      <author>
        <name>Thapa, Shree P</name>
      </author>
      <author>
        <name>Mulgaonkar, Nirmitee</name>
      </author>
      <author>
        <name>Ancona, Veronica</name>
      </author>
      <author>
        <name>He, Ping</name>
      </author>
      <author>
        <name>Coaker, Gitta</name>
        <uri>https://orcid.org/0000-0003-0899-2449</uri>
      </author>
      <author>
        <name>Fernando, Sandun</name>
      </author>
      <author>
        <name>Mandadi, Kranthi K</name>
      </author>
    </item>
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