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Hyperactive nanobacteria with host-dependent traits pervade Omnitrophota
- Seymour, Cale O;
- Palmer, Marike;
- Becraft, Eric D;
- Stepanauskas, Ramunas;
- Friel, Ariel D;
- Schulz, Frederik;
- Woyke, Tanja;
- Eloe-Fadrosh, Emiley;
- Lai, Dengxun;
- Jiao, Jian-Yu;
- Hua, Zheng-Shuang;
- Liu, Lan;
- Lian, Zheng-Han;
- Li, Wen-Jun;
- Chuvochina, Maria;
- Finley, Brianna K;
- Koch, Benjamin J;
- Schwartz, Egbert;
- Dijkstra, Paul;
- Moser, Duane P;
- Hungate, Bruce A;
- Hedlund, Brian P
- et al.
Published Web Location
https://doi.org/10.1038/s41564-022-01319-1Abstract
Candidate bacterial phylum Omnitrophota has not been isolated and is poorly understood. We analysed 72 newly sequenced and 349 existing Omnitrophota genomes representing 6 classes and 276 species, along with Earth Microbiome Project data to evaluate habitat, metabolic traits and lifestyles. We applied fluorescence-activated cell sorting and differential size filtration, and showed that most Omnitrophota are ultra-small (~0.2 μm) cells that are found in water, sediments and soils. Omnitrophota genomes in 6 classes are reduced, but maintain major biosynthetic and energy conservation pathways, including acetogenesis (with or without the Wood-Ljungdahl pathway) and diverse respirations. At least 64% of Omnitrophota genomes encode gene clusters typical of bacterial symbionts, suggesting host-associated lifestyles. We repurposed quantitative stable-isotope probing data from soils dominated by andesite, basalt or granite weathering and identified 3 families with high isotope uptake consistent with obligate bacterial predators. We propose that most Omnitrophota inhabit various ecosystems as predators or parasites.
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