- Džunková, Mária;
- La Clair, James J;
- Tyml, Tomáš;
- Doud, Devin;
- Schulz, Frederik;
- Piquer-Esteban, Samuel;
- Porcel Sanchis, Dafne;
- Osborn, Andrew;
- Robinson, David;
- Louie, Katherine B;
- Bowen, Ben P;
- Bowers, Robert M;
- Lee, Janey;
- Arnau, Vicente;
- Díaz-Villanueva, Wladimiro;
- Stepanauskas, Ramunas;
- Gosliner, Terrence;
- Date, Shailesh V;
- Northen, Trent R;
- Cheng, Jan-Fang;
- Burkart, Michael D;
- Woyke, Tanja
Background
Nudibranchs comprise a group of > 6000 marine soft-bodied mollusk species known to use secondary metabolites (natural products) for chemical defense. The full diversity of these metabolites and whether symbiotic microbes are responsible for their synthesis remains unexplored. Another issue in searching for undiscovered natural products is that computational analysis of genomes of uncultured microbes can result in detection of novel biosynthetic gene clusters; however, their in vivo functionality is not guaranteed which limits further exploration of their pharmaceutical or industrial potential. To overcome these challenges, we used a fluorescent pantetheine probe, which produces a fluorescent CoA-analog employed in biosynthesis of secondary metabolites, to label and capture bacterial symbionts actively producing these compounds in the mantle of the nudibranch Doriopsilla fulva.Results
We recovered the genome of Candidatus Doriopsillibacter californiensis from the Ca. Tethybacterales order, an uncultured lineage of sponge symbionts not found in nudibranchs previously. It forms part of the core skin microbiome of D. fulva and is nearly absent in its internal organs. We showed that crude extracts of D. fulva contained secondary metabolites that were consistent with the presence of a beta-lactone encoded in Ca. D. californiensis genome. Beta-lactones represent an underexplored group of secondary metabolites with pharmaceutical potential that have not been reported in nudibranchs previously.Conclusions
Altogether, this study shows how probe-based, targeted sorting approaches can capture bacterial symbionts producing secondary metabolites in vivo. Video Abstract.