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A multiproducer microbiome generates chemical diversity in the marine sponge Mycale hentscheli

Bacterial specialized metabolites are increasingly recognized as important factors in animal–microbiome interactions: for example, by providing the host with chemical defenses. Even in chemically rich animals, such compounds have been found to originate from individual members of more diverse microb...

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Autores principales: Rust, Michael, Helfrich, Eric J. N., Freeman, Michael F., Nanudorn, Pakjira, Field, Christopher M., Rückert, Christian, Kündig, Tomas, Page, Michael J., Webb, Victoria L., Kalinowski, Jörn, Sunagawa, Shinichi, Piel, Jörn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196800/
https://www.ncbi.nlm.nih.gov/pubmed/32291345
http://dx.doi.org/10.1073/pnas.1919245117
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author Rust, Michael
Helfrich, Eric J. N.
Freeman, Michael F.
Nanudorn, Pakjira
Field, Christopher M.
Rückert, Christian
Kündig, Tomas
Page, Michael J.
Webb, Victoria L.
Kalinowski, Jörn
Sunagawa, Shinichi
Piel, Jörn
author_facet Rust, Michael
Helfrich, Eric J. N.
Freeman, Michael F.
Nanudorn, Pakjira
Field, Christopher M.
Rückert, Christian
Kündig, Tomas
Page, Michael J.
Webb, Victoria L.
Kalinowski, Jörn
Sunagawa, Shinichi
Piel, Jörn
author_sort Rust, Michael
collection PubMed
description Bacterial specialized metabolites are increasingly recognized as important factors in animal–microbiome interactions: for example, by providing the host with chemical defenses. Even in chemically rich animals, such compounds have been found to originate from individual members of more diverse microbiomes. Here, we identified a remarkable case of a moderately complex microbiome in the sponge host Mycale hentscheli in which multiple symbionts jointly generate chemical diversity. In addition to bacterial pathways for three distinct polyketide families comprising microtubule-inhibiting peloruside drug candidates, mycalamide-type contact poisons, and the eukaryotic translation-inhibiting pateamines, we identified extensive biosynthetic potential distributed among a broad phylogenetic range of bacteria. Biochemical data on one of the orphan pathways suggest a previously unknown member of the rare polytheonamide-type cytotoxin family as its product. Other than supporting a scenario of cooperative symbiosis based on bacterial metabolites, the data provide a rationale for the chemical variability of M. hentscheli and could pave the way toward biotechnological peloruside production. Most bacterial lineages in the compositionally unusual sponge microbiome were not known to synthesize bioactive metabolites, supporting the concept that microbial dark matter harbors diverse producer taxa with as yet unrecognized drug discovery potential.
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spelling pubmed-71968002020-05-06 A multiproducer microbiome generates chemical diversity in the marine sponge Mycale hentscheli Rust, Michael Helfrich, Eric J. N. Freeman, Michael F. Nanudorn, Pakjira Field, Christopher M. Rückert, Christian Kündig, Tomas Page, Michael J. Webb, Victoria L. Kalinowski, Jörn Sunagawa, Shinichi Piel, Jörn Proc Natl Acad Sci U S A Biological Sciences Bacterial specialized metabolites are increasingly recognized as important factors in animal–microbiome interactions: for example, by providing the host with chemical defenses. Even in chemically rich animals, such compounds have been found to originate from individual members of more diverse microbiomes. Here, we identified a remarkable case of a moderately complex microbiome in the sponge host Mycale hentscheli in which multiple symbionts jointly generate chemical diversity. In addition to bacterial pathways for three distinct polyketide families comprising microtubule-inhibiting peloruside drug candidates, mycalamide-type contact poisons, and the eukaryotic translation-inhibiting pateamines, we identified extensive biosynthetic potential distributed among a broad phylogenetic range of bacteria. Biochemical data on one of the orphan pathways suggest a previously unknown member of the rare polytheonamide-type cytotoxin family as its product. Other than supporting a scenario of cooperative symbiosis based on bacterial metabolites, the data provide a rationale for the chemical variability of M. hentscheli and could pave the way toward biotechnological peloruside production. Most bacterial lineages in the compositionally unusual sponge microbiome were not known to synthesize bioactive metabolites, supporting the concept that microbial dark matter harbors diverse producer taxa with as yet unrecognized drug discovery potential. National Academy of Sciences 2020-04-28 2020-04-14 /pmc/articles/PMC7196800/ /pubmed/32291345 http://dx.doi.org/10.1073/pnas.1919245117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Rust, Michael
Helfrich, Eric J. N.
Freeman, Michael F.
Nanudorn, Pakjira
Field, Christopher M.
Rückert, Christian
Kündig, Tomas
Page, Michael J.
Webb, Victoria L.
Kalinowski, Jörn
Sunagawa, Shinichi
Piel, Jörn
A multiproducer microbiome generates chemical diversity in the marine sponge Mycale hentscheli
title A multiproducer microbiome generates chemical diversity in the marine sponge Mycale hentscheli
title_full A multiproducer microbiome generates chemical diversity in the marine sponge Mycale hentscheli
title_fullStr A multiproducer microbiome generates chemical diversity in the marine sponge Mycale hentscheli
title_full_unstemmed A multiproducer microbiome generates chemical diversity in the marine sponge Mycale hentscheli
title_short A multiproducer microbiome generates chemical diversity in the marine sponge Mycale hentscheli
title_sort multiproducer microbiome generates chemical diversity in the marine sponge mycale hentscheli
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196800/
https://www.ncbi.nlm.nih.gov/pubmed/32291345
http://dx.doi.org/10.1073/pnas.1919245117
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