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Metagenomic Exploration of the Marine Sponge Mycale hentscheli Uncovers Multiple Polyketide-Producing Bacterial Symbionts

Marine sponges have been a prolific source of unique bioactive compounds that are presumed to act as a deterrent to predation. Many of these compounds have potential therapeutic applications; however, the lack of efficient and sustainable synthetic routes frequently limits clinical development. Here...

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Autores principales: Storey, Mathew A., Andreassend, Sarah K., Bracegirdle, Joe, Brown, Alistair, Keyzers, Robert A., Ackerley, David F., Northcote, Peter T., Owen, Jeremy G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157528/
https://www.ncbi.nlm.nih.gov/pubmed/32209692
http://dx.doi.org/10.1128/mBio.02997-19
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author Storey, Mathew A.
Andreassend, Sarah K.
Bracegirdle, Joe
Brown, Alistair
Keyzers, Robert A.
Ackerley, David F.
Northcote, Peter T.
Owen, Jeremy G.
author_facet Storey, Mathew A.
Andreassend, Sarah K.
Bracegirdle, Joe
Brown, Alistair
Keyzers, Robert A.
Ackerley, David F.
Northcote, Peter T.
Owen, Jeremy G.
author_sort Storey, Mathew A.
collection PubMed
description Marine sponges have been a prolific source of unique bioactive compounds that are presumed to act as a deterrent to predation. Many of these compounds have potential therapeutic applications; however, the lack of efficient and sustainable synthetic routes frequently limits clinical development. Here, we describe a metagenomic investigation of Mycale hentscheli, a chemically gifted marine sponge that possesses multiple distinct chemotypes. We applied shotgun metagenomic sequencing, hybrid assembly of short- and long-read data, and metagenomic binning to obtain a comprehensive picture of the microbiome of five specimens, spanning three chemotypes. Our data revealed multiple producing species, each having relatively modest secondary metabolomes, that contribute collectively to the chemical arsenal of the holobiont. We assembled complete genomes for multiple new genera, including two species that produce the cytotoxic polyketides pateamine and mycalamide, as well as a third high-abundance symbiont harboring a proteusin-type biosynthetic pathway that appears to encode a new polytheonamide-like compound. We also identified an additional 188 biosynthetic gene clusters, including a pathway for biosynthesis of peloruside. These results suggest that multiple species cooperatively contribute to defensive symbiosis in M. hentscheli and reveal that the taxonomic diversity of secondary-metabolite-producing sponge symbionts is larger and richer than previously recognized.
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spelling pubmed-71575282020-04-15 Metagenomic Exploration of the Marine Sponge Mycale hentscheli Uncovers Multiple Polyketide-Producing Bacterial Symbionts Storey, Mathew A. Andreassend, Sarah K. Bracegirdle, Joe Brown, Alistair Keyzers, Robert A. Ackerley, David F. Northcote, Peter T. Owen, Jeremy G. mBio Research Article Marine sponges have been a prolific source of unique bioactive compounds that are presumed to act as a deterrent to predation. Many of these compounds have potential therapeutic applications; however, the lack of efficient and sustainable synthetic routes frequently limits clinical development. Here, we describe a metagenomic investigation of Mycale hentscheli, a chemically gifted marine sponge that possesses multiple distinct chemotypes. We applied shotgun metagenomic sequencing, hybrid assembly of short- and long-read data, and metagenomic binning to obtain a comprehensive picture of the microbiome of five specimens, spanning three chemotypes. Our data revealed multiple producing species, each having relatively modest secondary metabolomes, that contribute collectively to the chemical arsenal of the holobiont. We assembled complete genomes for multiple new genera, including two species that produce the cytotoxic polyketides pateamine and mycalamide, as well as a third high-abundance symbiont harboring a proteusin-type biosynthetic pathway that appears to encode a new polytheonamide-like compound. We also identified an additional 188 biosynthetic gene clusters, including a pathway for biosynthesis of peloruside. These results suggest that multiple species cooperatively contribute to defensive symbiosis in M. hentscheli and reveal that the taxonomic diversity of secondary-metabolite-producing sponge symbionts is larger and richer than previously recognized. American Society for Microbiology 2020-03-24 /pmc/articles/PMC7157528/ /pubmed/32209692 http://dx.doi.org/10.1128/mBio.02997-19 Text en Copyright © 2020 Storey et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Storey, Mathew A.
Andreassend, Sarah K.
Bracegirdle, Joe
Brown, Alistair
Keyzers, Robert A.
Ackerley, David F.
Northcote, Peter T.
Owen, Jeremy G.
Metagenomic Exploration of the Marine Sponge Mycale hentscheli Uncovers Multiple Polyketide-Producing Bacterial Symbionts
title Metagenomic Exploration of the Marine Sponge Mycale hentscheli Uncovers Multiple Polyketide-Producing Bacterial Symbionts
title_full Metagenomic Exploration of the Marine Sponge Mycale hentscheli Uncovers Multiple Polyketide-Producing Bacterial Symbionts
title_fullStr Metagenomic Exploration of the Marine Sponge Mycale hentscheli Uncovers Multiple Polyketide-Producing Bacterial Symbionts
title_full_unstemmed Metagenomic Exploration of the Marine Sponge Mycale hentscheli Uncovers Multiple Polyketide-Producing Bacterial Symbionts
title_short Metagenomic Exploration of the Marine Sponge Mycale hentscheli Uncovers Multiple Polyketide-Producing Bacterial Symbionts
title_sort metagenomic exploration of the marine sponge mycale hentscheli uncovers multiple polyketide-producing bacterial symbionts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157528/
https://www.ncbi.nlm.nih.gov/pubmed/32209692
http://dx.doi.org/10.1128/mBio.02997-19
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