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Metagenomic binning of a marine sponge microbiome reveals unity in defense but metabolic specialization
Marine sponges are ancient metazoans that are populated by distinct and highly diverse microbial communities. In order to obtain deeper insights into the functional gene repertoire of the Mediterranean sponge Aplysina aerophoba, we combined Illumina short-read and PacBio long-read sequencing followe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649159/ https://www.ncbi.nlm.nih.gov/pubmed/28696422 http://dx.doi.org/10.1038/ismej.2017.101 |
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author | Slaby, Beate M Hackl, Thomas Horn, Hannes Bayer, Kristina Hentschel, Ute |
author_facet | Slaby, Beate M Hackl, Thomas Horn, Hannes Bayer, Kristina Hentschel, Ute |
author_sort | Slaby, Beate M |
collection | PubMed |
description | Marine sponges are ancient metazoans that are populated by distinct and highly diverse microbial communities. In order to obtain deeper insights into the functional gene repertoire of the Mediterranean sponge Aplysina aerophoba, we combined Illumina short-read and PacBio long-read sequencing followed by un-targeted metagenomic binning. We identified a total of 37 high-quality bins representing 11 bacterial phyla and two candidate phyla. Statistical comparison of symbiont genomes with selected reference genomes revealed a significant enrichment of genes related to bacterial defense (restriction-modification systems, toxin-antitoxin systems) as well as genes involved in host colonization and extracellular matrix utilization in sponge symbionts. A within-symbionts genome comparison revealed a nutritional specialization of at least two symbiont guilds, where one appears to metabolize carnitine and the other sulfated polysaccharides, both of which are abundant molecules in the sponge extracellular matrix. A third guild of symbionts may be viewed as nutritional generalists that perform largely the same metabolic pathways but lack such extraordinary numbers of the relevant genes. This study characterizes the genomic repertoire of sponge symbionts at an unprecedented resolution and it provides greater insights into the molecular mechanisms underlying microbial-sponge symbiosis. |
format | Online Article Text |
id | pubmed-5649159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-56491592017-11-01 Metagenomic binning of a marine sponge microbiome reveals unity in defense but metabolic specialization Slaby, Beate M Hackl, Thomas Horn, Hannes Bayer, Kristina Hentschel, Ute ISME J Original Article Marine sponges are ancient metazoans that are populated by distinct and highly diverse microbial communities. In order to obtain deeper insights into the functional gene repertoire of the Mediterranean sponge Aplysina aerophoba, we combined Illumina short-read and PacBio long-read sequencing followed by un-targeted metagenomic binning. We identified a total of 37 high-quality bins representing 11 bacterial phyla and two candidate phyla. Statistical comparison of symbiont genomes with selected reference genomes revealed a significant enrichment of genes related to bacterial defense (restriction-modification systems, toxin-antitoxin systems) as well as genes involved in host colonization and extracellular matrix utilization in sponge symbionts. A within-symbionts genome comparison revealed a nutritional specialization of at least two symbiont guilds, where one appears to metabolize carnitine and the other sulfated polysaccharides, both of which are abundant molecules in the sponge extracellular matrix. A third guild of symbionts may be viewed as nutritional generalists that perform largely the same metabolic pathways but lack such extraordinary numbers of the relevant genes. This study characterizes the genomic repertoire of sponge symbionts at an unprecedented resolution and it provides greater insights into the molecular mechanisms underlying microbial-sponge symbiosis. Nature Publishing Group 2017-11 2017-07-11 /pmc/articles/PMC5649159/ /pubmed/28696422 http://dx.doi.org/10.1038/ismej.2017.101 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Slaby, Beate M Hackl, Thomas Horn, Hannes Bayer, Kristina Hentschel, Ute Metagenomic binning of a marine sponge microbiome reveals unity in defense but metabolic specialization |
title | Metagenomic binning of a marine sponge microbiome reveals unity in defense but metabolic specialization |
title_full | Metagenomic binning of a marine sponge microbiome reveals unity in defense but metabolic specialization |
title_fullStr | Metagenomic binning of a marine sponge microbiome reveals unity in defense but metabolic specialization |
title_full_unstemmed | Metagenomic binning of a marine sponge microbiome reveals unity in defense but metabolic specialization |
title_short | Metagenomic binning of a marine sponge microbiome reveals unity in defense but metabolic specialization |
title_sort | metagenomic binning of a marine sponge microbiome reveals unity in defense but metabolic specialization |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649159/ https://www.ncbi.nlm.nih.gov/pubmed/28696422 http://dx.doi.org/10.1038/ismej.2017.101 |
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