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Social networks predict gut microbiome composition in wild baboons

Social relationships have profound effects on health in humans and other primates, but the mechanisms that explain this relationship are not well understood. Using shotgun metagenomic data from wild baboons, we found that social group membership and social network relationships predicted both the ta...

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Autores principales: Tung, Jenny, Barreiro, Luis B, Burns, Michael B, Grenier, Jean-Christophe, Lynch, Josh, Grieneisen, Laura E, Altmann, Jeanne, Alberts, Susan C, Blekhman, Ran, Archie, Elizabeth A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379495/
https://www.ncbi.nlm.nih.gov/pubmed/25774601
http://dx.doi.org/10.7554/eLife.05224
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author Tung, Jenny
Barreiro, Luis B
Burns, Michael B
Grenier, Jean-Christophe
Lynch, Josh
Grieneisen, Laura E
Altmann, Jeanne
Alberts, Susan C
Blekhman, Ran
Archie, Elizabeth A
author_facet Tung, Jenny
Barreiro, Luis B
Burns, Michael B
Grenier, Jean-Christophe
Lynch, Josh
Grieneisen, Laura E
Altmann, Jeanne
Alberts, Susan C
Blekhman, Ran
Archie, Elizabeth A
author_sort Tung, Jenny
collection PubMed
description Social relationships have profound effects on health in humans and other primates, but the mechanisms that explain this relationship are not well understood. Using shotgun metagenomic data from wild baboons, we found that social group membership and social network relationships predicted both the taxonomic structure of the gut microbiome and the structure of genes encoded by gut microbial species. Rates of interaction directly explained variation in the gut microbiome, even after controlling for diet, kinship, and shared environments. They therefore strongly implicate direct physical contact among social partners in the transmission of gut microbial species. We identified 51 socially structured taxa, which were significantly enriched for anaerobic and non-spore-forming lifestyles. Our results argue that social interactions are an important determinant of gut microbiome composition in natural animal populations—a relationship with important ramifications for understanding how social relationships influence health, as well as the evolution of group living. DOI: http://dx.doi.org/10.7554/eLife.05224.001
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spelling pubmed-43794952015-04-02 Social networks predict gut microbiome composition in wild baboons Tung, Jenny Barreiro, Luis B Burns, Michael B Grenier, Jean-Christophe Lynch, Josh Grieneisen, Laura E Altmann, Jeanne Alberts, Susan C Blekhman, Ran Archie, Elizabeth A eLife Ecology Social relationships have profound effects on health in humans and other primates, but the mechanisms that explain this relationship are not well understood. Using shotgun metagenomic data from wild baboons, we found that social group membership and social network relationships predicted both the taxonomic structure of the gut microbiome and the structure of genes encoded by gut microbial species. Rates of interaction directly explained variation in the gut microbiome, even after controlling for diet, kinship, and shared environments. They therefore strongly implicate direct physical contact among social partners in the transmission of gut microbial species. We identified 51 socially structured taxa, which were significantly enriched for anaerobic and non-spore-forming lifestyles. Our results argue that social interactions are an important determinant of gut microbiome composition in natural animal populations—a relationship with important ramifications for understanding how social relationships influence health, as well as the evolution of group living. DOI: http://dx.doi.org/10.7554/eLife.05224.001 eLife Sciences Publications, Ltd 2015-03-16 /pmc/articles/PMC4379495/ /pubmed/25774601 http://dx.doi.org/10.7554/eLife.05224 Text en © 2015, Tung et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Ecology
Tung, Jenny
Barreiro, Luis B
Burns, Michael B
Grenier, Jean-Christophe
Lynch, Josh
Grieneisen, Laura E
Altmann, Jeanne
Alberts, Susan C
Blekhman, Ran
Archie, Elizabeth A
Social networks predict gut microbiome composition in wild baboons
title Social networks predict gut microbiome composition in wild baboons
title_full Social networks predict gut microbiome composition in wild baboons
title_fullStr Social networks predict gut microbiome composition in wild baboons
title_full_unstemmed Social networks predict gut microbiome composition in wild baboons
title_short Social networks predict gut microbiome composition in wild baboons
title_sort social networks predict gut microbiome composition in wild baboons
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379495/
https://www.ncbi.nlm.nih.gov/pubmed/25774601
http://dx.doi.org/10.7554/eLife.05224
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