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Individual diet has sex-dependent effects on vertebrate gut microbiota
Vertebrates harbour diverse communities of symbiotic gut microbes. Host diet is known to alter microbiota composition, implying that dietary treatments might alleviate diseases arising from altered microbial composition (‘dysbiosis’). However, it remains unclear whether diet effects are general or d...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279269/ https://www.ncbi.nlm.nih.gov/pubmed/25072318 http://dx.doi.org/10.1038/ncomms5500 |
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author | Bolnick, Daniel I. Snowberg, Lisa K. Hirsch, Philipp E. Lauber, Christian L. Org, Elin Parks, Brian Lusis, Aldons J. Knight, Rob Caporaso, J. Gregory Svanbäck, Richard |
author_facet | Bolnick, Daniel I. Snowberg, Lisa K. Hirsch, Philipp E. Lauber, Christian L. Org, Elin Parks, Brian Lusis, Aldons J. Knight, Rob Caporaso, J. Gregory Svanbäck, Richard |
author_sort | Bolnick, Daniel I. |
collection | PubMed |
description | Vertebrates harbour diverse communities of symbiotic gut microbes. Host diet is known to alter microbiota composition, implying that dietary treatments might alleviate diseases arising from altered microbial composition (‘dysbiosis’). However, it remains unclear whether diet effects are general or depend on host genotype. Here we show that gut microbiota composition depends on interactions between host diet and sex within populations of wild and laboratory fish, laboratory mice and humans. Within each of two natural fish populations (threespine stickleback and Eurasian perch), among-individual diet variation is correlated with individual differences in gut microbiota. However, these diet–microbiota associations are sex dependent. We document similar sex-specific diet–microbiota correlations in humans. Experimental diet manipulations in laboratory stickleback and mice confirmed that diet affects microbiota differently in males versus females. The prevalence of such genotype by environment (sex by diet) interactions implies that therapies to treat dysbiosis might have sex-specific effects. |
format | Online Article Text |
id | pubmed-4279269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42792692015-01-09 Individual diet has sex-dependent effects on vertebrate gut microbiota Bolnick, Daniel I. Snowberg, Lisa K. Hirsch, Philipp E. Lauber, Christian L. Org, Elin Parks, Brian Lusis, Aldons J. Knight, Rob Caporaso, J. Gregory Svanbäck, Richard Nat Commun Article Vertebrates harbour diverse communities of symbiotic gut microbes. Host diet is known to alter microbiota composition, implying that dietary treatments might alleviate diseases arising from altered microbial composition (‘dysbiosis’). However, it remains unclear whether diet effects are general or depend on host genotype. Here we show that gut microbiota composition depends on interactions between host diet and sex within populations of wild and laboratory fish, laboratory mice and humans. Within each of two natural fish populations (threespine stickleback and Eurasian perch), among-individual diet variation is correlated with individual differences in gut microbiota. However, these diet–microbiota associations are sex dependent. We document similar sex-specific diet–microbiota correlations in humans. Experimental diet manipulations in laboratory stickleback and mice confirmed that diet affects microbiota differently in males versus females. The prevalence of such genotype by environment (sex by diet) interactions implies that therapies to treat dysbiosis might have sex-specific effects. Nature Pub. Group 2014-07-29 /pmc/articles/PMC4279269/ /pubmed/25072318 http://dx.doi.org/10.1038/ncomms5500 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 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-nc-sa/4.0/ |
spellingShingle | Article Bolnick, Daniel I. Snowberg, Lisa K. Hirsch, Philipp E. Lauber, Christian L. Org, Elin Parks, Brian Lusis, Aldons J. Knight, Rob Caporaso, J. Gregory Svanbäck, Richard Individual diet has sex-dependent effects on vertebrate gut microbiota |
title | Individual diet has sex-dependent effects on vertebrate gut microbiota |
title_full | Individual diet has sex-dependent effects on vertebrate gut microbiota |
title_fullStr | Individual diet has sex-dependent effects on vertebrate gut microbiota |
title_full_unstemmed | Individual diet has sex-dependent effects on vertebrate gut microbiota |
title_short | Individual diet has sex-dependent effects on vertebrate gut microbiota |
title_sort | individual diet has sex-dependent effects on vertebrate gut microbiota |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4279269/ https://www.ncbi.nlm.nih.gov/pubmed/25072318 http://dx.doi.org/10.1038/ncomms5500 |
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