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Mammalian gut metabolomes mirror microbiome composition and host phylogeny

In the past decade, studies on the mammalian gut microbiome have revealed that different animal species have distinct gut microbial compositions. The functional ramifications of this variation in microbial composition remain unclear: do these taxonomic differences indicate microbial adaptations to h...

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Autores principales: Gregor, Rachel, Probst, Maraike, Eyal, Stav, Aksenov, Alexander, Sasson, Goor, Horovitz, Igal, Dorrestein, Pieter C., Meijler, Michael M., Mizrahi, Itzhak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038745/
https://www.ncbi.nlm.nih.gov/pubmed/34903850
http://dx.doi.org/10.1038/s41396-021-01152-0
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author Gregor, Rachel
Probst, Maraike
Eyal, Stav
Aksenov, Alexander
Sasson, Goor
Horovitz, Igal
Dorrestein, Pieter C.
Meijler, Michael M.
Mizrahi, Itzhak
author_facet Gregor, Rachel
Probst, Maraike
Eyal, Stav
Aksenov, Alexander
Sasson, Goor
Horovitz, Igal
Dorrestein, Pieter C.
Meijler, Michael M.
Mizrahi, Itzhak
author_sort Gregor, Rachel
collection PubMed
description In the past decade, studies on the mammalian gut microbiome have revealed that different animal species have distinct gut microbial compositions. The functional ramifications of this variation in microbial composition remain unclear: do these taxonomic differences indicate microbial adaptations to host-specific functionality, or are these diverse microbial communities essentially functionally redundant, as has been indicated by previous metagenomics studies? Here, we examine the metabolic content of mammalian gut microbiomes as a direct window into ecosystem function, using an untargeted metabolomics platform to analyze 101 fecal samples from a range of 25 exotic mammalian species in collaboration with a zoological center. We find that mammalian metabolomes are chemically diverse and strongly linked to microbiome composition, and that metabolome composition is further correlated to the phylogeny of the mammalian host. Specific metabolites enriched in different animal species included modified and degraded host and dietary compounds such as bile acids and triterpenoids, as well as fermentation products such as lactate and short-chain fatty acids. Our results suggest that differences in microbial taxonomic composition are indeed translated to host-specific metabolism, indicating that taxonomically distant microbiomes are more functionally diverse than redundant.
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spelling pubmed-90387452022-04-28 Mammalian gut metabolomes mirror microbiome composition and host phylogeny Gregor, Rachel Probst, Maraike Eyal, Stav Aksenov, Alexander Sasson, Goor Horovitz, Igal Dorrestein, Pieter C. Meijler, Michael M. Mizrahi, Itzhak ISME J Article In the past decade, studies on the mammalian gut microbiome have revealed that different animal species have distinct gut microbial compositions. The functional ramifications of this variation in microbial composition remain unclear: do these taxonomic differences indicate microbial adaptations to host-specific functionality, or are these diverse microbial communities essentially functionally redundant, as has been indicated by previous metagenomics studies? Here, we examine the metabolic content of mammalian gut microbiomes as a direct window into ecosystem function, using an untargeted metabolomics platform to analyze 101 fecal samples from a range of 25 exotic mammalian species in collaboration with a zoological center. We find that mammalian metabolomes are chemically diverse and strongly linked to microbiome composition, and that metabolome composition is further correlated to the phylogeny of the mammalian host. Specific metabolites enriched in different animal species included modified and degraded host and dietary compounds such as bile acids and triterpenoids, as well as fermentation products such as lactate and short-chain fatty acids. Our results suggest that differences in microbial taxonomic composition are indeed translated to host-specific metabolism, indicating that taxonomically distant microbiomes are more functionally diverse than redundant. Nature Publishing Group UK 2021-12-13 2022-05 /pmc/articles/PMC9038745/ /pubmed/34903850 http://dx.doi.org/10.1038/s41396-021-01152-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gregor, Rachel
Probst, Maraike
Eyal, Stav
Aksenov, Alexander
Sasson, Goor
Horovitz, Igal
Dorrestein, Pieter C.
Meijler, Michael M.
Mizrahi, Itzhak
Mammalian gut metabolomes mirror microbiome composition and host phylogeny
title Mammalian gut metabolomes mirror microbiome composition and host phylogeny
title_full Mammalian gut metabolomes mirror microbiome composition and host phylogeny
title_fullStr Mammalian gut metabolomes mirror microbiome composition and host phylogeny
title_full_unstemmed Mammalian gut metabolomes mirror microbiome composition and host phylogeny
title_short Mammalian gut metabolomes mirror microbiome composition and host phylogeny
title_sort mammalian gut metabolomes mirror microbiome composition and host phylogeny
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038745/
https://www.ncbi.nlm.nih.gov/pubmed/34903850
http://dx.doi.org/10.1038/s41396-021-01152-0
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