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Terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric Malagasy mammals
The gut microbiomes of mammals appear to mirror their hosts’ phylogeny, suggesting host-driven microbial community assembly. Yet, much of this evidence stems from comparative studies of distinct wild or captive populations that lack data for disentangling the relative influences of shared phylogeny...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299109/ https://www.ncbi.nlm.nih.gov/pubmed/30108305 http://dx.doi.org/10.1038/s41396-018-0251-5 |
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author | Perofsky, Amanda C. Lewis, Rebecca J. Meyers, Lauren Ancel |
author_facet | Perofsky, Amanda C. Lewis, Rebecca J. Meyers, Lauren Ancel |
author_sort | Perofsky, Amanda C. |
collection | PubMed |
description | The gut microbiomes of mammals appear to mirror their hosts’ phylogeny, suggesting host-driven microbial community assembly. Yet, much of this evidence stems from comparative studies of distinct wild or captive populations that lack data for disentangling the relative influences of shared phylogeny and environment. Here, we present phylogenetic and multivariate analyses of gut microbiomes from six sympatric (i.e., co-occurring) mammal species inhabiting a 1-km(2) area in western Madagascar—three lemur and three non-primate species—that consider genetic, dietary, and ecological predictors of microbiome functionality and composition. Host evolutionary history, indeed, appears to shape gut microbial patterns among both closely and distantly related species. However, we also find that diet—reliance on leaves versus fruit—is the best predictor of microbiome similarity among closely related lemur species, and that host substrate use—ground versus tree—constrains horizontal transmission via incidental contact with feces, with arboreal species harboring far more distinct communities than those of their terrestrial and semi-terrestrial counterparts. |
format | Online Article Text |
id | pubmed-6299109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62991092018-12-19 Terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric Malagasy mammals Perofsky, Amanda C. Lewis, Rebecca J. Meyers, Lauren Ancel ISME J Article The gut microbiomes of mammals appear to mirror their hosts’ phylogeny, suggesting host-driven microbial community assembly. Yet, much of this evidence stems from comparative studies of distinct wild or captive populations that lack data for disentangling the relative influences of shared phylogeny and environment. Here, we present phylogenetic and multivariate analyses of gut microbiomes from six sympatric (i.e., co-occurring) mammal species inhabiting a 1-km(2) area in western Madagascar—three lemur and three non-primate species—that consider genetic, dietary, and ecological predictors of microbiome functionality and composition. Host evolutionary history, indeed, appears to shape gut microbial patterns among both closely and distantly related species. However, we also find that diet—reliance on leaves versus fruit—is the best predictor of microbiome similarity among closely related lemur species, and that host substrate use—ground versus tree—constrains horizontal transmission via incidental contact with feces, with arboreal species harboring far more distinct communities than those of their terrestrial and semi-terrestrial counterparts. Nature Publishing Group UK 2018-08-14 2019-01 /pmc/articles/PMC6299109/ /pubmed/30108305 http://dx.doi.org/10.1038/s41396-018-0251-5 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Perofsky, Amanda C. Lewis, Rebecca J. Meyers, Lauren Ancel Terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric Malagasy mammals |
title | Terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric Malagasy mammals |
title_full | Terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric Malagasy mammals |
title_fullStr | Terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric Malagasy mammals |
title_full_unstemmed | Terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric Malagasy mammals |
title_short | Terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric Malagasy mammals |
title_sort | terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric malagasy mammals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299109/ https://www.ncbi.nlm.nih.gov/pubmed/30108305 http://dx.doi.org/10.1038/s41396-018-0251-5 |
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