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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...

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Autores principales: Perofsky, Amanda C., Lewis, Rebecca J., Meyers, Lauren Ancel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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