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Convergence of human and Old World monkey gut microbiomes demonstrates the importance of human ecology over phylogeny

BACKGROUND: Comparative data from non-human primates provide insight into the processes that shaped the evolution of the human gut microbiome and highlight microbiome traits that differentiate humans from other primates. Here, in an effort to improve our understanding of the human microbiome, we com...

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Autores principales: Amato, Katherine R., Mallott, Elizabeth K., McDonald, Daniel, Dominy, Nathaniel J., Goldberg, Tony, Lambert, Joanna E., Swedell, Larissa, Metcalf, Jessica L., Gomez, Andres, Britton, Gillian A. O., Stumpf, Rebecca M., Leigh, Steven R., Knight, Rob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781418/
https://www.ncbi.nlm.nih.gov/pubmed/31590679
http://dx.doi.org/10.1186/s13059-019-1807-z
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author Amato, Katherine R.
Mallott, Elizabeth K.
McDonald, Daniel
Dominy, Nathaniel J.
Goldberg, Tony
Lambert, Joanna E.
Swedell, Larissa
Metcalf, Jessica L.
Gomez, Andres
Britton, Gillian A. O.
Stumpf, Rebecca M.
Leigh, Steven R.
Knight, Rob
author_facet Amato, Katherine R.
Mallott, Elizabeth K.
McDonald, Daniel
Dominy, Nathaniel J.
Goldberg, Tony
Lambert, Joanna E.
Swedell, Larissa
Metcalf, Jessica L.
Gomez, Andres
Britton, Gillian A. O.
Stumpf, Rebecca M.
Leigh, Steven R.
Knight, Rob
author_sort Amato, Katherine R.
collection PubMed
description BACKGROUND: Comparative data from non-human primates provide insight into the processes that shaped the evolution of the human gut microbiome and highlight microbiome traits that differentiate humans from other primates. Here, in an effort to improve our understanding of the human microbiome, we compare gut microbiome composition and functional potential in 14 populations of humans from ten nations and 18 species of wild, non-human primates. RESULTS: Contrary to expectations from host phylogenetics, we find that human gut microbiome composition and functional potential are more similar to those of cercopithecines, a subfamily of Old World monkey, particularly baboons, than to those of African apes. Additionally, our data reveal more inter-individual variation in gut microbiome functional potential within the human species than across other primate species, suggesting that the human gut microbiome may exhibit more plasticity in response to environmental variation compared to that of other primates. CONCLUSIONS: Given similarities of ancestral human habitats and dietary strategies to those of baboons, these findings suggest that convergent ecologies shaped the gut microbiomes of both humans and cercopithecines, perhaps through environmental exposure to microbes, diet, and/or associated physiological adaptations. Increased inter-individual variation in the human microbiome may be associated with human dietary diversity or the ability of humans to inhabit novel environments. Overall, these findings show that diet, ecology, and physiological adaptations are more important than host-microbe co-diversification in shaping the human microbiome, providing a key foundation for comparative analyses of the role of the microbiome in human biology and health. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1807-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-67814182019-10-17 Convergence of human and Old World monkey gut microbiomes demonstrates the importance of human ecology over phylogeny Amato, Katherine R. Mallott, Elizabeth K. McDonald, Daniel Dominy, Nathaniel J. Goldberg, Tony Lambert, Joanna E. Swedell, Larissa Metcalf, Jessica L. Gomez, Andres Britton, Gillian A. O. Stumpf, Rebecca M. Leigh, Steven R. Knight, Rob Genome Biol Research BACKGROUND: Comparative data from non-human primates provide insight into the processes that shaped the evolution of the human gut microbiome and highlight microbiome traits that differentiate humans from other primates. Here, in an effort to improve our understanding of the human microbiome, we compare gut microbiome composition and functional potential in 14 populations of humans from ten nations and 18 species of wild, non-human primates. RESULTS: Contrary to expectations from host phylogenetics, we find that human gut microbiome composition and functional potential are more similar to those of cercopithecines, a subfamily of Old World monkey, particularly baboons, than to those of African apes. Additionally, our data reveal more inter-individual variation in gut microbiome functional potential within the human species than across other primate species, suggesting that the human gut microbiome may exhibit more plasticity in response to environmental variation compared to that of other primates. CONCLUSIONS: Given similarities of ancestral human habitats and dietary strategies to those of baboons, these findings suggest that convergent ecologies shaped the gut microbiomes of both humans and cercopithecines, perhaps through environmental exposure to microbes, diet, and/or associated physiological adaptations. Increased inter-individual variation in the human microbiome may be associated with human dietary diversity or the ability of humans to inhabit novel environments. Overall, these findings show that diet, ecology, and physiological adaptations are more important than host-microbe co-diversification in shaping the human microbiome, providing a key foundation for comparative analyses of the role of the microbiome in human biology and health. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-019-1807-z) contains supplementary material, which is available to authorized users. BioMed Central 2019-10-08 /pmc/articles/PMC6781418/ /pubmed/31590679 http://dx.doi.org/10.1186/s13059-019-1807-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Amato, Katherine R.
Mallott, Elizabeth K.
McDonald, Daniel
Dominy, Nathaniel J.
Goldberg, Tony
Lambert, Joanna E.
Swedell, Larissa
Metcalf, Jessica L.
Gomez, Andres
Britton, Gillian A. O.
Stumpf, Rebecca M.
Leigh, Steven R.
Knight, Rob
Convergence of human and Old World monkey gut microbiomes demonstrates the importance of human ecology over phylogeny
title Convergence of human and Old World monkey gut microbiomes demonstrates the importance of human ecology over phylogeny
title_full Convergence of human and Old World monkey gut microbiomes demonstrates the importance of human ecology over phylogeny
title_fullStr Convergence of human and Old World monkey gut microbiomes demonstrates the importance of human ecology over phylogeny
title_full_unstemmed Convergence of human and Old World monkey gut microbiomes demonstrates the importance of human ecology over phylogeny
title_short Convergence of human and Old World monkey gut microbiomes demonstrates the importance of human ecology over phylogeny
title_sort convergence of human and old world monkey gut microbiomes demonstrates the importance of human ecology over phylogeny
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781418/
https://www.ncbi.nlm.nih.gov/pubmed/31590679
http://dx.doi.org/10.1186/s13059-019-1807-z
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