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Butyrate Production Pathway Abundances Are Similar in Human and Nonhuman Primate Gut Microbiomes

Over the course of human evolution, shifts in dietary practices such as meat-eating and cooking, have resulted in reduced fiber intake, a trend that has been exaggerated more recently in industrialized populations. Reduced fiber consumption is associated with a loss of gut microbial taxa that degrad...

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Autores principales: Mallott, Elizabeth K, Amato, Katherine R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763029/
https://www.ncbi.nlm.nih.gov/pubmed/34542625
http://dx.doi.org/10.1093/molbev/msab279
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author Mallott, Elizabeth K
Amato, Katherine R
author_facet Mallott, Elizabeth K
Amato, Katherine R
author_sort Mallott, Elizabeth K
collection PubMed
description Over the course of human evolution, shifts in dietary practices such as meat-eating and cooking, have resulted in reduced fiber intake, a trend that has been exaggerated more recently in industrialized populations. Reduced fiber consumption is associated with a loss of gut microbial taxa that degrade fiber, particularly butyrate. Therefore, this dietary shift in humans may have altered the abundance of microbial genes involved in butyrate production. This study uses a gene-targeted alignment approach to quantify the abundance of butyrate production pathway genes from published wild nonhuman primate and human gut metagenomes. Surprisingly, humans have higher diversity and relative abundances of butyrate production pathways compared with all groups of nonhuman primates except cercopithecoids. Industrialized populations of humans also differ only slightly in butyrate pathway abundance from nonindustrialized populations. This apparent resilience of butyrate production pathways to shifts in human diet across both evolutionary and modern populations may signal an evolutionary shift in host–microbe interactions in humans that increased SCFA production. Such a shift could have contributed to meeting the increased energy requirements of humans relative to nonhuman primates.
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spelling pubmed-87630292022-01-19 Butyrate Production Pathway Abundances Are Similar in Human and Nonhuman Primate Gut Microbiomes Mallott, Elizabeth K Amato, Katherine R Mol Biol Evol Discoveries Over the course of human evolution, shifts in dietary practices such as meat-eating and cooking, have resulted in reduced fiber intake, a trend that has been exaggerated more recently in industrialized populations. Reduced fiber consumption is associated with a loss of gut microbial taxa that degrade fiber, particularly butyrate. Therefore, this dietary shift in humans may have altered the abundance of microbial genes involved in butyrate production. This study uses a gene-targeted alignment approach to quantify the abundance of butyrate production pathway genes from published wild nonhuman primate and human gut metagenomes. Surprisingly, humans have higher diversity and relative abundances of butyrate production pathways compared with all groups of nonhuman primates except cercopithecoids. Industrialized populations of humans also differ only slightly in butyrate pathway abundance from nonindustrialized populations. This apparent resilience of butyrate production pathways to shifts in human diet across both evolutionary and modern populations may signal an evolutionary shift in host–microbe interactions in humans that increased SCFA production. Such a shift could have contributed to meeting the increased energy requirements of humans relative to nonhuman primates. Oxford University Press 2021-09-20 /pmc/articles/PMC8763029/ /pubmed/34542625 http://dx.doi.org/10.1093/molbev/msab279 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Mallott, Elizabeth K
Amato, Katherine R
Butyrate Production Pathway Abundances Are Similar in Human and Nonhuman Primate Gut Microbiomes
title Butyrate Production Pathway Abundances Are Similar in Human and Nonhuman Primate Gut Microbiomes
title_full Butyrate Production Pathway Abundances Are Similar in Human and Nonhuman Primate Gut Microbiomes
title_fullStr Butyrate Production Pathway Abundances Are Similar in Human and Nonhuman Primate Gut Microbiomes
title_full_unstemmed Butyrate Production Pathway Abundances Are Similar in Human and Nonhuman Primate Gut Microbiomes
title_short Butyrate Production Pathway Abundances Are Similar in Human and Nonhuman Primate Gut Microbiomes
title_sort butyrate production pathway abundances are similar in human and nonhuman primate gut microbiomes
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763029/
https://www.ncbi.nlm.nih.gov/pubmed/34542625
http://dx.doi.org/10.1093/molbev/msab279
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