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The East Asian gut microbiome is distinct from colocalized White subjects and connected to metabolic health

East Asians (EAs) experience worse metabolic health outcomes compared to other ethnic groups at lower body mass indices; however, the potential role of the gut microbiota in contributing to these health disparities remains unknown. We conducted a multi-omic study of 46 lean and obese East Asian and...

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Autores principales: Ang, Qi Yan, Alba, Diana L, Upadhyay, Vaibhav, Bisanz, Jordan E, Cai, Jingwei, Lee, Ho Lim, Barajas, Eliseo, Wei, Grace, Noecker, Cecilia, Patterson, Andrew D, Koliwad, Suneil K, Turnbaugh, Peter J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612731/
https://www.ncbi.nlm.nih.gov/pubmed/34617511
http://dx.doi.org/10.7554/eLife.70349
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author Ang, Qi Yan
Alba, Diana L
Upadhyay, Vaibhav
Bisanz, Jordan E
Cai, Jingwei
Lee, Ho Lim
Barajas, Eliseo
Wei, Grace
Noecker, Cecilia
Patterson, Andrew D
Koliwad, Suneil K
Turnbaugh, Peter J
author_facet Ang, Qi Yan
Alba, Diana L
Upadhyay, Vaibhav
Bisanz, Jordan E
Cai, Jingwei
Lee, Ho Lim
Barajas, Eliseo
Wei, Grace
Noecker, Cecilia
Patterson, Andrew D
Koliwad, Suneil K
Turnbaugh, Peter J
author_sort Ang, Qi Yan
collection PubMed
description East Asians (EAs) experience worse metabolic health outcomes compared to other ethnic groups at lower body mass indices; however, the potential role of the gut microbiota in contributing to these health disparities remains unknown. We conducted a multi-omic study of 46 lean and obese East Asian and White participants living in the San Francisco Bay Area, revealing marked differences between ethnic groups in bacterial richness and community structure. White individuals were enriched for the mucin-degrading Akkermansia muciniphila. East Asian subjects had increased levels of multiple bacterial phyla, fermentative pathways detected by metagenomics, and the short-chain fatty acid end-products acetate, propionate, and isobutyrate. Differences in the gut microbiota between the East Asian and White subjects could not be explained by dietary intake, were more pronounced in lean individuals, and were associated with current geographical location. Microbiome transplantations into germ-free mice demonstrated stable diet- and host genotype-independent differences between the gut microbiotas of East Asian and White individuals that differentially impact host body composition. Taken together, our findings add to the growing body of literature describing microbiome variations between ethnicities and provide a starting point for defining the mechanisms through which the microbiome may shape disparate health outcomes in East Asians.
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spelling pubmed-86127312021-11-26 The East Asian gut microbiome is distinct from colocalized White subjects and connected to metabolic health Ang, Qi Yan Alba, Diana L Upadhyay, Vaibhav Bisanz, Jordan E Cai, Jingwei Lee, Ho Lim Barajas, Eliseo Wei, Grace Noecker, Cecilia Patterson, Andrew D Koliwad, Suneil K Turnbaugh, Peter J eLife Microbiology and Infectious Disease East Asians (EAs) experience worse metabolic health outcomes compared to other ethnic groups at lower body mass indices; however, the potential role of the gut microbiota in contributing to these health disparities remains unknown. We conducted a multi-omic study of 46 lean and obese East Asian and White participants living in the San Francisco Bay Area, revealing marked differences between ethnic groups in bacterial richness and community structure. White individuals were enriched for the mucin-degrading Akkermansia muciniphila. East Asian subjects had increased levels of multiple bacterial phyla, fermentative pathways detected by metagenomics, and the short-chain fatty acid end-products acetate, propionate, and isobutyrate. Differences in the gut microbiota between the East Asian and White subjects could not be explained by dietary intake, were more pronounced in lean individuals, and were associated with current geographical location. Microbiome transplantations into germ-free mice demonstrated stable diet- and host genotype-independent differences between the gut microbiotas of East Asian and White individuals that differentially impact host body composition. Taken together, our findings add to the growing body of literature describing microbiome variations between ethnicities and provide a starting point for defining the mechanisms through which the microbiome may shape disparate health outcomes in East Asians. eLife Sciences Publications, Ltd 2021-10-07 /pmc/articles/PMC8612731/ /pubmed/34617511 http://dx.doi.org/10.7554/eLife.70349 Text en © 2021, Ang et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Microbiology and Infectious Disease
Ang, Qi Yan
Alba, Diana L
Upadhyay, Vaibhav
Bisanz, Jordan E
Cai, Jingwei
Lee, Ho Lim
Barajas, Eliseo
Wei, Grace
Noecker, Cecilia
Patterson, Andrew D
Koliwad, Suneil K
Turnbaugh, Peter J
The East Asian gut microbiome is distinct from colocalized White subjects and connected to metabolic health
title The East Asian gut microbiome is distinct from colocalized White subjects and connected to metabolic health
title_full The East Asian gut microbiome is distinct from colocalized White subjects and connected to metabolic health
title_fullStr The East Asian gut microbiome is distinct from colocalized White subjects and connected to metabolic health
title_full_unstemmed The East Asian gut microbiome is distinct from colocalized White subjects and connected to metabolic health
title_short The East Asian gut microbiome is distinct from colocalized White subjects and connected to metabolic health
title_sort east asian gut microbiome is distinct from colocalized white subjects and connected to metabolic health
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612731/
https://www.ncbi.nlm.nih.gov/pubmed/34617511
http://dx.doi.org/10.7554/eLife.70349
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