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Phylogenetic signal in gut microbial community rather than in rodent metabolic traits

Host phylogeny and environment have all been implicated in shaping the gut microbiota and host metabolic traits of mammals. However, few studies have evaluated phylogeny-associated microbial assembly and host metabolic plasticity concurrently, and their relationships on both short-term and evolution...

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Autores principales: Zhang, Xue-Ying, Khakisahneh, Saeid, Liu, Wei, Zhang, Xinyi, Zhai, Weiwei, Cheng, Jilong, Speakman, John R, Wang, De-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625476/
https://www.ncbi.nlm.nih.gov/pubmed/37928774
http://dx.doi.org/10.1093/nsr/nwad209
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author Zhang, Xue-Ying
Khakisahneh, Saeid
Liu, Wei
Zhang, Xinyi
Zhai, Weiwei
Cheng, Jilong
Speakman, John R
Wang, De-Hua
author_facet Zhang, Xue-Ying
Khakisahneh, Saeid
Liu, Wei
Zhang, Xinyi
Zhai, Weiwei
Cheng, Jilong
Speakman, John R
Wang, De-Hua
author_sort Zhang, Xue-Ying
collection PubMed
description Host phylogeny and environment have all been implicated in shaping the gut microbiota and host metabolic traits of mammals. However, few studies have evaluated phylogeny-associated microbial assembly and host metabolic plasticity concurrently, and their relationships on both short-term and evolutionary timescales. We report that the branching order of a gut microbial dendrogram was nearly congruent with phylogenetic relationships of seven rodent species, and this pattern of phylosymbiosis was intact after diverse laboratory manipulations. Laboratory rearing, diet or air temperature (T(a)) acclimation induced alterations in gut microbial communities, but could not override host phylogeny in shaping microbial community assembly. A simulative heatwave reduced core microbiota diversity by 26% in these species, and led to an unmatched relationship between the microbiota and host metabolic phenotypes in desert species. Moreover, the similarity of metabolic traits across species at different Tas was not correlated with phylogenetic distance. These data demonstrated that the gut microbial assembly showed strong concordance with host phylogeny and may be shaped by environmental variables, whereas host metabolic traits did not seem to be linked with phylogeny.
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spelling pubmed-106254762023-11-05 Phylogenetic signal in gut microbial community rather than in rodent metabolic traits Zhang, Xue-Ying Khakisahneh, Saeid Liu, Wei Zhang, Xinyi Zhai, Weiwei Cheng, Jilong Speakman, John R Wang, De-Hua Natl Sci Rev Research Article Host phylogeny and environment have all been implicated in shaping the gut microbiota and host metabolic traits of mammals. However, few studies have evaluated phylogeny-associated microbial assembly and host metabolic plasticity concurrently, and their relationships on both short-term and evolutionary timescales. We report that the branching order of a gut microbial dendrogram was nearly congruent with phylogenetic relationships of seven rodent species, and this pattern of phylosymbiosis was intact after diverse laboratory manipulations. Laboratory rearing, diet or air temperature (T(a)) acclimation induced alterations in gut microbial communities, but could not override host phylogeny in shaping microbial community assembly. A simulative heatwave reduced core microbiota diversity by 26% in these species, and led to an unmatched relationship between the microbiota and host metabolic phenotypes in desert species. Moreover, the similarity of metabolic traits across species at different Tas was not correlated with phylogenetic distance. These data demonstrated that the gut microbial assembly showed strong concordance with host phylogeny and may be shaped by environmental variables, whereas host metabolic traits did not seem to be linked with phylogeny. Oxford University Press 2023-07-28 /pmc/articles/PMC10625476/ /pubmed/37928774 http://dx.doi.org/10.1093/nsr/nwad209 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Xue-Ying
Khakisahneh, Saeid
Liu, Wei
Zhang, Xinyi
Zhai, Weiwei
Cheng, Jilong
Speakman, John R
Wang, De-Hua
Phylogenetic signal in gut microbial community rather than in rodent metabolic traits
title Phylogenetic signal in gut microbial community rather than in rodent metabolic traits
title_full Phylogenetic signal in gut microbial community rather than in rodent metabolic traits
title_fullStr Phylogenetic signal in gut microbial community rather than in rodent metabolic traits
title_full_unstemmed Phylogenetic signal in gut microbial community rather than in rodent metabolic traits
title_short Phylogenetic signal in gut microbial community rather than in rodent metabolic traits
title_sort phylogenetic signal in gut microbial community rather than in rodent metabolic traits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625476/
https://www.ncbi.nlm.nih.gov/pubmed/37928774
http://dx.doi.org/10.1093/nsr/nwad209
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