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Mammals show distinct functional gut microbiome dynamics to identical series of environmental stressors

The ability of the gut microbiome has been posited as an additional axis of animals’ phenotypic plasticity. However, whether and how such plasticity varies across hosts with different biological features remains unclear. We performed a captivity experiment to compare how the taxonomic, phylogenetic,...

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Autores principales: Koziol, Adam, Odriozola, Iñaki, Leonard, Aoife, Eisenhofer, Raphael, San José, Carlos, Aizpurua, Ostaizka, Alberdi, Antton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653949/
https://www.ncbi.nlm.nih.gov/pubmed/37650630
http://dx.doi.org/10.1128/mbio.01606-23
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author Koziol, Adam
Odriozola, Iñaki
Leonard, Aoife
Eisenhofer, Raphael
San José, Carlos
Aizpurua, Ostaizka
Alberdi, Antton
author_facet Koziol, Adam
Odriozola, Iñaki
Leonard, Aoife
Eisenhofer, Raphael
San José, Carlos
Aizpurua, Ostaizka
Alberdi, Antton
author_sort Koziol, Adam
collection PubMed
description The ability of the gut microbiome has been posited as an additional axis of animals’ phenotypic plasticity. However, whether and how such plasticity varies across hosts with different biological features remains unclear. We performed a captivity experiment to compare how the taxonomic, phylogenetic, and functional microbial dynamics varied across a series of temperature and dietary disturbances in two mammals: the insectivorous-specialist Crocidura russula and the omnivorous-generalist Apodemus sylvaticus. Combining genome-resolved metagenomics, metabolic pathway distillation and joint species distribution modeling, we observed that, although microbiome alpha diversity of both species remained stable, C. russula exhibited substantially higher variability and directionality of microbial responses than A. sylvaticus. Our results indicate that the intrinsic properties (e.g., diversity and functional redundancy) of microbial communities coupled with physiological attributes (e.g., thermal plasticity) of hosts shape the taxonomic, phylogenetic, and functional response of gut microbiomes to environmental stressors, which might influence their contribution to the acclimation and adaptation capacity of animal hosts. IMPORTANCE: In our manuscript, we report the first interspecific comparative study about the plasticity of the gut microbiota. We conducted a captivity experiment that exposed wild-captured mammals to a series of environmental challenges over 45 days. We characterized their gut microbial communities using genome-resolved metagenomics and modeled how the taxonomic, phylogenetic, and functional microbial dynamics varied across a series of disturbances in both species. Our results indicate that the intrinsic properties (e.g., diversity and functional redundancy) of microbial communities coupled with physiological attributes (e.g., thermal plasticity) of hosts shape the taxonomic, phylogenetic, and functional response of gut microbiomes to environmental stressors, which might influence their contribution to the acclimation and adaptation capacity of animal hosts.
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spelling pubmed-106539492023-08-31 Mammals show distinct functional gut microbiome dynamics to identical series of environmental stressors Koziol, Adam Odriozola, Iñaki Leonard, Aoife Eisenhofer, Raphael San José, Carlos Aizpurua, Ostaizka Alberdi, Antton mBio Research Article The ability of the gut microbiome has been posited as an additional axis of animals’ phenotypic plasticity. However, whether and how such plasticity varies across hosts with different biological features remains unclear. We performed a captivity experiment to compare how the taxonomic, phylogenetic, and functional microbial dynamics varied across a series of temperature and dietary disturbances in two mammals: the insectivorous-specialist Crocidura russula and the omnivorous-generalist Apodemus sylvaticus. Combining genome-resolved metagenomics, metabolic pathway distillation and joint species distribution modeling, we observed that, although microbiome alpha diversity of both species remained stable, C. russula exhibited substantially higher variability and directionality of microbial responses than A. sylvaticus. Our results indicate that the intrinsic properties (e.g., diversity and functional redundancy) of microbial communities coupled with physiological attributes (e.g., thermal plasticity) of hosts shape the taxonomic, phylogenetic, and functional response of gut microbiomes to environmental stressors, which might influence their contribution to the acclimation and adaptation capacity of animal hosts. IMPORTANCE: In our manuscript, we report the first interspecific comparative study about the plasticity of the gut microbiota. We conducted a captivity experiment that exposed wild-captured mammals to a series of environmental challenges over 45 days. We characterized their gut microbial communities using genome-resolved metagenomics and modeled how the taxonomic, phylogenetic, and functional microbial dynamics varied across a series of disturbances in both species. Our results indicate that the intrinsic properties (e.g., diversity and functional redundancy) of microbial communities coupled with physiological attributes (e.g., thermal plasticity) of hosts shape the taxonomic, phylogenetic, and functional response of gut microbiomes to environmental stressors, which might influence their contribution to the acclimation and adaptation capacity of animal hosts. American Society for Microbiology 2023-08-31 /pmc/articles/PMC10653949/ /pubmed/37650630 http://dx.doi.org/10.1128/mbio.01606-23 Text en Copyright © 2023 Koziol et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Koziol, Adam
Odriozola, Iñaki
Leonard, Aoife
Eisenhofer, Raphael
San José, Carlos
Aizpurua, Ostaizka
Alberdi, Antton
Mammals show distinct functional gut microbiome dynamics to identical series of environmental stressors
title Mammals show distinct functional gut microbiome dynamics to identical series of environmental stressors
title_full Mammals show distinct functional gut microbiome dynamics to identical series of environmental stressors
title_fullStr Mammals show distinct functional gut microbiome dynamics to identical series of environmental stressors
title_full_unstemmed Mammals show distinct functional gut microbiome dynamics to identical series of environmental stressors
title_short Mammals show distinct functional gut microbiome dynamics to identical series of environmental stressors
title_sort mammals show distinct functional gut microbiome dynamics to identical series of environmental stressors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653949/
https://www.ncbi.nlm.nih.gov/pubmed/37650630
http://dx.doi.org/10.1128/mbio.01606-23
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