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Immunogenetic variation shapes the gut microbiome in a natural vertebrate population

BACKGROUND: The gut microbiome (GM) can influence many biological processes in the host, impacting its health and survival, but the GM can also be influenced by the host’s traits. In vertebrates, Major Histocompatibility Complex (MHC) genes play a pivotal role in combatting pathogens and are thought...

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Autores principales: Davies, Charli S., Worsley, Sarah F., Maher, Kathryn H., Komdeur, Jan, Burke, Terry, Dugdale, Hannah L., Richardson, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903650/
https://www.ncbi.nlm.nih.gov/pubmed/35256003
http://dx.doi.org/10.1186/s40168-022-01233-y
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author Davies, Charli S.
Worsley, Sarah F.
Maher, Kathryn H.
Komdeur, Jan
Burke, Terry
Dugdale, Hannah L.
Richardson, David S.
author_facet Davies, Charli S.
Worsley, Sarah F.
Maher, Kathryn H.
Komdeur, Jan
Burke, Terry
Dugdale, Hannah L.
Richardson, David S.
author_sort Davies, Charli S.
collection PubMed
description BACKGROUND: The gut microbiome (GM) can influence many biological processes in the host, impacting its health and survival, but the GM can also be influenced by the host’s traits. In vertebrates, Major Histocompatibility Complex (MHC) genes play a pivotal role in combatting pathogens and are thought to shape the host’s GM. Despite this—and the documented importance of both GM and MHC variation to individual fitness—few studies have investigated the association between the GM and MHC in the wild. RESULTS: We characterised MHC class I (MHC-I), MHC class II (MHC-II) and GM variation in individuals within a natural population of the Seychelles warbler (Acrocephalus sechellensis). We determined how the diversity and composition of the GM varied with MHC characteristics, in addition to environmental factors and other host traits. Our results show that the presence of specific MHC alleles, but not MHC diversity, influences both the diversity and composition of the GM in this population. MHC-I alleles, rather than MHC-II alleles, had the greatest impact on the GM. GM diversity was negatively associated with the presence of three MHC-I alleles (Ase-ua3, Ase-ua4, Ase-ua5), and one MHC-II allele (Ase-dab4), while changes in GM composition were associated with the presence of four different MHC-I alleles (Ase-ua1, Ase-ua7, Ase-ua10, Ase-ua11). There were no associations between GM diversity and TLR3 genotype, but GM diversity was positively correlated with genome-wide heterozygosity and varied with host age and field period. CONCLUSIONS: These results suggest that components of the host’s immune system play a role in shaping the GM of wild animals. Host genotype—specifically MHC-I and to a lesser degree MHC-II variation—can modulate the GM, although whether this occurs directly, or indirectly through effects on host health, is unclear. Importantly, if immune genes can regulate host health through modulation of the microbiome, then it is plausible that the microbiome could also influence selection on immune genes. As such, host–microbiome coevolution may play a role in maintaining functional immunogenetic variation within natural vertebrate populations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01233-y.
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spelling pubmed-89036502022-03-18 Immunogenetic variation shapes the gut microbiome in a natural vertebrate population Davies, Charli S. Worsley, Sarah F. Maher, Kathryn H. Komdeur, Jan Burke, Terry Dugdale, Hannah L. Richardson, David S. Microbiome Research BACKGROUND: The gut microbiome (GM) can influence many biological processes in the host, impacting its health and survival, but the GM can also be influenced by the host’s traits. In vertebrates, Major Histocompatibility Complex (MHC) genes play a pivotal role in combatting pathogens and are thought to shape the host’s GM. Despite this—and the documented importance of both GM and MHC variation to individual fitness—few studies have investigated the association between the GM and MHC in the wild. RESULTS: We characterised MHC class I (MHC-I), MHC class II (MHC-II) and GM variation in individuals within a natural population of the Seychelles warbler (Acrocephalus sechellensis). We determined how the diversity and composition of the GM varied with MHC characteristics, in addition to environmental factors and other host traits. Our results show that the presence of specific MHC alleles, but not MHC diversity, influences both the diversity and composition of the GM in this population. MHC-I alleles, rather than MHC-II alleles, had the greatest impact on the GM. GM diversity was negatively associated with the presence of three MHC-I alleles (Ase-ua3, Ase-ua4, Ase-ua5), and one MHC-II allele (Ase-dab4), while changes in GM composition were associated with the presence of four different MHC-I alleles (Ase-ua1, Ase-ua7, Ase-ua10, Ase-ua11). There were no associations between GM diversity and TLR3 genotype, but GM diversity was positively correlated with genome-wide heterozygosity and varied with host age and field period. CONCLUSIONS: These results suggest that components of the host’s immune system play a role in shaping the GM of wild animals. Host genotype—specifically MHC-I and to a lesser degree MHC-II variation—can modulate the GM, although whether this occurs directly, or indirectly through effects on host health, is unclear. Importantly, if immune genes can regulate host health through modulation of the microbiome, then it is plausible that the microbiome could also influence selection on immune genes. As such, host–microbiome coevolution may play a role in maintaining functional immunogenetic variation within natural vertebrate populations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01233-y. BioMed Central 2022-03-08 /pmc/articles/PMC8903650/ /pubmed/35256003 http://dx.doi.org/10.1186/s40168-022-01233-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Davies, Charli S.
Worsley, Sarah F.
Maher, Kathryn H.
Komdeur, Jan
Burke, Terry
Dugdale, Hannah L.
Richardson, David S.
Immunogenetic variation shapes the gut microbiome in a natural vertebrate population
title Immunogenetic variation shapes the gut microbiome in a natural vertebrate population
title_full Immunogenetic variation shapes the gut microbiome in a natural vertebrate population
title_fullStr Immunogenetic variation shapes the gut microbiome in a natural vertebrate population
title_full_unstemmed Immunogenetic variation shapes the gut microbiome in a natural vertebrate population
title_short Immunogenetic variation shapes the gut microbiome in a natural vertebrate population
title_sort immunogenetic variation shapes the gut microbiome in a natural vertebrate population
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903650/
https://www.ncbi.nlm.nih.gov/pubmed/35256003
http://dx.doi.org/10.1186/s40168-022-01233-y
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