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Microbial environment shapes immune function and cloacal microbiota dynamics in zebra finches Taeniopygia guttata

BACKGROUND: The relevance of the host microbiota to host ecology and evolution is well acknowledged. However, the effect of the microbial environment on host immune function and host microbiota dynamics is understudied in terrestrial vertebrates. Using a novel experimental approach centered on the m...

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Autores principales: van Veelen, H. Pieter J., Falcão Salles, Joana, Matson, Kevin D., van der Velde, Marco, Tieleman, B. Irene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807698/
https://www.ncbi.nlm.nih.gov/pubmed/33499970
http://dx.doi.org/10.1186/s42523-020-00039-3
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author van Veelen, H. Pieter J.
Falcão Salles, Joana
Matson, Kevin D.
van der Velde, Marco
Tieleman, B. Irene
author_facet van Veelen, H. Pieter J.
Falcão Salles, Joana
Matson, Kevin D.
van der Velde, Marco
Tieleman, B. Irene
author_sort van Veelen, H. Pieter J.
collection PubMed
description BACKGROUND: The relevance of the host microbiota to host ecology and evolution is well acknowledged. However, the effect of the microbial environment on host immune function and host microbiota dynamics is understudied in terrestrial vertebrates. Using a novel experimental approach centered on the manipulation of the microbial environment of zebra finches Taeniopygia guttata, we carried out a study to investigate effects of the host’s microbial environment on: 1) constitutive immune function, 2) the resilience of the host cloacal microbiota; and 3) the degree to which immune function and host microbiota covary in microbial environments that differ in diversity. RESULTS: We explored immune indices (hemagglutination, hemolysis, IgY levels and haptoglobin concentration) and host-associated microbiota (diversity and composition) in birds exposed to two experimental microbial environments differing in microbial diversity. According to our expectations, exposure to experimental microbial environments led to differences related to specific antibodies: IgY levels were elevated in the high diversity treatment, whereas we found no effects for the other immune indices. Furthermore, according to predictions, we found significantly increased richness of dominant OTUs for cloacal microbiota of birds of the high diversity compared with the low diversity group. In addition, cloacal microbiota of individual females approached their baseline state sooner in the low diversity environment than females in the high diversity environment. This result supported a direct phenotypically plastic response of host microbiota, and suggests that its resilience depends on environmental microbial diversity. Finally, immune indices and cloacal microbiota composition tend to covary within treatment groups, while at the same time, individuals exhibited consistent differences of immune indices and microbiota characteristics. CONCLUSION: We show that microbes in the surroundings of terrestrial vertebrates can influence immune function and host-associated microbiota dynamics over relatively short time scales. We suggest that covariation between immune indices and cloacal microbiota, in addition to large and consistent differences among individuals, provides potential for evolutionary adaptation. Ultimately, our study highlights that linking environmental and host microbiotas may help unravelling immunological variation within and potentially among species, and together these efforts will advance the integration of microbial ecology and ecological immunology.
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spelling pubmed-78076982021-01-19 Microbial environment shapes immune function and cloacal microbiota dynamics in zebra finches Taeniopygia guttata van Veelen, H. Pieter J. Falcão Salles, Joana Matson, Kevin D. van der Velde, Marco Tieleman, B. Irene Anim Microbiome Research Article BACKGROUND: The relevance of the host microbiota to host ecology and evolution is well acknowledged. However, the effect of the microbial environment on host immune function and host microbiota dynamics is understudied in terrestrial vertebrates. Using a novel experimental approach centered on the manipulation of the microbial environment of zebra finches Taeniopygia guttata, we carried out a study to investigate effects of the host’s microbial environment on: 1) constitutive immune function, 2) the resilience of the host cloacal microbiota; and 3) the degree to which immune function and host microbiota covary in microbial environments that differ in diversity. RESULTS: We explored immune indices (hemagglutination, hemolysis, IgY levels and haptoglobin concentration) and host-associated microbiota (diversity and composition) in birds exposed to two experimental microbial environments differing in microbial diversity. According to our expectations, exposure to experimental microbial environments led to differences related to specific antibodies: IgY levels were elevated in the high diversity treatment, whereas we found no effects for the other immune indices. Furthermore, according to predictions, we found significantly increased richness of dominant OTUs for cloacal microbiota of birds of the high diversity compared with the low diversity group. In addition, cloacal microbiota of individual females approached their baseline state sooner in the low diversity environment than females in the high diversity environment. This result supported a direct phenotypically plastic response of host microbiota, and suggests that its resilience depends on environmental microbial diversity. Finally, immune indices and cloacal microbiota composition tend to covary within treatment groups, while at the same time, individuals exhibited consistent differences of immune indices and microbiota characteristics. CONCLUSION: We show that microbes in the surroundings of terrestrial vertebrates can influence immune function and host-associated microbiota dynamics over relatively short time scales. We suggest that covariation between immune indices and cloacal microbiota, in addition to large and consistent differences among individuals, provides potential for evolutionary adaptation. Ultimately, our study highlights that linking environmental and host microbiotas may help unravelling immunological variation within and potentially among species, and together these efforts will advance the integration of microbial ecology and ecological immunology. BioMed Central 2020-06-03 /pmc/articles/PMC7807698/ /pubmed/33499970 http://dx.doi.org/10.1186/s42523-020-00039-3 Text en © The Author(s) 2020 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/.
spellingShingle Research Article
van Veelen, H. Pieter J.
Falcão Salles, Joana
Matson, Kevin D.
van der Velde, Marco
Tieleman, B. Irene
Microbial environment shapes immune function and cloacal microbiota dynamics in zebra finches Taeniopygia guttata
title Microbial environment shapes immune function and cloacal microbiota dynamics in zebra finches Taeniopygia guttata
title_full Microbial environment shapes immune function and cloacal microbiota dynamics in zebra finches Taeniopygia guttata
title_fullStr Microbial environment shapes immune function and cloacal microbiota dynamics in zebra finches Taeniopygia guttata
title_full_unstemmed Microbial environment shapes immune function and cloacal microbiota dynamics in zebra finches Taeniopygia guttata
title_short Microbial environment shapes immune function and cloacal microbiota dynamics in zebra finches Taeniopygia guttata
title_sort microbial environment shapes immune function and cloacal microbiota dynamics in zebra finches taeniopygia guttata
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807698/
https://www.ncbi.nlm.nih.gov/pubmed/33499970
http://dx.doi.org/10.1186/s42523-020-00039-3
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