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Caecal microbiota composition of experimental inbred MHC-B lines infected with IBV differs according to genetics and vaccination

Interactions between the gut microbiota and the immune system may be involved in vaccine and infection responses. In the present study, we studied the interactions between caecal microbiota composition and parameters describing the immune response in six experimental inbred chicken lines harboring d...

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Autores principales: Borey, Marion, Bed’Hom, Bertrand, Bruneau, Nicolas, Estellé, Jordi, Larsen, Frederik, Blanc, Fany, der Laan, Marie-Hélène Pinard-van, Dalgaard, Tina, Calenge, Fanny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9199466/
https://www.ncbi.nlm.nih.gov/pubmed/35705568
http://dx.doi.org/10.1038/s41598-022-13512-7
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author Borey, Marion
Bed’Hom, Bertrand
Bruneau, Nicolas
Estellé, Jordi
Larsen, Frederik
Blanc, Fany
der Laan, Marie-Hélène Pinard-van
Dalgaard, Tina
Calenge, Fanny
author_facet Borey, Marion
Bed’Hom, Bertrand
Bruneau, Nicolas
Estellé, Jordi
Larsen, Frederik
Blanc, Fany
der Laan, Marie-Hélène Pinard-van
Dalgaard, Tina
Calenge, Fanny
author_sort Borey, Marion
collection PubMed
description Interactions between the gut microbiota and the immune system may be involved in vaccine and infection responses. In the present study, we studied the interactions between caecal microbiota composition and parameters describing the immune response in six experimental inbred chicken lines harboring different MHC haplotypes. Animals were challenge-infected with the infectious bronchitis virus (IBV), and half of them were previously vaccinated against this pathogen. We explored to what extent the gut microbiota composition and the genetic line could be related to the immune response, evaluated through flow cytometry. To do so, we characterized the caecal bacterial communities with a 16S rRNA gene amplicon sequencing approach performed one week after the IBV infectious challenge. We observed significant effects of both the vaccination and the genetic line on the microbiota after the challenge infection with IBV, with a lower bacterial richness in vaccinated chickens. We also observed dissimilar caecal community profiles among the different lines, and between the vaccinated and non-vaccinated animals. The effect of vaccination was similar in all the lines, with a reduced abundance of OTU from the Ruminococcacea UCG-014 and Faecalibacterium genera, and an increased abundance of OTU from the Eisenbergiella genus. The main association between the caecal microbiota and the immune phenotypes involved TCR(ϒδ) expression on TCR(ϒδ)(+) T cells. This phenotype was negatively associated with OTU from the Escherichia-Shigella genus that were also less abundant in the lines with the highest responses to the vaccine. We proved that the caecal microbiota composition is associated with the IBV vaccine response level in inbred chicken lines, and that the TCR(ϒδ)(+) T cells (judged by TCR(ϒδ) expression) may be an important component involved in this interaction, especially with bacteria from the Escherichia-Shigella genus. We hypothesized that bacteria from the Escherichia-Shigella genus increased the systemic level of bacterial lipid antigens, which subsequently mitigated poultry γδ T cells.
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spelling pubmed-91994662022-06-17 Caecal microbiota composition of experimental inbred MHC-B lines infected with IBV differs according to genetics and vaccination Borey, Marion Bed’Hom, Bertrand Bruneau, Nicolas Estellé, Jordi Larsen, Frederik Blanc, Fany der Laan, Marie-Hélène Pinard-van Dalgaard, Tina Calenge, Fanny Sci Rep Article Interactions between the gut microbiota and the immune system may be involved in vaccine and infection responses. In the present study, we studied the interactions between caecal microbiota composition and parameters describing the immune response in six experimental inbred chicken lines harboring different MHC haplotypes. Animals were challenge-infected with the infectious bronchitis virus (IBV), and half of them were previously vaccinated against this pathogen. We explored to what extent the gut microbiota composition and the genetic line could be related to the immune response, evaluated through flow cytometry. To do so, we characterized the caecal bacterial communities with a 16S rRNA gene amplicon sequencing approach performed one week after the IBV infectious challenge. We observed significant effects of both the vaccination and the genetic line on the microbiota after the challenge infection with IBV, with a lower bacterial richness in vaccinated chickens. We also observed dissimilar caecal community profiles among the different lines, and between the vaccinated and non-vaccinated animals. The effect of vaccination was similar in all the lines, with a reduced abundance of OTU from the Ruminococcacea UCG-014 and Faecalibacterium genera, and an increased abundance of OTU from the Eisenbergiella genus. The main association between the caecal microbiota and the immune phenotypes involved TCR(ϒδ) expression on TCR(ϒδ)(+) T cells. This phenotype was negatively associated with OTU from the Escherichia-Shigella genus that were also less abundant in the lines with the highest responses to the vaccine. We proved that the caecal microbiota composition is associated with the IBV vaccine response level in inbred chicken lines, and that the TCR(ϒδ)(+) T cells (judged by TCR(ϒδ) expression) may be an important component involved in this interaction, especially with bacteria from the Escherichia-Shigella genus. We hypothesized that bacteria from the Escherichia-Shigella genus increased the systemic level of bacterial lipid antigens, which subsequently mitigated poultry γδ T cells. Nature Publishing Group UK 2022-06-15 /pmc/articles/PMC9199466/ /pubmed/35705568 http://dx.doi.org/10.1038/s41598-022-13512-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Borey, Marion
Bed’Hom, Bertrand
Bruneau, Nicolas
Estellé, Jordi
Larsen, Frederik
Blanc, Fany
der Laan, Marie-Hélène Pinard-van
Dalgaard, Tina
Calenge, Fanny
Caecal microbiota composition of experimental inbred MHC-B lines infected with IBV differs according to genetics and vaccination
title Caecal microbiota composition of experimental inbred MHC-B lines infected with IBV differs according to genetics and vaccination
title_full Caecal microbiota composition of experimental inbred MHC-B lines infected with IBV differs according to genetics and vaccination
title_fullStr Caecal microbiota composition of experimental inbred MHC-B lines infected with IBV differs according to genetics and vaccination
title_full_unstemmed Caecal microbiota composition of experimental inbred MHC-B lines infected with IBV differs according to genetics and vaccination
title_short Caecal microbiota composition of experimental inbred MHC-B lines infected with IBV differs according to genetics and vaccination
title_sort caecal microbiota composition of experimental inbred mhc-b lines infected with ibv differs according to genetics and vaccination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9199466/
https://www.ncbi.nlm.nih.gov/pubmed/35705568
http://dx.doi.org/10.1038/s41598-022-13512-7
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