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The association between microbial community and ileal gene expression on intestinal wall thickness alterations in chickens

The dynamic development of the animal intestine with a concurrent succession of microbiota and changes in microbial community and metabolite spectrum can exert far-reaching effects on host physiology. However, the precise mechanism of mutual response between microbiota and the gut is yet to be fully...

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Autores principales: Tang, Dazhi, Li, Zhui, Mahmood, Tahir, Liu, Dan, Hu, Yongfei, Guo, Yuming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587722/
https://www.ncbi.nlm.nih.gov/pubmed/32241465
http://dx.doi.org/10.1016/j.psj.2019.10.029
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author Tang, Dazhi
Li, Zhui
Mahmood, Tahir
Liu, Dan
Hu, Yongfei
Guo, Yuming
author_facet Tang, Dazhi
Li, Zhui
Mahmood, Tahir
Liu, Dan
Hu, Yongfei
Guo, Yuming
author_sort Tang, Dazhi
collection PubMed
description The dynamic development of the animal intestine with a concurrent succession of microbiota and changes in microbial community and metabolite spectrum can exert far-reaching effects on host physiology. However, the precise mechanism of mutual response between microbiota and the gut is yet to be fully elucidated. Broilers with varying developmental degrees of intestinal wall thickness were selected, and they were divided into the thick group (H type) and the thin group (B type), using multiomics data integration analysis to reveal the fundamental regulatory mechanisms of gut–microbiota interplay. Our data showed, in broilers with similar body weight, the intestinal morphological parameters were improved in H type and the diversity of microbial communities is distinguishable from each other. The beneficial bacteria such as Bifidobacterium breve was increased whereas avian endogenous retrovirus EAV-HP was decreased in the H type compared with the B type. Furthermore, microbial metabolic potentials were more active, especially the biosynthesis of folate was improved in the H type. Similarly, the consolidation of absorption, immunity, metabolism, and development was noticed in the thick group. Correlation analysis indicated that the expression levels of material transport and immunomodulatory-related genes were positively correlated with the relative abundance of several probiotics such as B. breve, Lactobacillus saerimneri, and Butyricicoccus pullicaecorum. Our findings suggest that the chickens with well-developed ileal thickness own exclusive microbial composition and metabolic potential, which is closely related to small intestinal morphogenesis and homeostasis.
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spelling pubmed-75877222020-10-27 The association between microbial community and ileal gene expression on intestinal wall thickness alterations in chickens Tang, Dazhi Li, Zhui Mahmood, Tahir Liu, Dan Hu, Yongfei Guo, Yuming Poult Sci Immunology, Health and Disease The dynamic development of the animal intestine with a concurrent succession of microbiota and changes in microbial community and metabolite spectrum can exert far-reaching effects on host physiology. However, the precise mechanism of mutual response between microbiota and the gut is yet to be fully elucidated. Broilers with varying developmental degrees of intestinal wall thickness were selected, and they were divided into the thick group (H type) and the thin group (B type), using multiomics data integration analysis to reveal the fundamental regulatory mechanisms of gut–microbiota interplay. Our data showed, in broilers with similar body weight, the intestinal morphological parameters were improved in H type and the diversity of microbial communities is distinguishable from each other. The beneficial bacteria such as Bifidobacterium breve was increased whereas avian endogenous retrovirus EAV-HP was decreased in the H type compared with the B type. Furthermore, microbial metabolic potentials were more active, especially the biosynthesis of folate was improved in the H type. Similarly, the consolidation of absorption, immunity, metabolism, and development was noticed in the thick group. Correlation analysis indicated that the expression levels of material transport and immunomodulatory-related genes were positively correlated with the relative abundance of several probiotics such as B. breve, Lactobacillus saerimneri, and Butyricicoccus pullicaecorum. Our findings suggest that the chickens with well-developed ileal thickness own exclusive microbial composition and metabolic potential, which is closely related to small intestinal morphogenesis and homeostasis. Elsevier 2020-02-24 /pmc/articles/PMC7587722/ /pubmed/32241465 http://dx.doi.org/10.1016/j.psj.2019.10.029 Text en © 2019 Published by Elsevier Inc. on behalf of Poultry Science Association Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Immunology, Health and Disease
Tang, Dazhi
Li, Zhui
Mahmood, Tahir
Liu, Dan
Hu, Yongfei
Guo, Yuming
The association between microbial community and ileal gene expression on intestinal wall thickness alterations in chickens
title The association between microbial community and ileal gene expression on intestinal wall thickness alterations in chickens
title_full The association between microbial community and ileal gene expression on intestinal wall thickness alterations in chickens
title_fullStr The association between microbial community and ileal gene expression on intestinal wall thickness alterations in chickens
title_full_unstemmed The association between microbial community and ileal gene expression on intestinal wall thickness alterations in chickens
title_short The association between microbial community and ileal gene expression on intestinal wall thickness alterations in chickens
title_sort association between microbial community and ileal gene expression on intestinal wall thickness alterations in chickens
topic Immunology, Health and Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587722/
https://www.ncbi.nlm.nih.gov/pubmed/32241465
http://dx.doi.org/10.1016/j.psj.2019.10.029
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