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Integrated multi-omics reveals novel microbe-host lipid metabolism and immune interactions in the donkey hindgut

Evidence has shown that gut microbiota play a key role in host metabolism and health; however, little is known about the microbial community in the donkey hindgut as well as the interactions that occur between gut microbes and the host. This study aimed to explore the gut microbiome differences by a...

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Autores principales: Li, Yan, Ma, Qingshan, Shi, Xiaoyuan, Liu, Guiqin, Wang, Changfa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9716284/
https://www.ncbi.nlm.nih.gov/pubmed/36466834
http://dx.doi.org/10.3389/fimmu.2022.1003247
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author Li, Yan
Ma, Qingshan
Shi, Xiaoyuan
Liu, Guiqin
Wang, Changfa
author_facet Li, Yan
Ma, Qingshan
Shi, Xiaoyuan
Liu, Guiqin
Wang, Changfa
author_sort Li, Yan
collection PubMed
description Evidence has shown that gut microbiota play a key role in host metabolism and health; however, little is known about the microbial community in the donkey hindgut as well as the interactions that occur between gut microbes and the host. This study aimed to explore the gut microbiome differences by analyzing the microbial community and differentially expressed genes (DEGs) related to lipid metabolism and the immune system along the donkey hindgut. The hindgut tissues (cecum, ventral colon, and dorsal colon) were separated, and the contents of each section were collected from six male donkeys for multi-omics analysis. There were significant differences in terms of dominant bacteria among the three sections, especially between the cecum and dorsal colon sites. For instance, species belonging to Prevotella and Treponema were most abundant in the cecum, while the Clostridiales_bacterium, Streptococcus_equinus, Ruminococcaceae_bacterium, etc., were more abundant in the dorsal colon. Apart from propionate, the concentrations of acetate, isobutyrate, valerate and isovalerate were all lower in the cecum than in the dorsal colon (p < 0.05). Furthermore, we identified some interesting DEGs related to lipid metabolism (e.g., ME1, MBOAT1, ACOX1, ACOX2 and LIPH) and the immune system (e.g., MUC3B, mucin-2-like, IL17RC, IL1R2, IL33, C1QA, and MMP9) between the cecum and dorsal colon and found that the PPAR pathway was mainly enriched in the cecum. Finally, we found a complex relationship between the gut microbiome and gene expression, especially with respect to the immune system, and combined with protein-protein interaction (PPI) data, suggesting that the PPAR pathway might be responsible, at least in part, for the role of the hindgut microbiota in the donkeys’ gut homeostasis. Our data provide an in-depth understanding of the interaction between the microbiota and function in the healthy equine hindgut and may also provide guidance for improving animal performance metrics (such as product quality) and equine welfare.
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spelling pubmed-97162842022-12-03 Integrated multi-omics reveals novel microbe-host lipid metabolism and immune interactions in the donkey hindgut Li, Yan Ma, Qingshan Shi, Xiaoyuan Liu, Guiqin Wang, Changfa Front Immunol Immunology Evidence has shown that gut microbiota play a key role in host metabolism and health; however, little is known about the microbial community in the donkey hindgut as well as the interactions that occur between gut microbes and the host. This study aimed to explore the gut microbiome differences by analyzing the microbial community and differentially expressed genes (DEGs) related to lipid metabolism and the immune system along the donkey hindgut. The hindgut tissues (cecum, ventral colon, and dorsal colon) were separated, and the contents of each section were collected from six male donkeys for multi-omics analysis. There were significant differences in terms of dominant bacteria among the three sections, especially between the cecum and dorsal colon sites. For instance, species belonging to Prevotella and Treponema were most abundant in the cecum, while the Clostridiales_bacterium, Streptococcus_equinus, Ruminococcaceae_bacterium, etc., were more abundant in the dorsal colon. Apart from propionate, the concentrations of acetate, isobutyrate, valerate and isovalerate were all lower in the cecum than in the dorsal colon (p < 0.05). Furthermore, we identified some interesting DEGs related to lipid metabolism (e.g., ME1, MBOAT1, ACOX1, ACOX2 and LIPH) and the immune system (e.g., MUC3B, mucin-2-like, IL17RC, IL1R2, IL33, C1QA, and MMP9) between the cecum and dorsal colon and found that the PPAR pathway was mainly enriched in the cecum. Finally, we found a complex relationship between the gut microbiome and gene expression, especially with respect to the immune system, and combined with protein-protein interaction (PPI) data, suggesting that the PPAR pathway might be responsible, at least in part, for the role of the hindgut microbiota in the donkeys’ gut homeostasis. Our data provide an in-depth understanding of the interaction between the microbiota and function in the healthy equine hindgut and may also provide guidance for improving animal performance metrics (such as product quality) and equine welfare. Frontiers Media S.A. 2022-11-18 /pmc/articles/PMC9716284/ /pubmed/36466834 http://dx.doi.org/10.3389/fimmu.2022.1003247 Text en Copyright © 2022 Li, Ma, Shi, Liu and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Li, Yan
Ma, Qingshan
Shi, Xiaoyuan
Liu, Guiqin
Wang, Changfa
Integrated multi-omics reveals novel microbe-host lipid metabolism and immune interactions in the donkey hindgut
title Integrated multi-omics reveals novel microbe-host lipid metabolism and immune interactions in the donkey hindgut
title_full Integrated multi-omics reveals novel microbe-host lipid metabolism and immune interactions in the donkey hindgut
title_fullStr Integrated multi-omics reveals novel microbe-host lipid metabolism and immune interactions in the donkey hindgut
title_full_unstemmed Integrated multi-omics reveals novel microbe-host lipid metabolism and immune interactions in the donkey hindgut
title_short Integrated multi-omics reveals novel microbe-host lipid metabolism and immune interactions in the donkey hindgut
title_sort integrated multi-omics reveals novel microbe-host lipid metabolism and immune interactions in the donkey hindgut
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9716284/
https://www.ncbi.nlm.nih.gov/pubmed/36466834
http://dx.doi.org/10.3389/fimmu.2022.1003247
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