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Impacts of diarrhea on the immune system, intestinal environment, and expression of PGRPs in New Zealand rabbits

Diarrhea is a syndrome of digestive disorders in young rabbits and may lead to secondary infections resulting in reduced immunity and higher mortality in baby rabbits, with serious impacts on rabbit farming. In this study, we investigated the effects of diarrhea on the health of baby rabbits in term...

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Autores principales: Chen, Yang, Zhao, Bohao, Wu, Yuwei, Hu, Shuaishuai, Mu, Lin, Zhu, Cigen, Pan, Yulai, Wu, Xinsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708184/
https://www.ncbi.nlm.nih.gov/pubmed/29201570
http://dx.doi.org/10.7717/peerj.4100
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author Chen, Yang
Zhao, Bohao
Wu, Yuwei
Hu, Shuaishuai
Mu, Lin
Zhu, Cigen
Pan, Yulai
Wu, Xinsheng
author_facet Chen, Yang
Zhao, Bohao
Wu, Yuwei
Hu, Shuaishuai
Mu, Lin
Zhu, Cigen
Pan, Yulai
Wu, Xinsheng
author_sort Chen, Yang
collection PubMed
description Diarrhea is a syndrome of digestive disorders in young rabbits and may lead to secondary infections resulting in reduced immunity and higher mortality in baby rabbits, with serious impacts on rabbit farming. In this study, we investigated the effects of diarrhea on the health of baby rabbits in terms of intestinal mucosal development, immune function, and intestinal microbial diversity. We found that the duodenal villus length and the villus/crypt ratio in rabbits with diarrhea were significantly reduced compared with those in healthy rabbits (P < 0.01). Rabbits with diarrhea had significantly lower concentrations of acetic acid (P < 0.05), higher pH levels (P < 0.05), and higher levels of ammonia nitrogen (P < 0.01) in the cecum. Moreover, diarrhea in baby rabbits led to significantly reduced levels of total serum protein (P < 0.05) and markedly increased levels of alkaline phosphatase, urea nitrogen, TNF-α, and IL-6 (P < 0.05). Transcriptional analysis of peptidoglycan recognition proteins (PGRPs, including PGLYRP-1, PGLYRP-2, and PGLYRP-3) using real-time PCR revealed that diarrhea induced the upregulation of PGRPs in the cecum and duodenum. Furthermore, through pyrosequencing of the 16S rRNA V4 region in cecum samples, we found that the total number and diversity of microbes were not significantly different between healthy rabbits and those with diarrhea, though there were noticeable differences in the prevalences of Clostridium, Roseburia, and Alistipes. Our results will contribute to a better understanding of the pathological mechanisms of diarrhea in young rabbits.
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spelling pubmed-57081842017-12-03 Impacts of diarrhea on the immune system, intestinal environment, and expression of PGRPs in New Zealand rabbits Chen, Yang Zhao, Bohao Wu, Yuwei Hu, Shuaishuai Mu, Lin Zhu, Cigen Pan, Yulai Wu, Xinsheng PeerJ Agricultural Science Diarrhea is a syndrome of digestive disorders in young rabbits and may lead to secondary infections resulting in reduced immunity and higher mortality in baby rabbits, with serious impacts on rabbit farming. In this study, we investigated the effects of diarrhea on the health of baby rabbits in terms of intestinal mucosal development, immune function, and intestinal microbial diversity. We found that the duodenal villus length and the villus/crypt ratio in rabbits with diarrhea were significantly reduced compared with those in healthy rabbits (P < 0.01). Rabbits with diarrhea had significantly lower concentrations of acetic acid (P < 0.05), higher pH levels (P < 0.05), and higher levels of ammonia nitrogen (P < 0.01) in the cecum. Moreover, diarrhea in baby rabbits led to significantly reduced levels of total serum protein (P < 0.05) and markedly increased levels of alkaline phosphatase, urea nitrogen, TNF-α, and IL-6 (P < 0.05). Transcriptional analysis of peptidoglycan recognition proteins (PGRPs, including PGLYRP-1, PGLYRP-2, and PGLYRP-3) using real-time PCR revealed that diarrhea induced the upregulation of PGRPs in the cecum and duodenum. Furthermore, through pyrosequencing of the 16S rRNA V4 region in cecum samples, we found that the total number and diversity of microbes were not significantly different between healthy rabbits and those with diarrhea, though there were noticeable differences in the prevalences of Clostridium, Roseburia, and Alistipes. Our results will contribute to a better understanding of the pathological mechanisms of diarrhea in young rabbits. PeerJ Inc. 2017-11-27 /pmc/articles/PMC5708184/ /pubmed/29201570 http://dx.doi.org/10.7717/peerj.4100 Text en ©2017 Chen et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Agricultural Science
Chen, Yang
Zhao, Bohao
Wu, Yuwei
Hu, Shuaishuai
Mu, Lin
Zhu, Cigen
Pan, Yulai
Wu, Xinsheng
Impacts of diarrhea on the immune system, intestinal environment, and expression of PGRPs in New Zealand rabbits
title Impacts of diarrhea on the immune system, intestinal environment, and expression of PGRPs in New Zealand rabbits
title_full Impacts of diarrhea on the immune system, intestinal environment, and expression of PGRPs in New Zealand rabbits
title_fullStr Impacts of diarrhea on the immune system, intestinal environment, and expression of PGRPs in New Zealand rabbits
title_full_unstemmed Impacts of diarrhea on the immune system, intestinal environment, and expression of PGRPs in New Zealand rabbits
title_short Impacts of diarrhea on the immune system, intestinal environment, and expression of PGRPs in New Zealand rabbits
title_sort impacts of diarrhea on the immune system, intestinal environment, and expression of pgrps in new zealand rabbits
topic Agricultural Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708184/
https://www.ncbi.nlm.nih.gov/pubmed/29201570
http://dx.doi.org/10.7717/peerj.4100
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