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Caecal infusion of the short‐chain fatty acid propionate affects the microbiota and expression of inflammatory cytokines in the colon in a fistula pig model

Short‐chain fatty acids (SCFAs), particularly butyrate, are known to suppress inflammation, and regulate the gut bacterial ecology. However, little is known about propionate. We report here that propionate infusion in the caecum dramatically affected the structure of colonic microbiota of pigs based...

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Autores principales: Zhang, Yanan, Yu, Kaifan, Chen, Huizi, Su, Yong, Zhu, Weiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116746/
https://www.ncbi.nlm.nih.gov/pubmed/29856120
http://dx.doi.org/10.1111/1751-7915.13282
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author Zhang, Yanan
Yu, Kaifan
Chen, Huizi
Su, Yong
Zhu, Weiyun
author_facet Zhang, Yanan
Yu, Kaifan
Chen, Huizi
Su, Yong
Zhu, Weiyun
author_sort Zhang, Yanan
collection PubMed
description Short‐chain fatty acids (SCFAs), particularly butyrate, are known to suppress inflammation, and regulate the gut bacterial ecology. However, little is known about propionate. We report here that propionate infusion in the caecum dramatically affected the structure of colonic microbiota of pigs based on 16s rRNA high‐throughput sequencing. Sixteen pig models were perfused with saline or sodium propionate by a fistula in the caecum. At d 28, all pigs were slaughtered for analysing bacterial metabolites, colonic microbiota and the expression of genes related to inflammation. The results showed that caecal infusion of sodium propionate increased the concentration of propionate and decreased the butyrate concentration in colonic content. For biogenic amines, the tyramine concentration was increased, while the concentration of cadaverine was decreased by infusion of sodium propionate. Furthermore, at the level of phylum, propionate increased the abundance of Bacteroidetes and reduced the abundance of Firmicutes. Prevotella and Bacteroides counts were increased, while Turicibacter abundance was decreased at the level of genus. Real‐time qPCR showed that the expression of NF‐κB and IL‐18 was upregulated by propionate infusion, whereas no significant differences were observed for the expression of other genes related to inflammatory processes. Taken together, these results provide a new evidence for the role of short‐chain fatty acid propionate on the composition of microbial community and inflammatory cytokines.
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spelling pubmed-61167462018-09-05 Caecal infusion of the short‐chain fatty acid propionate affects the microbiota and expression of inflammatory cytokines in the colon in a fistula pig model Zhang, Yanan Yu, Kaifan Chen, Huizi Su, Yong Zhu, Weiyun Microb Biotechnol Research Articles Short‐chain fatty acids (SCFAs), particularly butyrate, are known to suppress inflammation, and regulate the gut bacterial ecology. However, little is known about propionate. We report here that propionate infusion in the caecum dramatically affected the structure of colonic microbiota of pigs based on 16s rRNA high‐throughput sequencing. Sixteen pig models were perfused with saline or sodium propionate by a fistula in the caecum. At d 28, all pigs were slaughtered for analysing bacterial metabolites, colonic microbiota and the expression of genes related to inflammation. The results showed that caecal infusion of sodium propionate increased the concentration of propionate and decreased the butyrate concentration in colonic content. For biogenic amines, the tyramine concentration was increased, while the concentration of cadaverine was decreased by infusion of sodium propionate. Furthermore, at the level of phylum, propionate increased the abundance of Bacteroidetes and reduced the abundance of Firmicutes. Prevotella and Bacteroides counts were increased, while Turicibacter abundance was decreased at the level of genus. Real‐time qPCR showed that the expression of NF‐κB and IL‐18 was upregulated by propionate infusion, whereas no significant differences were observed for the expression of other genes related to inflammatory processes. Taken together, these results provide a new evidence for the role of short‐chain fatty acid propionate on the composition of microbial community and inflammatory cytokines. John Wiley and Sons Inc. 2018-06-01 /pmc/articles/PMC6116746/ /pubmed/29856120 http://dx.doi.org/10.1111/1751-7915.13282 Text en © 2018 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhang, Yanan
Yu, Kaifan
Chen, Huizi
Su, Yong
Zhu, Weiyun
Caecal infusion of the short‐chain fatty acid propionate affects the microbiota and expression of inflammatory cytokines in the colon in a fistula pig model
title Caecal infusion of the short‐chain fatty acid propionate affects the microbiota and expression of inflammatory cytokines in the colon in a fistula pig model
title_full Caecal infusion of the short‐chain fatty acid propionate affects the microbiota and expression of inflammatory cytokines in the colon in a fistula pig model
title_fullStr Caecal infusion of the short‐chain fatty acid propionate affects the microbiota and expression of inflammatory cytokines in the colon in a fistula pig model
title_full_unstemmed Caecal infusion of the short‐chain fatty acid propionate affects the microbiota and expression of inflammatory cytokines in the colon in a fistula pig model
title_short Caecal infusion of the short‐chain fatty acid propionate affects the microbiota and expression of inflammatory cytokines in the colon in a fistula pig model
title_sort caecal infusion of the short‐chain fatty acid propionate affects the microbiota and expression of inflammatory cytokines in the colon in a fistula pig model
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116746/
https://www.ncbi.nlm.nih.gov/pubmed/29856120
http://dx.doi.org/10.1111/1751-7915.13282
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