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A Class IIb Bacteriocin Plantaricin NC8 Modulates Gut Microbiota of Different Enterotypes in vitro
The gut microbiota is engaged in multiple interactions affecting host health. Bacteriocins showed the ability of impeding the growth of intestinal pathogenic bacteria and modulating gut microbiota in animals. Few studies have also discovered their regulation on human intestinal flora using an in vit...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280423/ https://www.ncbi.nlm.nih.gov/pubmed/35845772 http://dx.doi.org/10.3389/fnut.2022.877948 |
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author | Pu, Jiaqian Hang, Shuting Liu, Manman Chen, Ziqi Xiong, Jiayi Li, Yongquan Wu, Hongchen Zhao, Xiaodan Liu, Shuxun Gu, Qing Li, Ping |
author_facet | Pu, Jiaqian Hang, Shuting Liu, Manman Chen, Ziqi Xiong, Jiayi Li, Yongquan Wu, Hongchen Zhao, Xiaodan Liu, Shuxun Gu, Qing Li, Ping |
author_sort | Pu, Jiaqian |
collection | PubMed |
description | The gut microbiota is engaged in multiple interactions affecting host health. Bacteriocins showed the ability of impeding the growth of intestinal pathogenic bacteria and modulating gut microbiota in animals. Few studies have also discovered their regulation on human intestinal flora using an in vitro simulated system. However, little is known about their effect on gut microbiota of different enterotypes of human. This work evaluated the modification of the gut microbiota of two enterotypes (ET B and ET P) by the class IIb bacteriocin plantaricin NC8 (PLNC8) by using an in vitro fermentation model of the intestine. Gas chromatography results revealed that PLNC8 had no influence on the gut microbiota’s production of short-chain fatty acids in the subjects’ samples. PLNC8 lowered the Shannon index of ET B’ gut microbiota and the Simpson index of ET P’ gut microbiota, according to 16S rDNA sequencing. In ET B, PLNC8 enhanced the abundance of Bacteroides, Bifidobacterium, Megamonas, Escherichia-Shigella, Parabacteroides, and Lactobacillus while decreasing the abundance of Streptococcus. Prevotella_9, Bifidobacterium, Escherichia-Shigella, Mitsuokella, and Collinsella were found more abundant in ET P. The current study adds to our understanding of the impact of PLNC8 on the human gut microbiota and lays the groundwork for future research into PLNC8’s effects on human intestinal disease. |
format | Online Article Text |
id | pubmed-9280423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92804232022-07-15 A Class IIb Bacteriocin Plantaricin NC8 Modulates Gut Microbiota of Different Enterotypes in vitro Pu, Jiaqian Hang, Shuting Liu, Manman Chen, Ziqi Xiong, Jiayi Li, Yongquan Wu, Hongchen Zhao, Xiaodan Liu, Shuxun Gu, Qing Li, Ping Front Nutr Nutrition The gut microbiota is engaged in multiple interactions affecting host health. Bacteriocins showed the ability of impeding the growth of intestinal pathogenic bacteria and modulating gut microbiota in animals. Few studies have also discovered their regulation on human intestinal flora using an in vitro simulated system. However, little is known about their effect on gut microbiota of different enterotypes of human. This work evaluated the modification of the gut microbiota of two enterotypes (ET B and ET P) by the class IIb bacteriocin plantaricin NC8 (PLNC8) by using an in vitro fermentation model of the intestine. Gas chromatography results revealed that PLNC8 had no influence on the gut microbiota’s production of short-chain fatty acids in the subjects’ samples. PLNC8 lowered the Shannon index of ET B’ gut microbiota and the Simpson index of ET P’ gut microbiota, according to 16S rDNA sequencing. In ET B, PLNC8 enhanced the abundance of Bacteroides, Bifidobacterium, Megamonas, Escherichia-Shigella, Parabacteroides, and Lactobacillus while decreasing the abundance of Streptococcus. Prevotella_9, Bifidobacterium, Escherichia-Shigella, Mitsuokella, and Collinsella were found more abundant in ET P. The current study adds to our understanding of the impact of PLNC8 on the human gut microbiota and lays the groundwork for future research into PLNC8’s effects on human intestinal disease. Frontiers Media S.A. 2022-06-30 /pmc/articles/PMC9280423/ /pubmed/35845772 http://dx.doi.org/10.3389/fnut.2022.877948 Text en Copyright © 2022 Pu, Hang, Liu, Chen, Xiong, Li, Wu, Zhao, Liu, Gu and Li. 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 | Nutrition Pu, Jiaqian Hang, Shuting Liu, Manman Chen, Ziqi Xiong, Jiayi Li, Yongquan Wu, Hongchen Zhao, Xiaodan Liu, Shuxun Gu, Qing Li, Ping A Class IIb Bacteriocin Plantaricin NC8 Modulates Gut Microbiota of Different Enterotypes in vitro |
title | A Class IIb Bacteriocin Plantaricin NC8 Modulates Gut Microbiota of Different Enterotypes in vitro |
title_full | A Class IIb Bacteriocin Plantaricin NC8 Modulates Gut Microbiota of Different Enterotypes in vitro |
title_fullStr | A Class IIb Bacteriocin Plantaricin NC8 Modulates Gut Microbiota of Different Enterotypes in vitro |
title_full_unstemmed | A Class IIb Bacteriocin Plantaricin NC8 Modulates Gut Microbiota of Different Enterotypes in vitro |
title_short | A Class IIb Bacteriocin Plantaricin NC8 Modulates Gut Microbiota of Different Enterotypes in vitro |
title_sort | class iib bacteriocin plantaricin nc8 modulates gut microbiota of different enterotypes in vitro |
topic | Nutrition |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280423/ https://www.ncbi.nlm.nih.gov/pubmed/35845772 http://dx.doi.org/10.3389/fnut.2022.877948 |
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