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Saturated long-chain fatty acid-producing bacteria contribute to enhanced colonic motility in rats

BACKGROUND: The gut microbiota is closely associated with gastrointestinal (GI) motility disorder, but the mechanism(s) by which bacteria interact with and affect host GI motility remains unclear. In this study, through using metabolomic and metagenomic analyses, an animal model of neonatal maternal...

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Autores principales: Zhao, Ling, Huang, Yufen, Lu, Lin, Yang, Wei, Huang, Tao, Lin, Zesi, Lin, Chengyuan, Kwan, Hiuyee, Wong, Hoi Leong Xavier, Chen, Yang, Sun, Silong, Xie, Xuefeng, Fang, Xiaodong, Yang, Huanming, Wang, Jian, Zhu, Lixin, Bian, Zhaoxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003035/
https://www.ncbi.nlm.nih.gov/pubmed/29903041
http://dx.doi.org/10.1186/s40168-018-0492-6
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author Zhao, Ling
Huang, Yufen
Lu, Lin
Yang, Wei
Huang, Tao
Lin, Zesi
Lin, Chengyuan
Kwan, Hiuyee
Wong, Hoi Leong Xavier
Chen, Yang
Sun, Silong
Xie, Xuefeng
Fang, Xiaodong
Yang, Huanming
Wang, Jian
Zhu, Lixin
Bian, Zhaoxiang
author_facet Zhao, Ling
Huang, Yufen
Lu, Lin
Yang, Wei
Huang, Tao
Lin, Zesi
Lin, Chengyuan
Kwan, Hiuyee
Wong, Hoi Leong Xavier
Chen, Yang
Sun, Silong
Xie, Xuefeng
Fang, Xiaodong
Yang, Huanming
Wang, Jian
Zhu, Lixin
Bian, Zhaoxiang
author_sort Zhao, Ling
collection PubMed
description BACKGROUND: The gut microbiota is closely associated with gastrointestinal (GI) motility disorder, but the mechanism(s) by which bacteria interact with and affect host GI motility remains unclear. In this study, through using metabolomic and metagenomic analyses, an animal model of neonatal maternal separation (NMS) characterized by accelerated colonic motility and gut dysbiosis was used to investigate the mechanism underlying microbiota-driven motility dysfunction. RESULTS: An excess of intracolonic saturated long-chain fatty acids (SLCFAs) was associated with enhanced bowel motility in NMS rats. Heptadecanoic acid (C17:0) and stearic acid (C18:0), as the most abundant odd- and even-numbered carbon SLCFAs in the colon lumen, can promote rat colonic muscle contraction and increase stool frequency. Increase of SLCFAs was positively correlated with elevated abundances of Prevotella, Lactobacillus, and Alistipes. Functional annotation found that the level of bacterial LCFA biosynthesis was highly enriched in NMS group. Essential synthetic genes Fabs were largely identified from the genera Prevotella, Lactobacillus, and Alistipes. Pseudo germ-free (GF) rats receiving fecal microbiota from NMS donors exhibited increased defecation frequency and upregulated bacterial production of intracolonic SLCFAs. Modulation of gut dysbiosis by neomycin effectively attenuated GI motility and reduced bacterial SLCFA generation in the colon lumen of NMS rats. CONCLUSIONS: These findings reveal a previously unknown relationship between gut bacteria, intracolonic SLCFAs, and host GI motility, suggesting the importance of SLCFA-producing bacteria in GI motility disorders. Further exploration of this relationship could lead to a precise medication targeting the gut microbiota for treating GI motility disorders. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0492-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-60030352018-07-06 Saturated long-chain fatty acid-producing bacteria contribute to enhanced colonic motility in rats Zhao, Ling Huang, Yufen Lu, Lin Yang, Wei Huang, Tao Lin, Zesi Lin, Chengyuan Kwan, Hiuyee Wong, Hoi Leong Xavier Chen, Yang Sun, Silong Xie, Xuefeng Fang, Xiaodong Yang, Huanming Wang, Jian Zhu, Lixin Bian, Zhaoxiang Microbiome Research BACKGROUND: The gut microbiota is closely associated with gastrointestinal (GI) motility disorder, but the mechanism(s) by which bacteria interact with and affect host GI motility remains unclear. In this study, through using metabolomic and metagenomic analyses, an animal model of neonatal maternal separation (NMS) characterized by accelerated colonic motility and gut dysbiosis was used to investigate the mechanism underlying microbiota-driven motility dysfunction. RESULTS: An excess of intracolonic saturated long-chain fatty acids (SLCFAs) was associated with enhanced bowel motility in NMS rats. Heptadecanoic acid (C17:0) and stearic acid (C18:0), as the most abundant odd- and even-numbered carbon SLCFAs in the colon lumen, can promote rat colonic muscle contraction and increase stool frequency. Increase of SLCFAs was positively correlated with elevated abundances of Prevotella, Lactobacillus, and Alistipes. Functional annotation found that the level of bacterial LCFA biosynthesis was highly enriched in NMS group. Essential synthetic genes Fabs were largely identified from the genera Prevotella, Lactobacillus, and Alistipes. Pseudo germ-free (GF) rats receiving fecal microbiota from NMS donors exhibited increased defecation frequency and upregulated bacterial production of intracolonic SLCFAs. Modulation of gut dysbiosis by neomycin effectively attenuated GI motility and reduced bacterial SLCFA generation in the colon lumen of NMS rats. CONCLUSIONS: These findings reveal a previously unknown relationship between gut bacteria, intracolonic SLCFAs, and host GI motility, suggesting the importance of SLCFA-producing bacteria in GI motility disorders. Further exploration of this relationship could lead to a precise medication targeting the gut microbiota for treating GI motility disorders. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0492-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-14 /pmc/articles/PMC6003035/ /pubmed/29903041 http://dx.doi.org/10.1186/s40168-018-0492-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhao, Ling
Huang, Yufen
Lu, Lin
Yang, Wei
Huang, Tao
Lin, Zesi
Lin, Chengyuan
Kwan, Hiuyee
Wong, Hoi Leong Xavier
Chen, Yang
Sun, Silong
Xie, Xuefeng
Fang, Xiaodong
Yang, Huanming
Wang, Jian
Zhu, Lixin
Bian, Zhaoxiang
Saturated long-chain fatty acid-producing bacteria contribute to enhanced colonic motility in rats
title Saturated long-chain fatty acid-producing bacteria contribute to enhanced colonic motility in rats
title_full Saturated long-chain fatty acid-producing bacteria contribute to enhanced colonic motility in rats
title_fullStr Saturated long-chain fatty acid-producing bacteria contribute to enhanced colonic motility in rats
title_full_unstemmed Saturated long-chain fatty acid-producing bacteria contribute to enhanced colonic motility in rats
title_short Saturated long-chain fatty acid-producing bacteria contribute to enhanced colonic motility in rats
title_sort saturated long-chain fatty acid-producing bacteria contribute to enhanced colonic motility in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003035/
https://www.ncbi.nlm.nih.gov/pubmed/29903041
http://dx.doi.org/10.1186/s40168-018-0492-6
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