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Regulation of serotonin production by specific microbes from piglet gut

BACKGROUND: Serotonin is an important signaling molecule that regulates secretory and sensory functions in the gut. Gut microbiota has been demonstrated to affect serotonin synthesis in rodent models. However, how gut microbes regulate intestinal serotonin production in piglets remains vague. To inv...

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Autores principales: Liu, Ziyu, Ling, Yidan, Peng, Yu, Han, Shuibing, Ren, Yuting, Jing, Yujia, Fan, Wenlu, Su, Yong, Mu, Chunlong, Zhu, Weiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403853/
https://www.ncbi.nlm.nih.gov/pubmed/37542282
http://dx.doi.org/10.1186/s40104-023-00903-7
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author Liu, Ziyu
Ling, Yidan
Peng, Yu
Han, Shuibing
Ren, Yuting
Jing, Yujia
Fan, Wenlu
Su, Yong
Mu, Chunlong
Zhu, Weiyun
author_facet Liu, Ziyu
Ling, Yidan
Peng, Yu
Han, Shuibing
Ren, Yuting
Jing, Yujia
Fan, Wenlu
Su, Yong
Mu, Chunlong
Zhu, Weiyun
author_sort Liu, Ziyu
collection PubMed
description BACKGROUND: Serotonin is an important signaling molecule that regulates secretory and sensory functions in the gut. Gut microbiota has been demonstrated to affect serotonin synthesis in rodent models. However, how gut microbes regulate intestinal serotonin production in piglets remains vague. To investigate the relationship between microbiota and serotonin specifically in the colon, microbial composition and serotonin concentration were analyzed in ileum-cannulated piglets subjected to antibiotic infusion from the ileum when comparing with saline infusion. Microbes that correlated positively with serotonin production were isolated from piglet colon and were further used to investigate the regulation mechanisms on serotonin production in IPEC-J2 and a putative enterochromaffin cell line RIN-14B cells. RESULTS: Antibiotic infusion increased quantities of Lactobacillus amylovorus (LA) that positively correlated with increased serotonin concentrations in the colon, while no effects observed for Limosilactobacillus reuteri (LR). To understand how microbes regulate serotonin, representative strains of LA, LR, and Streptococcus alactolyticus (SA, enriched in feces from prior observation) were selected for cell culture studies. Compared to the control group, LA, LR and SA supernatants significantly up-regulated tryptophan hydroxylase 1 (TPH1) expression and promoted serotonin production in IPEC-J2 cells, while in RIN-14B cells only LA exerted similar action. To investigate potential mechanisms mediated by microbe-derived molecules, microbial metabolites including lactate, acetate, glutamine, and γ-aminobutyric acid were selected for cell treatment based on computational and metabolite profiling in bacterial supernatant. Among these metabolites, acetate upregulated the expression of free fatty acid receptor 3 and TPH1 while downregulated indoleamine 2,3-dioxygenase 1. Similar effects were also recapitulated when treating the cells with AR420626, an agonist targeting free fatty acid receptor 3. CONCLUSIONS: Overall, these results suggest that Lactobacillus amylovorus showed a positive correlation with serotonin production in the pig gut and exhibited a remarkable ability to regulate serotonin production in cell cultures. These findings provide evidence that microbial metabolites mediate the dialogue between microbes and host, which reveals a potential approach using microbial manipulation to regulate intestinal serotonin biosynthesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-023-00903-7.
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spelling pubmed-104038532023-08-06 Regulation of serotonin production by specific microbes from piglet gut Liu, Ziyu Ling, Yidan Peng, Yu Han, Shuibing Ren, Yuting Jing, Yujia Fan, Wenlu Su, Yong Mu, Chunlong Zhu, Weiyun J Anim Sci Biotechnol Research BACKGROUND: Serotonin is an important signaling molecule that regulates secretory and sensory functions in the gut. Gut microbiota has been demonstrated to affect serotonin synthesis in rodent models. However, how gut microbes regulate intestinal serotonin production in piglets remains vague. To investigate the relationship between microbiota and serotonin specifically in the colon, microbial composition and serotonin concentration were analyzed in ileum-cannulated piglets subjected to antibiotic infusion from the ileum when comparing with saline infusion. Microbes that correlated positively with serotonin production were isolated from piglet colon and were further used to investigate the regulation mechanisms on serotonin production in IPEC-J2 and a putative enterochromaffin cell line RIN-14B cells. RESULTS: Antibiotic infusion increased quantities of Lactobacillus amylovorus (LA) that positively correlated with increased serotonin concentrations in the colon, while no effects observed for Limosilactobacillus reuteri (LR). To understand how microbes regulate serotonin, representative strains of LA, LR, and Streptococcus alactolyticus (SA, enriched in feces from prior observation) were selected for cell culture studies. Compared to the control group, LA, LR and SA supernatants significantly up-regulated tryptophan hydroxylase 1 (TPH1) expression and promoted serotonin production in IPEC-J2 cells, while in RIN-14B cells only LA exerted similar action. To investigate potential mechanisms mediated by microbe-derived molecules, microbial metabolites including lactate, acetate, glutamine, and γ-aminobutyric acid were selected for cell treatment based on computational and metabolite profiling in bacterial supernatant. Among these metabolites, acetate upregulated the expression of free fatty acid receptor 3 and TPH1 while downregulated indoleamine 2,3-dioxygenase 1. Similar effects were also recapitulated when treating the cells with AR420626, an agonist targeting free fatty acid receptor 3. CONCLUSIONS: Overall, these results suggest that Lactobacillus amylovorus showed a positive correlation with serotonin production in the pig gut and exhibited a remarkable ability to regulate serotonin production in cell cultures. These findings provide evidence that microbial metabolites mediate the dialogue between microbes and host, which reveals a potential approach using microbial manipulation to regulate intestinal serotonin biosynthesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-023-00903-7. BioMed Central 2023-08-05 /pmc/articles/PMC10403853/ /pubmed/37542282 http://dx.doi.org/10.1186/s40104-023-00903-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Ziyu
Ling, Yidan
Peng, Yu
Han, Shuibing
Ren, Yuting
Jing, Yujia
Fan, Wenlu
Su, Yong
Mu, Chunlong
Zhu, Weiyun
Regulation of serotonin production by specific microbes from piglet gut
title Regulation of serotonin production by specific microbes from piglet gut
title_full Regulation of serotonin production by specific microbes from piglet gut
title_fullStr Regulation of serotonin production by specific microbes from piglet gut
title_full_unstemmed Regulation of serotonin production by specific microbes from piglet gut
title_short Regulation of serotonin production by specific microbes from piglet gut
title_sort regulation of serotonin production by specific microbes from piglet gut
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403853/
https://www.ncbi.nlm.nih.gov/pubmed/37542282
http://dx.doi.org/10.1186/s40104-023-00903-7
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