Identification of human gut bacteria that produce bioactive serotonin and promote colonic innervation.

IF 6.9 1区 生物学 Q1 CELL BIOLOGY
Chiara H Moretti, Estelle Grasset, Jiaying Zhu, Gaohua Yang, Louise E Olofsson, Muhammad Tanweer Khan, Per-Olof Bergh, Jee-Hwan Oh, Annika Lundqvist, Tom van Gils, Manuela Krämer, Lisa M Olsson, Piyush Patel, Matthias Mitteregger, Daysi Espinola Monges, Chinmay Dwibedi, Kimberly A Krautkramer, Nienke Koopman, Marcus Henricsson, Andrew J Macpherson, Thue Schwartz, Gianfranco Grompone, Jan-Peter van Pijkeren, Valentina Tremaroli, Stefan Roos, Magnus Simrén, Fredrik Bäckhed
{"title":"Identification of human gut bacteria that produce bioactive serotonin and promote colonic innervation.","authors":"Chiara H Moretti, Estelle Grasset, Jiaying Zhu, Gaohua Yang, Louise E Olofsson, Muhammad Tanweer Khan, Per-Olof Bergh, Jee-Hwan Oh, Annika Lundqvist, Tom van Gils, Manuela Krämer, Lisa M Olsson, Piyush Patel, Matthias Mitteregger, Daysi Espinola Monges, Chinmay Dwibedi, Kimberly A Krautkramer, Nienke Koopman, Marcus Henricsson, Andrew J Macpherson, Thue Schwartz, Gianfranco Grompone, Jan-Peter van Pijkeren, Valentina Tremaroli, Stefan Roos, Magnus Simrén, Fredrik Bäckhed","doi":"10.1016/j.celrep.2025.116434","DOIUrl":null,"url":null,"abstract":"<p><p>The gut microbiota regulates host intestinal serotonin synthesis, thereby promoting the development and maintenance of the enteric nervous system, which controls bowel motility. Functional bowel disorders, including irritable bowel syndrome, are associated with altered serotonin levels and gut microbiota composition. However, it is unclear if the gut microbiota can synthesize bioactive serotonin, which may affect enteric nervous system development. Here, we identify a consortium of the human gut bacteria Limosilactobacillus mucosae and Ligilactobacillus ruminis that synthesizes serotonin in vitro by decarboxylation of 5-hydroxytryptophan and elevates fecal serotonin levels, colonic neuronal density, and serotonin-immunoreactive neurons when introduced into germ-free, serotonin-deficient mice. The consortium normalizes intestinal transit time in germ-free wild-type mice, and we observe decreased fecal abundance of L. mucosae in individuals with irritable bowel syndrome. These findings suggest that specific members of the human gut microbiota synthesize bioactive serotonin that can contribute to gut health.</p>","PeriodicalId":9798,"journal":{"name":"Cell reports","volume":" ","pages":"116434"},"PeriodicalIF":6.9000,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell reports","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.celrep.2025.116434","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The gut microbiota regulates host intestinal serotonin synthesis, thereby promoting the development and maintenance of the enteric nervous system, which controls bowel motility. Functional bowel disorders, including irritable bowel syndrome, are associated with altered serotonin levels and gut microbiota composition. However, it is unclear if the gut microbiota can synthesize bioactive serotonin, which may affect enteric nervous system development. Here, we identify a consortium of the human gut bacteria Limosilactobacillus mucosae and Ligilactobacillus ruminis that synthesizes serotonin in vitro by decarboxylation of 5-hydroxytryptophan and elevates fecal serotonin levels, colonic neuronal density, and serotonin-immunoreactive neurons when introduced into germ-free, serotonin-deficient mice. The consortium normalizes intestinal transit time in germ-free wild-type mice, and we observe decreased fecal abundance of L. mucosae in individuals with irritable bowel syndrome. These findings suggest that specific members of the human gut microbiota synthesize bioactive serotonin that can contribute to gut health.

产生生物活性血清素并促进结肠神经支配的人类肠道细菌的鉴定。
肠道微生物群调节宿主肠道血清素合成,从而促进肠道神经系统的发育和维持,从而控制肠道运动。功能性肠道疾病,包括肠易激综合征,与血清素水平和肠道微生物群组成的改变有关。然而,目前尚不清楚肠道微生物群是否可以合成生物活性血清素,这可能会影响肠道神经系统的发育。在这里,我们鉴定了一个由人类肠道细菌粘膜乳酸杆菌和瘤胃乳酸杆菌组成的联合菌群,它们在体外通过5-羟色氨酸脱羧合成5-羟色胺,并在将其引入无菌、血清素缺乏的小鼠体内时,提高粪便血清素水平、结肠神经元密度和血清素免疫反应神经元。该联盟使无菌野生型小鼠的肠道运输时间正常化,我们观察到肠易激综合征患者粪便中粘膜乳杆菌的丰度降低。这些发现表明,人类肠道微生物群的特定成员可以合成生物活性血清素,有助于肠道健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信