| Literature DB >> 29902441 |
Yogesh Bhattarai1, Brianna B Williams2, Eric J Battaglioli1, Weston R Whitaker3, Lisa Till4, Madhusudan Grover5, David R Linden4, Yasutada Akiba6, Karunya K Kandimalla7, Nicholas C Zachos8, Jonathan D Kaunitz9, Justin L Sonnenburg3, Michael A Fischbach2, Gianrico Farrugia10, Purna C Kashyap11.
Abstract
Tryptamine, a tryptophan-derived monoamine similar to 5-hydroxytryptamine (5-HT), is produced by gut bacteria and is abundant in human and rodent feces. However, the physiologic effect of tryptamine in the gastrointestinal (GI) tract remains unknown. Here, we show that the biological effects of tryptamine are mediated through the 5-HT4 receptor (5-HT4R), a G-protein-coupled receptor (GPCR) uniquely expressed in the colonic epithelium. Tryptamine increases both ionic flux across the colonic epithelium and fluid secretion in colonoids from germ-free (GF) and humanized (ex-GF colonized with human stool) mice, consistent with increased intestinal secretion. The secretory effect of tryptamine is dependent on 5-HT4R activation and is blocked by 5-HT4R antagonist and absent in 5-HT4R-/- mice. GF mice colonized by Bacteroides thetaiotaomicron engineered to produce tryptamine exhibit accelerated GI transit. Our study demonstrates an aspect of host physiology under control of a bacterial metabolite that can be exploited as a therapeutic modality. VIDEO ABSTRACT.Entities:
Keywords: Bacteroides thetaiotaomicron; GI transit; IBS; constipation; genetically engineered; microbiome; motility; phage promoter; secretion; tryptophan
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Year: 2018 PMID: 29902441 PMCID: PMC6055526 DOI: 10.1016/j.chom.2018.05.004
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023