Journal Article
Fecal Clostridiales distribution and short‐chain fatty acids reflect bowel habits in irritable bowel syndrome
Giorgio Gargari; Valentina Taverniti; Claudio Gardana; Cesare Cremon; Filippo Canducci; Isabella Pagano; Maria Raffaella Barbaro; Lara Bellacosa; Anna Maria Castellazzi; Chiara Valsecchi; Sara Carlotta Tagliacarne; Massimo Bellini; Lorenzo Bertani; Dario Gambaccini; Santino Marchi; Michele Cicala; Bastianello Germanà; Elisabetta Dal Pont; Maurizio Vecchi; Cristina Ogliari; Walter Fiore; Vincenzo Stanghellini; Giovanni Barbara; Simone Guglielmetti
Environmental Microbiology · Vol. 20, Issue 9 · pp. 3201-3213 · 2018
Abstract
Summary Irritable bowel syndrome (IBS), a common functional gastrointestinal disorder, is classified according to bowel habits as IBS with constipation (IBS‐C), with diarrhea (IBS‐D), with alternating constipation and diarrhea (IBS‐M), and unsubtyped (IBS‐U). The mechanisms leading to the different IBS forms are mostly unknown. This study aims to evaluate whether specific fecal bacterial taxa and/or short‐chain fatty acids (SCFAs) can be used to distinguish IBS subtypes and are relevant for explaining the clinical differences between IBS subcategories. We characterized five fecal samples collected at 4‐weeks intervals from 40 IBS patients by 16S rRNA gene profiling and SCFA quantification. Finally, we investigated the potential correlations in IBS subtypes between the fecal microbial signatures and host physiological and clinical parameters. We found significant differences in the distribution of Clostridiales OTUs among IBS subtypes and reduced levels of SCFAs in IBS‐C compared to IBS‐U and IBS‐D patients. Correlation analyses showed that the diverse representation of Clostridiales OTUs between IBS subtypes was associated with altered levels of SCFAs; furthermore, the same OTUs and SCFAs were associated with the fecal cytokine levels and stool consistency. Our results suggest that intestinal Clostridiales and SCFAs might serve as potential mechanistic biomarkers of IBS subtypes and represent therapeutic targets.