Abstract

IntroductionInteractions between the gut microbiota and enteroendocrine cells play important role in irritable bowel syndrome (IBS). Reduced stem cell densities and their differentiation into enteroendocrine cells may cause abnormal densities of the duodenal enteroendocrine cells in IBS patients.Materials and MethodsWe aimed to investigate the effects of fecal microbiota transplantation (FMT) on stem cell differentiation into enteroendocrine cells as detected by neurogenin 3, stem cells as detected by Musashi 1, and the enteroendocrine cells in the duodenum of IBS patients. The study included 16 IBS patients according to Rome III criteria. Four patients were excluded. The remaining patients (n = 12, four females and eight males) were divided according to the cause of IBS into post-infectious (n = 6) and idiopathic (n = 6) IBS. They completed the following questionnaires before and 3 weeks after FMT: IBS-Symptom Severity Scoring system (IBS-SSS) and IBS-Symptom Questionnaire (IBS-SQ). Feces donated by healthy relatives of the patients were transplanted via gastroscope. Biopsies were taken from the descending part of the duodenum at baseline and 3 weeks after FMT. They were immunostained for neurogenin 3, Musashi 1, and all types of duodenal enteroendocrine cells and quantified by computerized image analysis. Microbiota analyses of feces collected just before and 3 weeks after FMT were performed using GA-map™ Dysbiosis test (Genetic Analysis AS, Oslo, Norway).ResultsThe total scores for IBS-SSS and IBS-SQ were significantly improved 3 weeks after receiving FMT, P = 0.0009 and <0.0001, respectively. The stem cell densities of neurogenin 3 increased significantly following FMT (P = 0.0006) but not for Musashi 1 (P = 0.42). The cell densities of chromogranin A, cholecystokinin, gastric inhibitory peptide, serotonin, and somatostatin, but not for secretin, have significantly changed in both IBS groups after 3 weeks from receiving FMT.ConclusionMore than two-thirds of IBS patients experienced improvement in their symptoms parallel to changes in the enteroendocrine cells densities 3 weeks after FMT. The changes in the enteroendocrine cell densities do not appear to be caused by changes in the stem cells or their early progenitors rather by changes in the differentiation progeny as detected by neurogenin 3. The study was retrospectively registered at ClinicalTrials.gov (ID: NCT03333291).Clinical Trial Registration ClinicalTrials.gov, identifier NCT03333291.

Highlights

  • Interactions between the gut microbiota and enteroendocrine cells play important role in irritable bowel syndrome (IBS)

  • Four out of the 16 originally included patients were excluded after withdrawing their consents to participate for practical reasons (n = 1), failed gastroscope intubation after Fecal microbiota transplantation (FMT) (n = 1), being diagnosed with functional dyspepsia (n = 1), and positive stool culture for Clostridium difficile (n = 1)

  • The densities of stem cells and enteroendocrine cells in the duodenum are abnormal in IBS patients before FMT, which is consistent with previous publications (El-Salhy et al, 2010; El-Salhy et al, 2014c; El-Salhy et al, 2015)

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Summary

Introduction

Interactions between the gut microbiota and enteroendocrine cells play important role in irritable bowel syndrome (IBS). Enteroendocrine cells, stem cells, and their progenitor cells are abnormal in the proximal and distal parts of the small intestine of patients with irritable bowel syndrome (IBS) (Dizdar et al, 2010; El-Salhy et al, 2010; El-Salhy et al, 2014a; El-Salhy, 2015; El-Salhy and Gilja, 2017). The abnormalities in enteroendocrine cells seem to explain the dysmotility, visceral hypersensitivity, and abnormal intestinal secretion seen in IBS patients (El-Salhy et al, 2014). Human feces from a healthy subject are used to treat patients

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