The Effects of Fecal Microbiota Transplantation on the Symptoms and the Duodenal Neurogenin 3, Musashi 1, and Enteroendocrine Cells in Patients With Diarrhea-Predominant Irritable Bowel Syndrome
- PMID: 34055657
- PMCID: PMC8149964
- DOI: 10.3389/fcimb.2021.524851
The Effects of Fecal Microbiota Transplantation on the Symptoms and the Duodenal Neurogenin 3, Musashi 1, and Enteroendocrine Cells in Patients With Diarrhea-Predominant Irritable Bowel Syndrome
Abstract
Introduction: Interactions 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 methods: We 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).
Results: The 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.
Conclusion: More 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.
Keywords: cell densities; duodenum; fecal microbiota transplantation; gut hormones; irritable bowel syndrome; microbiota; neuroendocrine; stem cells.
Copyright © 2021 Mazzawi, El-Salhy, Lied and Hausken.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Figures




Similar articles
-
The kinetics of gut microbial community composition in patients with irritable bowel syndrome following fecal microbiota transplantation.PLoS One. 2018 Nov 14;13(11):e0194904. doi: 10.1371/journal.pone.0194904. eCollection 2018. PLoS One. 2018. PMID: 30427836 Free PMC article.
-
Clinical response to fecal microbiota transplantation in patients with diarrhea-predominant irritable bowel syndrome is associated with normalization of fecal microbiota composition and short-chain fatty acid levels.Scand J Gastroenterol. 2019 Jun;54(6):690-699. doi: 10.1080/00365521.2019.1624815. Epub 2019 Jun 13. Scand J Gastroenterol. 2019. PMID: 31190584 Clinical Trial.
-
Changes in duodenal enteroendocrine cells in patients with irritable bowel syndrome following dietary guidance.Exp Biol Med (Maywood). 2017 Jul;242(13):1355-1362. doi: 10.1177/1535370217699537. Epub 2017 Mar 17. Exp Biol Med (Maywood). 2017. PMID: 28737477 Free PMC article.
-
Efficacy of Fecal Microbiota Transplantation in Irritable Bowel Syndrome Patients: An Updated Systematic Review and Meta-Analysis.Gastroenterol Nurs. 2022 Jan-Feb 01;45(1):11-20. doi: 10.1097/SGA.0000000000000652. Gastroenterol Nurs. 2022. PMID: 35108241
-
A meta-analysis of randomized controlled trials evaluating the effectiveness of fecal microbiota transplantation for patients with irritable bowel syndrome.BMC Gastroenterol. 2024 Jul 5;24(1):217. doi: 10.1186/s12876-024-03311-x. BMC Gastroenterol. 2024. PMID: 38970007 Free PMC article.
Cited by
-
Effects of faecal microbiota transplantation on the small intestinal mucosa in systemic sclerosis.Rheumatology (Oxford). 2023 Aug 1;62(8):2918-2929. doi: 10.1093/rheumatology/kead014. Rheumatology (Oxford). 2023. PMID: 36688692 Free PMC article.
-
Fecal microbiota transplantation for the treatment of irritable bowel syndrome: A systematic review and meta-analysis.World J Gastroenterol. 2023 May 28;29(20):3185-3202. doi: 10.3748/wjg.v29.i20.3185. World J Gastroenterol. 2023. PMID: 37346153 Free PMC article.
-
Gut Microbiota Manipulation in Irritable Bowel Syndrome.Microorganisms. 2022 Jun 30;10(7):1332. doi: 10.3390/microorganisms10071332. Microorganisms. 2022. PMID: 35889051 Free PMC article. Review.
-
Gut microbiota contributes to protection against porcine deltacoronavirus infection in piglets by modulating intestinal barrier and microbiome.Microbiome. 2025 Apr 7;13(1):93. doi: 10.1186/s40168-025-02092-z. Microbiome. 2025. PMID: 40189556 Free PMC article.
-
Gut microbiota: a new avenue to reveal pathological mechanisms of constipation.Appl Microbiol Biotechnol. 2022 Nov;106(21):6899-6913. doi: 10.1007/s00253-022-12197-2. Epub 2022 Oct 3. Appl Microbiol Biotechnol. 2022. PMID: 36190540 Review.
References
Publication types
MeSH terms
Associated data
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials