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Microbial dysbiosis in irritable bowel syndrome: A single‐center metagenomic study in Saudi Arabia

BACKGROUND: The focus of this study was to explore potential differences in colonic mucosal microbiota in irritable bowel syndrome (IBS) patients compared to a control group utilizing a metagenomic study. METHODS: Mucosal microbiota samples were collected from each IBS patient utilizing jet‐flushing...

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Autores principales: Masoodi, Ibrahim, Alshanqeeti, Ali S, Alyamani, Essam J, AlLehibi, Abed A, Alqutub, Adel N, Alsayari, Khalid N, Alomair, Ahmed O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7411548/
https://www.ncbi.nlm.nih.gov/pubmed/32782952
http://dx.doi.org/10.1002/jgh3.12313
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author Masoodi, Ibrahim
Alshanqeeti, Ali S
Alyamani, Essam J
AlLehibi, Abed A
Alqutub, Adel N
Alsayari, Khalid N
Alomair, Ahmed O
author_facet Masoodi, Ibrahim
Alshanqeeti, Ali S
Alyamani, Essam J
AlLehibi, Abed A
Alqutub, Adel N
Alsayari, Khalid N
Alomair, Ahmed O
author_sort Masoodi, Ibrahim
collection PubMed
description BACKGROUND: The focus of this study was to explore potential differences in colonic mucosal microbiota in irritable bowel syndrome (IBS) patients compared to a control group utilizing a metagenomic study. METHODS: Mucosal microbiota samples were collected from each IBS patient utilizing jet‐flushing colonic mucosa in unified segments of the colon with distilled water, followed by aspiration, during colonoscopy. All the purified dsDNA was extracted and quantified before metagenomic sequencing using an Illumina platform. An equal number of healthy age‐matched controls were also examined for colonic mucosal microbiota, which were obtained during screening colonoscopies. RESULTS: The microbiota data on 50 IBS patients (31 females), with a mean age 43.94 ± 14.50 (range19–65), were analyzed in comparison to 50 controls. Satisfactory DNA samples were subjected to metagenomics study, followed by comprehensive comparative phylogenetic analysis. Metagenomics analysis was carried out, and 3.58G reads were sequenced. Community richness (Chao) and microbial structure in IBS patients were shown to be significantly different from those in the control group. Enrichment of Oxalobacter formigenes, Sutterella wadsworthensis, and Bacteroides pectinophilus was significantly observed in controls, whereas enrichment of Collinsella aerofaciens, Gemella morbillorum, and Veillonella parvula Actinobacteria was observed significantly in the IBS cohort. CONCLUSION: The current study has demonstrated significant differences in the microbiota of IBS patients compared to controls.
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spelling pubmed-74115482020-08-10 Microbial dysbiosis in irritable bowel syndrome: A single‐center metagenomic study in Saudi Arabia Masoodi, Ibrahim Alshanqeeti, Ali S Alyamani, Essam J AlLehibi, Abed A Alqutub, Adel N Alsayari, Khalid N Alomair, Ahmed O JGH Open Original Articles BACKGROUND: The focus of this study was to explore potential differences in colonic mucosal microbiota in irritable bowel syndrome (IBS) patients compared to a control group utilizing a metagenomic study. METHODS: Mucosal microbiota samples were collected from each IBS patient utilizing jet‐flushing colonic mucosa in unified segments of the colon with distilled water, followed by aspiration, during colonoscopy. All the purified dsDNA was extracted and quantified before metagenomic sequencing using an Illumina platform. An equal number of healthy age‐matched controls were also examined for colonic mucosal microbiota, which were obtained during screening colonoscopies. RESULTS: The microbiota data on 50 IBS patients (31 females), with a mean age 43.94 ± 14.50 (range19–65), were analyzed in comparison to 50 controls. Satisfactory DNA samples were subjected to metagenomics study, followed by comprehensive comparative phylogenetic analysis. Metagenomics analysis was carried out, and 3.58G reads were sequenced. Community richness (Chao) and microbial structure in IBS patients were shown to be significantly different from those in the control group. Enrichment of Oxalobacter formigenes, Sutterella wadsworthensis, and Bacteroides pectinophilus was significantly observed in controls, whereas enrichment of Collinsella aerofaciens, Gemella morbillorum, and Veillonella parvula Actinobacteria was observed significantly in the IBS cohort. CONCLUSION: The current study has demonstrated significant differences in the microbiota of IBS patients compared to controls. Wiley Publishing Asia Pty Ltd 2020-02-25 /pmc/articles/PMC7411548/ /pubmed/32782952 http://dx.doi.org/10.1002/jgh3.12313 Text en © 2020 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Masoodi, Ibrahim
Alshanqeeti, Ali S
Alyamani, Essam J
AlLehibi, Abed A
Alqutub, Adel N
Alsayari, Khalid N
Alomair, Ahmed O
Microbial dysbiosis in irritable bowel syndrome: A single‐center metagenomic study in Saudi Arabia
title Microbial dysbiosis in irritable bowel syndrome: A single‐center metagenomic study in Saudi Arabia
title_full Microbial dysbiosis in irritable bowel syndrome: A single‐center metagenomic study in Saudi Arabia
title_fullStr Microbial dysbiosis in irritable bowel syndrome: A single‐center metagenomic study in Saudi Arabia
title_full_unstemmed Microbial dysbiosis in irritable bowel syndrome: A single‐center metagenomic study in Saudi Arabia
title_short Microbial dysbiosis in irritable bowel syndrome: A single‐center metagenomic study in Saudi Arabia
title_sort microbial dysbiosis in irritable bowel syndrome: a single‐center metagenomic study in saudi arabia
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7411548/
https://www.ncbi.nlm.nih.gov/pubmed/32782952
http://dx.doi.org/10.1002/jgh3.12313
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