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Ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut microbiota

BACKGROUND: Previous studies suggest a link between gut microbiota and the development of ulcerative colitis (UC) and irritable bowel syndrome (IBS). Our aim was to investigate any quantitative differences in faecal bacterial compositions in UC and IBS patients compared to healthy controls, and to i...

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Autores principales: Noor, Samah O, Ridgway, Karyn, Scovell, Louise, Kemsley, E Katherine, Lund, Elizabeth K, Jamieson, Crawford, Johnson, Ian T, Narbad, Arjan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002299/
https://www.ncbi.nlm.nih.gov/pubmed/21073731
http://dx.doi.org/10.1186/1471-230X-10-134
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author Noor, Samah O
Ridgway, Karyn
Scovell, Louise
Kemsley, E Katherine
Lund, Elizabeth K
Jamieson, Crawford
Johnson, Ian T
Narbad, Arjan
author_facet Noor, Samah O
Ridgway, Karyn
Scovell, Louise
Kemsley, E Katherine
Lund, Elizabeth K
Jamieson, Crawford
Johnson, Ian T
Narbad, Arjan
author_sort Noor, Samah O
collection PubMed
description BACKGROUND: Previous studies suggest a link between gut microbiota and the development of ulcerative colitis (UC) and irritable bowel syndrome (IBS). Our aim was to investigate any quantitative differences in faecal bacterial compositions in UC and IBS patients compared to healthy controls, and to identify individual bacterial species that contribute to these differences. METHODS: Faecal microbiota of 13 UC patients, 11 IBS patients and 22 healthy volunteers were analysed by PCR-Denaturing Gradient Gel Electrophoresis (DGGE) using universal and Bacteroides specific primers. The data obtained were normalized using in-house developed statistical method and interrogated by multivariate approaches. The differentiated bands were excised and identified by sequencing the V3 region of the 16S rRNA genes. RESULTS: Band profiles revealed that number of predominant faecal bacteria were significantly different between UC, IBS and control group (p < 10(-4)). By assessing the mean band numbers in UC (37 ± 5) and IBS (39 ± 6), compared to the controls (45 ± 3), a significant decrease in bacterial species is suggested (p = 0.01). There were no significant differences between IBS and UC. Biodiversity of the bacterial species was significantly lower in UC (μ = 2.94, σ = 0.29) and IBS patients (μ = 2.90, σ = 0.38) than controls (μ = 3.25, σ = 0.16; p = 0.01). Moreover, similarity indices revealed greater biological variability of predominant bacteria in UC and IBS compared to the controls (median Dice coefficients 76.1% (IQR 70.9 - 83.1), 73.8% (IQR 67.0 - 77.5) and 82.9% (IQR 79.1 - 86.7) respectively). DNA sequencing of discriminating bands suggest that the presence of Bacteroides vulgatus, B. ovatus, B. uniformis, and Parabacteroides sp. in healthy volunteers distinguishes them from IBS and UC patients. DGGE profiles of Bacteroides species revealed a decrease of Bacteroides community in UC relative to IBS and controls. CONCLUSION: Molecular profiling of faecal bacteria revealed abnormalities of intestinal microbiota in UC and IBS patients, while different patterns of Bacteroides species loss in particular, were associated with UC and IBS.
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spelling pubmed-30022992010-12-16 Ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut microbiota Noor, Samah O Ridgway, Karyn Scovell, Louise Kemsley, E Katherine Lund, Elizabeth K Jamieson, Crawford Johnson, Ian T Narbad, Arjan BMC Gastroenterol Research Article BACKGROUND: Previous studies suggest a link between gut microbiota and the development of ulcerative colitis (UC) and irritable bowel syndrome (IBS). Our aim was to investigate any quantitative differences in faecal bacterial compositions in UC and IBS patients compared to healthy controls, and to identify individual bacterial species that contribute to these differences. METHODS: Faecal microbiota of 13 UC patients, 11 IBS patients and 22 healthy volunteers were analysed by PCR-Denaturing Gradient Gel Electrophoresis (DGGE) using universal and Bacteroides specific primers. The data obtained were normalized using in-house developed statistical method and interrogated by multivariate approaches. The differentiated bands were excised and identified by sequencing the V3 region of the 16S rRNA genes. RESULTS: Band profiles revealed that number of predominant faecal bacteria were significantly different between UC, IBS and control group (p < 10(-4)). By assessing the mean band numbers in UC (37 ± 5) and IBS (39 ± 6), compared to the controls (45 ± 3), a significant decrease in bacterial species is suggested (p = 0.01). There were no significant differences between IBS and UC. Biodiversity of the bacterial species was significantly lower in UC (μ = 2.94, σ = 0.29) and IBS patients (μ = 2.90, σ = 0.38) than controls (μ = 3.25, σ = 0.16; p = 0.01). Moreover, similarity indices revealed greater biological variability of predominant bacteria in UC and IBS compared to the controls (median Dice coefficients 76.1% (IQR 70.9 - 83.1), 73.8% (IQR 67.0 - 77.5) and 82.9% (IQR 79.1 - 86.7) respectively). DNA sequencing of discriminating bands suggest that the presence of Bacteroides vulgatus, B. ovatus, B. uniformis, and Parabacteroides sp. in healthy volunteers distinguishes them from IBS and UC patients. DGGE profiles of Bacteroides species revealed a decrease of Bacteroides community in UC relative to IBS and controls. CONCLUSION: Molecular profiling of faecal bacteria revealed abnormalities of intestinal microbiota in UC and IBS patients, while different patterns of Bacteroides species loss in particular, were associated with UC and IBS. BioMed Central 2010-11-12 /pmc/articles/PMC3002299/ /pubmed/21073731 http://dx.doi.org/10.1186/1471-230X-10-134 Text en Copyright ©2010 Noor et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Noor, Samah O
Ridgway, Karyn
Scovell, Louise
Kemsley, E Katherine
Lund, Elizabeth K
Jamieson, Crawford
Johnson, Ian T
Narbad, Arjan
Ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut microbiota
title Ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut microbiota
title_full Ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut microbiota
title_fullStr Ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut microbiota
title_full_unstemmed Ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut microbiota
title_short Ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut microbiota
title_sort ulcerative colitis and irritable bowel patients exhibit distinct abnormalities of the gut microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002299/
https://www.ncbi.nlm.nih.gov/pubmed/21073731
http://dx.doi.org/10.1186/1471-230X-10-134
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