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Disease-Specific Enteric Microbiome Dysbiosis in Inflammatory Bowel Disease
Inflammatory Bowel disease (IBD) is traditionally divided into Crohn's disease (CD) and ulcerative colitis (UC). UC is a relapsing non-transmural inflammatory disease that is restricted to the colon and is characterized by flare-ups of bloody diarrhea. CD is a chronic, segmental localized granu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256240/ https://www.ncbi.nlm.nih.gov/pubmed/30525037 http://dx.doi.org/10.3389/fmed.2018.00304 |
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author | Mirsepasi-Lauridsen, Hengameh Chloé Vrankx, Katleen Engberg, Jørgen Friis-Møller, Alice Brynskov, Jørn Nordgaard-Lassen, Inge Petersen, Andreas Munk Krogfelt, Karen Angeliki |
author_facet | Mirsepasi-Lauridsen, Hengameh Chloé Vrankx, Katleen Engberg, Jørgen Friis-Møller, Alice Brynskov, Jørn Nordgaard-Lassen, Inge Petersen, Andreas Munk Krogfelt, Karen Angeliki |
author_sort | Mirsepasi-Lauridsen, Hengameh Chloé |
collection | PubMed |
description | Inflammatory Bowel disease (IBD) is traditionally divided into Crohn's disease (CD) and ulcerative colitis (UC). UC is a relapsing non-transmural inflammatory disease that is restricted to the colon and is characterized by flare-ups of bloody diarrhea. CD is a chronic, segmental localized granulomatous disease that can affect any part of the entire gastrointestinal tract. Ileo-anal pouch is a procedure restoring functionality of the rectum after a colectomy. IBD is a multifactorial disease and flares of IBD are probably triggered by changes in the intestinal microbiota followed by an abnormal immune response. In this study, we aim to analyze the intestinal bacterial diversity in IBD patients during various stages of disease compared with healthy controls. Permission for human experiments and recruitment of participants was obtained from the Ethic Committee for Copenhagen County hospitals (Permission no. KA-03019, Permission no. KA-20060159). Stools from 26 healthy controls, 42 CD, 38 UC and 18 pouch patients were collected. Stool DNA extraction was performed using Qiagen, DNA mini stool kit Denmark. DGGE-PCR amplifying the V2-V3 region of 16S-rDNA gene of the bacteria was amplified by universal primers HDA1 and HDA2. Analysis of DGGE was performed blinded using BioNumerics version 7.5. After normalization, a DGGE gel band matching was performed. The similarities between profiles were calculated with a ranked Pearson correlation coefficient based on the band matching results using band intensities. Simpson's index of diversity and Pielou's species evenness were calculated. Based on the Shannon Diversity Index, UC patients had lower species diversity and bacterial evenness in comparison to healthy persons, p < 0.05. However, only CD and disease pouch patients had lower species diversity compared to those with inactive disease and healthy controls. Well-functioning pouch patients had decreased species evenness in comparison to diseased pouch patients and control group. During the active disease stage in CD and pouch, the patients have a low bacterial diversity in their gut when compared to the inactive stage. In UC patients, a generally low diversity was observed at all stages of the disease compared to healthy controls. |
format | Online Article Text |
id | pubmed-6256240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62562402018-12-06 Disease-Specific Enteric Microbiome Dysbiosis in Inflammatory Bowel Disease Mirsepasi-Lauridsen, Hengameh Chloé Vrankx, Katleen Engberg, Jørgen Friis-Møller, Alice Brynskov, Jørn Nordgaard-Lassen, Inge Petersen, Andreas Munk Krogfelt, Karen Angeliki Front Med (Lausanne) Medicine Inflammatory Bowel disease (IBD) is traditionally divided into Crohn's disease (CD) and ulcerative colitis (UC). UC is a relapsing non-transmural inflammatory disease that is restricted to the colon and is characterized by flare-ups of bloody diarrhea. CD is a chronic, segmental localized granulomatous disease that can affect any part of the entire gastrointestinal tract. Ileo-anal pouch is a procedure restoring functionality of the rectum after a colectomy. IBD is a multifactorial disease and flares of IBD are probably triggered by changes in the intestinal microbiota followed by an abnormal immune response. In this study, we aim to analyze the intestinal bacterial diversity in IBD patients during various stages of disease compared with healthy controls. Permission for human experiments and recruitment of participants was obtained from the Ethic Committee for Copenhagen County hospitals (Permission no. KA-03019, Permission no. KA-20060159). Stools from 26 healthy controls, 42 CD, 38 UC and 18 pouch patients were collected. Stool DNA extraction was performed using Qiagen, DNA mini stool kit Denmark. DGGE-PCR amplifying the V2-V3 region of 16S-rDNA gene of the bacteria was amplified by universal primers HDA1 and HDA2. Analysis of DGGE was performed blinded using BioNumerics version 7.5. After normalization, a DGGE gel band matching was performed. The similarities between profiles were calculated with a ranked Pearson correlation coefficient based on the band matching results using band intensities. Simpson's index of diversity and Pielou's species evenness were calculated. Based on the Shannon Diversity Index, UC patients had lower species diversity and bacterial evenness in comparison to healthy persons, p < 0.05. However, only CD and disease pouch patients had lower species diversity compared to those with inactive disease and healthy controls. Well-functioning pouch patients had decreased species evenness in comparison to diseased pouch patients and control group. During the active disease stage in CD and pouch, the patients have a low bacterial diversity in their gut when compared to the inactive stage. In UC patients, a generally low diversity was observed at all stages of the disease compared to healthy controls. Frontiers Media S.A. 2018-11-20 /pmc/articles/PMC6256240/ /pubmed/30525037 http://dx.doi.org/10.3389/fmed.2018.00304 Text en Copyright © 2018 Mirsepasi-Lauridsen, Vrankx, Engberg, Friis-Møller, Brynskov, Nordgaard-Lassen, Petersen and Krogfelt. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Mirsepasi-Lauridsen, Hengameh Chloé Vrankx, Katleen Engberg, Jørgen Friis-Møller, Alice Brynskov, Jørn Nordgaard-Lassen, Inge Petersen, Andreas Munk Krogfelt, Karen Angeliki Disease-Specific Enteric Microbiome Dysbiosis in Inflammatory Bowel Disease |
title | Disease-Specific Enteric Microbiome Dysbiosis in Inflammatory Bowel Disease |
title_full | Disease-Specific Enteric Microbiome Dysbiosis in Inflammatory Bowel Disease |
title_fullStr | Disease-Specific Enteric Microbiome Dysbiosis in Inflammatory Bowel Disease |
title_full_unstemmed | Disease-Specific Enteric Microbiome Dysbiosis in Inflammatory Bowel Disease |
title_short | Disease-Specific Enteric Microbiome Dysbiosis in Inflammatory Bowel Disease |
title_sort | disease-specific enteric microbiome dysbiosis in inflammatory bowel disease |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256240/ https://www.ncbi.nlm.nih.gov/pubmed/30525037 http://dx.doi.org/10.3389/fmed.2018.00304 |
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