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Phylogenetic Analysis of Dysbiosis in Ulcerative Colitis During Remission

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2013
Authors
Rajilić-Stojanović, Mirjana
Shanahan, Fergus
Guarner, Francisco
de Vos, Willem M.
Article (Published version)
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Abstract
Background: Presence of intestinal microbes is a prerequisite for the development of ulcerative colitis (UC), although deviation of the normal intestinal microbiota composition, dysbiosis, is presumably implicated in the etiology of UC. Methods: The fecal microbiota of 30 UC samples obtained from 15 patients who were sampled twice and from 15 healthy control subjects originating from 2 geographic locations was analyzed using highly reproducible phylogenetic microarray that has the capacity for detection and quantification of more than 1000 intestinal bacteria in a wide dynamic range. Results: The fecal microbiota composition is not significantly influenced by geographic location, age, or gender, but it differs significantly between the patients with UC and the control subjects (P = 0.0004). UC-associated microbiota is stable during remission and similar among all patients with UC. Significant reduction of bacterial diversity of members of the Clostridium cluster IV and significant redu...ction in the abundance of bacteria involved in butyrate and propionate metabolism, including Ruminococcus bromii et rel. Eubacterium rectale et rel., Roseburia sp., and Akkermansia sp. are markers of dysbiosis in UC. Increased abundance of (opportunistic) pathogens including Fusobacterium sp., Peptostreptococcus sp., Helicobacter sp., and Campylobacter sp. as well as Clostridium difficile were found to be associated with UC. Conclusions: Dysbiosis in UC is stable in time and shared between patients from different geographic locations. The microbial alterations offer a mechanistic insight into the pathogenesis of the disease. (Inflamm Bowel Dis 2013;19:481-488)

Keywords:
microbiota / dysbiosis / ulcerative colitis / phylogenetic microarray / intestinal / bacteria
Source:
Inflammatory Bowel Diseases, 2013, 19, 3, 481-488
Publisher:
  • Lippincott Williams & Wilkins, Philadelphia

DOI: 10.1097/MIB.0b013e31827fec6d

ISSN: 1078-0998

PubMed: 23385241

WoS: 000316450200017

Scopus: 2-s2.0-84876375062
[ Google Scholar ]
243
209
URI
http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2551
Collections
  • Radovi istraživača / Researchers’ publications (TMF)
Institution/Community
Tehnološko-metalurški fakultet
TY  - JOUR
AU  - Rajilić-Stojanović, Mirjana
AU  - Shanahan, Fergus
AU  - Guarner, Francisco
AU  - de Vos, Willem M.
PY  - 2013
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2551
AB  - Background: Presence of intestinal microbes is a prerequisite for the development of ulcerative colitis (UC), although deviation of the normal intestinal microbiota composition, dysbiosis, is presumably implicated in the etiology of UC. Methods: The fecal microbiota of 30 UC samples obtained from 15 patients who were sampled twice and from 15 healthy control subjects originating from 2 geographic locations was analyzed using highly reproducible phylogenetic microarray that has the capacity for detection and quantification of more than 1000 intestinal bacteria in a wide dynamic range. Results: The fecal microbiota composition is not significantly influenced by geographic location, age, or gender, but it differs significantly between the patients with UC and the control subjects (P = 0.0004). UC-associated microbiota is stable during remission and similar among all patients with UC. Significant reduction of bacterial diversity of members of the Clostridium cluster IV and significant reduction in the abundance of bacteria involved in butyrate and propionate metabolism, including Ruminococcus bromii et rel. Eubacterium rectale et rel., Roseburia sp., and Akkermansia sp. are markers of dysbiosis in UC. Increased abundance of (opportunistic) pathogens including Fusobacterium sp., Peptostreptococcus sp., Helicobacter sp., and Campylobacter sp. as well as Clostridium difficile were found to be associated with UC. Conclusions: Dysbiosis in UC is stable in time and shared between patients from different geographic locations. The microbial alterations offer a mechanistic insight into the pathogenesis of the disease. (Inflamm Bowel Dis 2013;19:481-488)
PB  - Lippincott Williams & Wilkins, Philadelphia
T2  - Inflammatory Bowel Diseases
T1  - Phylogenetic Analysis of Dysbiosis in Ulcerative Colitis During Remission
EP  - 488
IS  - 3
SP  - 481
VL  - 19
DO  - 10.1097/MIB.0b013e31827fec6d
ER  - 
@article{
author = "Rajilić-Stojanović, Mirjana and Shanahan, Fergus and Guarner, Francisco and de Vos, Willem M.",
year = "2013",
abstract = "Background: Presence of intestinal microbes is a prerequisite for the development of ulcerative colitis (UC), although deviation of the normal intestinal microbiota composition, dysbiosis, is presumably implicated in the etiology of UC. Methods: The fecal microbiota of 30 UC samples obtained from 15 patients who were sampled twice and from 15 healthy control subjects originating from 2 geographic locations was analyzed using highly reproducible phylogenetic microarray that has the capacity for detection and quantification of more than 1000 intestinal bacteria in a wide dynamic range. Results: The fecal microbiota composition is not significantly influenced by geographic location, age, or gender, but it differs significantly between the patients with UC and the control subjects (P = 0.0004). UC-associated microbiota is stable during remission and similar among all patients with UC. Significant reduction of bacterial diversity of members of the Clostridium cluster IV and significant reduction in the abundance of bacteria involved in butyrate and propionate metabolism, including Ruminococcus bromii et rel. Eubacterium rectale et rel., Roseburia sp., and Akkermansia sp. are markers of dysbiosis in UC. Increased abundance of (opportunistic) pathogens including Fusobacterium sp., Peptostreptococcus sp., Helicobacter sp., and Campylobacter sp. as well as Clostridium difficile were found to be associated with UC. Conclusions: Dysbiosis in UC is stable in time and shared between patients from different geographic locations. The microbial alterations offer a mechanistic insight into the pathogenesis of the disease. (Inflamm Bowel Dis 2013;19:481-488)",
publisher = "Lippincott Williams & Wilkins, Philadelphia",
journal = "Inflammatory Bowel Diseases",
title = "Phylogenetic Analysis of Dysbiosis in Ulcerative Colitis During Remission",
pages = "488-481",
number = "3",
volume = "19",
doi = "10.1097/MIB.0b013e31827fec6d"
}
Rajilić-Stojanović, M., Shanahan, F., Guarner, F.,& de Vos, W. M.. (2013). Phylogenetic Analysis of Dysbiosis in Ulcerative Colitis During Remission. in Inflammatory Bowel Diseases
Lippincott Williams & Wilkins, Philadelphia., 19(3), 481-488.
https://doi.org/10.1097/MIB.0b013e31827fec6d
Rajilić-Stojanović M, Shanahan F, Guarner F, de Vos WM. Phylogenetic Analysis of Dysbiosis in Ulcerative Colitis During Remission. in Inflammatory Bowel Diseases. 2013;19(3):481-488.
doi:10.1097/MIB.0b013e31827fec6d .
Rajilić-Stojanović, Mirjana, Shanahan, Fergus, Guarner, Francisco, de Vos, Willem M., "Phylogenetic Analysis of Dysbiosis in Ulcerative Colitis During Remission" in Inflammatory Bowel Diseases, 19, no. 3 (2013):481-488,
https://doi.org/10.1097/MIB.0b013e31827fec6d . .

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