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Published Online First: 6 October 2006. doi:10.1136/gut.2006.099796
Gut 2007;56:669-675
Copyright © 2007 BMJ Publishing Group Ltd & British Society of Gastroenterology.

INFLAMMATORY BOWEL DISEASE

High prevalence of Escherichia coli belonging to the B2+D phylogenetic group in inflammatory bowel disease

Roman Kotlowski1, Charles N Bernstein3, Shadi Sepehri2, Denis O Krause3

1 Department of Animal Science, University of Manitoba, Winnipeg, Manitoba, Canada
2 Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Manitoba, Canada
3 Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada

Correspondence to:
Dr DO Krause
Department of Animal Science, 236 Animal Science Building, University of Manitoba, Winnipeg, MB, Canada R3T 2N2; denis_krause{at}umanitoba.ca

Background: It is not clear which species of bacteria may be involved in inflammatory bowel disease (IBD). One way of determining which bacteria might be likely candidates is to use culture-independent methods to identify microorganisms that are present in diseased tissues but not in controls.

Aims: (1) To assess the diversity of microbial communities of biopsy tissue using culture-independent methods; (2) to culture the bacteria found in the tissues of patients with IBD but not in the controls; (3) to identify potential virulence factors associated with cultured bacteria.

Methods: 84 biopsy specimens were collected from 15 controls, 13 patients with Crohn’s disease (CD) and 19 patients with ulcerative colitis (UC) from a population-based case–control study. Ribosomal intergenic spacer analysis (RISA) was conducted to identify unique DNA bands in tissues from patients with CD and UC that did not appear in controls.

Results: RISA followed by DNA sequencing identified unique bands in biopsy specimens from patients with IBD that were classified as Escherichia coli. Targeted culture showed a significantly (p<0.05) higher number of Enterobacteriaceae in specimens from patients with IBD. The B2+D phylogenetic group, serine protease autotransporters (SPATE) and adherence factors were more likely to be associated with tissues from patients with UC and CD than with controls.

Conclusions: The abundance of Enterobacteriaceae is 3–4 logs higher in tissues of patients with IBD and the B2+D phylogenetic groups are more prevalent in patients with UC and CD. The B2+D phylogenetic groups are associated with SPATE and adherence factors and may have a significant role in disease aetiology.

Abbreviations: CD, Crohn’s disease; IBD, inflammatory bowel disease; PAI, pathogenicity island; RFLP, restriction fragment length polymorphism; RISA, ribosomal intergenic spacer analysis; SPATE, serine protease autotransporters; UC, ulcerative colitis


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