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Reduced Mucosal Antimicrobial Activity in Crohn's Disease of the Colon

Overview
Journal Gut
Specialty Gastroenterology
Date 2007 Apr 26
PMID 17456510
Citations 47
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Abstract

Objectives: In order to maintain the mucosal barrier against luminal microorganisms the intestinal epithelial cells synthesise various broad-spectrum antimicrobial peptides including defensins and cathelicidins. Recent studies indicate that both may be deficient in Crohn's disease. To elucidate the possible functional consequences of this deficiency antimicrobial activity in colonic mucosa from patients with inflammatory bowel disease and healthy controls was investigated.

Methods: A flow cytometric assay was established to quantitate bacterial killing and test the antibacterial activity of cationic peptide extracts from colonic biopsies taken from patients with active or inactive ileocolonic or colonic Crohn's disease (n = 22), ulcerative colitis (n = 29) and controls (n = 13) against clinical isolates of Bacteroides vulgatus and Enterococcus faecalis or the reference strains Escherichia coli American Type Culture Collection (ATCC) 25922 and Staphylococcus aureus ATCC 25923.

Results: Compared with controls and ulcerative colitis there was a reduced antimicrobial effect in Crohn's disease extracts that was most evident against B. vulgatus. The antimicrobial effect against E. coli and E. faecalis was significantly lower in Crohn's disease compared with ulcerative colitis. Activity against S. aureus disclosed a similar pattern, but was less pronounced. The differences were independent of the inflammation status or concurrent steroid treatment. Bacteria incubated with biopsy extracts from ulcerative colitis patients frequently showed a characteristic change in cell size and granularity, compatible with more extensive membrane disintegration, compared with bacteria incubated with extracts from controls or Crohn's disease.

Conclusion: Crohn's disease of the colon is characterized by a diminished functional antimicrobial activity that is consistent with the reported low antibacterial peptide expression.

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References
1.
Swidsinski A, Ladhoff A, Pernthaler A, Swidsinski S, Loening-Baucke V, Ortner M . Mucosal flora in inflammatory bowel disease. Gastroenterology. 2002; 122(1):44-54. DOI: 10.1053/gast.2002.30294. View

2.
Mylonaki M, Rayment N, Rampton D, Hudspith B, Brostoff J . Molecular characterization of rectal mucosa-associated bacterial flora in inflammatory bowel disease. Inflamm Bowel Dis. 2005; 11(5):481-7. DOI: 10.1097/01.mib.0000159663.62651.4f. View

3.
Porter E, Poles M, Lee J, Naitoh J, Bevins C, Ganz T . Isolation of human intestinal defensins from ileal neobladder urine. FEBS Lett. 1998; 434(3):272-6. DOI: 10.1016/s0014-5793(98)00994-6. View

4.
Farrell R, Lamont J . Microbial factors in inflammatory bowel disease. Gastroenterol Clin North Am. 2002; 31(1):41-62. DOI: 10.1016/s0889-8553(01)00004-8. View

5.
Bevins C . The Paneth cell and the innate immune response. Curr Opin Gastroenterol. 2005; 20(6):572-80. DOI: 10.1097/00001574-200411000-00012. View