Literature DB >> 21807975

The insect peptide coprisin prevents Clostridium difficile-mediated acute inflammation and mucosal damage through selective antimicrobial activity.

Jin Ku Kang1, Jae Sam Hwang, Hyo Jung Nam, Keun Jae Ahn, Heon Seok, Sung-Kuk Kim, Eun Young Yun, Charalabos Pothoulakis, John Thomas Lamont, Ho Kim.   

Abstract

Clostridium difficile-associated diarrhea and pseudomembranous colitis are typically treated with vancomycin or metronidazole, but recent increases in relapse incidence and the emergence of drug-resistant strains of C. difficile indicate the need for new antibiotics. We previously isolated coprisin, an antibacterial peptide from Copris tripartitus, a Korean dung beetle, and identified a nine-amino-acid peptide in the α-helical region of it (LLCIALRKK) that had antimicrobial activity (J.-S. Hwang et al., Int. J. Pept., 2009, doi:10.1155/2009/136284). Here, we examined whether treatment with a coprisin analogue (a disulfide dimer of the nine peptides) prevented inflammation and mucosal damage in a mouse model of acute gut inflammation established by administration of antibiotics followed by C. difficile infection. In this model, coprisin treatment significantly ameliorated body weight decreases, improved the survival rate, and decreased mucosal damage and proinflammatory cytokine production. In contrast, the coprisin analogue had no apparent antibiotic activity against commensal bacteria, including Lactobacillus and Bifidobacterium, which are known to inhibit the colonization of C. difficile. The exposure of C. difficile to the coprisin analogue caused a marked increase in nuclear propidium iodide (PI) staining, indicating membrane damage; the staining levels were similar to those seen with bacteria treated with a positive control for membrane disruption (EDTA). In contrast, coprisin analogue treatment did not trigger increases in the nuclear PI staining of Bifidobacterium thermophilum. This observation suggests that the antibiotic activity of the coprisin analogue may occur through specific membrane disruption of C. difficile. Thus, these results indicate that the coprisin analogue may prove useful as a therapeutic agent for C. difficile infection-associated inflammatory diarrhea and pseudomembranous colitis.

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Year:  2011        PMID: 21807975      PMCID: PMC3186999          DOI: 10.1128/AAC.00177-11

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  49 in total

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Review 7.  Clostridium difficile colitis.

Authors:  C P Kelly; C Pothoulakis; J T LaMont
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9.  Rifalazil treats and prevents relapse of clostridium difficile-associated diarrhea in hamsters.

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Journal:  J Biol Chem       Date:  2015-12-11       Impact factor: 5.157

3.  Antimicrobial Peptide JH-3 Effectively Kills Salmonella enterica Serovar Typhimurium Strain CVCC541 and Reduces Its Pathogenicity in Mice.

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Journal:  Curr Pharm Des       Date:  2013       Impact factor: 3.116

5.  Anticancer activity of CopA3 dimer peptide in human gastric cancer cells.

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Review 6.  Antimicrobial proteins in intestine and inflammatory bowel diseases.

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Journal:  Intest Res       Date:  2014-01-28

Review 7.  Regulated Cell Death as a Therapeutic Target for Novel Antifungal Peptides and Biologics.

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8.  Effective inhibition of Clostridioides difficile by the novel peptide CM-A.

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9.  Protective Effects of Bifidobacterial Strains Against Toxigenic Clostridium difficile.

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