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J Bacteriol. 2012 Nov;194(22):6240-7. doi: 10.1128/JB.01272-12. Epub 2012 Sep 14.

Novel high-molecular-weight, R-type bacteriocins of Clostridium difficile.

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1
AvidBiotics Corporation, South San Francisco, California, USA.

Abstract

Clostridium difficile causes one of the leading nosocomial infections in developed countries, and therapeutic choices are limited. Some strains of C. difficile produce phage tail-like particles upon induction of the SOS response. These particles have bactericidal activity against other C. difficile strains and can therefore be classified as bacteriocins, similar to the R-type pyocins of Pseudomonas aeruginosa. These R-type bacteriocin particles, which have been purified from different strains, each have a different C. difficile-killing spectrum, with no one bacteriocin killing all C. difficile isolates tested. We have identified the genetic locus of these "diffocins" (open reading frames 1359 to 1376) and have found them to be common among the species. The entire diffocin genetic locus of more than 20 kb was cloned and expressed in Bacillus subtilis, and this resulted in production of bactericidal particles. One of the interesting features of these particles is a very large structural protein of ~200 kDa, the product of gene 1374. This large protein determines the killing spectrum of the particles and is likely the receptor-binding protein. Diffocins may provide an alternate bactericidal agent to prevent or treat infections and to decolonize individuals who are asymptomatic carriers.

PMID:
22984261
PMCID:
PMC3486368
DOI:
10.1128/JB.01272-12
[Indexed for MEDLINE]
Free PMC Article
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