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The α-toxin of Clostridium septicum is essential for virulence
Catherine L. Kennedy 1 , Efrosinia O. Krejany 1 , Lauren F. Young 1,2 , Jennifer R. O'Connor 1 , Milena M. Awad 1 , Richard L. Boyd 2 , John J. Emmins 2 , Dena Lyras 1 and Julian I. Rood 1 *
  1 Australian Bacterial Pathogenesis Program, Department of Microbiology, Monash University, Vic. 3800, Australia.
  2 Department of Immunology, Monash University, Alfred Medical Research and Education Precinct, Prahran Vic. 3161, Australia.
Correspondence to   *E-mail Julian.Rood@med.monash.edu.au; Tel. (+61) 3 9905 4825; Fax (+61) 3 9905 4811.
Copyright 2005 Blackwell Publishing Ltd

Summary

AbstractIntroductionResultsDiscussionExperimental proceduresAcknowledgementsReferences

Clostridium septicum is the causative agent of spontaneous gas gangrene or atraumatic myonecrosis, a sudden and frequently fatal infection that is increasingly associated with malignancy of the colon. Little is known about the disease process although the focus of virulence studies has been the α-toxin, a pore-forming cytolysin that is encoded by the csa gene and secreted as an inactive protoxin. Until now a lack of techniques for the genetic manipulation of C. septicum has hindered the use of molecular approaches to understand pathogenesis. By introducing plasmids by conjugation from Escherichia coli, we have developed methods for the genetic manipulation of C. septicum and constructed a chromosomal csa mutant by allelic exchange. Virulence testing of an isogenic series of strains consisting of the wild type, the csa mutant, and a csa mutant complemented with the wild-type csa gene revealed that the development of fulminant myonecrosis in mice was dependent on the ability to produce a functional haemolytic α-toxin. Furthermore, the inhibition of leukocyte influx into the lesion, which is very typical of clostridial myonecrosis, was also dependent on the ability to produce α-toxin. This study represents the first definitive identification of a virulence factor in this organism and opens the way for further studies that will delineate the role of other putative virulence factors in this significant pathogen.


Accepted 14 June, 2005.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-2958.2005.04774.x About DOI

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