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JB Accepts, published online ahead of print on 24 August 2007
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J. Bacteriol. doi:10.1128/JB.00767-07
Copyright (c) 2007, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Epsilon Toxin Plasmids of Clostridium perfringens Type D are Conjugative

Meredith L. Hughes, Rachael Poon, Vicki Adams, Sameera Sayeed, Juliann Saputo, Francisco A. Uzal, Bruce A. McClane, and Julian I. Rood*

Australian Research Council Centre of Excellence in Structural and Functional Microbial Genomics, Department of Microbiology, Monash University, Victoria, 3800, Australia, Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261, U.S.A., California Animal Health and Food Safety Laboratory, San Bernardino Branch, School of Veterinary Medicine, University of California, Davis, San Bernardino, California 92408, U.S.A.

* To whom correspondence should be addressed. Email: julian.rood{at}med.monash.edu.au.


   Abstract

Isolates of Clostridium perfringens type D produce the potent epsilon-toxin (a CDC/USDA overlap class B select agent) and are responsible for several economically significant enterotoxemias of domestic livestock. It is well established that the epsilon-toxin structural gene, etx, is encoded on large plasmids. We have now shown that at least two of these plasmids are conjugative. The etx gene on these plasmids was insertionally inactivated using a chloramphenicol resistance cassette to phenotypically tag the plasmid. High frequency conjugative transfer of these tagged plasmids into the C. perfringens type A strain JIR325 was demonstrated and the resultant transconjugants were shown to act as donors in subsequent mating experiments. We also demonstrated the transfer of "unmarked" native {epsilon}-toxin plasmids into strain JIR325, by exploiting the high transfer frequency. The transconjugants isolated from these experiments expressed functional {epsilon}-toxin since their supernatants caused cytopathic effects on MDCK cells and were toxic in mice. Using the widely accepted multiplex PCR approach to toxin genotyping, these type A-derived transconjugants were now genotypically type D. These findings have significant implications for the C. perfringens typing system since it is based on the toxin profile of each strain. Our study demonstrates the fluid nature of these toxinotypes and their dependence upon the presence or absence of toxin plasmids, some of which have for the first time been shown to be conjugative.




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