Journal article

Defining the roles of TcdA and TcdB in localized gastrointestinal disease, systemic organ damage, and the host response during Clostridium difficile infections

GP Carter, A Chakravorty, TAP Nguyen, S Mileto, F Schreiber, L Li, P Howarth, S Clare, B Cunningham, SP Sambol, A Cheknis, I Figueroa, S Johnson, D Gerding, JI Rood, G Dougan, TD Lawley, D Lyras

Mbio | AMER SOC MICROBIOLOGY | Published : 2015

Abstract

Clostridium difficile is a leading cause of antibiotic-associated diarrhea, a significant animal pathogen, and a worldwide public health burden. Most disease-causing strains secrete two exotoxins, TcdA and TcdB, which are considered to be the primary virulence factors. Understanding the role that these toxins play in disease is essential for the rational design of urgently needed new therapeutics. However, their relative contributions to disease remain contentious. Using three different animal models, we show that TcdA+ TcdB− mutants are attenuated in virulence in comparison to the wild-type (TcdA+ TcdB+) strain, whereas TcdA− TcdB+ mutants are fully virulent. We also show for the first time..

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Grants

Awarded by National Health and Medical Research Council


Funding Acknowledgements

Research at Monash University was supported by Project grants 545858 and APP1051584 (Australian National Health and Medical Research Council) and Discovery grant DP1093891 (Australian Research Council). D.L. was supported by Future fellowship FT120100779 (Australian Research Council). Research at the Sanger Institute was funded by the Wellcome Trust (grants 098051 and 086418) and the Medical Research Council New Investigator Research grant (grant 93614 to T.D.L.). S.J. and D.N.G. are funded by the VA Merit Review program.