Proteomic and Genomic Characterization of Highly Infectious Clostridium difficile 630 Spores

Author:

Lawley Trevor D.1,Croucher Nicholas J.2,Yu Lu3,Clare Simon1,Sebaihia Mohammed2,Goulding David1,Pickard Derek J.1,Parkhill Julian2,Choudhary Jyoti3,Dougan Gordon1

Affiliation:

1. Microbial Pathogenesis Laboratory

2. Pathogen Genomics

3. Proteomics Mass Spectrometry Laboratory, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, CB10 1SA, United Kingdom

Abstract

ABSTRACT Clostridium difficile , a major cause of antibiotic-associated diarrhea, produces highly resistant spores that contaminate hospital environments and facilitate efficient disease transmission. We purified C. difficile spores using a novel method and show that they exhibit significant resistance to harsh physical or chemical treatments and are also highly infectious, with <7 environmental spores per cm 2 reproducibly establishing a persistent infection in exposed mice. Mass spectrometric analysis identified ∼336 spore-associated polypeptides, with a significant proportion linked to translation, sporulation/germination, and protein stabilization/degradation. In addition, proteins from several distinct metabolic pathways associated with energy production were identified. Comparison of the C. difficile spore proteome to those of other clostridial species defined 88 proteins as the clostridial spore “core” and 29 proteins as C. difficile spore specific, including proteins that could contribute to spore-host interactions. Thus, our results provide the first molecular definition of C. difficile spores, opening up new opportunities for the development of diagnostic and therapeutic approaches.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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