Typing and subtyping of Clostridium difficile isolates by using multiple-locus variable-number tandem-repeat analysis

J Clin Microbiol. 2007 Mar;45(3):1024-8. doi: 10.1128/JCM.02023-06. Epub 2006 Dec 13.

Abstract

Using the genomic sequence of Clostridium difficile strain 630, we developed multiple-locus variable-number tandem-repeat analysis (MLVA) with automated fragment analysis and multicolored capillary electrophoresis as a typing method for C. difficile. All reference strains, representing 31 serogroups, 25 toxinotypes, and 7 known subtypes of PCR ribotype 001, could be discriminated from each other. Application of MLVA to 28 isolates from 7 outbreaks due to the emerging hypervirulent PCR ribotype 027-pulsed-field gel electrophoresis type NAP1 resulted in recognition of 13 clusters. Additionally, 29 toxin A-negative, toxin B-positive isolates belonging to PCR ribotype 017 from eight different countries revealed eight country-specific clusters. MLVA is a highly discriminatory genotyping method and a new tool for subtyping of newly emerging variants of C. difficile.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Automation
  • Bacterial Proteins / metabolism
  • Bacterial Toxins / metabolism
  • Bacterial Typing Techniques*
  • Clostridioides difficile / classification*
  • Clostridioides difficile / genetics*
  • Clostridioides difficile / isolation & purification
  • DNA, Bacterial / analysis
  • Electrophoresis, Capillary / methods*
  • Enterocolitis, Pseudomembranous / microbiology
  • Enterotoxins / metabolism
  • Genotype
  • Humans
  • Minisatellite Repeats*
  • Ribotyping

Substances

  • Bacterial Proteins
  • Bacterial Toxins
  • DNA, Bacterial
  • Enterotoxins
  • tcdA protein, Clostridium difficile
  • toxB protein, Clostridium difficile