Rapid diagnosis of toxinogenic Clostridium difficile in faecal samples with internally controlled real-time PCR

  • van den Berg, R.J.
  • Kuijper, E.J.
  • van Coppenraet, L.E.S. Bruijnesteijn
  • Claas, E.C.J.
Publication date
February 2006
Publisher
European Society of Clinical Infectious Diseases. Published by Elsevier Ltd.

Abstract

ABSTRACTA real-time PCR assay for Clostridium difficile was developed, based on the tcdB gene, which detected all known toxinogenic reference strains (n = 45), within 30 serogroups and 24 toxinotypes. The analytical sensitivity was 1 × 103 CFU/mL, and the detection limit in faeces was 1 × 105 CFU/g. The optimal protocol for DNA extraction from faecal samples involved use of the MagnaPure system with a Stool Transport and Recovery (STAR) buffer pre-treatment. In a 1-month prospective study of 85 patients with diarrhoea, the sensitivity, specificity and positive and negative predictive values of the assay were 100%, 94%, 55% and 100%, respectively, compared with the standard cell cytotoxicity assay

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