Real-time PCR for the rapid detection of vanA and vanB genes

Diagn Microbiol Infect Dis. 2003 Jan;45(1):81-4. doi: 10.1016/s0732-8893(02)00505-9.

Abstract

A real-time PCR assay suitable for use on the Roche LightCycler platform was developed to replace an existing gel-based PCR assay for the simultaneous detection of the vanA & vanB genes in enterococcal isolates. Novel Fluorescence Resonance Energy Transfer (FRET) hybridization probes were designed. The multiplex real-time PCR assay and the existing gel-based assay were 100% concordant and both correctly detected the vanA or vanB genes in 4/4 VanA E. faecium and 25/25 VanB E. faecium. Additionally, 1/1 VanC1 E. gallinarum, 1/1 VanC2 E. casseliflavus and 47/47 vancomycin susceptible enterococci were negative for the vanA and vanB genes in both PCR assays. Results were available within 1.5 h for the real-time PCR assay compared to up to 5.5 h for the conventional PCR assay.

Publication types

  • Comparative Study

MeSH terms

  • Base Sequence
  • Drug Resistance, Microbial
  • Enterococcus faecium / genetics*
  • Fluorescence Resonance Energy Transfer / methods*
  • Genes, Bacterial / drug effects
  • Humans
  • Molecular Sequence Data
  • Pharmacogenetics
  • Polymerase Chain Reaction / methods*
  • Sensitivity and Specificity
  • Vancomycin Resistance / genetics*