4.3 Article Proceedings Paper

Real-time TaqMan PCR for rapid detection and typing of genes encoding CTX-M extended-spectrum β-lactamases

Journal

JOURNAL OF MEDICAL MICROBIOLOGY
Volume 56, Issue 1, Pages 52-55

Publisher

MICROBIOLOGY SOC
DOI: 10.1099/jmm.0.46909-0

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The prevalence of CTX-M-producing members of the Enterobacteriaceae is increasing worldwide. A novel, multiplex, real-time TaqMan PCR assay to detect and type b/aCTX-M genes is described which is an improvement on previously described techniques with respect to reduced assay time, elimination of the need for protracted post-PCR processing and the convenience of a single reaction vessel. Based on beta-lactam antibiogram and MIC data, 478 of 1279 Enterobacteriaceae isolates from clinical blood and urine culture specimens were selected and tested for extended-spectrum beta-lactamase (ESBL) production using phenotypic methods. The new TaqMan assay detected and typed b/aCTX-M genes in 21 of 28 ESBL-producing isolates.

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