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

被引:115
作者
Birkett, Christopher I. [1 ]
Ludlam, Hugo A.
Woodford, Neil
Brown, Derek F. J.
Brown, Nicholas M.
Roberts, Mark T. M.
Milner, Nicola
Curran, Martin D.
机构
[1] Addenbrookes Hosp, Clin Microbiol & Publ Hlth Lab, Hlth Protect Agcy, Cambridge, England
[2] Hlth Protect Agcy, Ctr Infect, Antibiot Resistance Monitoring & Reference Lab, London, England
关键词
D O I
10.1099/jmm.0.46909-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:52 / 55
页数:4
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