Real-time PGR and melting curve analysis for reliable and rapid detection of SHV extended-spectrum beta-lactamases

Citation
Cc. Randegger et H. Hachler, Real-time PGR and melting curve analysis for reliable and rapid detection of SHV extended-spectrum beta-lactamases, ANTIM AG CH, 45(6), 2001, pp. 1730-1736
Citations number
38
Categorie Soggetti
Microbiology
Journal title
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
ISSN journal
00664804 → ACNP
Volume
45
Issue
6
Year of publication
2001
Pages
1730 - 1736
Database
ISI
SICI code
0066-4804(200106)45:6<1730:RPAMCA>2.0.ZU;2-6
Abstract
Extended-spectrum p-lactamases (ESBLs), e,g,, ESBLs of the TEM or SHV type, compromise the efficacies of expanded-spectrum cephalosporins, An SHV non- ESBL that hydrolyzes only narrow-spectrum cephalosporins can be converted i nto an SHV ESBL through substitutions at three amino acid positions, 179, 2 38, or 238-240, In order to improve detection of SHV ESBLs, a novel method, based on real-time PCR monitored with fluorescently labeled hybridization probes and followed by melting curve analysis, was developed. It is able to (i) detect bla(SHV) genes with high degrees of sensitivity and specificity , (ii) discriminate between bla(SHV non-ESBL) and bla(SHV ESBL) and (iii) c ategorize the SHV ESBL producers into three phenotypically relevant subgrou ps. This method, termed the SHV melting curve mutation defection method, re presents a powerful tool for epidemiological studies,vith SHV ESBLs. It eve n has the potential to be used in the diagnostic microbiology laboratory, b ecause up to 32 clinical isolates can be processed in less than 1 h by star ting with just a few bacterial colonies.