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

被引:41
作者
Randegger, CC [1 ]
Hächler, H [1 ]
机构
[1] Univ Zurich, Inst Med Microbiol, CH-8028 Zurich, Switzerland
关键词
D O I
10.1128/AAC.45.6.1730-1736.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 into an SHV ESBL through substitutions at three amino acid positions, 179, 238, 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) categorize the SHV ESBL producers into three phenotypically relevant subgroups. This method, termed the SHV melting curve mutation defection method, represents a powerful tool for epidemiological studies,vith SHV ESBLs. It even has the potential to be used in the diagnostic microbiology laboratory, because up to 32 clinical isolates can be processed in less than 1 h by starting with just a few bacterial colonies.
引用
收藏
页码:1730 / 1736
页数:7
相关论文
共 38 条
[1]  
ARLET G, 1995, FEMS MICROBIOL LETT, V134, P203, DOI 10.1111/j.1574-6968.1995.tb07938.x
[2]   DEVELOPMENT OF TEST PANEL OF BETA-LACTAMASES EXPRESSED IN A COMMON ESCHERICHIA-COLI HOST BACKGROUND FOR EVALUATION OF NEW BETA-LACTAM ANTIBIOTICS [J].
BRADFORD, PA ;
SANDERS, CC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (02) :308-313
[3]   SHV-7, A NOVEL CEFOTAXIME-HYDROLYZING BETA-LACTAMASE, IDENTIFIED IN ESCHERICHIA-COLI ISOLATES FROM HOSPITALIZED NURSING-HOME PATIENTS [J].
BRADFORD, PA ;
URBAN, C ;
JAISWAL, A ;
MARIANO, N ;
RASMUSSEN, BA ;
PROJAN, SJ ;
RAHAL, JJ ;
BUSH, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (04) :899-905
[5]   A FUNCTIONAL CLASSIFICATION SCHEME FOR BETA-LACTAMASES AND ITS CORRELATION WITH MOLECULAR-STRUCTURE [J].
BUSH, K ;
JACOBY, GA ;
MEDEIROS, AA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (06) :1211-1233
[6]   Detection of extended-spectrum β-lactamases in klebsiellae with the oxoid combination disk method [J].
Carter, MW ;
Oakton, KJ ;
Warner, M ;
Livermore, DM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (11) :4228-4232
[7]   Characterisation of extended-spectrum β-lactamases of the SHV family using a combination of PCR-single strand conformational polymorphism (PCR-SSCP) and PCR-restriction fragment length polymorphism (PCR-RFLP) [J].
Chanawong, A ;
M'Zali, FH ;
Heritage, J ;
Lulitanond, A ;
Hawkey, PM .
FEMS MICROBIOLOGY LETTERS, 2000, 184 (01) :85-89
[8]   Genetic methods for assessing antimicrobial resistance [J].
Cockerill, FR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (02) :199-212
[9]   Detection of extended-spectrum beta-lactamase (ESBL)-producing strains by the Etest ESBL screen [J].
Cormican, MG ;
Marshall, SA ;
Jones, RN .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (08) :1880-1884
[10]  
DUBOIS SK, 1995, J ANTIMICROB CHEMOTH, V35, P7