Multiplex PCR for Rapid Detection of Genes Encoding Class A Carbapenemases

被引:73
作者
Hong, Sang Sook [1 ]
Kim, Kyeongmi [1 ]
Huh, Ji Young [1 ]
Jung, Bochan [2 ]
Kang, Myung Sea [1 ]
Hong, Seong Geun [1 ]
机构
[1] CHA Univ, CHA Bundang Med Ctr, Dept Lab Med, Songnam 463712, South Korea
[2] CHA Univ, CHA Gumi Med Ctr, Dept Lab Med, Gumi, South Korea
关键词
Carbapenemase; Multiplex PCR; KPC; GES; KLEBSIELLA-PNEUMONIAE ISOLATE; HYDROLYZING BETA-LACTAMASE; ACQUIRED CARBAPENEMASES; ENTEROBACTERIACEAE; ISSUES; KOREA; KPC-2;
D O I
10.3343/alm.2012.32.5.359
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
In recent years, there have been increasing reports of KPC-producing Klebsiella pneumoniae in Korea. The modified Hodge test can be used as a phenotypic screening test for class A carbapenamase (CAC)-producing clinical isolates; however, it does not distinguish between carbapenemase types. The confirmation of type of CAC is important to ensure optimal therapy and to prevent transmission. This study applied a novel multiplex PCR assay to detect and differentiate CAC genes in a single reaction. Four primer pairs were designed to amplify fragments encoding 4 CAC families (SME, IMI/NMC-A, KPC, and GES). The multiplex PCR detected all genes tested for 4 CAC families that could be differentiated by fragment size according to gene type. This multiplex PCR offers a simple and useful approach for detecting and distinguishing CAC genes in carbapenem-resistant strains that are metallo-beta-lactamase nonproducers.
引用
收藏
页码:359 / 361
页数:3
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