Multiplex PCR for rapid detection of genes encoding class A carbapenemases

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Abstract

In recent years, there have been increasing reports of KPC-producing Klebsiella pneumoniae in Korea. The modifed 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 confrmation 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-β-lactamase nonproducers. © The Korean Society for Laboratory Medicine.

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APA

Hong, S. S., Kim, K., Huh, J. Y., Jung, B., Kang, M. S., & Hong, S. G. (2012). Multiplex PCR for rapid detection of genes encoding class A carbapenemases. Annals of Laboratory Medicine, 32(5), 359–361. https://doi.org/10.3343/alm.2012.32.5.359

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