Watahiki Masanori, Kawahara Ryuji, Suzuki Masahiro, Aoki Miyako, Uchida Kaoru, Matsumoto Yuko, Kumagai Yuko, Noda Makiko, Masuda Kanako, Fukuda Chiemi, Harada Seiya, Senba Keiko, Suzuki Masato, Matsui Mari, Suzuki Satowa, Shibayama Keigo, Shinomiya Hiroto
Department of Bacteriology, Toyama Institute of Health.
Division of Microbiology, Osaka Institute of Public Health.
Jpn J Infect Dis. 2020 Mar 24;73(2):166-172. doi: 10.7883/yoken.JJID.2019.041. Epub 2019 Nov 29.
A multiplex PCR assay in a single tube was developed for the detection of the carbapenemase genes of Enterobacteriaceae. Primers were designed to amplify the following six carbapenemase genes: bla, bla, bla, bla, bla, and bla. Of 70 bla variants, 67 subtypes were simulated to be PCR-positive based on in silico simulation and the primer-design strategy. After determining the optimal PCR conditions and performing in vitro assays, the performance of the PCR assay was evaluated using 51 and 91 clinical isolates with and without carbapenemase genes, respectively. In conclusion, the combination of multiplex PCR primers and QIAGEN Multiplex PCR Plus Kit was used to determine the best performance for the rapid and efficient screening of carbapenemase genes in Enterobacteriaceae. The assay had an overall sensitivity and specificity of 100%. This PCR assay compensates for the limitations of phenotypic testing, such as antimicrobial susceptibility testing and the modified carbapenem inactivation method, in clinical and public health settings.
开发了一种单管多重PCR检测方法,用于检测肠杆菌科细菌的碳青霉烯酶基因。设计引物以扩增以下六个碳青霉烯酶基因:bla、bla、bla、bla、bla和bla。基于计算机模拟和引物设计策略,在70个bla变体中,模拟了67个亚型为PCR阳性。确定最佳PCR条件并进行体外试验后,分别使用51株和91株携带和不携带碳青霉烯酶基因的临床分离株评估PCR检测方法的性能。总之,多重PCR引物与QIAGEN多重PCR Plus试剂盒相结合,用于确定在快速高效筛选肠杆菌科细菌碳青霉烯酶基因方面的最佳性能。该检测方法的总体灵敏度和特异性均为100%。这种PCR检测方法弥补了临床和公共卫生环境中表型检测(如抗菌药物敏感性检测和改良碳青霉烯灭活方法)的局限性。