Maggs A F, Logan J M, Carter P E, Pennington T H
Department of Medical Microbiology, University of Dundee Medical School, Ninewells Hospital, UK.
J Antimicrob Chemother. 1998 Sep;42(3):303-7. doi: 10.1093/jac/42.3.303.
Strains of penicillin-sensitive and -insensitive Neisseria meningitidis were examined using a range of polymerase chain reaction (PCR) primers directed at the meningococcal penicillin-binding protein 2 gene. DNA from isolates whose penicillin MIC was <0.2 mg/L yielded a product of the expected size with all the primers, but many amplification patterns were seen with DNA from isolates whose MIC was above this level. All strains whose MIC was >0.25 mg/L failed to produce a product of the expected size with at least one of the primers used. The changes seen in penicillin-insensitive strains were consistent with horizontal gene transfer from Neisseria flavescens in some isolates, although the source for others remains unknown. PCR-based methods for the detection of antibiotic resistance are becoming increasingly important with the expanding use of molecular techniques for bacteriological diagnosis.
使用一系列针对脑膜炎球菌青霉素结合蛋白2基因的聚合酶链反应(PCR)引物,对青霉素敏感和不敏感的脑膜炎奈瑟菌菌株进行了检测。青霉素最低抑菌浓度(MIC)<0.2mg/L的分离株的DNA,与所有引物均产生预期大小的产物,但MIC高于此水平的分离株的DNA出现了多种扩增模式。所有MIC>0.25mg/L的菌株,使用的至少一种引物未能产生预期大小的产物。在青霉素不敏感菌株中观察到的变化,在某些分离株中与微黄奈瑟菌的水平基因转移一致,尽管其他菌株的来源尚不清楚。随着分子技术在细菌学诊断中的广泛应用,基于PCR的抗生素耐药性检测方法变得越来越重要。