Zambardi G, Reverdy M E, Bland S, Bes M, Freney J, Fleurette J
Department of Studies and Research of Medical Bacteriology, Alexis Carrel Faculty of Medicine, Lyons, France.
Diagn Microbiol Infect Dis. 1994 May;19(1):25-31. doi: 10.1016/0732-8893(94)90047-7.
A polymerase chain reaction (PCR) test was developed in which the mecA gene responsible for the intrinsic resistance to oxacillin in Staphylococcus aureus and the gyrA gene, always present in this species, were amplified in one operation. Among the 468 clinical isolates tested, the results obtained for 454 of the isolates (97%) were consistent with those of MIC determination. Discrepant results were noted for strains with low-level oxacillin resistance (MICs, 4-8 micrograms/ml) and mecA gene negative. For these strains, susceptibility to oxacillin was restored in the presence of a beta-lactamase inhibitor, which suggested a resistance by penicillinase hyperproduction. In contrast, all of the high-level resistant strains (MICs, > 8 micrograms/ml) carried the mecA gene. The presence of this gene has frequently been associated with resistance to gentamicin, tetracycline, erythromycin, lincomycin, and pefloxacin. The PCR assay described in this study can be accomplished with ease and total confidence in the clinical microbiologic laboratory for a rapid and effective establishment of antistaphylococcal chemotherapy.
开发了一种聚合酶链反应(PCR)检测方法,可在一次操作中扩增负责金黄色葡萄球菌对苯唑西林固有耐药性的mecA基因以及该菌种中始终存在的gyrA基因。在所检测的468株临床分离株中,454株(97%)的检测结果与最低抑菌浓度(MIC)测定结果一致。对于低水平苯唑西林耐药(MIC为4 - 8微克/毫升)且mecA基因阴性的菌株,结果出现差异。对于这些菌株,在β-内酰胺酶抑制剂存在的情况下,对苯唑西林的敏感性得以恢复,这表明是由青霉素酶过度产生导致的耐药。相比之下,所有高水平耐药菌株(MIC > 8微克/毫升)都携带mecA基因。该基因的存在常常与对庆大霉素、四环素、红霉素、林可霉素和培氟沙星的耐药性相关。本研究中描述的PCR检测方法在临床微生物实验室中能够轻松且完全可靠地完成,以快速有效地确定抗葡萄球菌化疗方案。