首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Inhibitory effects of ciprofloxacin and sparfloxacin on DNA gyrase purified from fluoroquinolone-resistant strains of methicillin-resistant Staphylococcus aureus.
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Inhibitory effects of ciprofloxacin and sparfloxacin on DNA gyrase purified from fluoroquinolone-resistant strains of methicillin-resistant Staphylococcus aureus.

机译:环丙沙星和司帕沙星对从耐甲氧西林金黄色葡萄球菌的耐氟喹诺酮菌株中纯化的DNA促旋酶的抑制作用。

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摘要

The activities of new quinolones against 140 strains of methicillin-resistant Staphylococcus aureus were determined. From the relationship between the MICs of sparfloxacin and ciprofloxacin, fluoroquinolone-resistant S. aureus 6171 (MIC of sparfloxacin, 200 micrograms/ml; MIC of ciprofloxacin, 100 micrograms/ml) and fluoroquinolone-susceptible S. aureus FDA 209-P were selected for purification of the subunit A and B proteins of their DNA gyrases. The supercoiling activities of reconstituted ArBr (r, resistant) (from strain 6171) and ArBs (s, susceptible) gyrases were 40-fold more resistant to new quinolones than those of AsBs from FDA 209-P and AsBr gyrases. The 50% inhibitory doses of ciprofloxacin and sparfloxacin for AmBm (from mutant 19) and AmBs (m, moderately resistant) gyrases were 15- to 27-fold higher than those for AsBs and AsBm gyrases. These findings indicate that one of the resistance mechanisms of S. aureus against fluoroquinolones is a modification of the gyrase subunit A protein.
机译:测定了新喹诺酮类药物对140株耐甲氧西林金黄色葡萄球菌的活性。从司帕沙星和环丙沙星的MIC的关系中,选择耐氟喹诺酮的金黄色葡萄球菌6171(司帕沙星的MIC,200微克/毫升;环丙沙星的MIC,100微克/毫升)和氟喹诺酮敏感的金黄色葡萄球菌FDA 209-P用于纯化其DNA陀螺的亚基A和B蛋白。重组的ArBr(抗性)(来自6171菌株)和ArB(抗敏感)陀螺的超螺旋活性比来自FDA 209-P和AsBr的AsB的超喹诺酮抗性高40倍。环丙沙星和司帕沙星对AmBm(来自突变体19)和AmBs(m,中度耐药)陀螺的50%抑制剂量比对AsBs和AsBm陀螺的抑制剂量高15至27倍。这些发现表明,金黄色葡萄球菌对氟喹诺酮类药物的耐药机制之一是回旋酶亚基A蛋白的修饰。

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