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Mechanism of action of sparfloxacin against and mechanism of resistance in gram-negative and gram-positive bacteria.

机译:司帕沙星对革兰氏阴性和革兰氏阳性细菌的作用机理和耐药机理。

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摘要

The inhibition of DNA synthesis by sparfloxacin; accumulation of sparfloxacin into members of the family Enterobacteriaceae, Pseudomonas aeruginosa, and staphylococci; induction of recA in Escherichia coli; and the optimum bactericidal concentration (OBC) were measured, and killing kinetics at the OBC were estimated. The OBC and maximum recA-inducing concentration in E. coli were both 1 microgram of sparfloxacin per ml. Accumulation was rapid; two- to threefold more sparfloxacin than ciprofloxacin accumulated in staphylococci and more sparfloxacin accumulated in staphylococci than in gram-negative bacteria. Laboratory mutants with decreased susceptibilities to quinolones alone or multiply resistant were selected from the Enterobacteriaceae and Staphylococcus aureus by using sparfloxacin.
机译:司帕沙星对DNA合成的抑制;司帕沙星积累到肠杆菌科,铜绿假单胞菌和葡萄球菌中;在大肠杆菌中诱导recA;并测定最佳杀菌浓度(OBC),并估算OBC处的杀灭动力学。大肠杆菌中的OBC和最大recA诱导浓度均为每毫升1微克司帕沙星。积累迅速;在葡萄球菌中积累的环丙沙星比环丙沙星多两倍到三倍,而在葡萄球菌中积聚的斯帕沙星比革兰氏阴性细菌多。通过使用司帕沙星从肠杆菌科和金黄色葡萄球菌中选择对喹诺酮类药物敏感或单独耐药的实验室突变体。

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  • 作者

    Piddock, L J; Zhu, M;

  • 作者单位
  • 年度 1991
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  • 原文格式 PDF
  • 正文语种 en
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