首页> 外文期刊>Antimicrobial agents and chemotherapy. >Comparative activities of clinafloxacin, grepafloxacin, levofloxacin, moxifloxacin, ofloxacin, sparfloxacin, and trovafloxacin and nonquinolones linozelid, quinupristin-dalfopristin, gentamicin, and vancomycin against clinical isolates of ciprofloxac
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Comparative activities of clinafloxacin, grepafloxacin, levofloxacin, moxifloxacin, ofloxacin, sparfloxacin, and trovafloxacin and nonquinolones linozelid, quinupristin-dalfopristin, gentamicin, and vancomycin against clinical isolates of ciprofloxac

机译:克林沙星,格列氟沙星,左氧氟沙星,莫西沙星,氧氟沙星,司帕沙星和曲伐沙星与壬喹诺斯利诺齐尔,奎奴普丁-达福普汀,庆大霉素和万古霉素对环丙沙星临床分离株的比较活性

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摘要

The activities of eight fluoroquinolones and linezolid, quinupristin-dalfopristin (Synercid), gentamicin, and vancomycin were tested against 96 ciprofloxacin-susceptible and 205 ciprofloxacin-resistant Staphylococcus aureus strains. Overall, clinafloxacin, followed by moxifloxacin and trovafloxacin, was the most active quinolone tested. For all isolates, linezolid and quinupristin-dalfopristin showed activities that were at least comparable to vancomycin, with no cross-resistance to any other test compound.
机译:测试了八种氟喹诺酮和利奈唑胺,奎奴普丁-达福普汀(Synercid),庆大霉素和万古霉素对96例对环丙沙星敏感和205例对环丙沙星耐药的金黄色葡萄球菌的活性。总体而言,克林沙星,莫西沙星和曲伐沙星紧随其后,是测试的最有效的喹诺酮。对于所有分离株,利奈唑胺和奎奴普丁-达福普汀的活性至少与万古霉素相当,与其他任何测试化合物均无交叉抗性。

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