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抗生素组合对耐庆大霉素和耐甲氧西林金黄色葡萄球菌的体外活性

In vitro activity of combinations of antibiotics against Staphylococcus aureus resistant to gentamicin and methicillin.

作者信息

Dixson S, Brumfitt W, Hamilton-Miller J M

出版信息

Infection. 1985 Jan-Feb;13(1):35-8. doi: 10.1007/BF01643619.

Abstract

Twenty clinical isolates of Staphylococcus aureus, resistant to both gentamicin and methicillin, were tested in vitro for sensitivity to rifampicin, novobiocin, fusidic acid, vancomycin, teicoplanin and an extended range of aminoglycosides. Rifampicin was the most active compound tested, having an MIC of less than 0.02 mg/l. All the strains were inhibited by 1 mg/l of novobiocin, vancomycin and teicoplanin, and only one strain was resistant to fusidic acid. 50% of the strains were inhibited by less than 1 mg/l of amikacin and netilmicin, but other aminoglycosides were of poor activity. Resistant mutants were selected when strains were grown in the presence of rifampicin, novobiocin or fusidic acid alone, but this did not occur when rifampicin was combined with either novobiocin or vancomycin. Pharmacokinetic and other considerations suggest that a combination of rifampicin and novobiocin deserves further assessment for the treatment of infections caused by this type of organism.

摘要

对20株对庆大霉素和甲氧西林均耐药的金黄色葡萄球菌临床分离株进行了体外试验,检测其对利福平、新生霉素、夫西地酸、万古霉素、替考拉宁以及一系列氨基糖苷类药物的敏感性。利福平是所检测的活性最强的化合物,其最低抑菌浓度小于0.02mg/L。所有菌株均被1mg/L的新生霉素、万古霉素和替考拉宁抑制,只有1株对夫西地酸耐药。50%的菌株被小于1mg/L的阿米卡星和奈替米星抑制,但其他氨基糖苷类药物活性较差。当菌株单独在利福平、新生霉素或夫西地酸存在的情况下生长时,会筛选出耐药突变体,但当利福平与新生霉素或万古霉素联合使用时则不会出现这种情况。药代动力学和其他因素表明,利福平与新生霉素联合用药值得进一步评估用于治疗此类病原体引起的感染。

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