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新型半合成注射用普那霉素RP 59500对葡萄球菌的体外活性

In-vitro activity of RP 59500, a new semisynthetic injectable pristinamycin against staphylococci.

作者信息

von Eiff C, Peters G

机构信息

Institute of Medical Microbiology, Westfälische Wilhelms-Universität Münster, Germany.

出版信息

Zentralbl Bakteriol. 1996 Apr;283(4):497-501. doi: 10.1016/s0934-8840(96)80127-7.

Abstract

We compared the in vitro activity of RP 59500, a new streptogramin, with that of vancomycin and ciprofloxacin against 130 strains of S. aureus and 117 strains of coagulase-negative staphylococci, using the agar dilution method. The antistaphylococcal activity of RP 59500 was similar to that of vancomycin. All staphylococcal strains were inhibited by < or = 2 micrograms/mL, including 61 methicillin-resistant S. aureus, 28 methicillin-resistant S. epidermidis and 23 methicillin-resistant S. haemolyticus strains. In contrast to ciprofloxacin, the in vitro activity of RP 59500 as well as of vancomycin remained almost unchanged, irrespective of the resistance phenotype for methicillin.

摘要

我们采用琼脂稀释法,比较了新型链阳菌素RP 59500与万古霉素和环丙沙星对130株金黄色葡萄球菌及117株凝固酶阴性葡萄球菌的体外活性。RP 59500的抗葡萄球菌活性与万古霉素相似。所有葡萄球菌菌株均被≤2微克/毫升的浓度所抑制,其中包括61株耐甲氧西林金黄色葡萄球菌、28株耐甲氧西林表皮葡萄球菌和23株耐甲氧西林溶血葡萄球菌。与环丙沙星不同,RP 59500以及万古霉素的体外活性几乎不受甲氧西林耐药表型的影响,始终保持不变。

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