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磷霉素对甲氧西林敏感及耐甲氧西林金黄色葡萄球菌的体外活性

In vitro activity of fosfomycin against methicillin-susceptible and methicillin-resistant Staphylococcus aureus.

作者信息

Graninger W, Leitha T, Havel M, Georgopoulos A

出版信息

Infection. 1984 Jul-Aug;12(4):293-5. doi: 10.1007/BF01645964.

Abstract

The in vitro antibacterial activity of fosfomycin was compared to that of oxacillin, cefazolin, ceftriaxone and vancomycin against isolates of Staphylococcus aureus from patients treated at the University of Vienna General Hospital. Of 211 strains, 104 were methicillin-susceptible and 107 were methicillin-resistant. Fosfomycin inhibited over 90% of the strains at concentrations of less than or equal to 64 mg/l, independent of methicillin susceptibility or resistance. The minimal bactericidal concentrations (MBC) were one dilution above the minimal inhibitory concentrations (MIC). Vancomycin showed activity similar to fosfomycin while other beta-lactam antibiotics such as oxacillin, cefazolin and ceftriaxone were inactive against methicillin-resistant S. aureus. Fosfomycin at a high dosage seems to be a potential drug for the treatment of infections due to methicillin-resistant S. aureus.

摘要

将磷霉素的体外抗菌活性与苯唑西林、头孢唑林、头孢曲松和万古霉素针对维也纳大学总医院接受治疗患者的金黄色葡萄球菌分离株的抗菌活性进行了比较。在211株菌株中,104株对甲氧西林敏感,107株对甲氧西林耐药。磷霉素在浓度小于或等于64mg/L时可抑制超过90%的菌株,与甲氧西林敏感性或耐药性无关。最小杀菌浓度(MBC)比最小抑菌浓度(MIC)高一个稀释度。万古霉素显示出与磷霉素相似的活性,而其他β-内酰胺类抗生素如苯唑西林、头孢唑林和头孢曲松对耐甲氧西林金黄色葡萄球菌无活性。高剂量的磷霉素似乎是治疗耐甲氧西林金黄色葡萄球菌感染的一种潜在药物。

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