Antibacterial antagonism between fusidic acid and ciprofloxacin.

Acta microbiologica Hungarica Pub Date : 1993-01-01
J V Uri
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Abstract

A routine laboratory disk susceptibility testing of a resistant Staphylococcus aureus strain showed that around the ciprofloxacin disk, placed by chance in proximity to a fusidic acid disk, the inhibition zone was truncated. Follow-up of this observation by a planned disk approximation method showed that there is a real antagonism between these two antibacterial agents. The antagonism was observed while testing S. aureus isolates including the standard ATCC 25923 strain, with Bacillus subtilis ATCC 6633 spores and also with a mutant Escherichia coli made fusidic acid susceptible. The antagonistic property was found structure-specific, only associated with those fluoroquinolones containing the cyclopropyl substituent at the N1-position: ciprofloxacin, enrofloxacin, sparfloxacin and WIN 57273. Fluoroquinolones without this substituent such as enoxacin, norfloxacin, pefloxacin and ofloxacin were not antagonized by fusidic acid, the steroidal Gram-positive active antibiotic.

氟西地酸与环丙沙星的抗菌拮抗作用。
一株耐药金黄色葡萄球菌的常规实验室药盘药敏试验显示,偶然放置在靠近福西地酸药盘的环丙沙星药盘周围,抑制带被截断。用计划圆盘近似法对这一观察结果进行随访,表明这两种抗菌剂之间存在真正的拮抗作用。在测试金黄色葡萄球菌分离株时观察到拮抗作用,包括标准菌株ATCC 25923,枯草芽孢杆菌ATCC 6633孢子和突变的大肠杆菌使夫西地酸敏感。拮抗作用是结构特异性的,仅与含有n1位环丙基取代基的氟喹诺酮类药物有关:环丙沙星、恩诺沙星、斯帕沙星和WIN 57273。不含该取代基的氟喹诺酮类药物,如依诺沙星、诺氟沙星、培氟沙星和氧氟沙星,均不能被甾体革兰氏阳性活性抗生素氟西地酸拮抗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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