Effect of suprainhibitory concentrations of quinolones on hydrophobicity and motility of Serratia marcescens.

Microbios Pub Date : 2000-01-01
V Majtán, L Majtánová
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Abstract

The effect of suprainhibitory concentrations of quinolones (ciprofloxacin, enoxacin and norfloxacin) on the growth, hydrophobicity and motility of a nosocomial pathogen Serratia marcescens was studied. A postantibiotic effect (PAE) was induced by 2x of 4x MIC concentrations for 0.5 h. By using the 2x MIC concentrations all three quinolones induced equally long PAE approximately 1 h. The longest PAE of 5.4 h at 4x MIC concentration was induced by enoxacin. The results obtained showed that suprainhibitory concentrations of quinolones significantly stimulated the adhesion of S. marcescens to xylene, with the exception of enoxacin, which inhibited the adhesion to 61.2% at 4x MIC concentration. These results correlated with those in the salt aggregation test. The adhesion of strains to nitrocellulose filters did not influence the aftereffect of suprainhibitory concentrations of quinolones. Exposure of bacterial cells to suprainhibitory concentrations of ciprofloxacin and norfloxacin caused a reduction in motility, while this effect was more distinct at 4x MIC concentration. The results suggest that any consideration of postantibiotic effects should include the residual antibiotic effects on virulence factors, in addition to the defined suppression of bacterial regrowth.

喹诺酮类药物的超抑制浓度对粘质沙雷菌疏水性和运动性的影响。
研究了喹诺酮类药物(环丙沙星、依诺沙星和诺氟沙星)的超抑制浓度对粘质沙雷菌生长、疏水性和运动性的影响。在2倍MIC浓度下,三种喹诺酮类药物均可诱导相同长度的PAE(约1 h),在4倍MIC浓度下最长的PAE为5.4 h。结果表明,除依诺沙星外,喹诺酮类药物的超抑制浓度显著促进粘多糖对二甲苯的粘附,在4倍MIC浓度下,其粘附抑制率为61.2%。这些结果与盐聚集试验结果具有一定的相关性。菌株与硝化纤维素过滤器的粘附不影响喹诺酮类药物的超抑制效应。将细菌细胞暴露于环丙沙星和诺氟沙星的超抑制浓度下会导致细胞运动性降低,而这种影响在4倍MIC浓度下更为明显。结果表明,除抑制细菌再生外,任何对抗生素后效应的考虑都应包括对毒力因子的残留抗生素效应。
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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