铜绿假单胞菌毒力因子:卡比西林或庆大霉素亚抑制浓度的改变。

A R Ogaard, K Bjøro, G Bukholm, B P Berdal
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引用次数: 11

摘要

研究了一株毒力强的铜绿假单胞菌在卡比西林和庆大霉素亚抑制浓度下对HEp-2细胞的粘附、毒素A的产生和弹性蛋白酶的产生。两种抗生素在其最低杀菌浓度(MBC)的1:12浓度下均抑制毒素a的产生,庆大霉素在该浓度下完全消除弹性蛋白酶的产生,而卡比西林对该因素的影响很小或没有影响。两种抗生素都抑制了细菌的粘附,但方式不同。庆大霉素具有较强的慢起活性,而卡比西林具有短暂的快起活性,在90分钟的孵卵后恢复到正常值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pseudomonas aeruginosa virulence factors: modifications by sub-inhibitory concentrations of carbenicillin or gentamicin.

A virulent strain of Pseudomonas aeruginosa was assayed for adhesion to HEp-2 cells, production of toxin A, and production of elastase, in the presence of sub-inhibitory concentrations of carbenicillin and gentamicin. Both antibiotics, assayed in a concentration of 1:12 of their minimum bactericidal concentration (MBC), inhibited the production of toxin A. Gentamicin at this concentration totally abolished the production of elastase, whereas carbenicillin had little or no effect on this factor. Both antibiotics inhibited the bacterial adhesion, but in different ways. While gentamicin had a strong activity of slow onset, carbenicillin had a transitory activity of rapid onset, with return towards normal values after 90 min incubation.

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