穿透革兰氏阴性细胞壁:β -内酰胺类抗生素疗效的共同决定因素。

W Zimmermann
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引用次数: 0

摘要

革兰氏阴性菌对β -内酰胺类抗生素的耐药主要基于两种机制:β -内酰胺酶的水解和内膜靶点对抗生素的排斥。本文描述了使用铜绿假单胞菌k799 /WT和该菌株的突变体(K 799/61)来评估外膜作为青霉素和头孢菌素的通透性屏障的作用。这些数据证实了β -内酰胺对假单胞菌具有活性的良好穿透性的重要性。第二部分说明了β -内酰胺酶和外膜在大肠杆菌对β -内酰胺的耐药性中的相互作用。给出了一种确定膜透性参数的方法。研究结果支持这样一种观点,即只有结合灭活酶和渗透屏障才能更好地理解革兰氏阴性菌对β -内酰胺类抗生素的防御机制的效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Penetration through the gram-negative cell wall: a co-determinant of the efficacy of beta-lactam antibiotics.

Resistance of gram-negative bacteria to beta-lactam antibiotics is based mainly on two mechanisms: hydrolysis by beta-lactamases and exclusion of the antibiotics from their target sites in the inner membrane. This article describes the use of Pseudomonas aeruginosa K 799/WT and a mutant of this strain (K 799/61) to assess the role of the outer membrane as a permeability barrier to penicillins and cephalosporins. The data confirm the importance of good penetration for a beta-lactam to be active against Pseudomonas. The second part illustrates the interplay of beta-lactamases and the outer membrane in the resistance of Escherichia coli to beta-lactams. A method to determine membrane permeability parameters parameters is given. The results support the idea that only a combined consideration of inactivating enzymes and penetration barriers can lead to a better understanding of the efficiency of the defence mechanisms which gram-negative bacteria can invoke against beta-lactam antibiotics.

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