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白色念珠菌中对多烯或唑类抗真菌药物耐药的突变体以及双突变体白色念珠菌6.4中的甾醇

Sterols in Candida albicans mutants resistant to polyene or azole antifungals, and of a double mutant C. albicans 6.4.

作者信息

Hitchcock C A, Russell N J, Barrett-Bee K J

机构信息

Department of Biochemistry, University College, Cardiff, South Wales.

出版信息

Crit Rev Microbiol. 1987;15(1):111-5. doi: 10.3109/10408418709104454.

Abstract

Investigations of resistant mutants could help resolve differences and similarities in the action of azole and polyene antifungals whose modes of action are related; both disrupt membrane properties, such as permeability, by interfering with membrane sterols--polyenes by direct binding and azoles by inhibiting their synthesis. Studies of laboratory-derived mutants of Candida albicans which have an altered sterol content and/or an altered sterol composition do not provide evidence for a unified mechanism of polyene resistance. Clinical isolates of azole-resistant C. albicans have an increased or unaltered content of ergosterol and are impermeable to azoles. C. albicans 6.4, a laboratory-derived mutant resistant to both polyenes and azoles, is impermeable to azoles and has an increased content of methylated sterols. This unusual sterol composition resembles that of sensitive strains grown in the presence of azoles and may prevent polyene binding.

摘要

对耐药突变体的研究有助于解决作用方式相关的唑类和多烯类抗真菌药物在作用上的异同;二者均通过干扰膜甾醇来破坏膜特性,如通透性——多烯类通过直接结合,唑类通过抑制其合成。对白色念珠菌实验室衍生突变体的研究表明,这些突变体的甾醇含量和/或甾醇组成发生了改变,但并未为多烯耐药性的统一机制提供证据。对唑类耐药的白色念珠菌临床分离株中麦角甾醇含量增加或未改变,且对唑类不透性。白色念珠菌6.4是一种实验室衍生的对多烯类和唑类均耐药的突变体,对唑类不透性,且甲基化甾醇含量增加。这种不寻常的甾醇组成类似于在唑类存在下生长的敏感菌株,可能会阻止多烯类的结合。

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