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Antifungal Agents: Mode of Action Mechanisms of Resistance and Correlation of These Mechanisms with Bacterial Resistance

机译:抗真菌剂:作用方式耐药机制以及这些机制与细菌耐药性的关系

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摘要

The increased use of antibacterial and antifungal agents in recent years has resulted in the development of resistance to these drugs. The significant clinical implication of resistance has led to heightened interest in the study of antimicrobial resistance from different angles. Areas addressed include mechanisms underlying this resistance, improved methods to detect resistance when it occurs, alternate options for the treatment of infections caused by resistant organisms, and strategies to prevent and control the emergence and spread of resistance. In this review, the mode of action of antifungals and their mechanisms of resistance are discussed. Additionally, an attempt is made to discuss the correlation between fungal and bacterial resistance. Antifungals can be grouped into three classes based on their site of action: azoles, which inhibit the synthesis of ergosterol (the main fungal sterol); polyenes, which interact with fungal membrane sterols physicochemically; and 5-fluorocytosine, which inhibits macromolecular synthesis. Many different types of mechanisms contribute to the development of resistance to antifungals. These mechanisms include alteration in drug target, alteration in sterol biosynthesis, reduction in the intercellular concentration of target enzyme, and overexpression of the antifungal drug target. Although the comparison between the mechanisms of resistance to antifungals and antibacterials is necessarily limited by several factors defined in the review, a correlation between the two exists. For example, modification of enzymes which serve as targets for antimicrobial action and the involvement of membrane pumps in the extrusion of drugs are well characterized in both the eukaryotic and prokaryotic cells.
机译:近年来,抗菌和抗真菌剂的使用增加,导致了对这些药物的耐药性的发展。耐药性的重要临床意义已引起人们对不同角度的抗生素耐药性研究的兴趣。解决的领域包括抗药性的基础机制,改进的检测抗药性的方法,治疗由抗药性生物引起的感染的替代方案以及预防和控制抗药性的出现和扩散的策略。在这篇综述中,讨论了抗真菌药的作用方式及其耐药机制。另外,尝试讨论真菌和细菌抗性之间的相关性。根据其作用部位,抗真菌剂可分为三类:抑制麦角甾醇(主要真菌甾醇)合成的唑类;多烯,与真菌膜固醇发生物理化学反应;和5-氟胞嘧啶,抑制大分子合成。许多不同类型的机制有助于产生抗真菌性。这些机制包括药物靶标的改变,固醇生物合成的改变,靶标酶的细胞间浓度的降低以及抗真菌药物靶标的过表达。尽管对抗真菌药和抗菌剂的抗药性机制之间的比较必然受到本综述中定义的几个因素的限制,但两者之间存在相关性。例如,在真核和原核细胞中都很好地表征了用作抗微生物作用靶标的酶的修饰以及膜泵参与药物的挤出。

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