Metal-Based Combinations That Target Protein Synthesis by Fungi.

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Advances in Microbial Physiology Pub Date : 2017-01-01 Epub Date: 2017-02-11 DOI:10.1016/bs.ampbs.2017.01.001
Cindy Vallières, Simon V Avery
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引用次数: 7

Abstract

A wide range of fungicides (or antifungals) are used in agriculture and medicine, with activities against a spectrum of fungal pathogens. Unfortunately, the evolution of fungicide resistance has become a major issue. Therefore, there is an urgent need for new antifungal treatments. Certain metals have been used for decades as efficient fungicides in agriculture. However, concerns over metal toxicity have escalated over this time. Recent studies have revealed that metals like copper and chromate can impair functions required for the fidelity of protein synthesis in fungi. This occurs through different mechanisms, based on targeting of iron-sulphur cluster integrity or competition for uptake with amino acid precursors. Moreover, chromate at least acts synergistically with other agents known to target translation fidelity, like aminoglycoside antibiotics, causing dramatic and selective growth inhibition of several fungal pathogens of humans and plants. As such synergy allows the application of decreased amounts of metals for effective inhibition, it lessens concerns about nonspecific toxicity and opens new possibilities for metal applications in combinatorial fungicides targeting protein synthesis.

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以真菌合成蛋白质为目标的金属基组合。
广泛的杀菌剂(或抗真菌剂)用于农业和医学,具有对抗真菌病原体的活性。不幸的是,杀菌剂耐药性的演变已成为一个主要问题。因此,迫切需要新的抗真菌治疗方法。某些金属作为高效的杀菌剂已经在农业中使用了几十年。然而,在这段时间里,对金属毒性的担忧已经升级。最近的研究表明,铜和铬酸盐等金属会损害真菌中蛋白质合成保真度所需的功能。这通过不同的机制发生,基于铁硫簇完整性的靶向或与氨基酸前体的摄取竞争。此外,铬酸盐至少与其他已知的靶向翻译保真度的药物协同作用,如氨基糖苷类抗生素,对人类和植物的几种真菌病原体产生显著的选择性生长抑制。由于这种协同作用允许使用较少数量的金属进行有效抑制,它减少了对非特异性毒性的担忧,并为金属在靶向蛋白质合成的组合杀菌剂中的应用开辟了新的可能性。
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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来源期刊
Advances in Microbial Physiology
Advances in Microbial Physiology 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
16
期刊介绍: Advances in Microbial Physiology publishes topical and important reviews, interpreting physiology to include all material that contributes to our understanding of how microorganisms and their component parts work. First published in 1967, the editors have always striven to interpret microbial physiology in the broadest context and have never restricted the contents to traditional views of whole cell physiology.
期刊最新文献
Preface. Biological functions of bacterial lysophospholipids. Redefining the bacterial Type I protein secretion system. Purine catabolism by enterobacteria. Fumarate, a central electron acceptor for Enterobacteriaceae beyond fumarate respiration and energy conservation.
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