Beyond ergosterol: Strategies for combatting antifungal resistance in Aspergillus fumigatus and Candida auris

被引:10
|
作者
Cruz, Ricardo [1 ]
Wuest, William M. [1 ]
机构
[1] Emory Univ, Dept Chem, 1515 Dickey Dr, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
Antifungals; Antimicrobial resistance; Natural products; Total synthesis; BROAD-SPECTRUM ANTIFUNGAL; IN-VITRO; ACETOHYDROXYACID SYNTHASE; AMPHOTERICIN-B; NIKKOMYCIN Z; INHIBITOR; ALBICANS; DRUG; TETRANDRINE; PRODUCT;
D O I
10.1016/j.tet.2023.133268
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Aspergillus fumigatus and Candida auris are historically problematic fungal pathogens responsible for systemic infections and high mortality rates, especially in immunocompromised populations. The three antifungal classes that comprise our present day armamentarium have facilitated efficacious treatment of these fungal infections in past decades, but their potency has steadily declined over the years as resistance to these compounds has accumulated. Importantly, pan-resistant strains of Candida auris have been observed in clinical settings, leaving affected patients with no treatment options and a death sentence. Many compounds in the ongoing antifungal drug discovery pipeline, similar to those within our aforementioned trinity, are predicated on the binding or inhibition of ergosterol. Recurring accounts of resistance to antifungals targeting this pathway suggest optimization of ergosterol-dependent anti-fungals is likely not the best solution for the long-term. This review aims to present several natural products with novel or underexplored biological targets, as well as similarly underutilized drug discovery strategies to inspire future biological investigations and medicinal chemistry campaigns.(c) 2023 Elsevier Ltd. All rights reserved.
引用
收藏
页数:13
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