Department of Microbiology, Immunology and Molecular Genetics, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Curr Opin Microbiol. 2019 Dec;52:27-34. doi: 10.1016/j.mib.2019.04.005. Epub 2019 May 24.
Candida albicans, a major human fungal pathogen, can cause a wide variety of both mucosal and systemic infections, particularly in immunocompromised individuals. Multiple lines of evidence suggest a strong association between virulence and the ability of C. albicans to undergo a reversible morphological transition from yeast to filamentous cells in response to host environmental cues. Most previous studies on mechanisms important for controlling the C. albicans morphological transition have focused on signaling pathways and sequence-specific transcription factors. However, in recent years a variety of novel mechanisms have been reported, including those involving global transcriptional regulation and translational control. A large-scale functional genomics screen has also revealed new roles in filamentation for certain key biosynthesis pathways. This review article will highlight several of these exciting recent discoveries and discuss how they are relevant to the development of novel antifungal strategies. Ultimately, components of mechanisms that control C. albicans morphogenesis and pathogenicity could potentially serve as viable antifungal targets.
白色念珠菌是一种主要的人类真菌病原体,可引起广泛的黏膜和系统性感染,尤其是在免疫功能低下的个体中。多项证据表明,毒力与白色念珠菌在宿主环境线索的作用下发生可逆形态转变的能力之间存在很强的关联。大多数关于控制白色念珠菌形态转变的重要机制的先前研究都集中在信号通路和序列特异性转录因子上。然而,近年来已经报道了多种新的机制,包括涉及全局转录调控和翻译控制的机制。大规模的功能基因组筛选也揭示了某些关键生物合成途径在菌丝形成中的新作用。本文综述将重点介绍其中的一些令人兴奋的最新发现,并讨论它们与新型抗真菌策略的相关性。最终,控制白色念珠菌形态发生和致病性的机制成分可能成为可行的抗真菌靶标。