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Sphingolipids: Regulators of azole drug resistance and fungal pathogenicity

期刊

MOLECULAR MICROBIOLOGY
卷 114, 期 6, 页码 891-905

出版社

WILEY
DOI: 10.1111/mmi.14586

关键词

antifungal therapeutic target; azole resistance; ergosterol; fungal pathogenicity; sphingolipids

资金

  1. National Natural Science Foundation of China [NSFC31800058, NSFC81703569, 81870005]

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In recent years, the role of sphingolipids in pathogenic fungi, in terms of pathogenicity and resistance to azole drugs, has been a rapidly growing field. This review describes evidence about the roles of sphingolipids in azole resistance and fungal virulence. Sphingolipids can serve as signaling molecules that contribute to azole resistance through modulation of the expression of drug efflux pumps. They also contribute to azole resistance by participating in various microbial pathways such as the unfolded protein response (UPR), pH-responsive Rim pathway, and pleiotropic drug resistance (PDR) pathway. In addition, sphingolipid signaling and eisosomes also coordinately regulate sphingolipid biosynthesis in response to azole-induced membrane stress. Sphingolipids are important for fungal virulence, playing roles during growth in hosts under stressful conditions, maintenance of cell wall integrity, biofilm formation, and production of various virulence factors. Finally, we discuss the possibility of exploiting fungal sphingolipids for the development of new therapeutic strategies to treat infections caused by pathogenic fungi.

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