Roles for Stress Response and Cell Wall Biosynthesis Pathways in Caspofungin Tolerance in Cryptococcus neoformans. Issue 1 (1st September 2019)

• Record Type: Journal Article
• Authors: Pianalto, Kaila M; Billmyre, R Blake; Telzrow, Calla L; Alspaugh, J Andrew
• Is Part Of: Genetics. Volume 213:Issue 1(2019)
• Page Start: 213
• Page End: 227
• Publication Date: 2019-09-01
• Subjects: antifungal -- chitin -- calcineurin -- signalosome -- Ras; Genetics -- Periodicals; 576.5
• DOI: 10.1534/genetics.119.302290
• Languages: English
• ISSNs: 0016-6731

Abstract

Abstract: Limited antifungal diversity and availability are growing problems for the treatment of fungal infections in the face of increasing drug resistance. The echinocandins, one of the newest classes of antifungal drugs, inhibit production of a crucial cell wall component. However, these compounds do not effectively inhibit the growth of the opportunistic fungal pathogen Cryptococcus neoformans, despite potent inhibition of the target enzyme in vitro . Therefore, we performed a forward genetic screen to identify cellular processes that mediate the relative tolerance of this organism to the echinocandin drug caspofungin. Through these studies, we identified 14 genetic mutants that enhance caspofungin antifungal activity. Rather than directly affecting caspofungin antifungal activity, these mutations seem to prevent the activation of various stress-induced compensatory cellular processes. For example, the pfa4 Δ mutant has defects in the palmitoylation and localization of many of its target proteins, including the Ras1 GTPase and the Chs3 chitin synthase, which are both required for caspofungin tolerance. Similarly, we have confirmed the link between caspofungin treatment and calcineurin signaling in this organism, but we suggest a deeper mechanism in which caspofungin tolerance is mediated by multiple pathways downstream of calcineurin function. In summary, we describe here several pathways in C. neoformans that contribute to the complex caspofungin tolerance phenotype in this organism.