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Unlabelled: The fungal pathogen represents a severe threat to hospitalized patients. Its resistance to multiple classes of antifungal drugs and ability to spread and resist decontamination in health-care settings make it especially dangerous. We screened 1,990 clinically approved and late-stage investigational compounds for the potential to be repurposed as antifungal drugs targeting and narrowed our focus to five FDA-approved compounds with inhibitory concentrations under 10 µM for and significantly lower toxicity to three human cell lines. These compounds, some of which had been previously identified in independent screens, include three dihalogenated 8-hydroxyquinolines: broxyquinoline, chloroxine, and clioquinol. A subsequent structure-activity study of 32 quinoline derivatives found that 8-hydroxyquinolines, especially those dihalogenated at the C5 and C7 positions, were the most effective inhibitors of . To pursue these compounds further, we exposed to clioquinol in an extended experimental evolution study and found that developed only 2- to 5-fold resistance to the compound. DNA sequencing of resistant strains and subsequent verification by directed mutation in naive strains revealed that resistance was due to mutations in the transcriptional regulator (causing upregulation of the drug transporter ) and in the drug transporter . These mutations had only modest effects on resistance to traditional antifungal agents, and the mutation rendered more sensitive to posaconazole. This observation raises the possibility that a combination treatment involving an 8-hydroxyquinoline and posaconazole might prevent from developing resistance to this established antifungal agent.
Abstract Importance: The rapidly emerging fungal pathogen represents a growing threat to hospitalized patients, in part due to frequent resistance to multiple classes of antifungal drugs. We identify a class of compounds, the dihalogenated hydroxyquinolines, with broad fungistatic ability against a diverse collection of 13 strains of . Although this compound has been identified in previous screens, we extended the analysis by showing that developed only modest 2- to 5-fold increases in resistance to this class of compounds despite long-term exposure; a noticeable difference from the 30- to 500- fold increases in resistance reported for similar studies with commonly used antifungal drugs. We also identify the mutations underlying the resistance. These results suggest that the dihalogenated hydroxyquinolines are working inside the fungal cell and should be developed further to combat and other fungal pathogens.
Tweet: Lohse and colleagues characterize a class of compounds that inhibit the fungal pathogen . Unlike many other antifungal drugs, does not readily develop resistance to this class of compounds.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949084 | PMC |
http://dx.doi.org/10.1101/2023.02.16.528905 | DOI Listing |
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