PubMed · 5088525
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M E Kirk, J Lough, H A Warner. 1971. Histoplasma colitis: an electron microscopic study.. https://pubmed.ncbi.nlm.nih.gov/5088525/
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Clinical isolates of Candida auris show a high prevalence of resistance to Amphotericin B (AmB)-an uncommon trait in most Candida species. Alterations in ergosterol biosynthesis can contribute to acquired AmB resistance in C. auris laboratory strains but are rarely seen in clinical isolates. In this study, we experimentally evolved two drug-susceptible Clade II isolates of C. auris to develop AmB resistance. The evolved strains displayed a four to eight fold increase in MIC50 compared to the parental cells. We analyzed changes in their karyotype, genome, lipidome, and transcriptome associated with this acquired resistance. In one lineage, AOX2 was upregulated, and its deletion reversed the AmB resistance phenotype. The aox2Δ mutant also failed to evolve AmB resistance under experimental conditions. In the same lineage, restoring the UPC2 S332R and RTG3 S101T mutations to the wild-type allele restored AmB susceptibility. In another lineage, the ergosterol and sphingolipid pathways were observed to play a critical role, and upregulation of the ERG genes elevated the total sterol content, while significant downregulation of HSX11 (glucosylceramide synthase) resulted in lower levels of glucosylceramides. To our knowledge, this study is the first to show that AmB resistance in C. auris can be acquired through mechanisms both dependent on or independent of sterol content modulation, highlighting Aox2 and Upc2 as key regulators of amphotericin resistance.
UNLABELLED: The post-antifungal effect (PAFE) of amphotericin B and voriconazole, either alone or in combination, on Aspergillus fumigatus was studied using an automated system based on fungal CO2 production. METHODS: Conidia of A. fumigatus were exposed to concentrations of 1-10 x MIC of amphotericin B and 1-40 x MIC of voriconazole for 1, 2 and 4 h. After a washing step, exposed and control conidia were inoculated into Pedi-BacT culture bottles. CO2 production was automatically monitored until the bottles signalled positive. The difference in time span for positive signals in drug-exposed and control bottles was used to calculate PAFE. RESULTS: There was a linear relationship between inoculum size and time to positive signal (r2=0.99). The precision of duplicate analyses was 1.5%. Longer exposure times increased the amphotericin B-induced PAFE (P<0.001), whereas concentrations above the MIC did not. Voriconazole after 4 h of exposure induced a short dose-independent PAFE. The combination with amphotericin B did not prolong the PAFE over that caused by amphotericin B alone. CONCLUSIONS: This automated method can be used for determination of PAFE. In contrast to Candida spp., in which amphotericin B-induced PAFE is mainly related to the area under the curve, the effect on A. fumigatus was more dependent on the exposure time. This implies that pharmacodynamic data obtained from Candida experiments cannot be directly extrapolated to Aspergillus.
Melanin is made by several important pathogenic fungi and is implicated in the pathogenesis of a number of mycoses. This study investigates whether the thermally dimorphic fungal pathogen Blastomyces dermatitidis produces melanin. Using techniques developed to study melanization in other fungi, we demonstrate that B. dermatitidis conidia and yeast produce melanin in vitro and that yeast cells synthesize melanin or melanin-like pigment in vivo. Melanization reduced susceptibility to amphotericin B, but not to itraconazole or voriconazole. Since melanin is an important virulence factor in other pathogenic fungi, this pigment may affect the pathogenesis of blastomycosis.