Litcius/Paper detail

Impact of Erg11 Amino Acid Substitutions Identified in Candida auris Clade III Isolates on Triazole Drug Susceptibility

Williamson, Benjamin, Wilk, Adam, Guerrero, Kevin D., Mikulski, Timothy D., Elias, Tony N., Sawh, Indira, Cancino-Prado, Geselle, Gardam, Dianne, Heath, Christopher H., Govender, Nelesh P., Perlin, David S., Kordalewska, Milena, Healey, Kelley R., Williamson, Benjamin, Wilk, Adam, Guerrero, Kevin D., Mikulski, Timothy D., Elias, Tony N., Sawh, Indira, Cancino-Prado, Geselle, Gardam, Dianne, Heath, Christopher H., Govender, Nelesh P., Perlin, David S., Kordalewska, Milena, Healey, Kelley R.

2021UWA Profiles and Research Repository (UWA)20 citationsOpen Access PDF

Abstract

ERG11 sequencing of 28 Candida auris clade III isolates revealed the presence of concomitant V125A and F126L substitutions. Heterologous expression of Erg11-V125A/F126L in Saccharomyces cerevisiae led to reduced fluconazole and voriconazole susceptibilities. Generation of single substitution gene variants through site-directed mutagenesis uncovered that F126L primarily contributes to the elevated triazole MICs. A similar yet diminished pattern of reduced susceptibility was observed with the long-tailed triazoles posaconazole and itraconazole for the V125A/F126L, F126L, Y132F, and K143R alleles.

Topics & Concepts

PosaconazoleCandida aurisFluconazoleItraconazoleBiologyVoriconazoleTriazoleCladeGeneticsGeneMicrobiologyPhylogenetic treeAntifungalChemistryOrganic chemistryAntifungal resistance and susceptibilityFungal Infections and StudiesPneumocystis jirovecii pneumonia detection and treatment