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An Erg11 lanosterol 14-alpha-demethylase-Arv1 complex is required forCandida albicansvirulence
Journal article   Open access   Peer reviewed

An Erg11 lanosterol 14-alpha-demethylase-Arv1 complex is required forCandida albicansvirulence

Michelle L. Villasmil, Antonio Daniel Barbosa, Jessie Lee Cunningham, Symeon Siniossoglou and Joseph T. Nickels
PloS one, v 15(7), 0235746
17 Jul 2020
PMID: 32678853
url
https://doi.org/10.1371/journal.pone.0235746View
Published, Version of Record (VoR) Open

Abstract

Multidisciplinary Sciences Science & Technology Science & Technology - Other Topics
Azole resistant fungal infections remain a health problem for the immune compromised. Current therapies are limited due to rises in new resistance mechanisms. Therefore, it is important to identify new drug targets for drug discovery and novel therapeutics. Arv1 (are1 are2required forviability1) function is highly conserved between multiple pathogenic fungal species.Candida albicans(C.albicans) cells lacking CaArv1 are azole hypersusceptible and lack virulence.Saccharomyces cerevisiae(S.cerevisiae)Scarv1cells are also azole hypersusceptible, a phenotype reversed by expression of CaArv1, indicating conservation in the molecular mechanism for azole susceptibility. To define the relationship between Arv1 function and azole susceptibility, we undertook a structure/function analysis of ScArv1. We identified several conserved amino acids within the ScArv1homologydomain (ScAhd) required for maintaining normal azole susceptibility. Erg11 lanosterol 14-alpha-demethylase is the rate-limiting enzyme in sterol biosynthesis and is the direct target of azole antifungals, so we used our ScArv1 mutants in order to explore the relationship between ScArv1 and ScErg11. Specific ScArv1 mutants ectopically expressed from a low copy plasmid were unable to restore normal azole susceptibility toScarv1cells and had reduced Erg11 protein levels. Erg11 protein stability depended on its ability to form a heterodimeric complex with Arv1. Complex formation was required for maintaining normal azole susceptibility.Scarv1cells expressing orthologous CaArv1 mutants also had reduced CaErg11 levels, were unable to form a CaArv1-CaErg11 complex, and were azole hypersusceptible.Scarv1cells expressing CaArv1 mutants unable to interact with CaErg11 could not sustain proper levels of the azole resistant CaErg11(Y132F F145L)protein.Caarv1/Caarv1cells expressing CaArv1 mutants unable to interact with CaErg11 were found to lack virulence using a disseminated candidiasis mouse model. Expressing CaErg11(Y132F F145L)did not reverse the lack of virulence. We hypothesize that the role of Arv1 in Erg11-dependent azole resistance is to stabilize Erg11 protein level. Arv1 inhibition may represent an avenue for treating azole resistance.

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Web of Science research areas
Biochemistry & Molecular Biology
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