The good, the bad and the hazardous: comparative genomic analysis unveils cell wall features in the pathogen Candidozyma auris typical for both baker´s yeast and Candida

The drug-resistant pathogenic yeast Candidozyma auris (formerly named Candida auris) is considered a critical health problem of global importance. As the cell wall plays a crucial role in pathobiology, here we performed a detailed bioinformatic analysis of its biosynthesis in C. auris and related Ca...

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Bibliographic Details
Authors: Alvarado González, María, Gómez Navajas, Jesús Alberto, Blázquez Muñoz, María Teresa, Gómez Molero, Emilia, Fernández Sánchez, Sebastián, Eraso Barrio, Elena, Munro, Carol Anne, Valentín Gomez, Eulogio, Mateo Alesanco, Estíbaliz, de Groot, Petrus Wilhelmus Johannes
Format: article
Publication Date:2024
Country:España
Institution:Universidad de Castilla-La Mancha
Repository:RUIdeRA. Repositorio Institucional de la UCLM
OAI Identifier:oai:ruidera.uclm.es:10578/46308
Online Access:https://academic.oup.com/femsyr/article/doi/10.1093/femsyr/foae039/7916657
https://hdl.handle.net/10578/46308
Access Level:Open access
Keyword:Adhesins
Candida auris
Candidiasis
Cell wall
Glucan
GPI proteins
Mannosylation
Description
Summary:The drug-resistant pathogenic yeast Candidozyma auris (formerly named Candida auris) is considered a critical health problem of global importance. As the cell wall plays a crucial role in pathobiology, here we performed a detailed bioinformatic analysis of its biosynthesis in C. auris and related Candidozyma haemuli complex species using Candida albicans and Saccharomyces cerevisiae as references. Our data indicate that the cell wall architecture described for these reference yeasts is largely conserved in Candidozyma spp.; however, expansions or reductions in gene families point to subtle alterations, particularly with respect to ß­-1,3-­glucan synthesis and remodeling, phosphomannosylation, ß-mannosylation, and glycosylphosphatidylinositol (GPI) proteins. In several aspects, C. auris holds a position in between C. albicans and S. cerevisiae, consistent with being classified in a separate genus. Strikingly, among the identified putative GPI proteins in C. auris are adhesins typical for both Candida (Als and Hyr/Iff) and Saccharomyces (Flo11 and Flo5-like flocculins). Further, 26 putative C. auris GPI proteins lack homologs in Candida genus species. Phenotypic analysis of one such gene, QG37_05701, showed mild phenotypes implicating a role associated with cell wall ß-1,3-glucan. Altogether, our study uncovered a wealth of information relevant for the pathogenicity of C. auris as well as targets for follow-up studies.