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Published on: October 12, 2022
Ume6-dependent pathways of morphogenesis and biofilm formation in Candida auris
Marine Louvet1, Jizhou Li1, Danielle Brandalise1
1Institute of Microbiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Abstract:
Candida auris is a yeast pathogen causing nosocomial outbreaks of candidemia. Its ability to adhere to inert surfaces and to be transmitted from one patient to another via medical devices is of particular concern. Like other Candida spp., C. auris has the ability to transition from the yeast form to pseudohyphae and to build biofilms. Moreover, some isolates have a unique capacity to form aggregates. These morphogenetic changes may impact virulence. In this study, we demonstrated the role of the transcription factor Ume6 in C. auris morphogenesis. Genetic hyperactivation of Ume6 induced filamentation and aggregation. The Ume6-hyperactivated strain (UME6HA) also exhibited increased adhesion to inert surface and formed biofilms of higher biomass compared to the parental strain. Transcriptomic analyses of UME6HA revealed enrichment of genes encoding for adhesins, proteins involved in cell wall organization, sterol biosynthesis, and aspartic protease activities. The three most upregulated genes compared to wild-type were those encoding for the agglutin-like sequence adhesin Als4498, the C. auris-specific adhesin Scf1, and the hypha-specific G1 cyclin-related protein Hgc1. The deletion of these genes in the UME6HA background showed that Ume6 controls filamentation via Hgc1 and aggregation via Als4498 and Scf1. Adhesion to inert surface was essentially triggered by Scf1. However, Als4498 and Hgc1 were also crucial for biofilm formation. Our data show that Ume6 is a universal regulator of C. auris morphogenesis via distinct modulators.IMPORTANCEC. auris represents a public health threat because of its ability to cause difficult-to-treat infections and hospital outbreaks. The morphogenetic plasticity of C. auris, including its ability to filament, to form aggregates or biofilms on inert surfaces, is important to the fungus for interhuman transmission, skin or catheter colonization, tissue invasion, antifungal resistance, and escape of the host immune system. This work deciphered the importance of Ume6 in the control of distinct pathways involved in filamentation, aggregation, adhesion, and biofilm formation of C. auris. A better understanding of the mechanisms of C. auris morphogenesis may help identify novel antifungal targets.
Insights
The transcription factor Ume6 controls Candida auris morphogenesis, including filamentation and aggregation. Ume6 hyperactivation enhances adhesion and biofilm formation, crucial for this public health threat.
Area of Science:
- Medical Mycology
- Molecular Biology
- Pathogenesis
Background:
- * Candida auris is an emerging yeast pathogen responsible for nosocomial candidemia outbreaks.
- * Its ability to adhere to surfaces and form biofilms contributes to patient-to-patient transmission via medical devices.
- * Morphogenetic changes like filamentation and aggregation are linked to C. auris virulence.
Purpose of the Study:
- * To investigate the role of the transcription factor Ume6 in regulating Candida auris morphogenesis.
- * To identify the specific pathways and genes controlled by Ume6 during morphogenetic transitions.
- * To understand how Ume6 influences C. auris adhesion and biofilm formation.
Main Methods:
- * Genetic manipulation to hyperactivate Ume6 in C. auris.
- * Phenotypic analysis of Ume6-hyperactivated strains for filamentation, aggregation, adhesion, and biofilm formation.
- * Transcriptomic analysis to identify Ume6-regulated genes.
- * Gene deletion studies to confirm the role of specific Ume6-regulated genes.
Main Results:
- * Ume6 hyperactivation induced filamentation and aggregation in C. auris.
- * The Ume6-hyperactivated strain showed increased adhesion to inert surfaces and higher biofilm biomass.
- * Transcriptomic analysis revealed Ume6 upregulates genes involved in adhesion (Als4498, Scf1) and filamentation (Hgc1).
- * Ume6 controls filamentation via Hgc1, aggregation via Als4498 and Scf1, and adhesion primarily via Scf1.
Conclusions:
- * Ume6 is a key regulator of Candida auris morphogenesis, controlling distinct pathways.
- * Ume6 orchestrates filamentation, aggregation, adhesion, and biofilm formation through specific downstream effectors.
- * Understanding Ume6's regulatory role provides insights into C. auris pathogenesis and potential antifungal targets.
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