Abstract

First described in 2009 in Japan, the emerging multidrug-resistant fungal pathogen Candida auris is becoming a worldwide public health threat that has been attracting considerable attention due to its rapid and widespread emergence over the past decade. The reasons behind the recent emergence of this fungus remain a mystery to date. Genetic analyses indicate that this fungal pathogen emerged simultaneously in several different continents, where 5 genetically distinct clades of C. auris were isolated from distinct geographical locations. Although C. auris belongs to the CTG clade (its constituent species translate the CTG codon as serine instead of leucine, as in the standard code), C. auris is a haploid fungal species that is more closely related to the haploid and often multidrug-resistant species Candida haemulonii and Candida lusitaniae and is distantly related to the diploid and clinically common fungal pathogens Candida albicans and Candida tropicalis. Infections and outbreaks caused by C. auris in hospitals settings have been rising over the past several years. Difficulty in its identification, multidrug resistance properties, evolution of virulence factors, associated high mortality rates in patients, and long-term survival on surfaces in the environment make C. auris particularly problematic in clinical settings. Here, we review progress made over the past decade on the biological and clinical aspects of C. auris. Future efforts should be directed toward understanding the mechanistic details of its biology, epidemiology, antifungal resistance, and pathogenesis with a goal of developing novel tools and methods for the prevention, diagnosis, and treatment of C. auris infections.

Highlights

  • Fungal infections are increasingly recognized as a worldwide threat to human health

  • A comparative study of European Committee on Antimicrobial Susceptibility Testing (EUCAST) and Clinical and Laboratory Standards Institute (CLSI) methods revealed that C. auris isolates have a remarkably similar fluconazole resistance but a wide range of minimum inhibitory concentrations (MICs) for the other antifungal drug classes [67]

  • Comparative genomic analyses indicate that the C. auris genome contains conserved genes within the CTG clade that are associated with virulence and antifungal resistance [13,14]

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Summary

Introduction

Fungal infections are increasingly recognized as a worldwide threat to human health. About 1.7 billion people worldwide suffer from a fungal infection, most of which are superficial infections of the skin and mucosa (reviewed by [1]). Pathogenic Candida species, such as C. albicans, C. tropicalis, C. parapsilosis, and C. auris, but not C. glabrata, belong to the CTG clade. Similar to other Candida species, C. auris can form biofilms, undergo filamentation, and phenotypically change between specific cell types [12,32,43,44,45].

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