Clade II Candida auris possess genomic structural variations related to an ancestral strain.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 18 07 2019
accepted: 20 09 2019
entrez: 10 10 2019
pubmed: 10 10 2019
medline: 10 3 2020
Statut: epublish

Résumé

Candida auris is an invasive and multidrug-resistant ascomycetous yeast that is under global surveillance. All clinical cases of C. auris infection diagnosed from 1997 to 2019 in Japan were non-invasive and sporadic otitis media cases. In the present study, we performed whole-genome sequencing of seven C. auris strains isolated from patients with otitis media in Japan, all of which belonged to clade II. Comparative genome analysis using the high-quality draft genome sequences JCM 15448T revealed that single nucleotide variations (SNVs), clade-specific accessory genes, and copy number variations (CNVs) were identified in each C. auris clade. A total of 61 genes involved in cell wall and stress response-related functions was absent in clade II, and the pattern of conserved CNVs in each clade was more stable in clade II than in other clades. Our data suggest that the genomic structural diversity is stable in C. auris isolated from each biogeographic location, and Japanese strains isolated from patients with otitis media might belong to an ancestral type of C. auris. One Japanese strain, TWCC 58362, with reduced susceptibility to fluconazole, exhibited no mutation in ergosterol biosynthesis-related genes (ERG). However, TWCC 58362-specific variations, including SNVs, indels, and CNVs were detected, suggesting that gene duplication events in C. auris might contribute to antifungal drug resistance. Taken together, we demonstrated that genomic structural variations in C. auris could correlate to geographical dissemination, epidemiology, lesions in the host, and antifungal resistance.

Identifiants

pubmed: 31596885
doi: 10.1371/journal.pone.0223433
pii: PONE-D-19-20377
pmc: PMC6785063
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0223433

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Tsuyoshi Sekizuka (T)

Pathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan.

Shigekazu Iguchi (S)

Department of Infectious Diseases, Tokyo Women's Medical University, Tokyo, Japan.

Takashi Umeyama (T)

Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Tokyo, Japan.

Yuba Inamine (Y)

Pathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan.

Koichi Makimura (K)

Department of Medical Mycology, Graduate School of Medicine, Teikyo University, Tokyo, Japan.

Makoto Kuroda (M)

Pathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan.

Yoshitsugu Miyazaki (Y)

Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Tokyo, Japan.

Ken Kikuchi (K)

Department of Infectious Diseases, Tokyo Women's Medical University, Tokyo, Japan.

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Classifications MeSH