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

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 se...

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Autores principales: Sekizuka, Tsuyoshi, Iguchi, Shigekazu, Umeyama, Takashi, Inamine, Yuba, Makimura, Koichi, Kuroda, Makoto, Miyazaki, Yoshitsugu, Kikuchi, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785063/
https://www.ncbi.nlm.nih.gov/pubmed/31596885
http://dx.doi.org/10.1371/journal.pone.0223433
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author Sekizuka, Tsuyoshi
Iguchi, Shigekazu
Umeyama, Takashi
Inamine, Yuba
Makimura, Koichi
Kuroda, Makoto
Miyazaki, Yoshitsugu
Kikuchi, Ken
author_facet Sekizuka, Tsuyoshi
Iguchi, Shigekazu
Umeyama, Takashi
Inamine, Yuba
Makimura, Koichi
Kuroda, Makoto
Miyazaki, Yoshitsugu
Kikuchi, Ken
author_sort Sekizuka, Tsuyoshi
collection PubMed
description 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 15448(T) 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.
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spelling pubmed-67850632019-10-19 Clade II Candida auris possess genomic structural variations related to an ancestral strain Sekizuka, Tsuyoshi Iguchi, Shigekazu Umeyama, Takashi Inamine, Yuba Makimura, Koichi Kuroda, Makoto Miyazaki, Yoshitsugu Kikuchi, Ken PLoS One Research Article 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 15448(T) 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. Public Library of Science 2019-10-09 /pmc/articles/PMC6785063/ /pubmed/31596885 http://dx.doi.org/10.1371/journal.pone.0223433 Text en © 2019 Sekizuka et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sekizuka, Tsuyoshi
Iguchi, Shigekazu
Umeyama, Takashi
Inamine, Yuba
Makimura, Koichi
Kuroda, Makoto
Miyazaki, Yoshitsugu
Kikuchi, Ken
Clade II Candida auris possess genomic structural variations related to an ancestral strain
title Clade II Candida auris possess genomic structural variations related to an ancestral strain
title_full Clade II Candida auris possess genomic structural variations related to an ancestral strain
title_fullStr Clade II Candida auris possess genomic structural variations related to an ancestral strain
title_full_unstemmed Clade II Candida auris possess genomic structural variations related to an ancestral strain
title_short Clade II Candida auris possess genomic structural variations related to an ancestral strain
title_sort clade ii candida auris possess genomic structural variations related to an ancestral strain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785063/
https://www.ncbi.nlm.nih.gov/pubmed/31596885
http://dx.doi.org/10.1371/journal.pone.0223433
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