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Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris
BACKGROUND: Candida auris is a multidrug resistant, emerging agent of fungemia in humans. Its actual global distribution remains obscure as the current commercial methods of clinical diagnosis misidentify it as C. haemulonii. Here we report the first draft genome of C. auris to explore the genomic b...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562351/ https://www.ncbi.nlm.nih.gov/pubmed/26346253 http://dx.doi.org/10.1186/s12864-015-1863-z |
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author | Chatterjee, Sharanya Alampalli, Shuba Varshini Nageshan, Rishi Kumar Chettiar, Sivarajan T. Joshi, Sangeeta Tatu, Utpal S. |
author_facet | Chatterjee, Sharanya Alampalli, Shuba Varshini Nageshan, Rishi Kumar Chettiar, Sivarajan T. Joshi, Sangeeta Tatu, Utpal S. |
author_sort | Chatterjee, Sharanya |
collection | PubMed |
description | BACKGROUND: Candida auris is a multidrug resistant, emerging agent of fungemia in humans. Its actual global distribution remains obscure as the current commercial methods of clinical diagnosis misidentify it as C. haemulonii. Here we report the first draft genome of C. auris to explore the genomic basis of virulence and unique differences that could be employed for differential diagnosis. RESULTS: More than 99.5 % of the C. auris genomic reads did not align to the current whole (or draft) genome sequences of Candida albicans, Candida lusitaniae, Candida glabrata and Saccharomyces cerevisiae; thereby indicating its divergence from the active Candida clade. The genome spans around 12.49 Mb with 8527 predicted genes. Functional annotation revealed that among the sequenced Candida species, it is closest to the hemiascomycete species Clavispora lusitaniae. Comparison with the well-studied species Candida albicans showed that it shares significant virulence attributes with other pathogenic Candida species such as oligopeptide transporters, mannosyl transfersases, secreted proteases and genes involved in biofilm formation. We also identified a plethora of transporters belonging to the ABC and major facilitator superfamily along with known MDR transcription factors which explained its high tolerance to antifungal drugs. CONCLUSIONS: Our study emphasizes an urgent need for accurate fungal screening methods such as PCR and electrophoretic karyotyping to ensure proper management of fungemia. Our work highlights the potential genetic mechanisms involved in virulence and pathogenicity of an important emerging human pathogen namely C. auris. Owing to its diversity at the genomic scale; we expect the genome sequence to be a useful resource to map species specific differences that will help develop accurate diagnostic markers and better drug targets. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1863-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4562351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45623512015-09-09 Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris Chatterjee, Sharanya Alampalli, Shuba Varshini Nageshan, Rishi Kumar Chettiar, Sivarajan T. Joshi, Sangeeta Tatu, Utpal S. BMC Genomics Research Article BACKGROUND: Candida auris is a multidrug resistant, emerging agent of fungemia in humans. Its actual global distribution remains obscure as the current commercial methods of clinical diagnosis misidentify it as C. haemulonii. Here we report the first draft genome of C. auris to explore the genomic basis of virulence and unique differences that could be employed for differential diagnosis. RESULTS: More than 99.5 % of the C. auris genomic reads did not align to the current whole (or draft) genome sequences of Candida albicans, Candida lusitaniae, Candida glabrata and Saccharomyces cerevisiae; thereby indicating its divergence from the active Candida clade. The genome spans around 12.49 Mb with 8527 predicted genes. Functional annotation revealed that among the sequenced Candida species, it is closest to the hemiascomycete species Clavispora lusitaniae. Comparison with the well-studied species Candida albicans showed that it shares significant virulence attributes with other pathogenic Candida species such as oligopeptide transporters, mannosyl transfersases, secreted proteases and genes involved in biofilm formation. We also identified a plethora of transporters belonging to the ABC and major facilitator superfamily along with known MDR transcription factors which explained its high tolerance to antifungal drugs. CONCLUSIONS: Our study emphasizes an urgent need for accurate fungal screening methods such as PCR and electrophoretic karyotyping to ensure proper management of fungemia. Our work highlights the potential genetic mechanisms involved in virulence and pathogenicity of an important emerging human pathogen namely C. auris. Owing to its diversity at the genomic scale; we expect the genome sequence to be a useful resource to map species specific differences that will help develop accurate diagnostic markers and better drug targets. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1863-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-07 /pmc/articles/PMC4562351/ /pubmed/26346253 http://dx.doi.org/10.1186/s12864-015-1863-z Text en © Chatterjee et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Chatterjee, Sharanya Alampalli, Shuba Varshini Nageshan, Rishi Kumar Chettiar, Sivarajan T. Joshi, Sangeeta Tatu, Utpal S. Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris |
title | Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris |
title_full | Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris |
title_fullStr | Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris |
title_full_unstemmed | Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris |
title_short | Draft genome of a commonly misdiagnosed multidrug resistant pathogen Candida auris |
title_sort | draft genome of a commonly misdiagnosed multidrug resistant pathogen candida auris |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562351/ https://www.ncbi.nlm.nih.gov/pubmed/26346253 http://dx.doi.org/10.1186/s12864-015-1863-z |
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