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Use of the VITEK 2 system to identify and test the antifungal susceptibility of clinically relevant yeast species

Eleven quality control isolates (Candida albicans ATCC 64548, C. tropicalis ATCC 200956, C. glabrata ATCC 90030, C. lusitaniae ATCC 200951, C. parapsilosis ATCC 22019, C. krusei ATCC 6258, C. dubliniensis ATCC 6330, Saccharomyces cerevisiae ATCC 9763, Cryptococcus neoformans ATCC 90012, C. gattii FI...

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Autores principales: Melhem, MSC, Bertoletti, A, Lucca, HRL, Silva, RBO, Meneghin, FA, Szeszs, MW
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Society of Microbiology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958196/
https://www.ncbi.nlm.nih.gov/pubmed/24688520
http://dx.doi.org/10.1590/S1517-83822014005000018
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author Melhem, MSC
Bertoletti, A
Lucca, HRL
Silva, RBO
Meneghin, FA
Szeszs, MW
author_facet Melhem, MSC
Bertoletti, A
Lucca, HRL
Silva, RBO
Meneghin, FA
Szeszs, MW
author_sort Melhem, MSC
collection PubMed
description Eleven quality control isolates (Candida albicans ATCC 64548, C. tropicalis ATCC 200956, C. glabrata ATCC 90030, C. lusitaniae ATCC 200951, C. parapsilosis ATCC 22019, C. krusei ATCC 6258, C. dubliniensis ATCC 6330, Saccharomyces cerevisiae ATCC 9763, Cryptococcus neoformans ATCC 90012, C. gattii FIOCRUZ-CPF 60, and Trichosporon mucoides ATCC 204094) and 32 bloodstream isolates, including C. albicans, C. tropicalis, C. parapsilosis, C. glabrata, C. krusei, C. guilliermondii, C. pelliculosa (Pichia anomala), C. haemulonii, C. lusitaniae, and C. kefyr were identified at the species level by the VITEK 2 system. A set of clinical isolates (32 total) were used as challenge strains to evaluate the ability of the VITEK 2 system to determine the antifungal susceptibility of yeasts compared with the CLSI and EUCAST BMD reference standards. The VITEK 2 system correctly identified 100% of the challenge strains. The identification of yeast species and the evaluation of their susceptibility profiles were performed in an automated manner by the VITEK 2 system after approximately 15 h of growth for most species of Candida. The VITEK 2 system ensures that each test is performed in a standardized manner and provides quantitative MIC results that are reproducible and accurate when compared with the BMD reference methods. This system was able to determine the MICs of amphotericin B, flucytosine, voriconazole, and fluconazole in 15 h or less for the most common clinically relevant Candida species. In addition, the VITEK 2 system could reliably identify resistance to flucytosine, voriconazole, and fluconazole and exhibits excellent quantitative and qualitative agreement with the CLSI or EUCAST broth microdilution reference methods.
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spelling pubmed-39581962014-04-10 Use of the VITEK 2 system to identify and test the antifungal susceptibility of clinically relevant yeast species Melhem, MSC Bertoletti, A Lucca, HRL Silva, RBO Meneghin, FA Szeszs, MW Braz J Microbiol Research Paper Eleven quality control isolates (Candida albicans ATCC 64548, C. tropicalis ATCC 200956, C. glabrata ATCC 90030, C. lusitaniae ATCC 200951, C. parapsilosis ATCC 22019, C. krusei ATCC 6258, C. dubliniensis ATCC 6330, Saccharomyces cerevisiae ATCC 9763, Cryptococcus neoformans ATCC 90012, C. gattii FIOCRUZ-CPF 60, and Trichosporon mucoides ATCC 204094) and 32 bloodstream isolates, including C. albicans, C. tropicalis, C. parapsilosis, C. glabrata, C. krusei, C. guilliermondii, C. pelliculosa (Pichia anomala), C. haemulonii, C. lusitaniae, and C. kefyr were identified at the species level by the VITEK 2 system. A set of clinical isolates (32 total) were used as challenge strains to evaluate the ability of the VITEK 2 system to determine the antifungal susceptibility of yeasts compared with the CLSI and EUCAST BMD reference standards. The VITEK 2 system correctly identified 100% of the challenge strains. The identification of yeast species and the evaluation of their susceptibility profiles were performed in an automated manner by the VITEK 2 system after approximately 15 h of growth for most species of Candida. The VITEK 2 system ensures that each test is performed in a standardized manner and provides quantitative MIC results that are reproducible and accurate when compared with the BMD reference methods. This system was able to determine the MICs of amphotericin B, flucytosine, voriconazole, and fluconazole in 15 h or less for the most common clinically relevant Candida species. In addition, the VITEK 2 system could reliably identify resistance to flucytosine, voriconazole, and fluconazole and exhibits excellent quantitative and qualitative agreement with the CLSI or EUCAST broth microdilution reference methods. Brazilian Society of Microbiology 2014-03-10 /pmc/articles/PMC3958196/ /pubmed/24688520 http://dx.doi.org/10.1590/S1517-83822014005000018 Text en Copyright © 2013, Sociedade Brasileira de Microbiologia All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License CC BY-NC.
spellingShingle Research Paper
Melhem, MSC
Bertoletti, A
Lucca, HRL
Silva, RBO
Meneghin, FA
Szeszs, MW
Use of the VITEK 2 system to identify and test the antifungal susceptibility of clinically relevant yeast species
title Use of the VITEK 2 system to identify and test the antifungal susceptibility of clinically relevant yeast species
title_full Use of the VITEK 2 system to identify and test the antifungal susceptibility of clinically relevant yeast species
title_fullStr Use of the VITEK 2 system to identify and test the antifungal susceptibility of clinically relevant yeast species
title_full_unstemmed Use of the VITEK 2 system to identify and test the antifungal susceptibility of clinically relevant yeast species
title_short Use of the VITEK 2 system to identify and test the antifungal susceptibility of clinically relevant yeast species
title_sort use of the vitek 2 system to identify and test the antifungal susceptibility of clinically relevant yeast species
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958196/
https://www.ncbi.nlm.nih.gov/pubmed/24688520
http://dx.doi.org/10.1590/S1517-83822014005000018
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