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Comparison of Two Commercially Available qPCR Kits for the Detection of Candida auris

Candida auris is an emerging pathogen with resistance to many commonly used antifungal agents. Infections with C. auris require rapid and reliable detection methods to initiate successful medical treatment and contain hospital outbreaks. Conventional identification methods are prone to errors and ca...

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Autores principales: Sattler, Janko, Noster, Janina, Brunke, Anne, Plum, Georg, Wiegel, Pia, Kurzai, Oliver, Meis, Jacques F., Hamprecht, Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926799/
https://www.ncbi.nlm.nih.gov/pubmed/33671676
http://dx.doi.org/10.3390/jof7020154
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author Sattler, Janko
Noster, Janina
Brunke, Anne
Plum, Georg
Wiegel, Pia
Kurzai, Oliver
Meis, Jacques F.
Hamprecht, Axel
author_facet Sattler, Janko
Noster, Janina
Brunke, Anne
Plum, Georg
Wiegel, Pia
Kurzai, Oliver
Meis, Jacques F.
Hamprecht, Axel
author_sort Sattler, Janko
collection PubMed
description Candida auris is an emerging pathogen with resistance to many commonly used antifungal agents. Infections with C. auris require rapid and reliable detection methods to initiate successful medical treatment and contain hospital outbreaks. Conventional identification methods are prone to errors and can lead to misidentifications. PCR-based assays, in turn, can provide reliable results with low turnaround times. However, only limited data are available on the performance of commercially available assays for C. auris detection. In the present study, the two commercially available PCR assays AurisID (OLM, Newcastle Upon Tyne, UK) and Fungiplex Candida Auris RUO Real-Time PCR (Bruker, Bremen, Germany) were challenged with 29 C. auris isolates from all five clades and eight other Candida species as controls. AurisID reliably detected C. auris with a limit of detection (LoD) of 1 genome copies/reaction. However, false positive results were obtained with high DNA amounts of the closely related species C. haemulonii, C. duobushaemulonii and C. pseudohaemulonii. The Fungiplex Candida Auris RUO Real-Time PCR kit detected C. auris with an LoD of 9 copies/reaction. No false positive results were obtained with this assay. In addition, C. auris could also be detected in human blood samples spiked with pure fungal cultures by both kits. In summary, both kits could detect C. auris-DNA at low DNA concentrations but differed slightly in their limits of detection and specificity.
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spelling pubmed-79267992021-03-04 Comparison of Two Commercially Available qPCR Kits for the Detection of Candida auris Sattler, Janko Noster, Janina Brunke, Anne Plum, Georg Wiegel, Pia Kurzai, Oliver Meis, Jacques F. Hamprecht, Axel J Fungi (Basel) Article Candida auris is an emerging pathogen with resistance to many commonly used antifungal agents. Infections with C. auris require rapid and reliable detection methods to initiate successful medical treatment and contain hospital outbreaks. Conventional identification methods are prone to errors and can lead to misidentifications. PCR-based assays, in turn, can provide reliable results with low turnaround times. However, only limited data are available on the performance of commercially available assays for C. auris detection. In the present study, the two commercially available PCR assays AurisID (OLM, Newcastle Upon Tyne, UK) and Fungiplex Candida Auris RUO Real-Time PCR (Bruker, Bremen, Germany) were challenged with 29 C. auris isolates from all five clades and eight other Candida species as controls. AurisID reliably detected C. auris with a limit of detection (LoD) of 1 genome copies/reaction. However, false positive results were obtained with high DNA amounts of the closely related species C. haemulonii, C. duobushaemulonii and C. pseudohaemulonii. The Fungiplex Candida Auris RUO Real-Time PCR kit detected C. auris with an LoD of 9 copies/reaction. No false positive results were obtained with this assay. In addition, C. auris could also be detected in human blood samples spiked with pure fungal cultures by both kits. In summary, both kits could detect C. auris-DNA at low DNA concentrations but differed slightly in their limits of detection and specificity. MDPI 2021-02-22 /pmc/articles/PMC7926799/ /pubmed/33671676 http://dx.doi.org/10.3390/jof7020154 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sattler, Janko
Noster, Janina
Brunke, Anne
Plum, Georg
Wiegel, Pia
Kurzai, Oliver
Meis, Jacques F.
Hamprecht, Axel
Comparison of Two Commercially Available qPCR Kits for the Detection of Candida auris
title Comparison of Two Commercially Available qPCR Kits for the Detection of Candida auris
title_full Comparison of Two Commercially Available qPCR Kits for the Detection of Candida auris
title_fullStr Comparison of Two Commercially Available qPCR Kits for the Detection of Candida auris
title_full_unstemmed Comparison of Two Commercially Available qPCR Kits for the Detection of Candida auris
title_short Comparison of Two Commercially Available qPCR Kits for the Detection of Candida auris
title_sort comparison of two commercially available qpcr kits for the detection of candida auris
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926799/
https://www.ncbi.nlm.nih.gov/pubmed/33671676
http://dx.doi.org/10.3390/jof7020154
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