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

被引:15
|
作者
Sattler, Janko [1 ,2 ]
Noster, Janina [3 ]
Brunke, Anne [1 ,2 ]
Plum, Georg [1 ]
Wiegel, Pia [1 ]
Kurzai, Oliver [4 ,5 ]
Meis, Jacques F. [6 ,7 ]
Hamprecht, Axel [1 ,2 ,3 ]
机构
[1] Univ Cologne, Univ Hosp Cologne, Inst Med Microbiol Immunol & Hyg, D-50935 Cologne, Germany
[2] German Ctr Infect Res, Partner Site Bonn Cologne, D-50937 Cologne, Germany
[3] Carl von Ossietzky Univ Oldenburg, Inst Med Microbiol & Virol, D-26129 Oldenburg, Germany
[4] Univ Wurzburg, Inst Hyg & Microbiol, D-97080 Wurzburg, Germany
[5] Hans Knoell Inst, Leibniz Inst Nat Prod Res & Infect Biol, German Natl Reference Ctr Invas Fungal Infect, D-07745 Jena, Germany
[6] Radboud Univ Nijmegen, Med Ctr, Canisius Wilhelmina Hosp, Ctr Expertise Mycol, NL-6532 SZ Nijmegen, Netherlands
[7] Canisius Wilhelmina Hosp, Dept Med Microbiol & Infect Dis, NL-6532 SZ Nijmegen, Netherlands
关键词
qPCR; detection limits; sensitivity; strain specificity; commercial kits; Candida auris; Fungiplex Candida Auris; AurisID;
D O I
10.3390/jof7020154
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
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页码:1 / 7
页数:7
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