Novel Multiplex Real-Time Quantitative PCR Detecting System Approach for Direct Detection of Candida Auris and its Relatives in Spiked Serum Samples
Author(s) -
Amir Arastehfar,
Wenjie Fang,
Farnaz Daneshnia,
Abdullah M. S. AlHatmi,
Wanqing Liao,
Weihua Pan,
Ziauddin Khan,
Suhail Ahmad,
Katharina Rosam,
Michaela Lackner,
Cornelia LassFlörl,
Ferry Hagen,
Teun Boekhout
Publication year - 2018
Publication title -
future microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.797
H-Index - 82
eISSN - 1746-0921
pISSN - 1746-0913
DOI - 10.2217/fmb-2018-0227
Subject(s) - candida auris , multiplex polymerase chain reaction , multiplex , biology , microbiology and biotechnology , genome , real time polymerase chain reaction , yeast , polymerase chain reaction , genetics , gene , antifungal
The multidrug-resistant opportunistic yeast species of Candida auris, Candida haemulonii, Candida duobushaemulonii and Candida pseudohaemulonii continue to endanger the healthcare settings around the globe. Due to the lack of a specific qPCR assay for detection of these species from clinical samples, we developed a multiplex qPCR assay. Analytical specificity and sensitivity showed 100% specificity and the sensitivity of up to ten genomes of target species with a high value of reproducibility (R 2 >0.99). Subsequently, from spiked serum samples, our qPCR specifically could detect up to ten genomes of C. auris and one genome of C. haemulonii, C. duobushaemulonii and C. pseudohaemulonii (R 2 >0.98). Lack of cross reaction with the human DNA, a high degree of specificity and sensitivity, showed the potential of our multiplex PCR for direct detection of C. auris and closely related species from serum samples of suspected patients. Future studies are warranted to assure its applicability in clinical settings.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom