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Novel multiplex real-time quantitative PCR detecting system approach for direct detection of Candida auris and its relatives in spiked serum samples

机译:用于直接检测Candida Auris及其在尖刺血清样品中的亲属的新型多重实时定量PCR检测系统方法

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摘要

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.
机译:Candida Auris,Candida Haemulonii,Candida Duobushaemulonii和CandidaPseudohaemulonii的多药抗性机会酵母种类继续危及全球的医疗保健环境。由于缺乏针对临床样品检测这些物种的特异性QPCR测定,我们开发了多重QPCR测定。分析特异性和敏感性显示出100%的特异性和靶物种的最多10种基因组的敏感性,具有高重现性(R-2> 0.99)。随后,来自尖刺的血清样品,我们的QPCR明确可以检测到C. auris的10个基因组和C. haemulonii,C. duobushaemulonii和C.Pseudohaemulonii(R-2> 0.98)的1个基因组。缺乏与人DNA的交叉反应,高度的特异性和敏感性,表明我们的多重PCR用于直接检测疑似患者的血清样品的C. auris和密切相关的物种。未来的研究是有必要确保其在临床环境中的适用性。

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