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Rapid Detection and Identification of Aspergillus from Lower Respiratory Tract Specimens by Use of a Combined Probe–High-Resolution Melting Analysis

机译:使用组合探针快速检测和鉴定下呼吸道标本中的曲霉菌-高分辨率熔解分析

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摘要

Diagnosis of invasive aspergillosis (IA) requires increasingly rapid molecular methods that enable sensitive detection and discrimination between species. We designed and evaluated a real-time PCR-based method that combined melting temperature (Tm) calling analysis of a specific probe with high-resolution melting analysis of the full amplicon. The test correctly identified 78 isolates of Aspergillus section Fumigati and non-Fumigati sections of Aspergillus with a limit of detection of 102 conidia/ml (102 fg/ml). No cross-reactivity with other fungi was found. The assay was further validated on lower respiratory tract specimens containing Aspergillus or not. It successfully identified Aspergillus to section level in 56 of 59 specimens. With culture as the gold standard, our assay shows 100% sensitivity and specificity and constitutes an efficient alternative for identification of Aspergillus in lower respiratory tract samples.
机译:侵袭性曲霉病(IA)的诊断需要越来越快的分子方法,以实现灵敏的检测和物种间的区分。我们设计和评估了一种基于实时PCR的方法,该方法将特定探针的解链温度(Tm)调用分析与整个扩增子的高分辨率解链分析相结合。该测试正确鉴定了78株曲霉烟曲霉菌和非烟曲霉菌的分离株,其检出限为10 2 分生孢子/ ml(10 2 fg / ml)。未发现与其他真菌的交叉反应。该试验进一步在含有或不含曲霉菌的下呼吸道标本上进行了验证。它成功地在59个标本中的56个标本中将曲霉菌鉴定为切片水平。以培养物为金标准,我们的测定法显示出100%的敏感性和特异性,是鉴定下呼吸道样品中曲霉的有效替代方法。

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