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Colorimetric Nucleic Acid Testing Assay for RNA Virus Detection Based on Circle-to-Circle Amplification of Padlock Probes

机译:基于挂锁探针环间扩增的RNA病毒检测比色核酸测试方法

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摘要

We developed a molecular diagnostic method for detection of RNA virus based on padlock probes and colorimetric readout. The feasibility of our approach was demonstrated by using detection of Crimean-Congo hemorrhagic fever (CCHF) virus as a model. Compared with conventional PCR-based methods, our approach does not require advanced equipment, involves easier assay design, and has a sensitivity of 103 viral copies/ml. By using a cocktail of padlock probes, synthetic templates representing different viral strain variants could be detected. We analyzed 34 CCHF patient samples, and all patients were correctly diagnosed when the results were compared to those of the current real-time PCR method. This is the first time that highly specific padlock probes have been applied to detection of a highly variable target sequence typical of RNA viruses.
机译:我们开发了一种基于挂锁探针和比色读数的分子诊断方法,用于检测RNA病毒。通过使用克里米亚-刚果出血热(CCHF)病毒检测作为模型,证明了我们方法的可行性。与传统的基于PCR的方法相比,我们的方法不需要先进的设备,涉及到更简便的测定设计,并且具有10 3 病毒拷贝/ ml的灵敏度。通过使用一系列挂锁探针,可以检测到代表不同病毒株变异的合成模板。我们分析了34个CCHF患者样本,并将结果与​​当前实时PCR方法的结果进行比较后,所有患者均被正确诊断。这是首次将高度特异性的挂锁探针用于检测典型的RNA病毒的高度可变靶序列。

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