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Evaluation of droplet digital PCR for quantification of SARS-CoV-2 Virus in discharged COVID-19 patients

机译:液滴数码PCR评价SARS-COV-2病毒在排出的Covid-19患者中的定量

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摘要

The worldwide severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) outbreak has led to the rapid spread of coronavirus disease (COVID-19). The quantitative real time PCR (qPCR) is widely used as the gold standard for clinical detection of SARS-CoV-2. However, more and more infected patients are relapsing after discharge, which suggests qPCR may fail to detect the virus in some cases. In this study, we selected 74 clinical samples from 43 recovering inpatients for qPCR and Droplet Digital PCR (ddPCR) synchronous blind detection, and established a cutoff value for ddPCR diagnosis of COVID-19. The results showed that at a cutoff value of 0.04 copies/μL, the ddPCR sensitivity and specificity are 97.6% and 100%, respectively. In addition, we also analyzed 18 retained samples from 9 discharged patients who relapsed. Although qPCR showed all 18 samples to be negative, ddPCR showed 12 to be positive, and there was only one patient with two negative samples; the other eight patients had at least one positive sample. These results indicate that ddPCR could significantly improve the accuracy of COVID-19 diagnosis, especially for discharged patients with a low viral load, and help to reduce misdiagnosis during recovery.
机译:全球严重的急性呼吸综合征冠状病毒2(SARS-COV-2)爆发导致了冠状病毒疾病的迅速传播(Covid-19)。定量实时PCR(QPCR)被广泛用作SARS-COV-2的临床检测金标准。然而,越来越多的感染患者在放电后复发,这表明在某些情况下QPCR可能无法检测到病毒。在这项研究中,我们选择了43种临床样品,从43次回收QPCR和液滴数字PCR(DDPCR)同步盲检测,并建立了Covid-19的DDPCR诊断的截止值。结果表明,在0.04拷贝/μL的截止值下,DDPCR敏感性和特异性分别为97.6%和100%。此外,我们还分析了来自9名已排列的9名患者的保留样品。虽然QPCR显示所有18个样品为阴性,但DDPCR显示12呈阳性,只有一名患者有两个阴性样品;另外8名患者至少有一个阳性样品。这些结果表明,DDPCR可以显着提高Covid-19诊断的准确性,特别是对于病毒载荷低的患者,并有助于减少恢复过程中的误诊。

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