实时聚合酶链反应
化学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒学
分子生物学
2019年冠状病毒病(COVID-19)
金标准(测试)
假阳性悖论
生物
基因
医学
传染病(医学专业)
病理
内科学
疾病
机器学习
生物化学
计算机科学
作者
Ji Wang,Kun Cai,Ruiqing Zhang,Xiaozhou He,Xinxin Shen,Jun Liu,Junqiang Xu,Feng Qiu,Wenwen Lei,Jinrong Wang,Xinna Li,Yuan Gao,Yongzhong Jiang,Wenbo Xu,Xuejun Ma
标识
DOI:10.1021/acs.analchem.0c01884
摘要
Coronavirus disease 2019 (COVID-19) has become a public health emergency. The reverse transcriptase real-time quantitative PCR (qRT-PCR) test is currently considered as the gold standard in the laboratory for the etiological detection of COVID-19. However, qRT-PCR results could be false-negative due to the inadequate sensitivity of qRT-PCR. In this study, we have developed and evaluated a novel one-step single-tube nested quantitative real-time PCR (OSN-qRT-PCR) assay for the highly sensitive detection of SARS-CoV-2 targeting the ORF1ab and N genes. The sensitivity of the OSN-qRT-PCR assay was 1 copy/reaction and 10-fold higher than that of the commercial qRT-PCR kit (10 copies/reaction). The clinical performance of the OSN-qRT-PCR assay was evaluated using 181 clinical samples. Among them, 14 qRT-PCR-negative samples (7 had no repetitive results and 7 had no cycle threshold (CT) values) were detected by OSN-qRT-PCR. Moreover, the 7 qRT-PCR-positives in the qRT-PCR gray zone (CT values of ORF1ab ranged from 37.48 to 39.07, and CT values of N ranged from 37.34 to 38.75) were out of the gray zone and thus were deemed to be positive by OSN-qRT-PCR, indicating that the positivity of these samples is confirmative. Compared to the qRT-PCR kit, the OSN-qRT-PCR assay revealed higher sensitivity and specificity, showing better suitability to clinical applications for the detection of SARS-CoV-2 in patients with low viral load.
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