病毒学
环介导等温扩增
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019年冠状病毒病(COVID-19)
重组酶聚合酶扩增
医学
生物
作者
Yong Sun,Panzhu Qin,Jun He,Weiwei Li,Yonglin Shi,Jianguo Xu,Qian Wu,Qingqing Chen,Li Weidong,Xinxin Wang,Guodong Liu,Wei Chen
标识
DOI:10.1016/j.bios.2021.113771
摘要
Due to the similar clinical symptoms of influenza (Flu) and coronavirus disease 2019 (COVID-19), there is a looming infection threat of concurrent Flu viruses and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In this work, we introduce a customized isothermal amplification integrated lateral flow strip (LFS) that is capable performing duplex reverse transcription–recombinase polymerase amplification (RT-RPA) and colorimetric LFS in a sequential manner. With customized amplification primer sets targeted to SARS-CoV-2 (opening reading frame 1a/b and nucleoprotein genes) and Flu viruses (Flu A and Flu B), the platform allows the rapid and simultaneous visual screening of SARS-CoV-2 and Flu viruses (Flu A and Flu B) without cross reactivity, false positives, and false negatives. Moreover, it maximally eases the detection, reduces the detection time (1 h), and improves the assay performance to detect as low as 10 copies of the viral RNA. Its clinical application is powerfully demonstrated with 100% accuracy for evaluating 15 SARS-CoV-2-positive clinical samples, 10 Flu viruses-positive clinical samples, and 5 negative clinical samples, which were pre-confirmed by standard qRT-PCR. We envision this portable device can meet the increasing need of online monitoring the serious infectious diseases that substantially affects health care systems worldwide. • Constructing method for rapid and simultaneous screening both COVID-19 and common Flu A and B. • N and ORF1ab as the dual-index for COVID-19 while Flue A & B for common flu in 1 h. • As low as 10 copies of the viral RNA can be well measured with constructed method. • Both clinical COVID-19 and flu samples have been measured with this reported method. • COVID-19 and common flu can be easily distinguished.
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