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)
2019-20冠状病毒爆发
病毒学
生物
计算生物学
医学
爆发
传染病(医学专业)
疾病
病理
作者
Xinge Wang,Yangcan Chen,Xue-Jia Cheng,Siqi Wang,Yanping Hu,Yingmei Feng,Ronghua Jin,Kangping Zhou,Qingmei Sui,Jianxin Wang,Kai Pan,Bing Liu,Jie Xiang,Yanping Wang,Qi Zhou,Ying Zhang,Weiye Pan,Wei Li
标识
DOI:10.3389/fmicb.2023.1158163
摘要
The ongoing 2019 coronavirus disease pandemic (COVID-19), caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and its variants, is a global public health threat. Early diagnosis and identification of SARS-CoV-2 and its variants plays a critical role in COVID-19 prevention and control. Currently, the most widely used technique to detect SARS-CoV-2 is quantitative reverse transcription real-time quantitative PCR (RT-qPCR), which takes nearly 1 hour and should be performed by experienced personnel to ensure the accuracy of results. Therefore, the development of a nucleic acid detection kit with higher sensitivity, faster detection and greater accuracy is important.Here, we optimized the system components and reaction conditions of our previous detection approach by using RT-RAA and Cas12b.We developed a Cas12b-assisted one-pot detection platform (CDetection.v2) that allows rapid detection of SARS-CoV-2 in 30 minutes. This platform was able to detect up to 5,000 copies/ml of SARS-CoV-2 without cross-reactivity with other viruses. Moreover, the sensitivity of this CRISPR system was comparable to that of RT-qPCR when tested on 120 clinical samples.The CDetection.v2 provides a novel one-pot detection approach based on the integration of RT-RAA and CRISPR/Cas12b for detecting SARS-CoV-2 and screening of large-scale clinical samples, offering a more efficient strategy for detecting various types of viruses.
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