清脆的
核糖核酸
环介导等温扩增
2019年冠状病毒病(COVID-19)
计算生物学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
基因组
生物
病毒学
分子生物学
DNA
基因
遗传学
医学
病理
传染病(医学专业)
疾病
作者
Kean Hean Ooi,Mengying Mandy Liu,Douglas Jie Wen Tay,Seok Yee Teo,Pornchai Kaewsapsak,Jin Sheng-yang,Chun Kiat Lee,Jingwen Hou,Sebastian Maurer‐Stroh,Weisi Lin,Benedict Yan,Gabriel Yan,Yong‐Gui Gao,Meng How Tan
标识
DOI:10.1038/s41467-021-21996-6
摘要
Abstract Extensive testing is essential to break the transmission of SARS-CoV-2, which causes the ongoing COVID-19 pandemic. Here, we present a CRISPR-based diagnostic assay that is robust to viral genome mutations and temperature, produces results fast, can be applied directly on nasopharyngeal (NP) specimens without RNA purification, and incorporates a human internal control within the same reaction. Specifically, we show that the use of an engineered AsCas12a enzyme enables detection of wildtype and mutated SARS-CoV-2 and allows us to perform the detection step with loop-mediated isothermal amplification (LAMP) at 60-65 °C. We also find that the use of hybrid DNA-RNA guides increases the rate of reaction, enabling our test to be completed within 30 minutes. Utilizing clinical samples from 72 patients with COVID-19 infection and 57 healthy individuals, we demonstrate that our test exhibits a specificity and positive predictive value of 100% with a sensitivity of 50 and 1000 copies per reaction (or 2 and 40 copies per microliter) for purified RNA samples and unpurified NP specimens respectively.
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