| Literature DB >> 33741959 |
Kean Hean Ooi1,2, Mengying Mandy Liu1,2, Jie Wen Douglas Tay1,2,3, Seok Yee Teo1,2,3, Pornchai Kaewsapsak2, Shengyang Jin3, Chun Kiat Lee4, Jingwen Hou5, Sebastian Maurer-Stroh6, Weisi Lin5, Benedict Yan4, Gabriel Yan7, Yong-Gui Gao3, Meng How Tan8,9.
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.Entities:
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Year: 2021 PMID: 33741959 DOI: 10.1038/s41467-021-21996-6
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919