清脆的
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
对偶(语法数字)
基因
生物
2019年冠状病毒病(COVID-19)
计算生物学
病毒学
遗传学
医学
病理
传染病(医学专业)
疾病
艺术
文学类
作者
Erhu Xiong,Ling Jiang,Tian Tian,Menglu Hu,Huahua Yue,Mengqi Huang,Wei Lin,Yongzhong Jiang,Debin Zhu,Xiaoming Zhou
标识
DOI:10.1002/anie.202014506
摘要
Few methods for the detection of SARS-CoV-2 currently have the capability to simultaneously detect two genes in a single test, which is a key measure to improve detection accuracy, as adopted by the gold standard RT-qPCR method. Developed here is a CRISPR/Cas9-mediated triple-line lateral flow assay (TL-LFA) combined with multiplex reverse transcription-recombinase polymerase amplification (RT-RPA) for rapid and simultaneous dual-gene detection of SARS-CoV-2 in a single strip test. This assay is characterized by the detection of envelope (E) and open reading frame 1ab (Orf1ab) genes from cell-cultured SARS-CoV-2 and SARS-CoV-2 viral RNA standards, showing a sensitivity of 100 RNA copies per reaction (25 μL). Furthermore, dual-gene analysis of 64 nasopharyngeal swab samples showed 100 % negative predictive agreement and 97.14 % positive predictive agreement. This platform will provide a more accurate and convenient pathway for diagnosis of COVID-19 or other infectious diseases in low-resource regions.
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