Osborn Mark J, Bhardwaj Akshay, Bingea Samuel P, Knipping Friederike, Feser Colby J, Lees Christopher J, Collins Daniel P, Steer Clifford J, Blazar Bruce R, Tolar Jakub
Department of Pediatrics, Division of Blood and Marrow Transplant & Cellular Therapy, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Cytomedical Design Group, LLC, Saint Paul, MN 55127, USA.
Bioengineering (Basel). 2021 Feb 12;8(2):23. doi: 10.3390/bioengineering8020023.
Clustered regularly interspaced short palindromic repeat (CRISPR/Cas) proteins can be designed to bind specified DNA and RNA sequences and hold great promise for the accurate detection of nucleic acids for diagnostics. We integrated commercially available reagents into a CRISPR/Cas9-based lateral flow assay that can detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) sequences with single-base specificity. This approach requires minimal equipment and represents a simplified platform for field-based deployment. We also developed a rapid, multiplex fluorescence CRISPR/Cas9 nuclease cleavage assay capable of detecting and differentiating SARS-CoV-2, influenza A and B, and respiratory syncytial virus in a single reaction. Our findings provide proof-of-principle for CRISPR/Cas9 point-of-care diagnosis as well as a scalable fluorescent platform for identifying respiratory viral pathogens with overlapping symptomology.
成簇规律间隔短回文重复序列(CRISPR/Cas)蛋白可被设计用于结合特定的DNA和RNA序列,在核酸精确检测用于诊断方面具有巨大潜力。我们将市售试剂整合到基于CRISPR/Cas9的侧向流动分析中,该分析能够以单碱基特异性检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)序列。这种方法所需设备最少,代表了一种用于现场部署的简化平台。我们还开发了一种快速、多重荧光CRISPR/Cas9核酸酶切割分析方法,能够在单一反应中检测和区分SARS-CoV-2、甲型和乙型流感病毒以及呼吸道合胞病毒。我们的研究结果为CRISPR/Cas9即时诊断提供了原理证明,以及一个用于识别具有重叠症状的呼吸道病毒病原体的可扩展荧光平台。