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用于快速灵敏检测新型冠状病毒2的数字CRISPR/Cas辅助检测法

Digital CRISPR/Cas-Assisted Assay for Rapid and Sensitive Detection of SARS-CoV-2.

作者信息

Park Joon Soo, Hsieh Kuangwen, Chen Liben, Kaushik Aniruddha, Trick Alexander Y, Wang Tza-Huei

机构信息

Department of Biomedical Engineering Johns Hopkins University Baltimore MD 21218 USA.

Department of Mechanical Engineering Johns Hopkins University Baltimore MD 21218 USA.

出版信息

Adv Sci (Weinh). 2021 Jan 12;8(5):2003564. doi: 10.1002/advs.202003564. eCollection 2021 Mar.

Abstract

The unprecedented demand for rapid diagnostics in response to the COVID-19 pandemic has brought the spotlight onto clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated systems (Cas)-assisted nucleic acid detection assays. Already benefitting from an elegant detection mechanism, fast assay time, and low reaction temperature, these assays can be further advanced via integration with powerful, digital-based detection. Thus motivated, the first digital CRISPR/Cas-assisted assay-coined digitization-enhanced CRISPR/Cas-assisted one-pot virus detection (deCOViD)-is developed and applied toward SARS-CoV-2 detection. deCOViD is realized through tuning and discretizing a one-step, fluorescence-based, CRISPR/Cas12a-assisted reverse transcription recombinase polymerase amplification assay into sub-nanoliter reaction wells within commercially available microfluidic digital chips. The uniformly elevated digital concentrations enable deCOViD to achieve qualitative detection in <15 min and quantitative detection in 30 min with high signal-to-background ratio, broad dynamic range, and high sensitivity-down to 1 genome equivalent (GE) µL of SARS-CoV-2 RNA and 20 GE µL of heat-inactivated SARS-CoV-2, which outstrips its benchtop-based counterpart and represents one of the fastest and most sensitive CRISPR/Cas-assisted SARS-CoV-2 detection to date. Moreover, deCOViD can detect RNA extracts from clinical samples. Taken together, deCOViD opens a new avenue for advancing CRISPR/Cas-assisted assays and combating the COVID-19 pandemic and beyond.

摘要

为应对新冠疫情而对快速诊断产生的前所未有的需求,使成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关系统(Cas)辅助的核酸检测分析方法受到关注。这些分析方法已经受益于其精妙的检测机制、快速的检测时间和较低的反应温度,通过与强大的基于数字的检测方法相结合,还可以进一步改进。因此,我们开发了首个数字CRISPR/Cas辅助分析方法——数字化增强CRISPR/Cas辅助单管病毒检测(deCOViD),并将其应用于严重急性呼吸综合征冠状病毒2(SARS-CoV-2)检测。deCOViD是通过将基于荧光的一步法CRISPR/Cas12a辅助逆转录重组酶聚合酶扩增分析方法进行调整和离散化,使其在市售微流控数字芯片内的亚纳升反应孔中实现的。均匀提高的数字浓度使deCOViD能够在不到15分钟内实现定性检测,在30分钟内实现定量检测,具有高信噪比、宽动态范围和高灵敏度——低至每微升1个基因组当量(GE)的SARS-CoV-2 RNA和每微升20个GE的热灭活SARS-CoV-2,超过了其基于台式仪器的同类方法,是迄今为止最快、最灵敏的CRISPR/Cas辅助SARS-CoV-2检测方法之一。此外,deCOViD可以检测临床样本的RNA提取物。综上所述,deCOViD为推进CRISPR/Cas辅助分析方法以及抗击新冠疫情及其他疫情开辟了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d62f/7927608/867b54f837fc/ADVS-8-2003564-g001.jpg

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