Park Joon Soo, Hsieh Kuangwen, Chen Liben, Kaushik Aniruddha, Trick Alexander Y, Wang Tza-Huei
Department of Biomedical Engineering Johns Hopkins University Baltimore MD 21218 USA.
Department of Mechanical Engineering Johns Hopkins University Baltimore MD 21218 USA.
Adv Sci (Weinh). 2021 Jan 12;8(5):2003564. doi: 10.1002/advs.202003564. eCollection 2021 Mar.
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.
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。