Division of Biological Sciences, Section of Cell and Developmental Biology, University of California San Diego, La Jolla, California 92093, United States.
Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, California 92092, United States.
ACS Sens. 2021 Nov 26;6(11):3957-3966. doi: 10.1021/acssensors.1c01088. Epub 2021 Oct 29.
The development of an extensive toolkit for potential point-of-care diagnostics that is expeditiously adaptable to new emerging pathogens is of critical public health importance. Recently, a number of novel CRISPR-based diagnostics have been developed to detect SARS-CoV-2. Herein, we outline the development of an alternative CRISPR nucleic acid diagnostic utilizing a Cas13d ribonuclease derived from XPD3002 (CasRx) to detect SARS-CoV-2, an approach we term SENSR (sensitive enzymatic nucleic acid sequence reporter) that can detect attomolar concentrations of SARS-CoV-2. We demonstrate 100% sensitivity in patient-derived samples by lateral flow and fluorescence readout with a detection limit of 45 copy/μL. This technology expands the available nucleic acid diagnostic toolkit, which can be adapted to combat future pandemics.
开发一个广泛的工具包,用于潜在的即时诊断,并且能够迅速适应新出现的病原体,这对公共卫生至关重要。最近,已经开发了许多基于 CRISPR 的新型诊断方法来检测 SARS-CoV-2。在此,我们概述了一种利用源自 XPD3002 的 Cas13d 核糖核酸酶(CasRx)来检测 SARS-CoV-2 的替代 CRISPR 核酸诊断方法的开发,我们将其称为 SENSR(敏感酶核酸序列报告),该方法可以检测到 SARS-CoV-2 的皮摩尔浓度。我们通过侧流和荧光读数在患者样本中证明了 100%的灵敏度,检测限为 45 拷贝/μL。这项技术扩展了现有的核酸诊断工具包,可以用于应对未来的大流行。