Qin Xiaochen, Paul Ratul, Zhou Yuyuan, Wu Yue, Cheng Xuanhong, Liu Yaling
Department of Bioengineering, Lehigh University, Bethlehem, PA, 18015, USA.
Department of Mechanical Engineering & Mechanics, Lehigh University, Bethlehem, PA, 18015, USA.
Biosens Bioelectron X. 2023 Sep;14. doi: 10.1016/j.biosx.2023.100381. Epub 2023 Jul 10.
The COVID-19 pandemic has presented a significant challenge to the world's public health and led to over 6.9 million deaths reported to date. A rapid, sensitive, and cost-effective point-of-care virus detection device is essential for the control and surveillance of the contagious severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic. The study presented here aimed to demonstrate a solid-phase isothermal recombinase polymerase amplification coupled CRISPR-based (spRPA-CRISPR) assay for on-chip multiplexed, sensitive and visual COVID-19 DNA detection. The assay targets the SARS-CoV-2 structure protein encoded genomes and can simultaneously detect two specific genes without cross-interaction. The amplified target sequences were immobilized on the one-pot device surface and detected using the mixed Cas12a-crRNA collateral cleavage of reporter-released fluorescent signal when specific genes were recognized. The endpoint signal can be directly visualized for rapid detection of COVID-19. The system was tested with samples of a broad range of concentrations (20 to 2 × 10 copies) and showed analytical sensitivity down to 20 copies per microliter. Furthermore, a low-cost blue LED flashlight (~$12) was used to provide a visible SARS-CoV-2 detection signal of the spRPA-CRISPR assay which could be purchased online easily. Thus, our platform provides a sensitive and easy-to-read multiplexed gene detection method that can specifically identify low concentration genes.
新冠疫情给全球公共卫生带来了巨大挑战,截至目前已导致超过690万人死亡。一种快速、灵敏且经济高效的即时检测病毒装置对于控制和监测传染性严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫情至关重要。本文介绍的研究旨在展示一种基于固相等温重组酶聚合酶扩增与CRISPR技术结合的(spRPA-CRISPR)检测方法,用于芯片上多重、灵敏且可视化的新冠病毒DNA检测。该检测方法针对SARS-CoV-2结构蛋白编码的基因组,能够同时检测两个特定基因且无交叉干扰。扩增后的目标序列固定在一体化装置表面,当识别到特定基因时,利用混合的Cas12a-crRNA旁切裂解报告基因释放荧光信号进行检测。终点信号可直接可视化,用于快速检测新冠病毒。该系统用一系列浓度范围(20至2×10拷贝)的样本进行了测试,分析灵敏度低至每微升20拷贝。此外,使用一种低成本的蓝色LED手电筒(约12美元)为spRPA-CRISPR检测提供可见的SARS-CoV-2检测信号,该手电筒可轻松在网上购买。因此,我们的平台提供了一种灵敏且易于读取的多重基因检测方法,能够特异性识别低浓度基因。