CASPR Biotech, San Francisco, CA 94103, USA.
Genetics and Molecular Biology Laboratory, Hospital Municipal de Trauma y Emergencias Dr. Federico Abete, Malvinas Argentinas, Buenos Aires 1615, Argentina.
Viruses. 2021 Mar 5;13(3):420. doi: 10.3390/v13030420.
We evaluated a lyophilized CRISPR-Cas12 assay for SARS-CoV-2 detection (Lyo-CRISPR SARS-CoV-2 kit) based on reverse transcription, isothermal amplification, and CRISPR-Cas12 reaction. From a total of 210 RNA samples extracted from nasopharyngeal swabs using spin columns, the Lyo-CRISPR SARS-CoV-2 kit detected 105/105 (100%; 95% confidence interval (CI): 96.55-100) positive samples and 104/105 (99.05%; 95% CI: 94.81-99.97) negative samples that were previously tested using commercial RT-qPCR. The estimated overall Kappa index was 0.991, reflecting an almost perfect concordance level between the two diagnostic tests. An initial validation test was also performed on 30 nasopharyngeal samples collected in lysis buffer, in which the Lyo-CRISPR SARS-CoV-2 kit detected 20/21 (95.24%; 95% CI: 76.18-99.88) positive samples and 9/9 (100%; 95% CI: 66.37-100) negative samples. The estimated Kappa index was 0.923, indicating a strong concordance between the test procedures. The Lyo-CRISPR SARS-CoV-2 kit was suitable for detecting a wide range of RT-qPCR-positive samples (cycle threshold range: 11.45-36.90) and dilutions of heat-inactivated virus (range: 2.5-100 copies/µL); no cross-reaction was observed with the other respiratory pathogens tested. We demonstrated that the performance of the Lyo-CRISPR SARS-CoV-2 kit was similar to that of commercial RT-qPCR, as the former was highly sensitive and specific, timesaving (1.5 h), inexpensive, and did not require sophisticated equipment. The use of this kit would reduce the time taken for diagnosis and facilitate molecular diagnosis in low-resource laboratories.
我们评估了一种基于逆转录、等温扩增和 CRISPR-Cas12 反应的冻干 CRISPR-Cas12 检测试剂盒(Lyo-CRISPR SARS-CoV-2 试剂盒)用于检测 SARS-CoV-2。总共从使用离心柱提取的 210 个鼻咽拭子 RNA 样本中,Lyo-CRISPR SARS-CoV-2 试剂盒检测到 105/105(100%;95%置信区间(CI):96.55-100)阳性样本和 104/105(99.05%;95%CI:94.81-99.97)阴性样本,这些样本先前使用商业 RT-qPCR 进行了检测。估计的总体 Kappa 指数为 0.991,反映了两种诊断测试之间几乎完美的一致性水平。我们还对 30 个在裂解缓冲液中收集的鼻咽样本进行了初步验证测试,其中 Lyo-CRISPR SARS-CoV-2 试剂盒检测到 20/21(95.24%;95%CI:76.18-99.88)阳性样本和 9/9(100%;95%CI:66.37-100)阴性样本。估计的 Kappa 指数为 0.923,表明测试程序之间具有很强的一致性。Lyo-CRISPR SARS-CoV-2 试剂盒适用于检测广泛的 RT-qPCR 阳性样本(循环阈值范围:11.45-36.90)和热灭活病毒的稀释度(范围:2.5-100 拷贝/µL);与测试的其他呼吸道病原体没有交叉反应。我们证明了 Lyo-CRISPR SARS-CoV-2 试剂盒的性能与商业 RT-qPCR 相似,因为前者具有高度的灵敏度和特异性、省时(1.5 小时)、价格低廉,并且不需要复杂的设备。该试剂盒的使用将缩短诊断时间,并促进低资源实验室的分子诊断。