Xiao Huyan, Hu Jianyu, Huang Camille, Feng Wei, Liu Yanming, Kumblathan Teresa, Tao Jeffrey, Xu Jingyang, Le X Chris, Zhang Hongquan
Division of Analytical and Environmental Toxicology, Department of Laboratory Medicine and Pathology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, T6G 2G3, Canada.
Trends Analyt Chem. 2023 Apr;161:117000. doi: 10.1016/j.trac.2023.117000. Epub 2023 Mar 2.
The continuing evolution of the SARS-CoV-2 virus has led to the emergence of many variants, including variants of concern (VOCs). CRISPR-Cas systems have been used to develop techniques for the detection of variants. These techniques have focused on the detection of variant-specific mutations in the spike protein gene of SARS-CoV-2. These sequences mostly carry single-nucleotide mutations and are difficult to differentiate using a single CRISPR-based assay. Here we discuss the specificity of the Cas9, Cas12, and Cas13 systems, important considerations of mutation sites, design of guide RNA, and recent progress in CRISPR-based assays for SARS-CoV-2 variants. Strategies for discriminating single-nucleotide mutations include optimizing the position of mismatches, modifying nucleotides in the guide RNA, and using two guide RNAs to recognize the specific mutation sequence and a conservative sequence. Further research is needed to confront challenges in the detection and differentiation of variants and sublineages of SARS-CoV-2 in clinical diagnostic and point-of-care applications.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒的持续进化导致了许多变体的出现,包括关注变体(VOC)。CRISPR-Cas系统已被用于开发检测变体的技术。这些技术主要集中于检测SARS-CoV-2刺突蛋白基因中的变体特异性突变。这些序列大多携带单核苷酸突变,使用单一的基于CRISPR的检测方法难以区分。在此,我们讨论了Cas9、Cas12和Cas13系统的特异性、突变位点的重要考量因素、向导RNA的设计以及基于CRISPR的SARS-CoV-2变体检测方法的最新进展。区分单核苷酸突变的策略包括优化错配位置、修饰向导RNA中的核苷酸,以及使用两个向导RNA来识别特定突变序列和保守序列。在临床诊断和即时检测应用中,仍需要进一步研究以应对SARS-CoV-2变体和亚谱系检测与区分方面的挑战。