State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Collaborative Innovation Center for Green Transformation of Bio-resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, Hubei, PR China.
Hubei Provincial Center for Disease Control and Prevention, Wuhan, Hubei, PR China.
Talanta. 2021 May 15;227:122154. doi: 10.1016/j.talanta.2021.122154. Epub 2021 Feb 11.
Infectious diseases caused by viruses such as SARS-CoV-2 and HPV have greatly endangered human health. The nucleic acid detection is essential for the early diagnosis of diseases. Here, we propose a method called PLCR (PfAgo coupled with modified Ligase Chain Reaction for nucleic acid detection) which utilizes PfAgo to only use DNA guides longer than 14-mer to specifically cleave DNA and LCR to precisely distinguish single-base mismatch. PLCR can detect DNA or RNA without PCR at attomolar sensitivities, distinguish single base mutation between the genome of wild type SARS-CoV-2 and its mutant spike D614G, effectively distinguish the novel coronavirus from other coronaviruses and finally achieve multiplexed detection in 70 min. Additionally, LCR products can be directly used as DNA guides without additional input guides to simplify primer design. With desirable sensitivity, specificity and simplicity, the method can be extended for detecting other pathogenic microorganisms.
由 SARS-CoV-2 和 HPV 等病毒引起的传染病极大地危及了人类健康。核酸检测对于疾病的早期诊断至关重要。在这里,我们提出了一种称为 PLCR(PfAgo 与改良的连接酶链反应相结合用于核酸检测)的方法,该方法利用 PfAgo 仅使用长度大于 14 个碱基的 DNA 向导特异性切割 DNA,而 LCR 则精确区分单碱基错配。PLCR 可以在皮摩尔灵敏度下检测 DNA 或 RNA,无需 PCR,能够区分野生型 SARS-CoV-2 基因组与其突变刺突 D614G 之间的单碱基突变,能够有效区分新型冠状病毒与其他冠状病毒,并最终在 70 分钟内实现多重检测。此外,LCR 产物可直接用作 DNA 向导,无需额外输入向导,从而简化了引物设计。该方法具有良好的灵敏度、特异性和简单性,可扩展用于检测其他致病微生物。