Hu Ge, Wei Zhijie, Guo Jinlei, Zhao Kangchen, Qiao Qiao, Zhu Xiaojuan, Wu Tao, Rong Heng, Ning Shuo, Hao Ziyang, Chi Ying, Cui Lunbiao, Ge Yiyue
School of Public Health, Nanjing Medical University, Nanjing 211166, China.
NHC Key Laboratory of Enteric Pathogenic Microbiology, Jiangsu Provincial Medical Key Laboratory of Pathogenic Microbiology in Emerging Major Infectious Diseases, Jiangsu Provincial Center for Disease Control and Prevention, Nanjing 210009, China.
Viruses. 2025 Jun 12;17(6):841. doi: 10.3390/v17060841.
Mpox is a zoonotic disease caused by the Mpox virus (MPXV). The rapid and accurate diagnosis of MPXV is essential for the timely and effective prevention, control, and treatment of the disease. In this study, we combined Multienzyme Isothermal Rapid Amplification (MIRA) (at 42 °C) and Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR-associated protein 12b(CRISPR/Cas12b) (at 60 °C) to develop a single-tube two-step assay for rapid MPXV detection, leveraging the distinct physical states of tricosane at these temperatures. MIRA amplification primers and CRISPR/cas12b SgRNA were designed based on the MPXV F3L gene. After screening the primers and sgRNAs, the reaction conditions were optimized, and the performances of the assay were evaluated. The detection limit (LOD) of this single-tube two-step MIRA-CRISPR/Cas12b assay for MPXV is four copies of DNA molecules. No cross-reactivity with other pathogens (herpes simplex virus (HSV), Epstein-Barr virus (EBV), Coxsackievirus A16 (CVA16), Enterovirus A71 (EV-A71), and measles virus (MeV)) was found. The assay also showed good consistency with quantitative real-time PCR (qPCR) (Kappa = 0.9547, < 0.05, = 100) in the detection of clinical samples, with a sensitivity of 98.5% and a specificity of 97.0%. The single-tube two-step MIRA-CRISPR/Cas12b assay permits the rapid (within 45 min), sensitive, and specific detection of MPXV. The lack of need for opening the reaction tube eliminates the risk of product contamination.
猴痘是一种由猴痘病毒(MPXV)引起的人畜共患病。MPXV的快速准确诊断对于及时有效地预防、控制和治疗该疾病至关重要。在本研究中,我们结合多酶等温快速扩增(MIRA)(42℃)和成簇规律间隔短回文重复序列/CRISPR相关蛋白12b(CRISPR/Cas12b)(60℃),利用三癸烷在这些温度下的不同物理状态,开发了一种用于快速检测MPXV的单管两步检测法。基于MPXV F3L基因设计了MIRA扩增引物和CRISPR/cas12b SgRNA。在筛选引物和sgRNA后,优化了反应条件,并评估了该检测法的性能。这种用于MPXV的单管两步MIRA-CRISPR/Cas12b检测法的检测限为四个DNA分子拷贝。未发现与其他病原体(单纯疱疹病毒(HSV)、爱泼斯坦-巴尔病毒(EBV)、柯萨奇病毒A16(CVA16)、肠道病毒A71(EV-A71)和麻疹病毒(MeV))有交叉反应。该检测法在临床样本检测中与定量实时PCR(qPCR)也显示出良好的一致性(Kappa = 0.9547,<0.05,=100),灵敏度为98.5%,特异性为97.0%。单管两步MIRA-CRISPR/Cas12b检测法能够快速(45分钟内)、灵敏且特异性地检测MPXV。无需打开反应管消除了产物污染的风险。