Guo Jinlei, Shan Yunfeng, Hu Ge, Zhu Xiaojuan, Zhao Kangchen, Wu Tao, Qiao Qiao, Chi Ying, Cui Lunbiao, Ge Yiyue
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.
Virol J. 2025 May 20;22(1):151. doi: 10.1186/s12985-025-02780-0.
Monkeypox virus (MPXV) infection has garnered significant global attention due to its rising incidence and substantial public health implications. A rapid, sensitive, and accurate diagnostic method is urgently required to enable early intervention and effective management of MPXV outbreaks.
In this study, we developed a novel one-step assay that integrates loop-mediated isothermal amplification (LAMP) with CRISPR/Cas12b in one-pot for the detection of MPXV. The entire detection process did not require opening the lid of the reaction tube and could be completed within 40 min using extracted viral nucleic acids, which is faster than real-time quantitative PCR (qPCR). And the results could be interpreted through either real-time fluorescence or naked-eye visualization. The limit of detection (LOD) of the assay was demonstrated to be 6.5 copies per reaction and no cross-reactivity with other pathogens such as HSV, EBV, CVA16, EV-A71, and MV was found. Furthermore, when evaluated using 113 clinical samples, the assay achieved 100% sensitivity (71/71) and 100% specificity (42/42) compared to the qPCR.
In resource-limited settings, our method requires only a portable heat block or water bath and a blue light or ultraviolet flashlight for visual detection of MPXV, making it highly accessible. The integration of LAMP and CRISPR/Cas12b provides a robust, user-friendly platform for point-of-care testing, with promising potential for the rapid molecular diagnosis of infectious diseases.
猴痘病毒(MPXV)感染因其发病率上升及重大公共卫生影响而受到全球广泛关注。迫切需要一种快速、灵敏且准确的诊断方法,以便对MPXV疫情进行早期干预和有效管理。
在本研究中,我们开发了一种新颖的一步法检测技术,将环介导等温扩增(LAMP)与CRISPR/Cas12b整合于一锅反应中用于检测MPXV。整个检测过程无需打开反应管盖子,使用提取的病毒核酸可在40分钟内完成,比实时定量PCR(qPCR)更快。结果可通过实时荧光或肉眼可视化进行解读。该检测方法的检测限被证明为每个反应6.5个拷贝,未发现与其他病原体如单纯疱疹病毒(HSV)、 Epstein-Barr病毒(EBV)、柯萨奇病毒A16型(CVA16)、肠道病毒A71型(EV-A71)和麻疹病毒(MV)有交叉反应。此外,在使用113份临床样本进行评估时,与qPCR相比,该检测方法的灵敏度达到100%(71/71),特异性达到100%(42/42)。
在资源有限的环境中,我们的方法仅需一个便携式加热块或水浴以及一个蓝光或紫外线手电筒用于MPXV的可视化检测,使其易于获得。LAMP与CRISPR/Cas12b的整合为即时检测提供了一个强大、用户友好的平台,在传染病快速分子诊断方面具有广阔的应用前景。