Ma Xue, Ma Yanlong, Wang Ziqiao, Feng Fei, Han Yutong, Sun Xinran, Li Liushuai, Gao Zhichao, Wang Manli, Zhang Rong
Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS), School of Basic Medical Sciences, Shanghai Frontiers Science Center of Pathogenic Microorganisms and Infection, Shanghai Institute of Infectious Disease and Biosecurity, Shanghai Medical College, Fudan University, Shanghai, China.
State Key Laboratory of Virology, Center for Biosafety Mega-Science, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
J Med Virol. 2025 Jun;97(6):e70457. doi: 10.1002/jmv.70457.
Crimean-Congo hemorrhagic fever virus (CCHFV) is a medically important tick-borne virus, causing severe hemorrhagic diseases in humans. There are no approved vaccines and therapeutics for CCHFV infection. The study of CCHFV authentic virus requires biosafety level 3 facilities, hindering the research and development of antivirals. Here we report the generation of a recombinant vesicular stomatitis virus (VSV) bearing both CCHFV glycoprotein precursor (GPC) and EGFP reporter (rVSV-CCHFV-GFP). We also find that the acquisition of an unexpected single R516K mutation in the GPC protein enables the packaging of high-titer pseudotyped particles. The replication-competent rVSV-CCHFV-GFP reporter virus resembles the entry properties of the authentic virus and allows for rapid assessment of susceptible cell lines, neutralizing antibodies, and host entry factors such as heparan sulfate in fluorescence-based assays. This study provides a valuable strategy for packaging of high-titer CCHFV pseudovirus, and the tool generated here can be served for the identification and evaluation of countermeasures against the cell entry of CCHFV.
克里米亚-刚果出血热病毒(CCHFV)是一种具有重要医学意义的蜱传病毒,可导致人类严重出血性疾病。目前尚无针对CCHFV感染的获批疫苗和治疗方法。对CCHFV活病毒的研究需要生物安全3级设施,这阻碍了抗病毒药物的研发。在此,我们报告了一种携带CCHFV糖蛋白前体(GPC)和EGFP报告基因的重组水疱性口炎病毒(VSV)(rVSV-CCHFV-GFP)的产生。我们还发现,GPC蛋白中意外出现的单个R516K突变使得高滴度假型颗粒得以包装。具有复制能力的rVSV-CCHFV-GFP报告病毒类似于活病毒的进入特性,并允许在基于荧光的检测中快速评估易感细胞系、中和抗体以及诸如硫酸乙酰肝素等宿主进入因子。本研究为高滴度CCHFV假病毒的包装提供了一种有价值的策略,此处产生的工具可用于鉴定和评估针对CCHFV细胞进入的对策。