Division of Life Science and Medicine, University of Science and Technology of China, Hefei 230027, China.
State Key Laboratory of Virology, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan 430071, China.
Viruses. 2023 May 10;15(5):1147. doi: 10.3390/v15051147.
Severe fever with thrombocytopenia syndrome (SFTS) caused by a novel bunyavirus (SFTSV) is an emerging infectious disease with up to 30% case fatality. Currently, there are no specific antiviral drugs or vaccines for SFTS. Here, we constructed a reporter SFTSV in which the virulent factor nonstructural protein (NSs) was replaced by eGFP for drug screening. First, we developed a reverse genetics system based on the SFTSV HBMC5 strain. Then, the reporter virus SFTSV-delNSs-eGFP was constructed, rescued, and characterized in vitro. SFTSV-delNSs-eGFP showed similar growth kinetics with the wild-type virus in Vero cells. We further detected the antiviral efficacy of favipiravir and chloroquine against wild-type and recombinant SFTSV by the quantification of viral RNA, and compared the results with that of fluorescent assay using high-content screening. The results showed that SFTSV-delNSs-eGFP could be used as a reporter virus for antiviral drug screening in vitro. In addition, we analyzed the pathogenesis of SFTSV-delNSs-eGFP in interferon receptor-deficient (IFNAR) C57BL/6J mice and found that unlike the fatal infection of the wild-type virus, no obvious pathological change or viral replication were observed in SFTSV-delNSs-eGFP-infected mice. Taken together, the green fluorescence and attenuated pathogenicity make SFTSV-delNSs-eGFP a potent tool for the future high-throughput screening of antiviral drugs.
严重发热伴血小板减少综合征(SFTS)由一种新型布尼亚病毒(SFTSV)引起,是一种具有高达 30%病死率的新发传染病。目前,SFTS 尚无特效抗病毒药物或疫苗。在这里,我们构建了一种报告 SFTSV,其中毒力因子非结构蛋白(NSs)被 eGFP 取代,用于药物筛选。首先,我们基于 SFTSV HBMC5 株开发了一种反向遗传学系统。然后,构建、拯救并表征了报告病毒 SFTSV-delNSs-eGFP。SFTSV-delNSs-eGFP 在 Vero 细胞中与野生型病毒具有相似的生长动力学。我们进一步通过定量检测病毒 RNA 来检测利巴韦林和氯喹对野生型和重组 SFTSV 的抗病毒功效,并将结果与使用高内涵筛选的荧光测定法进行比较。结果表明,SFTSV-delNSs-eGFP 可作为体外抗病毒药物筛选的报告病毒。此外,我们在干扰素受体缺陷(IFNAR)C57BL/6J 小鼠中分析了 SFTSV-delNSs-eGFP 的发病机制,结果发现,与野生型病毒的致死性感染不同,SFTSV-delNSs-eGFP 感染的小鼠未观察到明显的病理变化或病毒复制。总之,绿色荧光和减弱的致病性使 SFTSV-delNSs-eGFP 成为未来高通量筛选抗病毒药物的有力工具。