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严重发热伴血小板减少综合征病毒荧光报告基因的构建与鉴定及其在抗病毒药物筛选中的应用

Construction and Characterization of Severe Fever with Thrombocytopenia Syndrome Virus with a Fluorescent Reporter for Antiviral Drug Screening.

机构信息

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.

出版信息

Viruses. 2023 May 10;15(5):1147. doi: 10.3390/v15051147.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7120/10222071/6e14371fcced/viruses-15-01147-g001.jpg

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