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

被引:2
|
作者
Wang, Xiao [1 ,2 ]
Xu, Mingyue [2 ]
Ke, Huanhuan [2 ]
Ma, Longda [2 ,3 ]
Li, Liushuai [2 ]
Li, Jiang [2 ]
Deng, Fei [2 ]
Wang, Manli [2 ,4 ]
Hu, Zhihong [1 ,2 ]
Liu, Jia [2 ]
机构
[1] Univ Sci & Technol China, Div Life Sci & Med, Hefei 230027, Peoples R China
[2] Chinese Acad Sci, Wuhan Inst Virol, Ctr Biosafety Mega Sci, State Key Lab Virol, Wuhan 430071, Peoples R China
[3] Huazhong Univ Sci & Technol, Dept Forens Med, Tongji Med Coll, Wuhan 430030, Peoples R China
[4] Hubei Jiangxia Lab, Wuhan 430200, Peoples R China
来源
VIRUSES-BASEL | 2023年 / 15卷 / 05期
基金
中国国家自然科学基金;
关键词
severe fever with thrombocytopenia syndrome virus; fluorescent virus; NSs deletion; attenuated virulence; high-content antiviral drugs screening; INTERFERON; BUNYAVIRUS;
D O I
10.3390/v15051147
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页数:16
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