Department of Virology I, National Institute of Infectious Diseases, Tokyo, Japan; Department of Virology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Department of Virology I, National Institute of Infectious Diseases, Tokyo, Japan; Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Virology. 2019 Sep;535:102-110. doi: 10.1016/j.virol.2019.06.014. Epub 2019 Jun 27.
Severe fever with thrombocytopenia syndrome (SFTS) is an infectious disease with a high fatality rate, caused by SFTS virus (SFTSV). Because little is known about the nature of SFTSV, basic studies are required for the developments of vaccines and effective therapies. In the present study, we identified the amino acid residue important for membrane fusion induced by the SFTSV glycoprotein (GP). Syncytium formations were observed in cells expressing the GPs of SFTSV Japanese strain (YG-1 and SPL030). In contrast, no or only weak syncytium formations were induced in cells expressing GP of SFTSV Chinese strain (HB29). The replacement of arginine at amino acid residue 962 with serine in HB29 GP (R962S) induced membrane fusion, while the replacement of serine at residue 962 with arginine in YG1 GP (S962R) did not. These data indicate that serine at residue 962 in the SFTSV-GP is critical for inducing membrane fusion and viral infection.
严重发热伴血小板减少综合征(SFTS)是一种由SFTS 病毒(SFTSV)引起的高死亡率传染病。由于对 SFTSV 的性质知之甚少,因此需要进行基础研究,以开发疫苗和有效的治疗方法。在本研究中,我们确定了 SFTSV 糖蛋白(GP)诱导膜融合所必需的氨基酸残基。在表达 SFTSV 日本株(YG-1 和 SPL030)GP 的细胞中观察到合胞体形成。相比之下,在表达 SFTSV 中国株(HB29)GP 的细胞中,几乎没有或只有弱的合胞体形成。HB29 GP 中氨基酸残基 962 的精氨酸替换为丝氨酸(R962S)诱导膜融合,而 YG1 GP 中残基 962 的丝氨酸替换为精氨酸(S962R)则没有。这些数据表明,SFTSV-GP 中残基 962 的丝氨酸对于诱导膜融合和病毒感染至关重要。