CCR2型
严重发热伴血小板减少综合征
病毒学
生物
静脉病毒
趋化因子受体
发病机制
病毒病机
病毒复制
病毒载量
趋化因子
免疫学
受体
病毒
遗传学
布尼亚病毒科
作者
Leike Zhang,Xue-Fang Peng,Qingxing Wang,Jin Li,Shou-Ming Lv,Shuo Han,Lingyu Zhang,Heng Ding,Cong Yi Wang,Gengfu Xiao,Xuguang Du,Ke Peng,Hao Li,Liu Wei
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2023-08-02
卷期号:9 (31)
被引量:4
标识
DOI:10.1126/sciadv.adg6856
摘要
Severe fever with thrombocytopenia syndrome virus (SFTSV) is an emerging tick-borne bunyavirus causing a high fatality rate of up to 30%. To date, the receptor mediating SFTSV entry remained uncharacterized, hindering the understanding of disease pathogenesis. Here, C-C motif chemokine receptor 2 (CCR2) was identified as a host receptor for SFTSV based on a genome-wide CRISPR-Cas9 screen. Knockout of CCR2 substantially reduced viral binding and infection. CCR2 enhanced SFTSV binding through direct binding to SFTSV glycoprotein N (Gn), which is mediated by its N-terminal extracellular domain. Depletion of CCR2 in C57BL/6J mouse model attenuated SFTSV replication and pathogenesis. The peripheral blood primary monocytes from elderly individuals or subjects with underlying diabetes mellitus showed higher CCR2 surface expression and supported stronger binding and replication of SFTSV. Together, these data indicate that CCR2 is a host entry receptor for SFTSV infection and a novel target for developing anti-SFTSV therapeutics.
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