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发热伴血小板减少综合征布尼亚病毒的呼吸道传播潜力:来自人源化小鼠模型鼻内暴露的证据

Respiratory transmission potential of severe fever with thrombocytopenia syndrome bunyavirus: evidence from intranasal exposure in a humanized mouse model.

作者信息

Lu Dafeng, Han Yifang, Xu Ruowei, Wang Chunfang, Qin Mingke, Shi Jianwei, Ye Fuqiang, Zhang Jinhai, Luo Zhenghan, Wang Yuhe, Lin Hong, Jia Peiqi, Zhu Jin, Wang Chunhui

机构信息

School of Public Health, Capital Medical University, Beijing, People's Republic of China.

Department of infectious Disease Prevention and Control, Nanjing Bioengineering (Gene) Technology Centre for Medicine, Nanjing, People's Republic of China.

出版信息

Emerg Microbes Infect. 2025 Dec;14(1):2511134. doi: 10.1080/22221751.2025.2511134. Epub 2025 Jun 19.

DOI:10.1080/22221751.2025.2511134
PMID:40407816
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12180321/
Abstract

Severe Fever with Thrombocytopenia Syndrome Bunyavirus (SFTSV) is a highly lethal pathogen with expanding endemic regions in Asia. While primarily transmitted by ticks, recent evidence suggests potential airborne transmission, raising significant public health concerns. This study investigates the potential for respiratory transmission and pathogenesis using humanized NCG mice inoculated with SFTSV via subcutaneous injection challenge (SIC) or intranasal drop challenge (IDC). Both groups demonstrated rapid systemic dissemination, marked by viremia, weight loss, and multi-organ injury, with hemorrhagic manifestations observed in high-dose infection groups. Histopathological evaluations revealed lung pathology in the intranasal drop challenge mice, including extensive alveolar disruption and inflammatory cell infiltration. Transcriptomic analyses further confirmed that respiratory route inoculation resulted in heightened expression of inflammatory signalling pathways such as IL-17 and NF-κB, potentially contributing to severe local immunopathology. Subcutaneous infection provoked an earlier systemic immune response, with significant upregulation of antigen-processing genes in peripheral blood mononuclear cells. Nevertheless, both routes ultimately culminated in widespread injury to the liver, spleen, kidney, highlighting the systemic nature of SFTSV pathogenesis. These findings underscore the need for preventive strategies addressing respiratory spread.

摘要

严重发热伴血小板减少综合征布尼亚病毒(SFTSV)是一种高致死性病原体,在亚洲的流行区域不断扩大。虽然主要通过蜱传播,但最近的证据表明存在潜在的空气传播,这引起了重大的公共卫生关注。本研究使用经皮下注射攻击(SIC)或滴鼻攻击(IDC)接种SFTSV的人源化NCG小鼠,研究其呼吸道传播和发病机制的可能性。两组均表现出快速的全身播散,表现为病毒血症、体重减轻和多器官损伤,在高剂量感染组中观察到出血表现。组织病理学评估显示滴鼻攻击小鼠出现肺部病变,包括广泛的肺泡破坏和炎性细胞浸润。转录组分析进一步证实,呼吸道途径接种导致炎性信号通路如IL-17和NF-κB的表达升高,可能导致严重的局部免疫病理学。皮下感染引发了更早的全身免疫反应,外周血单核细胞中的抗原加工基因显著上调。然而,两种途径最终都导致肝脏、脾脏、肾脏的广泛损伤,突出了SFTSV发病机制的全身性。这些发现强调了针对呼吸道传播采取预防策略的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/296f72462719/TEMI_A_2511134_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/4c0d17b1fa1a/TEMI_A_2511134_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/fb4c585a73ad/TEMI_A_2511134_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/c9d5fd5ca94c/TEMI_A_2511134_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/ea0ff9380667/TEMI_A_2511134_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/296f72462719/TEMI_A_2511134_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/4c0d17b1fa1a/TEMI_A_2511134_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/fb4c585a73ad/TEMI_A_2511134_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/c9d5fd5ca94c/TEMI_A_2511134_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/ea0ff9380667/TEMI_A_2511134_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54ec/12180321/296f72462719/TEMI_A_2511134_F0005_OC.jpg

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Bioact Mater. 2024 Dec 3;45:401-416. doi: 10.1016/j.bioactmat.2024.11.016. eCollection 2025 Mar.
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Adenovirus type 5-expressing Gn induces better protective immunity than Gc against SFTSV infection in mice.在小鼠中,表达5型腺病毒的Gn比Gc能诱导更好的针对发热伴血小板减少综合征病毒(SFTSV)感染的保护性免疫。
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Global epidemiology of severe fever with thrombocytopenia syndrome virus in human and animals: a systematic review and meta-analysis.
全球人类和动物中严重发热伴血小板减少综合征病毒的流行病学:一项系统综述和荟萃分析。
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Inhibition of SFTSV replication in humanized mice by a subcutaneously administered anti-PD1 nanobody.皮下注射抗 PD1 纳米抗体抑制人源化小鼠中的 SFTSV 复制。
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