He Yingying, Shen Min, Wang Xiaohe, Yin Anqi, Liu Bingyan, Zhu Jie, Zhang Zhenhua
Institute of Clinical Virology, Department of Infectious Diseases, The Second Affiliated Hospital of Anhui Medical University, Hefei 230601, China.
Department of Clinical Medicine, Anhui Medical University, Hefei 230032, China.
Trop Med Infect Dis. 2024 Sep 7;9(9):205. doi: 10.3390/tropicalmed9090205.
The order Bunyavirales belongs to the class of Ellioviricetes and is classified into fourteen families. Some species of the order Bunyavirales pose potential threats to human health. The continuously increasing research reveals that various viruses within this order achieve immune evasion in the host through suppressing interferon (IFN) response. As the types and nodes of the interferon response pathway are continually updated or enriched, the IFN suppression mechanisms and target points of different virus species within this order are also constantly enriched and exhibit variations. For instance, Puumala virus (PUUV) and Tula virus (TULV) can inhibit IFN response through their functional NSs inhibiting downstream factor IRF3 activity. Nevertheless, the IFN suppression mechanisms of Dabie bandavirus (DBV) and Guertu virus (GTV) are mostly mediated by viral inclusion bodies (IBs) or filamentous structures (FSs). Currently, there are no effective drugs against several viruses belonging to this order that pose significant threats to society and human health. While the discovery, development, and application of antiviral drugs constitute a lengthy process, our focus on key targets in the IFN response suppression process of the virus leads to potential antiviral strategies, which provide references for both basic research and practical applications.
布尼亚病毒目属于埃利奥病毒纲,分为十四个科。布尼亚病毒目中的一些病毒种类对人类健康构成潜在威胁。不断增加的研究表明,该目中的各种病毒通过抑制干扰素(IFN)反应在宿主体内实现免疫逃逸。随着干扰素反应途径的类型和节点不断更新或丰富,该目中不同病毒种类的IFN抑制机制和靶点也不断丰富并呈现出差异。例如,普马拉病毒(PUUV)和图拉病毒(TULV)可通过其功能性NSs抑制下游因子IRF3活性来抑制IFN反应。然而,大别山病毒(DBV)和古尔图病毒(GTV)的IFN抑制机制大多由病毒包涵体(IBs)或丝状结构(FSs)介导。目前,针对该目中几种对社会和人类健康构成重大威胁的病毒尚无有效药物。虽然抗病毒药物的发现、开发和应用是一个漫长的过程,但我们对病毒IFN反应抑制过程中关键靶点的关注产生了潜在的抗病毒策略,这为基础研究和实际应用都提供了参考。