Evasion mechanisms of the type I interferons responses by influenza A virus

被引:23
作者
Li, Chengye [1 ,2 ]
Wang, Tong [3 ,4 ]
Zhang, Yuying [5 ]
Wei, Fanhua [2 ]
机构
[1] Ningxia Univ, Minist Educ Conservat & Utilizat Special Biol Res, Key Lab, Yinchuan, Ningxia, Peoples R China
[2] Ningxia Univ, Coll Agr, Yinchuan 750021, Ningxia, Peoples R China
[3] China Agr Univ, Coll Vet Med, Minist Agr, Key Lab Anim Epidemiol & Zoonosis, Beijing, Peoples R China
[4] China Agr Univ, State Key Lab Agrobiotechnol, Beijing, Peoples R China
[5] Univ Jinan, Sch Biol Sci & Technol, Jinan, Peoples R China
基金
中国国家自然科学基金;
关键词
Influenza virus; antiviral; immune evasion; PRR; type I interferons; INNATE IMMUNE-RESPONSE; RNA-POLYMERASE; NS1; PROTEIN; RIG-I; UBIQUITIN LIGASE; VIRAL REPLICATION; ACTIVATION; RECOGNITION; INFECTION; VIRULENCE;
D O I
10.1080/1040841X.2020.1794791
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The type I interferons (IFNs) represent the first line of host defense against influenza virus infection, and the precisely control of the type I IFNs responses is a central event of the immune defense against influenza viral infection. Influenza viruses are one of the leading causes of respiratory tract infections in human and are responsible for seasonal epidemics and occasional pandemics, leading to a serious threat to global human health due to their antigenic variation and interspecies transmission. Although the host cells have evolved sophisticated antiviral mechanisms based on sensing influenza viral products and triggering of signalling cascades resulting in secretion of the type I IFNs (IFN-alpha/beta), influenza viruses have developed many strategies to counteract this mechanism and circumvent the type I IFNs responses, for example, by inducing host shut-off, or by regulating the polyubiquitination of viral and host proteins. This review will summarise the current knowledge of how the host cells recognise influenza viruses to induce the type I IFNs responses and the strategies that influenza viruses exploited to evade the type I IFNs signalling pathways, which will be helpful for the development of antivirals and vaccines.
引用
收藏
页码:420 / 432
页数:13
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