Peng Shuwei, Wang Yiming, Zhang Yu, Song Xu, Zou Yuanfeng, Li Lixia, Zhao Xinghong, Yin Zhongqiong
Natural Medicine Research Center, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Front Vet Sci. 2022 Apr 8;9:820625. doi: 10.3389/fvets.2022.820625. eCollection 2022.
Infectious bronchitis virus (IBV) is the first coronavirus discovered in the world, which is also the prototype of gamma-coronaviruses. Nowadays, IBV is widespread all over the world and has become one of the causative agent causing severe economic losses in poultry industry. Generally, it is believed that the viral replication and immune evasion functions of IBV were modulated by non-structural and accessory proteins, which were also considered as the causes for its pathogenicity. In this study, we summarized the current knowledge about the immune evasion functions of IBV non-structural and accessory proteins. Some non-structural proteins such as nsp2, nsp3, and nsp15 have been shown to antagonize the host innate immune response. Also, nsp7 and nsp16 can block the antigen presentation to inhibit the adapted immune response. In addition, nsp13, nsp14, and nsp16 are participating in the formation of viral mRNA cap to limit the recognition by innate immune system. In conclusion, it is of vital importance to understand the immune evasion functions of IBV non-structural and accessory proteins, which could help us to further explore the pathogenesis of IBV and provide new horizons for the prevention and treatment of IBV in the future.
传染性支气管炎病毒(IBV)是世界上发现的第一种冠状病毒,也是γ冠状病毒的原型。如今,IBV在全球广泛传播,已成为导致家禽业严重经济损失的病原体之一。一般认为,IBV的病毒复制和免疫逃避功能由非结构蛋白和辅助蛋白调节,这些蛋白也被认为是其致病性的原因。在本研究中,我们总结了目前关于IBV非结构蛋白和辅助蛋白免疫逃避功能的知识。一些非结构蛋白,如nsp2、nsp3和nsp15,已被证明可拮抗宿主先天免疫反应。此外,nsp7和nsp16可阻断抗原呈递以抑制适应性免疫反应。此外,nsp13、nsp14和nsp16参与病毒mRNA帽的形成,以限制先天免疫系统的识别。总之,了解IBV非结构蛋白和辅助蛋白的免疫逃避功能至关重要,这有助于我们进一步探索IBV的发病机制,并为未来IBV的预防和治疗提供新的思路。