Key Laboratory of Animal Epidemiology and Zoonosis, Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing 100193, PR China.
Key Laboratory of Animal Epidemiology and Zoonosis, Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing 100193, PR China.
Vet Microbiol. 2020 Jun;245:108669. doi: 10.1016/j.vetmic.2020.108669. Epub 2020 Apr 30.
Influenza virus hemagglutinin (HA) plays an important role in viral antigenicity, replication and host range. However, few amino acid positions in HA were reported to play multiple functions in both viral antigenicity and replication. In the present study, through analyzing the amino acid sequences of H9N2 avian influenza viruses (AIVs) isolated from China, we identified a multi-functional substitution of D200N in HA1 protein. Firstly, the substitution of D200N changed the antigenicity of H9N2 AIVs. Secondly, the D200N increased the HA cleavage efficiency and reduced acid and thermal stability of HA protein, which triggered viral-endosomal membrane fusion whereby promoted the release of viral genome into the host cytoplasm. Finally, residue 200-N increased the replication of H9N2 viruses in both chicken embryo fibroblast (CEF) cells and chicken embryonated eggs. In summary, the D200N substitution is a newly identified antigenicity and replication determinant of H9N2 AIVs, which should be paid more attention during surveillance.
流感病毒血凝素 (HA) 在病毒抗原性、复制和宿主范围方面发挥着重要作用。然而,HA 中的少数氨基酸位置被报道在病毒抗原性和复制中发挥多种功能。在本研究中,通过分析从中国分离的 H9N2 禽流感病毒 (AIV) 的氨基酸序列,我们鉴定出 HA1 蛋白中 D200N 的多功能取代。首先,D200N 的取代改变了 H9N2 AIV 的抗原性。其次,D200N 增加了 HA 的切割效率,降低了 HA 蛋白的酸稳定性和热稳定性,触发了病毒-内体膜融合,从而促进了病毒基因组进入宿主细胞质。最后,残基 200-N 增加了 H9N2 病毒在鸡胚成纤维细胞 (CEF) 和鸡胚中的复制。总之,D200N 取代是 H9N2 AIV 的一个新鉴定的抗原性和复制决定因素,在监测过程中应予以更多关注。