Division of Avian Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150001, China.
Viruses. 2020 Feb 23;12(2):249. doi: 10.3390/v12020249.
Infectious bursal disease (IBD) is an immunosuppressive, highly contagious, and lethal disease of young chickens caused by IBD virus (IBDV). It results in huge economic loss to the poultry industry worldwide. Infection caused by very virulent IBDV (vvIBDV) strains results in high mortality in young chicken flocks. However, the replication characteristics of vvIBDV are not well studied. Publications have shown that virus protein 3 (VP3) binds to VP1 and viral double-stranded RNA, and together they form a ribonucleoprotein complex that plays a key role in virus replication. In this study, vvIBDV VP3 was used to identify host proteins potentially involved in modulating vvIBDV replication. Chicken eukaryotic translation elongation factor 1α (cheEF1α) was chosen to further investigate effects on vvIBDV replication. By small interfering RNA-mediated knockdown, we demonstrated the possibility of significantly reducing viral polymerase activity, with a subsequent reduction in virus yields. Conversely, over-expression of significantly increased viral polymerase activity and virus replication. Further study confirmed that cheEF1α interacted only with vvIBDV VP3 but not with attenuated IBDV (aIBDV) VP3. Furthermore, the amino acids at the N- and C-termini were important in the interaction between vvIBDV VP3 and cheEF1α. Domain III was essential for interactions between cheEF1α and vvIBDV VP3. In summary, cheEF1α enhances vvIBDV replication by promoting the activity of virus polymerase. Our study indicates cheEF1α is a potential target for limiting vvIBDV infection.
传染性法氏囊病(IBD)是一种由传染性法氏囊病病毒(IBDV)引起的、具有免疫抑制性、高度传染性和致死性的幼鸡疾病。它会给全球家禽业造成巨大的经济损失。强毒力 IBDV(vvIBDV)株引起的感染会导致幼鸡群死亡率很高。然而,vvIBDV 的复制特征尚未得到很好的研究。出版物表明,病毒蛋白 3(VP3)与 VP1 和病毒双链 RNA 结合,它们共同形成核糖核蛋白复合物,在病毒复制中起关键作用。在这项研究中,vvIBDV VP3 被用于鉴定可能参与调节 vvIBDV 复制的宿主蛋白。鸡真核翻译延伸因子 1α(cheEF1α)被选为进一步研究其对 vvIBDV 复制的影响。通过小干扰 RNA 介导的敲低,我们证明了显著降低病毒聚合酶活性的可能性,随后病毒产量降低。相反,过表达 显著增加了病毒聚合酶活性和病毒复制。进一步的研究证实 cheEF1α 仅与 vvIBDV VP3 相互作用,而不与弱毒 IBDV(aIBDV)VP3 相互作用。此外,N-和 C-末端的氨基酸在 vvIBDV VP3 和 cheEF1α 之间的相互作用中很重要。结构域 III 对于 cheEF1α 和 vvIBDV VP3 之间的相互作用至关重要。总之,cheEF1α 通过促进病毒聚合酶的活性增强 vvIBDV 的复制。我们的研究表明 cheEF1α 是限制 vvIBDV 感染的潜在靶点。