National Research Center for Wildlife Borne Diseases, Institute of Zoology, Chinese Academy of Sciences, No.1-5 Beichenxilu, Chaoyang District, Beijing, 100101, People's Republic of China.
University of the Chinese Academy of Sciences, Beijing, 100101, China.
Virol J. 2018 Nov 8;15(1):172. doi: 10.1186/s12985-018-1079-3.
Influenza A virus (IAV) is an important pathogen that poses a severe threat to the health of humans. Nucleoprotein (NP) of IAV plays crucial roles in the viral life cycle by interacting with various cellular factors. Histone Acetyl Transferase TIP60 is a key target of several viral proteins during infection, including HIV-1 Tat, HPV E6, HTLV-1 p30 and HCMV UL27 proteins. However, Whether the interaction between the IAV NP and TIP60, and the role of TIP60 in IAV life cycle are largely unknown. Here, we showed that IAV infection up-regulated TIP60 protein and RNA expression. Overexpression of TIP60 inhibited viral protein and RNA expression and reduced the progeny viral titer. Further study revealed that TIP60 inhibited viral replication through activation of TBK1-IRF3 signaling pathway. Furthermore, we demonstrated that the NP protein of IAV interacted with TIP60. Together, these results indicate that TIP60 play a repressor in IAV infection, and it may be a possible target for antiviral drugs.
甲型流感病毒(IAV)是一种重要的病原体,对人类健康构成严重威胁。IAV 的核蛋白(NP)在病毒生命周期中通过与各种细胞因子相互作用发挥关键作用。组蛋白乙酰转移酶 TIP60 是感染过程中几种病毒蛋白的关键靶标,包括 HIV-1 Tat、HPV E6、HTLV-1 p30 和 HCMV UL27 蛋白。然而,IAV NP 与 TIP60 之间的相互作用以及 TIP60 在 IAV 生命周期中的作用在很大程度上尚不清楚。在这里,我们表明 IAV 感染上调了 TIP60 蛋白和 RNA 的表达。TIP60 的过表达抑制了病毒蛋白和 RNA 的表达,并降低了子代病毒滴度。进一步的研究表明,TIP60 通过激活 TBK1-IRF3 信号通路抑制病毒复制。此外,我们证明了 IAV 的 NP 蛋白与 TIP60 相互作用。总之,这些结果表明 TIP60 在 IAV 感染中发挥抑制作用,它可能是抗病毒药物的一个潜在靶点。