Wang Xingbo, Zheng Tuyuan, Lin Lulu, Zhang Yina, Peng Xiran, Yan Yan, Lei Jing, Zhou Jiyong, Hu Boli
MOA Key Laboratory of Animal Virology, Department of Veterinary Medicine and Center of Veterinary Medical Sciences, Zhejiang University, Hangzhou, China.
Institute of Immunology and College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, China.
Front Microbiol. 2020 Oct 7;11:566348. doi: 10.3389/fmicb.2020.566348. eCollection 2020.
Autophagy can be utilized by the influenza A virus (IAV) to facilitate its replication. However, whether autophagy is induced at the stage of IAV entry is still unclear. Here, we report that IAV induces autophagy by hemagglutinin (HA) binding to heat shock protein 90AA1 (HSP90AA1) distributed on the cell surface. Virus overlay protein binding assay and pull-down assay indicated that IAV HA bound directly to cell surface HSP90AA1. Knockdown of HSP90AA1 weakened H1N1 infection. Incubation of IAV viral particles with recombinant HSP90AA1 or prior blockade of A549 cells with an anti-HSP90AA1 antibody could inhibit attachment of IAV. Moreover, we found that recombinant HA1 protein binding to cell surface HSP90AA1 was sufficient to induce autophagy through the AKT-MTOR pathway. Our study reveals that the HSP90AA1 on cell surface participates in IAV entry by directing binding to the HA1 subunit of IAV and subsequently induces autophagy.
甲型流感病毒(IAV)可利用自噬促进其复制。然而,IAV进入阶段是否诱导自噬仍不清楚。在此,我们报告IAV通过血凝素(HA)与分布在细胞表面的热休克蛋白90AA1(HSP90AA1)结合来诱导自噬。病毒覆盖蛋白结合试验和下拉试验表明,IAV HA直接与细胞表面HSP90AA1结合。敲低HSP90AA1会减弱H1N1感染。用重组HSP90AA1孵育IAV病毒颗粒或先用抗HSP90AA1抗体阻断A549细胞可抑制IAV的附着。此外,我们发现重组HA1蛋白与细胞表面HSP90AA1结合足以通过AKT - MTOR途径诱导自噬。我们的研究表明,细胞表面的HSP90AA1通过指导与IAV的HA1亚基结合参与IAV进入,随后诱导自噬。