Cao Lei, Wang Ting, Ren Peilei, Cheng Chuxing, Mao Haiying, Hui Xianfeng, Lin Xian, Hu Xiaotong, Sun Xiaomei, Huang Kun, Jin Meilin
State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
College of Animal Medicine, Huazhong Agricultural University, Wuhan, China.
Microbiol Spectr. 2025 Jul;13(7):e0312024. doi: 10.1128/spectrum.03120-24. Epub 2025 May 23.
The H5N6 avian influenza virus, a highly pathogenic strain, poses a significant threat to poultry production and public health. The RNA-dependent RNA polymerase (comprising PB1, PB2, and PA proteins) and nucleoprotein of highly pathogenic avian influenza viruses interact with avian host proteins, influencing the efficiency of viral RNA synthesis and severity of infection. To comprehensively understand how H5N6 avian influenza virus interfaces with host cellular mechanisms during infection and replication, it is essential to identify which host proteins physically associate with viral polymerase proteins. In this study, affinity purification mass spectrometry was used to identify physical interactions between H5N6-JX polymerase proteins (PB1, PB2, PA, and nucleoprotein) and host proteins in chicken DF-1 cells. We identified 455 H5N6-chicken interacting proteins and successfully cloned 231 of these genes. Overexpression experiments revealed several host proteins involved in viral replication in DF-1 cells. Specifically, nine host genes were found to promote avian influenza virus proliferation, whereas 20 inhibited it. Furthermore, we demonstrated that avian NUP93 interacts with the viral PB1 protein, enhancing polymerase transcriptional activity and promoting viral proliferation. These findings provide a more comprehensive understanding of how host mechanisms are manipulated during H5N6 avian influenza viral infection and replication, providing insights into the mechanisms of avian influenza virus cross-species transmission.IMPORTANCEThe RNA-dependent interaction of RNA polymerase with avian host protein determines the efficiency of viral RNA synthesis and the severity of infection. However, the strain-specific interactions of the avian influenza virus (AIV) remain unclear. In this study, we identified 455 H5N6-chicken interacting proteins and successfully cloned 231 of them. Nine host genes that promote the proliferation of avian influenza virus and 20 host genes that inhibit the proliferation of avian influenza virus were identified through overexpression experiments. In addition, we demonstrated that avian NUP93 interacts with viral PB1 protein to enhance polymerase transcriptional activity and promote viral proliferation. This study contributes to a more comprehensive and detailed understanding of the molecular mechanisms of host utilization during the H5N6 highly pathogenic avian influenza virus infection and replication.
H5N6禽流感病毒是一种高致病性毒株,对家禽生产和公共卫生构成重大威胁。高致病性禽流感病毒的RNA依赖性RNA聚合酶(由PB1、PB2和PA蛋白组成)和核蛋白与禽类宿主蛋白相互作用,影响病毒RNA合成效率和感染的严重程度。为了全面了解H5N6禽流感病毒在感染和复制过程中如何与宿主细胞机制相互作用,确定哪些宿主蛋白与病毒聚合酶蛋白发生物理关联至关重要。在本研究中,利用亲和纯化质谱法鉴定了H5N6-JX聚合酶蛋白(PB1、PB2、PA和核蛋白)与鸡DF-1细胞中宿主蛋白之间的物理相互作用。我们鉴定出455种H5N6-鸡相互作用蛋白,并成功克隆了其中231个基因。过表达实验揭示了DF-1细胞中几种参与病毒复制的宿主蛋白。具体而言,发现9个宿主基因促进禽流感病毒增殖,而20个宿主基因抑制其增殖。此外,我们证明禽类NUP93与病毒PB1蛋白相互作用,增强聚合酶转录活性并促进病毒增殖。这些发现为更全面地了解H5N6禽流感病毒感染和复制过程中宿主机制如何被操纵提供了依据,为禽流感病毒跨物种传播机制提供了见解。
RNA聚合酶与禽类宿主蛋白的RNA依赖性相互作用决定了病毒RNA合成效率和感染的严重程度。然而,禽流感病毒(AIV)的毒株特异性相互作用仍不清楚。在本研究中,我们鉴定出455种H5N6-鸡相互作用蛋白,并成功克隆了其中231个。通过过表达实验鉴定出9个促进禽流感病毒增殖的宿主基因和20个抑制禽流感病毒增殖的宿主基因。此外,我们证明禽类NUP93与病毒PB1蛋白相互作用以增强聚合酶转录活性并促进病毒增殖。本研究有助于更全面、详细地了解H5N6高致病性禽流感病毒感染和复制过程中宿主利用的分子机制。