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核 NS1 蛋白在高致病性 H5N1 流感病毒中的作用。

The role of nuclear NS1 protein in highly pathogenic H5N1 influenza viruses.

机构信息

State Key Laboratory for Emerging Infectious Diseases and Department of Microbiology, The University of Hong Kong, Hong Kong, China.

State Key Laboratory for Emerging Infectious Diseases and Department of Microbiology, The University of Hong Kong, Hong Kong, China.

出版信息

Microbes Infect. 2017 Dec;19(12):587-596. doi: 10.1016/j.micinf.2017.08.011. Epub 2017 Sep 10.

DOI:10.1016/j.micinf.2017.08.011
PMID:28903072
Abstract

The non-structural protein (NS1) of influenza A viruses (IAV) performs multiple functions during viral infection. NS1 contains two nuclear localization signals (NLS): NLS1 and NLS2. The NS1 protein is located predominantly in the nucleus during the early stages of infection and subsequently exported to the cytoplasm. A nonsense mutation that results in a large deletion in the carboxy-terminal region of the NS1 protein that contains the NLS2 domain was found in some IAV subtypes, including highly pathogenic avian influenza (HPAI) H7N9 and H5N1 viruses. We introduced different mutations into the NLS domains of NS1 proteins in various strains of IAV, and demonstrated that mutation of the NLS2 region in the NS1 protein of HPAI H5N1 viruses severely affects its nuclear localization pattern. H5N1 viruses expressing NS1 protein that is unable to localize to the nucleus are less potent in antagonizing cellular antiviral responses than viruses expressing wild-type NS1. However, no significant difference was observed with respect to viral replication and pathogenesis. In contrast, the replication and antiviral defenses of H1N1 viruses are greatly attenuated when nuclear localization of the NS1 protein is blocked. Our data reveals a novel functional plasticity for NS1 proteins among different IAV subtypes.

摘要

甲型流感病毒(IAV)的非结构蛋白(NS1)在病毒感染过程中发挥多种功能。NS1 包含两个核定位信号(NLS):NLS1 和 NLS2。NS1 蛋白在感染早期主要位于细胞核内,随后输出到细胞质。在某些 IAV 亚型中,包括高致病性禽流感(HPAI)H7N9 和 H5N1 病毒,发现 NS1 蛋白羧基末端区域的无义突变导致大片段缺失,该区域包含 NLS2 结构域。我们在各种 IAV 株系的 NS1 蛋白的 NLS 结构域中引入不同的突变,并证实 HPAI H5N1 病毒 NS1 蛋白 NLS2 区域的突变严重影响其核定位模式。与表达野生型 NS1 的病毒相比,无法定位到细胞核的 H5N1 病毒表达的 NS1 蛋白拮抗细胞抗病毒反应的能力较弱。然而,在病毒复制和发病机制方面没有观察到显著差异。相比之下,当 NS1 蛋白的核定位被阻断时,H1N1 病毒的复制和抗病毒防御能力大大减弱。我们的数据揭示了不同 IAV 亚型的 NS1 蛋白的一种新的功能可塑性。

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