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新型突变 N588 残基在猫细小病毒 NS1 蛋白中极大地增强了病毒复制。

Novel mutation N588 residue in the NS1 protein of feline parvovirus greatly augments viral replication.

机构信息

State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.

Key Laboratory of Preventive Veterinary Medicine in Hubei Province, The Cooperative Innovation Center for Sustainable Pig Production, Wuhan, China.

出版信息

J Virol. 2024 May 14;98(5):e0009324. doi: 10.1128/jvi.00093-24. Epub 2024 Apr 9.

Abstract

Feline parvovirus (FPV) infection is highly fatal in felines. NS1, which is a key nonstructural protein of FPV, can inhibit host innate immunity and promote viral replication, which is the main reason for the severe pathogenicity of FPV. However, the mechanism by which the NS1 protein disrupts host immunity and regulates viral replication is still unclear. Here, we identified an FPV M1 strain that is regulated by the NS1 protein and has more pronounced suppression of innate immunity, resulting in robust replication. We found that the neutralization titer of the FPV M1 strain was significantly lower than that of the other strains. Moreover, FPV M1 had powerful replication ability, and the FPV M1-NS1 protein had heightened efficacy in repressing interferon-stimulated genes (ISGs) expression. Subsequently, we constructed an FPV reverse genetic system, which confirmed that the N588 residue of FPV M1-NS1 protein is a key amino acid that bolsters viral proliferation. Recombinant virus containing N588 also had stronger ability to inhibit ISGs, and lower ISGs levels promoted viral replication and reduced the neutralization titer of the positive control serum. Finally, we confirmed that the difference in viral replication was abolished in type I IFN receptor knockout cell lines. In conclusion, our results demonstrate that the N588 residue of the NS1 protein is a critical amino acid that promotes viral proliferation by increasing the inhibition of ISGs expression. These insights provide a reference for studying the relationship between parvovirus-mediated inhibition of host innate immunity and viral replication while facilitating improved FPV vaccine production.IMPORTANCEFPV infection is a viral infectious disease with the highest mortality rate in felines. A universal feature of parvovirus is its ability to inhibit host innate immunity, and its ability to suppress innate immunity is mainly accomplished by the NS1 protein. In the present study, FPV was used as a viral model to explore the mechanism by which the NS1 protein inhibits innate immunity and regulates viral replication. Studies have shown that the FPV-NS1 protein containing the N588 residue strongly inhibits the expression of host ISGs, thereby increasing the viral proliferation titer. In addition, the presence of the N588 residue can increase the proliferation titer of the strain 5- to 10-fold without affecting its virulence and immunogenicity. In conclusion, our findings provide new insights and guidance for studying the mechanisms by which parvoviruses suppress innate immunity and for developing high-yielding FPV vaccines.

摘要

猫细小病毒(FPV)感染对猫具有高度致命性。 NS1 是 FPV 的关键非结构蛋白,它可以抑制宿主固有免疫并促进病毒复制,这是 FPV 严重致病性的主要原因。然而,NS1 蛋白破坏宿主免疫和调节病毒复制的机制仍不清楚。在这里,我们鉴定了一种受 NS1 蛋白调控且对固有免疫抑制作用更明显的 FPV M1 株,导致其具有更强的复制能力。我们发现,FPV M1 株的中和效价明显低于其他株。此外,FPV M1 具有强大的复制能力,FPV M1-NS1 蛋白在抑制干扰素刺激基因(ISGs)表达方面具有更高的功效。随后,我们构建了 FPV 反向遗传系统,该系统证实 FPV M1-NS1 蛋白的 N588 残基是增强病毒增殖的关键氨基酸。含有 N588 的重组病毒也具有更强的抑制 ISGs 的能力,较低的 ISGs 水平促进了病毒复制并降低了阳性对照血清的中和效价。最后,我们证实 I 型 IFN 受体敲除细胞系中病毒复制的差异被消除。总之,我们的结果表明,NS1 蛋白的 N588 残基是通过增加对 ISGs 表达的抑制来促进病毒增殖的关键氨基酸。这些发现为研究细小病毒介导的抑制宿主固有免疫与病毒复制之间的关系提供了参考,同时有助于改进 FPV 疫苗的生产。

重要性

FPV 感染是一种猫科动物死亡率最高的病毒性传染病。细小病毒的一个普遍特征是能够抑制宿主固有免疫,其抑制固有免疫的能力主要由 NS1 蛋白完成。在本研究中,FPV 被用作病毒模型来探索 NS1 蛋白抑制固有免疫和调节病毒复制的机制。研究表明,含有 N588 残基的 FPV-NS1 蛋白强烈抑制宿主 ISGs 的表达,从而增加病毒的增殖滴度。此外,存在 N588 残基可以在不影响其毒力和免疫原性的情况下使株的增殖滴度增加 5-10 倍。总之,我们的发现为研究细小病毒抑制固有免疫的机制和开发高产量 FPV 疫苗提供了新的见解和指导。

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