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鸟苷酸结合蛋白 1 通过破坏肌动蛋白丝的结构来抑制伪狂犬病病毒的核内运输。

Guanylate-binding protein 1 inhibits nuclear delivery of pseudorabies virus by disrupting structure of actin filaments.

机构信息

College of Veterinary Medicine, Northwest A&F University, Yangling, China.

出版信息

Vet Res. 2023 Mar 14;54(1):21. doi: 10.1186/s13567-023-01154-0.

Abstract

The alphaherpesvirus pseudorabies virus (PRV) is the causative agent of pseudorabies, responsible for severe economic losses to the swine industry worldwide. The interferon-inducible GTPase guanylate-binding protein 1 (GBP1) exhibits antiviral immunity. Our findings show that there is a robust upregulation in the expression of porcine GBP1 during PRV infection. GBP1 knockout promotes PRV infection, while GBP1 overexpression restricts it. Importantly, we found that GBP1 impeded the normal structure of actin filaments in a GTPase-dependent manner, preventing PRV virions from reaching the nucleus. We also discovered that viral US3 protein bound GBP1 to interfere with its GTPase activity. Finally, the interaction between US3 and GBP1 requires US3 serine/threonine kinase activity sites and the GTPase domain (aa 1 to 308) of GBP1. Taken together, this study offers fresh perspectives on how PRV manipulates the host's antiviral immune system.

摘要

α疱疹病毒伪狂犬病病毒(PRV)是伪狂犬病的病原体,导致全球养猪业遭受严重的经济损失。干扰素诱导的鸟嘌呤核苷酸结合蛋白 1(GBP1)具有抗病毒免疫作用。我们的研究结果表明,在 PRV 感染过程中,猪 GBP1 的表达水平会出现明显的上调。GBP1 敲除会促进 PRV 感染,而过表达 GBP1 则会限制 PRV 的感染。重要的是,我们发现 GBP1 以 GTPase 依赖的方式干扰肌动蛋白丝的正常结构,阻止 PRV 病毒颗粒到达细胞核。我们还发现,病毒 US3 蛋白结合 GBP1 以干扰其 GTPase 活性。最后,US3 和 GBP1 之间的相互作用需要 US3 丝氨酸/苏氨酸激酶活性位点和 GBP1 的 GTPase 结构域(aa1 到 308)。综上所述,这项研究为 PRV 如何操纵宿主的抗病毒免疫系统提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c1/10015811/3fe486ed8359/13567_2023_1154_Fig1_HTML.jpg

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