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细胞中间丝蛋白 vimentin 通过靶向 HN 蛋白调节新城疫病毒的感染力。

Cellular vimentin regulates the infectivity of Newcastle disease virus through targeting of the HN protein.

机构信息

Animal Infectious Disease Laboratory, College of Veterinary Medicine, Yangzhou University, No.48 East Wenhui Road, Yangzhou, 225009, China.

Jiangsu Key Laboratory of Zoonosis, Yangzhou University, Yangzhou, 225009, China.

出版信息

Vet Res. 2023 Oct 17;54(1):92. doi: 10.1186/s13567-023-01230-5.

DOI:10.1186/s13567-023-01230-5
PMID:37848995
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10580610/
Abstract

The haemagglutinin-neuraminidase (HN) protein plays a crucial role in the infectivity and virulence of Newcastle disease virus (NDV). In a previous study, the mutant HN protein was identified as a crucial virulence factor for the velogenic variant NDV strain JS/7/05/Ch, which evolved from the prototypic vaccine strain Mukteswar. Furthermore, macrophages are the main susceptible target cells of NDV. However, the possible involvement of cellular molecules in viral infectivity remains unclear. Herein, we elucidate the crucial role of vimentin, an intermediate filament protein, in regulating NDV infectivity through targeting of the HN protein. Using LC‒MS/MS mass spectrometry and coimmunoprecipitation assays, we identified vimentin as a host protein that differentially interacted with prototypic and mutant HN proteins. Further analysis revealed that the variant NDV strain induced more significant rearrangement of vimentin fibres compared to the prototypic NDV strain and showed an interdependence between vimentin rearrangement and virus replication. Notably, these mutual influences were pronounced in HD11 chicken macrophages. Moreover, vimentin was required for multiple infection processes of the variant NDV strain in HD11 cells, including viral internalization, fusion, and release, while it was not necessary for those of the prototypic NDV strain. Collectively, these findings underscore the pivotal role of vimentin in NDV infection through targeting of the HN protein, providing novel targets for antiviral treatment strategies for NDV.

摘要

血凝素-神经氨酸酶(HN)蛋白在新城疫病毒(NDV)的感染性和毒力中起着至关重要的作用。在之前的研究中,突变的 HN 蛋白被鉴定为毒力很强的新城疫病毒 JS/7/05/Ch 变异株的关键毒力因子,该变异株源自原型疫苗株 Mukteswar。此外,巨噬细胞是 NDV 的主要易感靶细胞。然而,细胞分子在病毒感染性中的可能作用仍不清楚。在这里,我们通过靶向 HN 蛋白,阐明了中间丝蛋白波形蛋白在调节 NDV 感染性中的关键作用。通过使用 LC-MS/MS 质谱和共免疫沉淀实验,我们鉴定出波形蛋白是一种与原型和突变 HN 蛋白差异相互作用的宿主蛋白。进一步的分析表明,与原型 NDV 株相比,变异株 NDV 诱导了更显著的波形蛋白纤维重排,并显示出波形蛋白重排与病毒复制之间的相互依赖关系。值得注意的是,这些相互影响在 HD11 鸡巨噬细胞中更为明显。此外,在 HD11 细胞中,波形蛋白对于变异株 NDV 的多个感染过程都是必需的,包括病毒内化、融合和释放,而对于原型 NDV 株则不是必需的。总的来说,这些发现强调了波形蛋白通过靶向 HN 蛋白在 NDV 感染中的关键作用,为 NDV 的抗病毒治疗策略提供了新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/221a5701f4cb/13567_2023_1230_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/f94256b7da91/13567_2023_1230_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/a770bbf6dfe1/13567_2023_1230_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/7658d56222f3/13567_2023_1230_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/a6828c5f81ce/13567_2023_1230_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/aeea04df496f/13567_2023_1230_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/5337ce679490/13567_2023_1230_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/221a5701f4cb/13567_2023_1230_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/f94256b7da91/13567_2023_1230_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/45272e7d34c5/13567_2023_1230_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/1d70af74208f/13567_2023_1230_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/a770bbf6dfe1/13567_2023_1230_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/7658d56222f3/13567_2023_1230_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/a6828c5f81ce/13567_2023_1230_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/aeea04df496f/13567_2023_1230_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/5337ce679490/13567_2023_1230_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f7/10580610/221a5701f4cb/13567_2023_1230_Fig9_HTML.jpg

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