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猪德尔塔冠状病毒核衣壳蛋白与宿主细胞蛋白的网络相互作用。

The network interactions between the porcine deltacoronavirus nucleocapsid protein and host cellular proteins.

机构信息

Institute of Pathogenic Microorganism, Jiangxi Agricultural University, Nanchang 330045, China; Department of Avian Infectious Diseases, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Science, Shanghai 200241, China.

Institute of Pathogenic Microorganism, Jiangxi Agricultural University, Nanchang 330045, China; College of Bioscience and Engineering, Jiangxi Agricultural University, Nanchang 330045, China.

出版信息

Vet Microbiol. 2024 Nov;298:110225. doi: 10.1016/j.vetmic.2024.110225. Epub 2024 Aug 17.

Abstract

Porcine deltacoronavirus (PDCoV) is an emerging swine coronavirus that can cause diarrhea in pigs of all ages with varying severity. Host-virus protein interactions are critical for intracellular viral replication. Elucidating the interactions between cellular and viral proteins can help us to design antiviral strategies. PDCoV N protein is the most abundant and vital regulator in virus replication. In this study, 604 host proteins were identified to interact with PDCoV N protein by Co-IP combined with LC-MS, of which 243 proteins were specifically bound to N protein. PPI analysis revealed that the N-interacting host proteins are categorized into three groups: ribonucleoprotein complex biogenesis modulation, cellular nitrogen compound metabolism, and nucleic acid binding. GO and KEGG analyses showed that the host proteins are primarily involved in mRNA splicing, stress granule assembly, spliceosomal snRNP assembly. Additionally, four host proteins-TRIM25, HNRNPUL1, RPS27A, and SLC3A2-were selected to validate the interactome data through Co-IP and Confocal assays. This study can help in designing anti-PDCoV strategies and understanding the replication mechanism of PDCoV.

摘要

猪德尔塔冠状病毒(PDCoV)是一种新兴的猪冠状病毒,可引起不同严重程度各年龄段猪的腹泻。宿主-病毒蛋白相互作用对细胞内病毒复制至关重要。阐明细胞和病毒蛋白之间的相互作用可以帮助我们设计抗病毒策略。PDCoV N 蛋白是病毒复制中最丰富和最重要的调节蛋白。在这项研究中,通过 Co-IP 结合 LC-MS 鉴定了 604 种与 PDCoV N 蛋白相互作用的宿主蛋白,其中 243 种蛋白特异性结合 N 蛋白。PPI 分析表明,与 N 相互作用的宿主蛋白分为三组:核糖核蛋白复合物生物发生调节、细胞氮化合物代谢和核酸结合。GO 和 KEGG 分析表明,宿主蛋白主要参与 mRNA 剪接、应激颗粒组装、剪接体 snRNP 组装。此外,通过 Co-IP 和共聚焦检测,选择了四个宿主蛋白(TRIM25、HNRNPUL1、RPS27A 和 SLC3A2)来验证互作组数据。这项研究有助于设计抗 PDCoV 策略和理解 PDCoV 的复制机制。

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