畜牧兽医学报 ›› 2025, Vol. 56 ›› Issue (11): 5839-5851.doi: 10.11843/j.issn.0366-6964.2025.11.040

• 基础兽医 • 上一篇    下一篇

稳定表达猪瘟病毒NS3-NS4A和NS3pro-NS4A蛋白巨噬细胞系的构建及蛋白质组学分析

郑晓茹(), 王一丹, 张丽红, 杨莹莹, 赵欣如, 李敏, 黄娟, 张乔亚*(), 曹志*()   

  1. 青岛农业大学动物医学院, 青岛 266109
  • 收稿日期:2024-07-29 出版日期:2025-11-23 发布日期:2025-11-27
  • 通讯作者: 张乔亚,曹志 E-mail:zzwyyxrr@163.com;201801056@qau.edu.cn;201901252@qau.edu.cn
  • 作者简介:郑晓茹(2000-),女,山东聊城人,硕士,主要从事病毒感染与免疫调控机制研究,E-mail:zzwyyxrr@163.com
  • 基金资助:
    国家自然科学基金青年科学项目(32002269);山东省生猪产业技术体系疫病控制岗位(SDAIT-08-07)

Construction and Proteomic Analysis of Macrophage Cell Lines Stably Expressing NS3-NS4A and NS3pro-NS4A of Classical Swine Fever Virus

ZHENG Xiaoru(), WANG Yidan, ZHANG Lihong, YANG Yingying, ZHAO Xinru, LI Min, HUANG Juan, ZHANG Qiaoya*(), CAO Zhi*()   

  1. College of Veterinary Medicine, Qingdao Agricultural University, Qingdao 266109, China
  • Received:2024-07-29 Online:2025-11-23 Published:2025-11-27
  • Contact: ZHANG Qiaoya, CAO Zhi E-mail:zzwyyxrr@163.com;201801056@qau.edu.cn;201901252@qau.edu.cn

摘要:

本研究旨在通过构建稳定表达的猪瘟病毒(classical swine fever virus, CSFV)NS3-NS4A和NS3pro-NS4A蛋白巨噬细胞系,以期更好地探索宿主天然免疫与CSFV的相互作用关系。利用琼脂糖凝胶电泳、连接与转化和提取质粒等方法对重组表达载体进行构建,将构建好的pCMV-CBH-GFP-2A-Puro-CSFV NS3pro-NS4A、pCMV-CBH-GFP-2A-Puro-CSFV NS3-NS4A和pCMV-CBH-GFP-2A-Puro重组表达载体分别感染HEK-293T细胞包装出慢病毒。然后利用包装成功的慢病毒感染猪肺泡巨噬细胞(3D4/21),对感染细胞进行单克隆筛选得到稳定转染细胞系,最后用Western blot方法验证稳定细胞系蛋白表达。对其进行蛋白组学分析,筛选出MAPK、PI3K通路的相互作用蛋白,并进行功能分析,利用Western blot检测CDK4、CDC37、CASP3、IKBKG、NFκB1蛋白表达量。结果表明,经MegAlign分析构建的过表达CSFV非结构蛋白NS3-NS4A以及NS3pro-NS4A慢病毒载体氨基酸序列全部正确,无移码;重组表达载体感染293T细胞24 h后,感染效率可达90%以上,慢病毒包装成功;Western blot分析成功获得稳定表达CSFV NS3-NS4A、NS3pro-NS4A巨噬细胞系;通过蛋白组学分析,筛选出NS3-NS4A/mock组中MAPK与PI3K通路中上调蛋白11个,下调蛋白24个;经Western blot检测CSFV NS3-NS4A显著降低了MAPK通路中CASP3、NFκB1、IKBKG的表达,PI3K通路中CDK4、CDC37的表达。本研究成功构建了稳定表达NS3-NS4A、NS3pro-NS4A蛋白的3D4/21细胞系,并对蛋白组学筛选的关键蛋白进行功能分析,为研究CSFV NS3-NS4A调控宿主天然免疫应答的机制提供物质基础。

关键词: 猪瘟病毒, NS3-NS4A, NS3pro-NS4A, 猪肺泡巨噬细胞, 稳定表达

Abstract:

The purpose of this study is to better explore the interaction between host innate immunity and classical swine fever virus (CSFV) by constructing a stable expressing CSFV NS3/NS4A and pCMV-CBH-GFP-2A-Puro-CSFV NS3pro-NS4A, pCMV-CBH-GFP-2A-Puro-CSFV NS3-NS4A and pCMV-CBH-GFP-2A-Puro recombinant expression vector were separately infected with HEK-293T cells packaged out of the lentivirus. Then, packaged lentivirus was used to infect porcine alveolar macrophages (3D4/21), monoclonal screening of infected cell lines was performed to obtain stable cell lines, and the protein expression of stable cell lines was verified by Western blot. Proteomic analysis was conducted on it to screen out the interacting proteins of MAPK and PI3K pathways, and functional analysis was carried out. Detection of CDK4, CDC37, CASP3, IKBKG, and NFκB1 Protein Expression Levels via Western blot Analysis. The results showed that the amino acid sequences of NS3-NS4A and NS3pro-NS4A lentiviral vectors constructed by MegAlign analysis were correct without frameshift. After the recombinant expression vector infected 293T cells for 24 hours, the infection efficiency could reach more than 90%, the lentvirus was successfully packaged, and the stable expression of CSFV NS3-NS4A and NS3pro-NS4A macrophage cell lines were successfully obtained by Western blot analysis. Through proteomic analysis, 11 up-regulated and 24 down-regulated proteins in the MAPK and PI3K pathways were screened out in the NS3-NS4A/mock group. Western blot analysis revealed that CSFV NS3-NS4A significantly reduced the expression of CASP3, NFκB1, and IKBKG in the MAPK pathway, as well as CDK4 and CDC37 in the PI3K pathway. In this study, 3D4/21 cell lines stably expressing NS3-NS4A and NS3pro-NS4A proteins were successfully constructed, and conducted functional analysis on the key proteins screened by proteomics, which provides a material basis for studying the mechanism of CSFV NS3-NS4A regulating the host innate immune responses.

Key words: classical swine fever virus, NS3-NS4A, NS3pro-NS4A, porcine alveolar macrophages, stably expressing

中图分类号: