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检测PRRSV-NSP4酶活性的FlipNLuc报告系统的构建与应用

董楠 井汇源 彭志锋 王瑞宁 杨昆 盛亚敏 王梦迪 张哲玮

中国兽医杂志2026,Vol.62Issue(9):64-71,8.
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中国兽医杂志2026,Vol.62Issue(9):64-71,8.DOI:10.20157/j.cnki.zgsyzz.2026.sf.035

检测PRRSV-NSP4酶活性的FlipNLuc报告系统的构建与应用

Construction and Application of a FlipNLuc System for Detecting PRRSV-NSP4 Protease Activity

董楠 1井汇源 2彭志锋 2王瑞宁 2杨昆 2盛亚敏 2王梦迪 2张哲玮2

作者信息

  • 1. 中牧实业股份有限公司,北京 丰台 100070
  • 2. 河南牧业经济学院动物医药学院,河南 郑州 450046
  • 折叠

摘要

Abstract

To establish a FlipNLuc reporter system for detecting the enzymatic activity of non-structural protein 4(NSP4)of porcine reproductive and respiratory syndrome virus(PRRSV),a nanoluciferase-based reporter plasmid,pCMV-NLuc-Flag,was constructed in this study.The optimal cleavage sequence for the FlipNLuc reporter system was screened,and the system was subsequently characterized and optimized with respect to its operating conditions and compatibility.Furthermore,the established system was used to screen compounds targeting NSP4 protease activity and to evaluate their antiviral effects.The results showed that among the NSP4 cleavage sequences derived from the PRRSV polyprotein,GSLLE/GAFR was identified as the optimal cleavage sequence.The optimal detection performance was achieved when the pCMV-NLuc-Flag reporter plasmid and the pCMV-NSP4-HA eukaryotic expression plasmid were co-transfected at a ratio of 1:1 for 24-36 h.The system efficiently accommodated NSP4 proteases from both PRRSV-1 and PRRSV-2 strains.Using this system,one NSP4 protease inhibitor,tanshinone IIA,was successfully identified.Treatment of porcine alveolar macrophages(PAMs)with tanshinone IIA at concentrations below 50 μmol/L for 24 h showed no obvious cytotoxicity(P>0.05).In contrast,treatment with 50 μmol/L tanshinone IIA for 24 h significantly reduced the mRNA expression level of the PRRSV-2 open reading frame 7(ORF7)gene,N protein expression level,and viral titer(P<0.01),indicating that the compound possessed anti-PRRSV-2 activity.In conclusion,this study successfully established a FlipNLuc reporter system for detecting NSP4 enzymatic activity.The system can be used not only for high-throughput screening of anti-PRRSV compounds targeting NSP4 protease at the cellular level,but also as a methodological reference for activity detection of other viral proteases.

关键词

猪繁殖与呼吸综合征病毒(PRRSV)/非结构蛋白4(NSP4)/蛋白酶/纳米荧光素酶/丹参酮IIA

Key words

porcine reproductive and respiratory syndrome virus(PRRSV)/non-structural protein 4(NSP4)/protease/nano luciferase(NLuc)/tanshinone IIA

分类

农业科技

引用本文复制引用

董楠,井汇源,彭志锋,王瑞宁,杨昆,盛亚敏,王梦迪,张哲玮..检测PRRSV-NSP4酶活性的FlipNLuc报告系统的构建与应用[J].中国兽医杂志,2026,62(9):64-71,8.

基金项目

国家自然科学基金项目(32402849) (32402849)

河南省自然科学基金项目(262300421455) (262300421455)

河南省重点研发项目(251111113600,261111110600) (251111113600,261111110600)

河南省科技攻关项目(262102111017) (262102111017)

中国兽医杂志

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