• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一种用于检测牛病毒性腹泻病毒感染抗体的新型竞争性酶联免疫吸附测定法。

A novel competitive ELISA for detection of antibodies against bovine viral diarrhea virus infection.

作者信息

Seyfi Abad Shapouri Masoud Reza, Mahmoodi Pezhman, Ghorbanpour Najafabadi Masoud, Haji Haji-Kolaei Mohammad Rahim, Moradi Choghakabodi Parastoo, Lotfi Mohsen, Pourmahdi Boroujeni Mahdi, Ekhtelat Maryam, Daghari Maryam

机构信息

Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran.

Department of Pathobiology, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan, Iran.

出版信息

Vet Res Forum. 2022 Sep;13(3):403-407. doi: 10.30466/vrf.2021.521500.3135. Epub 2022 Sep 15.

DOI:10.30466/vrf.2021.521500.3135
PMID:36320291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9548221/
Abstract

Diagnosis of bovine viral diarrhea (BVD) relies on the detection of antibodies against its viral causing agent, bovine viral diarrhea virus (BVDV). Here, we designed a novel competitive ELISA (cELISA) using the most immunogenic part of BVDV nonstructural protein 3 (NS), as a single ELISA recombinant antigen, along with a monoclonal antibody to detect antibodies against BVDV in sera of infected animals. Hence, 197 serum samples were tested by this cELISA and the results were compared to the results obtained from virus neutralization test (VNT) as the gold standard method for diagnosis of BVD. McNemar's test indicated that there was no significant difference between the results of this newly designed cELISA and VNT. Meanwhile, kappa coefficients showed that there was a high correlation between these two assays. The relative sensitivity and specificity of cELISA with respect to VNT were 93.90% and 100%, respectively, suggesting that this newly designed cELISA could be a useful diagnostic tool for detection of BVDV infection. Moreover, as NS is highly conserved among Pestiviruses and the developed ELISA is a competitive one, it could potentially be applied to detect BVDV infection in other domestic and wildlife species.

摘要

牛病毒性腹泻(BVD)的诊断依赖于针对其致病病毒——牛病毒性腹泻病毒(BVDV)的抗体检测。在此,我们设计了一种新型竞争酶联免疫吸附测定法(cELISA),使用BVDV非结构蛋白3(NS)最具免疫原性的部分作为单一酶联免疫吸附测定重组抗原,以及一种单克隆抗体来检测感染动物血清中针对BVDV的抗体。因此,用这种cELISA对197份血清样本进行了检测,并将结果与作为BVD诊断金标准方法的病毒中和试验(VNT)所得结果进行了比较。McNemar检验表明,这种新设计的cELISA结果与VNT结果之间没有显著差异。同时,kappa系数表明这两种检测方法之间存在高度相关性。相对于VNT,cELISA的相对敏感性和特异性分别为93.90%和100%,这表明这种新设计的cELISA可能是检测BVDV感染的一种有用诊断工具。此外,由于NS在瘟病毒中高度保守,且所开发的酶联免疫吸附测定法是一种竞争法,它有可能应用于检测其他家养和野生动物物种中的BVDV感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/9548221/d677389a8ca2/vrf-13-403-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/9548221/d677389a8ca2/vrf-13-403-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/9548221/d677389a8ca2/vrf-13-403-g001.jpg

相似文献

1
A novel competitive ELISA for detection of antibodies against bovine viral diarrhea virus infection.一种用于检测牛病毒性腹泻病毒感染抗体的新型竞争性酶联免疫吸附测定法。
Vet Res Forum. 2022 Sep;13(3):403-407. doi: 10.30466/vrf.2021.521500.3135. Epub 2022 Sep 15.
2
Simple Indirect Enzyme-Linked Immunosorbent Assay to Detect Antibodies Against Bovine Viral Diarrhea Virus, Based on Prokaryotically Expressed Recombinant MBP-NS3 Protein.基于原核表达的重组MBP-NS3蛋白的简易间接酶联免疫吸附测定法检测牛病毒性腹泻病毒抗体
Jundishapur J Microbiol. 2015 Jan 14;8(3):e14311. doi: 10.5812/jjm.14311. eCollection 2015 Mar.
3
Evaluation of currently available bovine viral diarrhoea virus (BVDV) and HoBi-like pestivirus (HoBiPeV) specific diagnostic tests in detection of highly divergent HoBiPeVs in cattle.评估现有的牛病毒性腹泻病毒(BVDV)和 HoBi 样瘟病毒(HoBiPeV)特异性诊断检测方法,以检测牛中高度分化的 HoBiPeV。
J Virol Methods. 2019 Oct;272:113707. doi: 10.1016/j.jviromet.2019.113707. Epub 2019 Jul 24.
4
Epitope mapping of bovine viral diarrhea virus nonstructural protein 3.牛病毒性腹泻病毒非结构蛋白3的表位作图
Vet Immunol Immunopathol. 2014 Oct 15;161(3-4):232-9. doi: 10.1016/j.vetimm.2014.08.012. Epub 2014 Aug 27.
5
International proficiency trial for bovine viral diarrhea virus (BVDV) antibody detection: limitations of milk serology.牛病毒性腹泻病毒(BVDV)抗体检测国际能力验证试验:乳血清学的局限性。
BMC Vet Res. 2022 May 6;18(1):168. doi: 10.1186/s12917-022-03265-w.
6
The recombinant E and truncated E2-based indirect enzyme-linked immunosorbent assays to distinguishably test specific antibodies against classical swine fever virus and bovine viral diarrhea virus.基于重组 E 和截短 E2 的间接酶联免疫吸附试验可区分检测针对经典猪瘟病毒和牛病毒性腹泻病毒的特异性抗体。
Virol J. 2022 Jul 22;19(1):121. doi: 10.1186/s12985-022-01851-w.
7
Development of an in-house Indirect ELISA for detection of bovine viral diarrhoea virus antibodies in bovine sera.
J Virol Methods. 2022 Oct;308:114576. doi: 10.1016/j.jviromet.2022.114576. Epub 2022 Jul 8.
8
A neutralizing monoclonal antibody-based competitive ELISA for classical swine fever C-strain post-vaccination monitoring.用于监测猪瘟 C 株疫苗接种后免疫反应的基于中和单克隆抗体的竞争性 ELISA。
BMC Vet Res. 2020 Jan 14;16(1):14. doi: 10.1186/s12917-020-2237-6.
9
Application of recombinant bovine viral diarrhea virus proteins in the diagnosis of bovine viral diarrhea infection in cattle.重组牛病毒性腹泻病毒蛋白在牛群牛病毒性腹泻感染诊断中的应用。
Vet Microbiol. 1997 Sep;57(2-3):119-33. doi: 10.1016/s0378-1135(97)00128-4.
10
Development and evaluation of a truncated recombinant NS3 antigen-based indirect ELISA for detection of pestivirus antibodies in sheep and goats.
J Immunoassay Immunochem. 2015;36(3):312-23. doi: 10.1080/15321819.2014.947433.

引用本文的文献

1
Development of a pan-genotypic monoclonal antibody-based competitive ELISA for the detection of antibodies against Bovine viral diarrhea virus.开发一种基于泛基因型单克隆抗体的竞争性ELISA,用于检测牛病毒性腹泻病毒抗体。
Front Immunol. 2024 Nov 25;15:1504115. doi: 10.3389/fimmu.2024.1504115. eCollection 2024.
2
Diagnosis of bovine viral diarrhea virus: an overview of currently available methods.牛病毒性腹泻病毒的诊断:现有方法概述
Front Microbiol. 2024 Apr 5;15:1370050. doi: 10.3389/fmicb.2024.1370050. eCollection 2024.

本文引用的文献

1
Epitope mapping of bovine viral diarrhea virus nonstructural protein 3.牛病毒性腹泻病毒非结构蛋白3的表位作图
Vet Immunol Immunopathol. 2014 Oct 15;161(3-4):232-9. doi: 10.1016/j.vetimm.2014.08.012. Epub 2014 Aug 27.
2
BVD eradication in Switzerland--a new approach.瑞士的 BVD 根除计划——一种新方法。
Vet Microbiol. 2010 Apr 21;142(1-2):137-42. doi: 10.1016/j.vetmic.2009.09.054. Epub 2009 Oct 1.
3
Development and evaluation of a MAb based competitive-ELISA using helicase domain of NS3 protein for sero-diagnosis of bovine viral diarrhea in cattle and buffaloes.
基于单克隆抗体的竞争酶联免疫吸附测定法的开发与评估:利用NS3蛋白解旋酶结构域进行牛和水牛牛病毒性腹泻的血清学诊断
Res Vet Sci. 2008 Aug;85(1):39-45. doi: 10.1016/j.rvsc.2007.09.013. Epub 2007 Nov 5.
4
Multiple recombinant ELISA for the detection of bovine viral diarrhoea virus antibodies in cattle sera.用于检测牛血清中牛病毒性腹泻病毒抗体的多重重组酶联免疫吸附测定法
J Virol Methods. 2006 Dec;138(1-2):99-108. doi: 10.1016/j.jviromet.2006.07.025. Epub 2006 Sep 8.
5
Mapping of two antigenic domains on the NS3 protein of the pestivirus bovine viral diarrhea virus.
Vet Microbiol. 2005 Jun 15;108(1-2):13-22. doi: 10.1016/j.vetmic.2005.02.010. Epub 2005 Mar 17.
6
Bovine viral diarrhoea eradication and control programmes in Europe.欧洲牛病毒性腹泻根除与控制计划
Biologicals. 2003 Jun;31(2):113-8. doi: 10.1016/s1045-1056(03)00025-3.
7
Laboratory diagnostic investigations for bovine viral diarrhoea virus infections in cattle.牛病毒性腹泻病毒感染牛的实验室诊断研究
Vet Microbiol. 1999 Jan;64(2-3):123-34. doi: 10.1016/s0378-1135(98)00264-8.
8
Application of recombinant bovine viral diarrhea virus proteins in the diagnosis of bovine viral diarrhea infection in cattle.重组牛病毒性腹泻病毒蛋白在牛群牛病毒性腹泻感染诊断中的应用。
Vet Microbiol. 1997 Sep;57(2-3):119-33. doi: 10.1016/s0378-1135(97)00128-4.
9
Bovine viral diarrhea virus proteins and their antigenic analyses.
Arch Virol Suppl. 1991;3:29-40. doi: 10.1007/978-3-7091-9153-8_4.
10
Bovine viral diarrhea virus genomic organization.牛病毒性腹泻病毒基因组结构
Arch Virol Suppl. 1991;3:19-27. doi: 10.1007/978-3-7091-9153-8_3.