Validation of ELISA for the detection of African horse sickness virus antigens and antibodies.

C Rubio, M A Cubillo, H Hooghuis, J M Sanchez-Vizcaino, M Diaz-Laviada, E Plateau, S Zientara, C Crucière, C Hamblin
{"title":"Validation of ELISA for the detection of African horse sickness virus antigens and antibodies.","authors":"C Rubio,&nbsp;M A Cubillo,&nbsp;H Hooghuis,&nbsp;J M Sanchez-Vizcaino,&nbsp;M Diaz-Laviada,&nbsp;E Plateau,&nbsp;S Zientara,&nbsp;C Crucière,&nbsp;C Hamblin","doi":"10.1007/978-3-7091-6823-3_27","DOIUrl":null,"url":null,"abstract":"<p><p>The mortality rate in susceptible populations of horses during an epizootic of African horse sickness (AHS) may be in excess of 90%. Rapid and reliable assays are therefore essential for the confirmation of clinical diagnoses and to enable control strategies to be implemented without undue delay. One of the major objectives of a recent European Union funded project was the validation of newly developed diagnostic assays which are rapid, sensitive, highly reproducible and inexpensive, for the detection of African horse sickness virus (AHSV) antigens and antibodies. The Laboratorio de Sanidad y Produccion Animal (LSPA) in Algete, Spain was charged with the responsibility of co-ordinating and supplying samples of viruses and antisera to the participating laboratories in Spain, France and the United Kingdom. The panels comprised 76 antigen samples for assay by indirect sandwich ELISAs and 53 serum samples for antibody detection by either indirect or competitive ELISAs. Results generated by ELISA for each laboratory were analysed in LSPA in terms of their relative sensitivities and specificities. There was a good agreement between the ELISAs used for either antigen or antibody detection. The participating groups agreed that any field sample giving a doubtful result would always be retested by ELISA and an alternative assay.</p>","PeriodicalId":77010,"journal":{"name":"Archives of virology. Supplementum","volume":"14 ","pages":"311-5"},"PeriodicalIF":0.0000,"publicationDate":"1998-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of virology. Supplementum","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/978-3-7091-6823-3_27","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

Abstract

The mortality rate in susceptible populations of horses during an epizootic of African horse sickness (AHS) may be in excess of 90%. Rapid and reliable assays are therefore essential for the confirmation of clinical diagnoses and to enable control strategies to be implemented without undue delay. One of the major objectives of a recent European Union funded project was the validation of newly developed diagnostic assays which are rapid, sensitive, highly reproducible and inexpensive, for the detection of African horse sickness virus (AHSV) antigens and antibodies. The Laboratorio de Sanidad y Produccion Animal (LSPA) in Algete, Spain was charged with the responsibility of co-ordinating and supplying samples of viruses and antisera to the participating laboratories in Spain, France and the United Kingdom. The panels comprised 76 antigen samples for assay by indirect sandwich ELISAs and 53 serum samples for antibody detection by either indirect or competitive ELISAs. Results generated by ELISA for each laboratory were analysed in LSPA in terms of their relative sensitivities and specificities. There was a good agreement between the ELISAs used for either antigen or antibody detection. The participating groups agreed that any field sample giving a doubtful result would always be retested by ELISA and an alternative assay.

ELISA检测非洲马病病毒抗原和抗体的验证。
在非洲马病(AHS)兽疫期间,易感人群的死亡率可能超过90%。因此,快速和可靠的检测对于确认临床诊断和使控制战略能够在没有不当延误的情况下实施至关重要。最近欧洲联盟资助的一个项目的主要目标之一是验证新开发的快速、敏感、高度可重复和廉价的诊断分析方法,以检测非洲马病病毒(AHSV)抗原和抗体。位于西班牙阿尔代特的动物生产实验室负责协调并向西班牙、法国和联合王国的参与实验室提供病毒和抗血清样本。样本包括76份用于间接夹心elisa检测的抗原样本和53份用于间接或竞争性elisa检测的血清样本。在LSPA中分析每个实验室ELISA产生的结果的相对敏感性和特异性。用于抗原或抗体检测的elisa之间有很好的一致性。参与小组同意,任何给出可疑结果的现场样本都必须通过ELISA和另一种检测方法重新检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书