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使用单克隆抗体对来自津巴布韦的SAT 2血清型口蹄疫病毒分离株进行抗原分析。

Antigenic analysis of SAT 2 serotype foot-and-mouth disease virus isolates from Zimbabwe using monoclonal antibodies.

作者信息

Davidson F L, Crowther J R, Nqindi J, Knowles N J, Thevasagayam S J, Van Vuuren C J

机构信息

BBSRC, Institute for Animal Health (IAH), Pirbright Laboratory, Woking, Surrey, UK.

出版信息

Epidemiol Infect. 1995 Aug;115(1):193-205. doi: 10.1017/s095026880005826x.

Abstract

This paper compares strains of foot-and-mouth disease (FMD) serotype SAT (South African Territories) 2 viruses isolated from Zimbabwe and other African countries using monoclonal antibodies (MAb). A sandwich-ELISA was used to examine the relative binding of anti-SAT 2 MAb to the various viruses. The MAb-binding profiles of viruses isolated from field samples were compared using hierarchical cluster analysis. Viruses were obtained from game animals, mainly African buffalo (Syncerus caffer) which is the natural host and reservoir for SAT serotypes in Africa, and from cattle showing clinical signs of FMD, as well as from animals suspected of carrying the virus subclinically. Some isolates have been adapted for use as vaccine strains. The results showed that most of the Zimbabwe isolates collected between 1989 and 1992 were an antigenically closely-related group. Although differences were observed between Zimbabwe isolates collected between 1989 and 1992 and those collected in 1987, there was no correlation with the different MAb binding patterns within the 1987 group and the epidemiological information received from the field. Similar profiles were observed for many SAT 2 viruses, including viruses isolated over a 50-year period and from geographically distant areas. This indicates an inherent stability in antigenic profiles of SAT 2 viruses. The MAb panel was capable of assessing antigenic variation, since very different profiles were obtained for some isolates. The work also allowed comparison and characterization of anti-type SAT 2 MAb from different laboratories. The findings are discussed with reference to selection of vaccine strains.

摘要

本文使用单克隆抗体(MAb)比较了从津巴布韦和其他非洲国家分离出的口蹄疫(FMD)南非领土(SAT)2型病毒毒株。采用夹心酶联免疫吸附测定(ELISA)检测抗SAT 2单克隆抗体与各种病毒的相对结合情况。使用层次聚类分析比较了从现场样本中分离出的病毒的单克隆抗体结合谱。病毒取自野生动物,主要是非洲水牛(非洲野水牛),它是非洲SAT血清型的天然宿主和储存宿主,也取自表现出口蹄疫临床症状的牛,以及疑似亚临床携带该病毒的动物。一些分离株已被用作疫苗毒株。结果表明,1989年至1992年间收集的大多数津巴布韦分离株是抗原密切相关的一组。虽然观察到1989年至1992年间收集的津巴布韦分离株与1987年收集的分离株之间存在差异,但1987年组内不同的单克隆抗体结合模式与从现场获得的流行病学信息之间没有相关性。许多SAT 2病毒都观察到了类似的谱,包括在50年期间从地理上遥远的地区分离出的病毒。这表明SAT 2病毒抗原谱具有内在稳定性。该单克隆抗体组能够评估抗原变异,因为一些分离株获得了非常不同的谱。这项工作还允许对来自不同实验室的抗SAT 2单克隆抗体进行比较和表征。结合疫苗毒株的选择对这些发现进行了讨论。

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