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利用中和性单克隆抗体和中和逃逸变异体鉴定蓝舌病病毒10型的四个不同中和表位

Identification of four distinct neutralizing epitopes on bluetongue virus serotype 10 using neutralizing monoclonal antibodies and neutralization-escape variants.

作者信息

Heidner H W, Rossitto P V, MacLachlan N J

机构信息

Department of Veterinary Pathology, School of Veterinary Medicine, University of California, Davis 95616.

出版信息

Virology. 1990 Jun;176(2):658-61. doi: 10.1016/0042-6822(90)90041-o.

DOI:10.1016/0042-6822(90)90041-o
PMID:1693250
Abstract

Neutralizing sites on bluetongue virus serotype 10 (BTV-10) were investigated with a panel of seven neutralizing monoclonal antibodies (MAbs). Each MAb was coupled to agarose beads and tested against the other MAbs and a nonneutralizing control MAb in a competitive immueprecipitation assay. In addition, neutralization-escape viral variants of BTV-10 were identified and cloned by selecting individual plaques that formed in the presence of neutralizing MAbs. Four antigenic variants were isolated, each under the selective pressure of a different MAb. Parental BTV-10 and the four antigenic variants were compared by microneutralization assay using the MAb panel. The panel of neutralizing MAbs was subdivided into four groups on the basis of these assays, indicating that at least four distinct neutralizing epitopes exist on the BTV-10 virion. These epitopes are individually defined by representative MAbs 034, 039, 041, and 045, and the results indicate that the four epitopes are interacting sites within a single antigenic domain on BTV-10 outer capsid protein VP2. This conclusion is further supported by the fact that a double-site neutralization-escape variant designated DE34/39 (sequentially produced against MAbs 034 and 039) was not neutralized by any MAb of the panel.

摘要

利用一组七种中和单克隆抗体(MAb)对蓝舌病毒10型(BTV - 10)的中和位点进行了研究。每种单克隆抗体与琼脂糖珠偶联,并在竞争性免疫沉淀试验中与其他单克隆抗体和一种非中和对照单克隆抗体进行测试。此外,通过选择在中和单克隆抗体存在下形成的单个噬斑,鉴定并克隆了BTV - 10的中和逃逸病毒变体。分离出四种抗原变体,每种变体都处于不同单克隆抗体的选择压力下。使用该单克隆抗体组通过微量中和试验比较了亲本BTV - 10和四种抗原变体。基于这些试验,将中和单克隆抗体组分为四组,这表明BTV - 10病毒粒子上至少存在四个不同的中和表位。这些表位分别由代表性单克隆抗体034、039、041和045定义,结果表明这四个表位是BTV - 10外 capsid 蛋白VP2上单个抗原域内的相互作用位点。一个名为DE34/39(依次针对单克隆抗体034和039产生)的双位点中和逃逸变体不能被该组中的任何单克隆抗体中和,这一事实进一步支持了这一结论。

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Identification of four distinct neutralizing epitopes on bluetongue virus serotype 10 using neutralizing monoclonal antibodies and neutralization-escape variants.利用中和性单克隆抗体和中和逃逸变异体鉴定蓝舌病病毒10型的四个不同中和表位
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