Suppr超能文献

GP4 特异性中和抗体可能是 PRRSV 进化的驱动力。

GP4-specific neutralizing antibodies might be a driving force in PRRSV evolution.

机构信息

Laboratory of Virology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.

出版信息

Virus Res. 2010 Dec;154(1-2):104-13. doi: 10.1016/j.virusres.2010.08.026. Epub 2010 Sep 15.

Abstract

The structural envelope glycoprotein GP4 of European porcine reproductive and respiratory syndrome virus (PRRSV) strains contains a highly variable neutralizing epitope that is susceptible to neutralizing antibody-mediated selective pressure in vitro. In this study, it was analyzed what happens with this neutralizing epitope during infection in vivo in the presence of neutralizing antibodies. A neutralizing antibody-mediated selective pressure was created in 30 pigs by vaccination prior to inoculation with infectious Lelystad virus (LV). Nine viable neutralizing antibody-escape variants were isolated from 9 of these pigs and their neutralizing antibody-escape mutant-identity was confirmed by the acquired resistance to neutralization by autologous neutralizing sera. Six out of 9 neutralizing antibody-escape variants contained aa substitutions in the GP4 neutralizing epitope and had become resistant to neutralization by a monoclonal antibody (mAb) against this epitope. In addition, in all 6 corresponding pigs, antibodies against this epitope were detected early in infection. In contrast to these 6 virus variants, the 3 other antibody-escape variants did not contain aa substitutions in the GP4 neutralizing epitope and were still sensitive to neutralization by the GP4-specific mAb. These antibody-escape variants were isolated from pigs that did not contain antibodies against this epitope early in infection. All these findings together strongly indicate that aa substitutions in the GP4 neutralizing epitope can abrogate antibody recognition, and that neutralizing antibodies might be responsible for the selection of neutralizing antibody-resistant variants with aa substitutions in the neutralizing epitope on GP4. In conclusion, this study indicates that neutralizing antibodies in pigs might be a driving force in the rapid evolution of the neutralizing epitope on GP4 of European PRRSV strains.

摘要

欧洲猪繁殖与呼吸综合征病毒(PRRSV)株的结构包膜糖蛋白 GP4 含有一个高度可变的中和表位,该表位易受中和抗体介导的体外选择压力的影响。在本研究中,分析了在存在中和抗体的情况下,该中和表位在体内感染过程中会发生什么变化。通过在接种传染性莱利斯塔德病毒(LV)之前接种疫苗,在 30 头猪中产生了中和抗体介导的选择压力。从其中 9 头猪中分离出 9 个具有中和活性的逃逸变异株,通过对同源中和血清的中和抗性获得,证实了其中和抗体逃逸突变体的身份。在 9 个中和抗体逃逸变异株中,有 6 个含有 GP4 中和表位的 aa 取代,并且对针对该表位的单克隆抗体(mAb)的中和作用产生了抗性。此外,在所有 6 头相应的猪中,在感染早期就检测到针对该表位的抗体。与这 6 个病毒变异株不同,另外 3 个抗体逃逸变异株在 GP4 中和表位中没有 aa 取代,仍然对 GP4 特异性 mAb 的中和作用敏感。这些抗体逃逸变异株是从感染早期未检测到针对该表位的抗体的猪中分离出来的。所有这些发现都强烈表明,GP4 中和表位中的 aa 取代可以消除抗体的识别,中和抗体可能是导致 GP4 中和表位发生 aa 取代的中和抗体抗性变异株选择的原因。总之,本研究表明,猪体内的中和抗体可能是欧洲 PRRSV 株 GP4 中和表位快速进化的驱动力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验