首页> 美国卫生研究院文献>Journal of Virology >Open reading frame 5 of porcine reproductive and respiratory syndrome virus as a cause of virus-induced apoptosis.
【2h】

Open reading frame 5 of porcine reproductive and respiratory syndrome virus as a cause of virus-induced apoptosis.

机译:猪繁殖与呼吸综合征病毒的开放阅读框5是病毒诱导的细胞凋亡的原因。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The gene product of open reading frame 5 (p25) of porcine reproductive and respiratory syndrome (PRRS) virus has been expressed by coinfection of culture cells with vaccinia virus expressing the T7 RNA polymerase and a recombinant vaccinia virus encoding the open reading frame 5 gene under the T7 promoter and the encephalomyocarditis virus internal ribosome entry site. In spite of the reported efficiency of the expression system, very poor accumulation of p25 protein was observed and a strong cytotoxicity was produced in the doubly infected cells. This cell toxicity was shown to occur by induction of apoptosis, as indicated by nucleosome ladder formation, chromatin condensation, and rRNA degradation. Apoptosis induction was also observed after infection of cultured cells with an adapted PRRS virus strain and after infection of swine macrophage cells with a PRRS virus field strain. Contrary to the observations made for other cases of virus-induced apoptosis, we could not prevent p25 protein-induced apoptosis by using a cell line permanently expressing Bcl-2 protein.
机译:猪生殖与呼吸综合症(PRRS)病毒的开放阅读框5(p25)的基因产物已通过培养细胞与表达T7 RNA聚合酶的牛痘病毒和重组牛痘病毒共同编码,表达载体是在以下条件下表达的: T7启动子和脑心肌炎病毒内部核糖体进入位点。尽管报道了表达系统的效率,但观察到p25蛋白的积累非常差,并且在双重感染的细胞中产生了很强的细胞毒性。该细胞毒性显示出通过诱导凋亡而发生,如核小体梯形成,染色质浓缩和rRNA降解所表明。在用适应的PRRS病毒株感染培养的细胞后和用PRRS病毒野毒株感染猪巨噬细胞后,也观察到凋亡诱导。与其他病毒诱导的细胞凋亡案例相反,我们无法通过使用永久表达Bcl-2蛋白的细胞系来预防p25蛋白诱导的细胞凋亡。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号