首页> 外文OA文献 >Prevention of foot-and-mouth disease in cattle using a prime-boot-vaccination strategy
【2h】

Prevention of foot-and-mouth disease in cattle using a prime-boot-vaccination strategy

机译:使用主要疫苗接种策略预防牛的口蹄疫

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

Foot-and-mouth disease (FMD) is one of the most economically important infectious diseases of production animals globally. Vaccination can help to control this disease, however, current vaccines are imperfect. They are made using chemically inactivated FMD virus (FMDV) that is produced in mammalian cell culture under high containment. Here, we have expressed the FMDV capsid protein precursor (P1-2A) of strain O1 Manisa alone or with the FMDV 3C protease (3Cpro) using a “single cycle” packaged alphavirus self-replicating RNA based on Semliki Forest virus (SFV). When the FMDV P1-2A was expressed with 3Cpro then processing of the FMDV capsid precursor protein is observed within cells and the proteins assemble into empty capsid particles. In cattle vaccinated once with these rSFV-FMDV vectors alone, anti-FMDV antibodies were elicited but the immune response was insufficient to give protection against FMDV challenge. However, the prior vaccination with these vectors resulted in a much stronger immune response against FMDV post-challenge and the viremia observed was decreased in level and duration. In subsequent experiments, cattle were sequentially vaccinated with a rSFV-FMDV followed by recombinant FMDV empty capsid particles, or vice versa, prior to challenge. Animals given a primary vaccination with the rSFV-FMDV vector and then boosted with FMDV empty capsids showed a strong anti-FMDV antibody response prior to challenge. Following challenge with FMDV, the cattle were protected against disease and no FMDV RNA was detected in their sera. Initial inoculation with empty capsids followed by the rSFV-FMDV was much less effective at combating the FMDV challenge and a large post-challenge boost to the level of anti-FMDV antibodies was observed and clinical disease occurred. This prime-boost system, using reagents that can be generated outside of high-containment facilities, offers significant advantages to achieve control of FMD by vaccination.
机译:口蹄疫(FMD)是全球生产性动物中最经济重要的传染病之一。疫苗接种可以帮助控制这种疾病,但是,目前的疫苗还不完善。它们是使用化学灭活的口蹄疫病毒(FMDV)制成的,该病毒是在高度封闭的条件下在哺乳动物细胞培养物中产生的。在这里,我们已经表达了O1 Manisa菌株的FMDV衣壳蛋白前体(P1-2A)或与FMDV 3C蛋白酶(3Cpro)一起使用了基于Semliki Forest病毒(SFV)的“单周期”包装的α病毒自我复制RNA。当FMDV P1-2A用3Cpro表达时,可在细胞内观察到FMDV衣壳前体蛋白的加工,并且该蛋白组装成空的衣壳颗粒。在仅用这些rSFV-FMDV载体接种一次的牛中,产生了抗FMDV抗体,但免疫应答不足以提供针对FMDV攻击的保护。但是,事先用这些载体接种疫苗后,对FMDV的攻击产生了更强的免疫反应,观察到的病毒血症水平和持续时间均降低了。在随后的实验中,在攻击前,先向牛先接种rSFV-FMDV,然后再接种重组FMDV空衣壳颗粒,反之亦然。接种rSFV-FMDV载体的初次疫苗接种,然后用FMDV空衣壳加强免疫的动物在攻击前表现出强烈的抗FMDV抗体反应。用FMDV攻击后,牛被保护免受疾病侵害,并且其血清中未检测到FMDV RNA。最初用空衣壳接种,然后用rSFV-FMDV接种对付FMDV攻击的效果要差得多,并且在攻击后大大提高了抗FMDV抗体的水平,并发生了临床疾病。这种初免-升压系统使用的试剂可以在高安全性设施之外产生,具有显着的优势,可以通过疫苗接种来控制口蹄疫。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

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