Department of Biomedical Sciences and Pathobiology, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Department of Computer Science, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Virology. 2014 Feb;450-451:132-9. doi: 10.1016/j.virol.2013.12.009. Epub 2013 Dec 31.
Synthetic attenuated virus engineering (SAVE) is an emerging technology that enables rapid attenuation of viruses. In this study, by using SAVE we demonstrated rapid attenuation of an arterivirus, porcine reproductive and respiratory syndrome virus (PRRSV). The major envelope GP5 gene of PRRSV was codon-pair deoptimized aided by a computer algorithm. The codon-pair deoptimized virus, designated as SAVE5 with a deoptimized GP5 gene, was successfully rescued in vitro. The SAVE5 virus replicated at a lower level in vitro with a significant decrease of GP5 protein expression compared to the wild-type PRRSV VR2385 virus. Pigs experimentally infected with the SAVE5 virus had significantly lower viremia level up to 14 days post-infection as well as significantly reduced gross and histological lung lesions when compared to wild-type PRRSV VR2385 virus-infected pigs, indicating the attenuation of the SAVE5 virus. This study proved the feasibility of rapidly attenuating PRRSV by SAVE.
合成减毒病毒工程(SAVE)是一种新兴技术,可实现病毒的快速减毒。在这项研究中,我们通过使用 SAVE 成功地快速减毒了动脉炎病毒,猪繁殖与呼吸综合征病毒(PRRSV)。使用计算机算法辅助对 PRRSV 的主要包膜 GP5 基因进行密码子对去优化。成功地在体外拯救了去优化的 GP5 基因的减毒病毒,命名为 SAVE5。与野生型 PRRSV VR2385 病毒相比,SAVE5 病毒在体外的复制水平较低,GP5 蛋白表达显著降低。与感染野生型 PRRSV VR2385 病毒的猪相比,实验感染 SAVE5 病毒的猪的病毒血症水平在感染后 14 天内显著降低,肺部大体和组织学病变也显著减少,表明 SAVE5 病毒的减毒效果。本研究证明了通过 SAVE 快速减毒 PRRSV 的可行性。