Department of Biomedical Sciences and Pathobiology, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, USA.
J Virol. 2013 Jan;87(1):304-13. doi: 10.1128/JVI.01789-12. Epub 2012 Oct 17.
Molecular breeding via DNA shuffling can direct the evolution of viruses with desired traits. By using a positive-strand RNA virus, porcine reproductive and respiratory syndrome virus (PRRSV), as a model, rapid attenuation of the virus was achieved in this study by DNA shuffling of the viral envelope genes from multiple strains. The GP5 envelope genes of 7 genetically divergent PRRSV strains and the GP5-M genes of 6 different PRRSV strains were molecularly bred by DNA shuffling and iteration of the process, and the shuffled genes were cloned into the backbone of a DNA-launched PRRSV infectious clone. Two representative chimeric viruses, DS722 with shuffled GP5 genes and DS5M3 with shuffled GP5-M genes, were rescued and shown to replicate at a lower level and to form smaller plaques in vitro than their parental virus. An in vivo pathogenicity study revealed that pigs infected with the two chimeric viruses had significant reductions in viral-RNA loads in sera and lungs and in gross and microscopic lung lesions, indicating attenuation of the chimeric viruses. Furthermore, pigs vaccinated with the chimeric virus DS722, but not pigs vaccinated with DS5M3, still acquired protection against PRRSV challenge at a level similar to that of the parental virus. Therefore, this study reveals a unique approach through DNA shuffling of viral envelope genes to attenuate a positive-strand RNA virus. The results have important implications for future vaccine development and will generate broad general interest in the scientific community in rapidly attenuating other important human and veterinary viruses.
通过 DNA 重排进行分子育种可以指导具有所需特性的病毒进化。本研究以正链 RNA 病毒猪繁殖与呼吸综合征病毒(PRRSV)为模型,通过对来自多个毒株的病毒包膜基因进行 DNA 重排,实现了病毒的快速衰减。7 个遗传分化的 PRRSV 毒株的 GP5 包膜基因和 6 个不同 PRRSV 毒株的 GP5-M 基因通过 DNA 重排和迭代过程进行了分子育种,重排的基因被克隆到 DNA 启动的 PRRSV 感染性克隆的骨架中。两个代表性嵌合病毒,DS722(GP5 基因重排)和 DS5M3(GP5-M 基因重排)被拯救并显示在体外复制水平较低,形成的噬菌斑较小。体内致病性研究表明,感染两种嵌合病毒的猪血清和肺组织中的病毒 RNA 载量以及大体和显微镜下的肺病变显著减少,表明嵌合病毒的衰减。此外,接种嵌合病毒 DS722 的猪,而不是接种 DS5M3 的猪,仍然获得了与亲本病毒相似水平的 PRRSV 攻毒保护。因此,本研究通过 DNA 重排病毒包膜基因揭示了一种独特的方法来衰减正链 RNA 病毒。研究结果对未来疫苗的开发具有重要意义,并将在科学界引起广泛关注,迅速衰减其他重要的人类和兽医病毒。