Tian Debin, Cao Dianjun, Lynn Heffron C, Yugo Danielle M, Rogers Adam J, Overend Christopher, Matzinger Shannon R, Subramaniam Sakthivel, Opriessnig Tanja, LeRoith Tanya, Meng Xiang-Jin
Department of Biomedical Sciences and Pathobiology, College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Roslin Institute, University of Edinburgh, Midlothian, Scotland, UK.
Vaccine. 2017 Apr 25;35(18):2427-2434. doi: 10.1016/j.vaccine.2017.03.046. Epub 2017 Mar 23.
Porcine reproductive and respiratory syndrome virus (PRRSV) is the causative agent of arguably the most economically important global swine disease. The extensive genetic variation of PRRSV strains is a major obstacle for heterologous protection of current vaccines. Previously, we constructed a panel of chimeric viruses containing only the ectodomain sequences of DNA-shuffled structural genes of different PRRSV strains in the backbone of a commercial vaccine, and found that one chimeric virus had an improved cross-protection efficacy. In this present study, to further enhance the cross-protective efficacy against heterologous strains, we constructed a novel chimeric virus VR2385-S3456 containing the full-length sequences of shuffled structural genes (ORFs 3-6) from 6 heterologous PRRSV strains in the backbone of PRRSV strain VR2385. We showed that the chimeric virus VR2385-S3456 induced a high level of neutralizing antibodies in pigs against two heterologous strains. A subsequent vaccination and challenge study in 48 pigs revealed that the chimeric virus VR2385-S3456 conferred an enhanced cross-protection when challenged with heterologous virus strain NADC20 or a contemporary heterologous strain RFLP 1-7-4. The results suggest that the chimera VR2385-S3456 may be a good PRRSV vaccine candidate for further development to confer heterologous protection.
猪繁殖与呼吸综合征病毒(PRRSV)是全球最具经济重要性的猪病的病原体。PRRSV毒株广泛的基因变异是当前疫苗进行异源保护的主要障碍。此前,我们构建了一组嵌合病毒,其仅在商业疫苗的骨架中包含不同PRRSV毒株DNA改组结构基因的胞外域序列,并发现一种嵌合病毒具有提高的交叉保护效力。在本研究中,为进一步增强针对异源毒株的交叉保护效力,我们构建了一种新型嵌合病毒VR2385-S3456,其在PRRSV毒株VR2385的骨架中包含来自6种异源PRRSV毒株的改组结构基因(开放阅读框3-6)的全长序列。我们发现嵌合病毒VR2385-S3456在猪体内诱导产生了针对两种异源毒株的高水平中和抗体。随后对48头猪进行的疫苗接种和攻毒研究表明,当用异源病毒毒株NADC20或当代异源毒株RFLP 1-7-4进行攻毒时,嵌合病毒VR2385-S3456提供了增强的交叉保护。结果表明,嵌合体VR2385-S3456可能是一种良好的PRRSV疫苗候选物,可进一步开发以提供异源保护。