Division of Swine Infectious Diseases, National Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150001, China.
Vet Microbiol. 2011 Apr 21;149(1-2):104-12. doi: 10.1016/j.vetmic.2010.11.001. Epub 2010 Nov 9.
Porcine reproductive and respiratory syndrome virus (PRRSV), the causative agent of porcine reproductive and respiratory syndrome, is responsible for serious disease in pigs resulting in substantial economic losses in the porcine industry. An attenuated vaccine strain, HuN4-F112, was obtained by passaging virulent PRRSV strain HuN4 on Marc-145 cells (for 112 passages), and the full-genomic sequence was determined. To understand the molecular basis of attenuation of PRRSV, we compared and analyzed the genomic sequences of HuN4/HuN4-F112, together with those of other four virulent parental/attenuated vaccine strains. Among the 19 PRRSV proteins, two (NSP6 and NSP8) were highly conserved, without any mutations and considered irrelative to attenuation. The mutation rates of envelope-associated structural proteins were obviously higher than those of most non-structural proteins. It is interesting that the gene of the smallest structural protein, E protein, had the highest mutation rate among all of the structural genes analyzed, and also harbored a highly variable region. Our results indicate that determinants of PRRSV attenuation are multigenic products of both non-structural and structural genes. To our knowledge, this is the first report showing that the envelope-associated structural proteins (including E and GP2-GP5 proteins) may play a significant role. These findings contribute towards our understanding of PRRSV attenuation and will provide an important clue for further study.
猪繁殖与呼吸综合征病毒(PRRSV)是引起猪繁殖与呼吸综合征的病原体,可导致猪的严重疾病,给养猪业造成重大经济损失。一种减毒疫苗株 HuN4-F112 是通过在 Marc-145 细胞上传代强毒 PRRSV 株 HuN4(传代 112 代)获得的,并确定了其全基因组序列。为了了解 PRRSV 减毒的分子基础,我们比较和分析了 HuN4/HuN4-F112 的基因组序列,以及其他 4 株强毒亲本/减毒疫苗株的基因组序列。在 19 种 PRRSV 蛋白中,有两种(NSP6 和 NSP8)高度保守,没有任何突变,被认为与减毒无关。包膜相关结构蛋白的突变率明显高于大多数非结构蛋白。有趣的是,最小结构蛋白 E 蛋白的基因在所有分析的结构基因中具有最高的突变率,并且还具有高度可变区。我们的研究结果表明,PRRSV 减毒的决定因素是结构基因和非结构基因的多基因产物。据我们所知,这是第一个表明包膜相关结构蛋白(包括 E 和 GP2-GP5 蛋白)可能发挥重要作用的报告。这些发现有助于我们了解 PRRSV 减毒的机制,并为进一步研究提供了重要线索。