Chen Zhenhai, Collin Emily, Peddireddi Lalitha, Clement Travis, Gauger Phillip, Hause Ben M
College of Veterinary Medicine, Yangzhou University, Yangzhou, JS, China; Department of Diagnostic Medicine and Pathobiology, Kansas State University, Manhattan, KS, USA.
Kansas State Veterinary Diagnostic Laboratory, Kansas State University, Manhattan, KS, USA.
Res Vet Sci. 2017 Dec;115:432-441. doi: 10.1016/j.rvsc.2017.07.027. Epub 2017 Jul 26.
Porcine reproductive and respiratory syndrome (PRRS) is one of the most economically important diseases in swine caused by porcine reproductive and respiratory syndrome virus (PRRSV). Genome sequences of sixty-six PRRSV strains were obtained using metagenomic sequencing of serum samples collected in the U.S. in 2014 to explore contemporary genetic diversity. Phylogenetic analysis of the genes encoding the envelope proteins identified four to eight distinct lineages with >87% intraclade identity. To explore the effect of the observed genetic diversity on antigenicity, the genome regions encoding either GP2a-GP3-GP4 or GP5-M in strain SD95-21 were replaced with alleles from each of eight distinct PRRSV strains using reverse genetics. The GP2a-GP3-GP4 region from only four of the eight strains yielded viable recombinant virus. When viable, both GP2a-GP3-GP4 and GP5-M variably affected antigenicity. A strain-dependent significant loss in cross reactivity was variably observed by indirect immunofluorescence assays using antisera from pigs vaccinated with commercial modified-live vaccines following replacement of GP2a-GP3-GP4 or GP5-M. Significantly reduced neutralization titers were similarly measured using antisera from naturally PRRSV-exposed pigs. These results illustrate the need to consider genomic regions besides GP5 for PRRSV epidemiology and vaccination.
猪繁殖与呼吸综合征(PRRS)是由猪繁殖与呼吸综合征病毒(PRRSV)引起的猪群中最具经济重要性的疾病之一。2014年在美国采集血清样本,通过宏基因组测序获得了66株PRRSV毒株的基因组序列,以探索当代的遗传多样性。对编码包膜蛋白的基因进行系统发育分析,确定了4至8个不同分支,分支内同一性>87%。为了探究观察到的遗传多样性对抗原性的影响,利用反向遗传学方法,将SD95-21毒株中编码GP2a-GP3-GP4或GP5-M的基因组区域替换为8个不同PRRSV毒株各自的等位基因。8个毒株中只有4个的GP2a-GP3-GP4区域产生了有活力的重组病毒。当有活力时,GP2a-GP3-GP4和GP5-M对抗原性均有不同程度的影响。在用商业改良活疫苗免疫的猪的抗血清进行间接免疫荧光试验时,在替换GP2a-GP3-GP4或GP5-M后,观察到交叉反应性出现了因毒株而异的显著降低。用自然感染PRRSV的猪的抗血清进行中和试验时,也同样测得中和效价显著降低。这些结果表明,在PRRSV流行病学和疫苗接种研究中,除了GP5之外,还需要考虑其他基因组区域。