Department of Swine Infectious Diseases, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, 200241, China.
Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou, 225009, China.
Virol Sin. 2021 Dec;36(6):1611-1625. doi: 10.1007/s12250-021-00453-0. Epub 2021 Oct 12.
Currently, various porcine reproductive and respiratory syndrome virus (PRRSV) variants emerged worldwide with different genetic characteristics and pathogenicity, increasing the difficulty of PRRS control. In this study, a PRRSV strain named HBap4-2018 was isolated from swine herds suffering severe respiratory disease with high morbidity in Hebei Province of China in 2018. The genome of HBap4-2018 is 15,003 nucleotides in length, and compared with NADC30-like PRRSV, nsp2 of HBap4-2018 has an additional continuous deletion of five amino acids. Phylogenetic analysis based on complete genome and ORF5 showed that HBap4-2018 belonged to lineage 8 of PRRSV-2, which was characterized by highly variable genome. However, HBap4-2018 was classified into lineage 1 based on phylogenetic analysis of nsp2, sharing higher amino acid homology (85.3%-85.5%) with NADC30-like PRRSV. Further analysis suggested that HBap4-2018 was a novel natural recombinant PRRSV with three recombinant fragments in the genome, of which highly pathogenic PRRSV (HP-PRRSV) served as the major parental strains, while NADC30-like PRRSV served as the minor parental strains. Five recombination break points were identified in nsp2, nsp3, nsp5, nsp9 and ORF6, respectively, presenting a novel recombinant pattern in the genome. Piglets inoculated with HBap4-2018 presented typical clinical signs with a mortality rate of 60%. High levels of viremia and obvious macroscopic and histopathological lesions in the lungs were observed, revealing the high pathogenicity of HBap4-2018 in piglets.
目前,世界各地出现了多种具有不同遗传特征和致病性的猪繁殖与呼吸综合征病毒(PRRSV)变异株,增加了 PRRS 控制的难度。本研究中,2018 年从中国河北省暴发严重呼吸道疾病且发病率高的猪群中分离到一株 PRRSV 毒株,命名为 HBap4-2018。HBap4-2018 的基因组全长为 15003 个核苷酸,与 NADC30 样 PRRSV 相比,HBap4-2018 的 nsp2 有 5 个连续氨基酸缺失。基于全基因组和 ORF5 的系统进化分析表明,HBap4-2018 属于 PRRSV-2 第 8 谱系,该谱系基因组高度可变。然而,根据 nsp2 的系统进化分析,HBap4-2018 被归类为 1 谱系,与 NADC30 样 PRRSV 具有较高的氨基酸同源性(85.3%-85.5%)。进一步分析表明,HBap4-2018 是一株新型天然重组 PRRSV,基因组中存在 3 个重组片段,其中高致病性 PRRSV(HP-PRRSV)为主要亲本株,而 NADC30 样 PRRSV 为次要亲本株。在 nsp2、nsp3、nsp5、nsp9 和 ORF6 中分别鉴定出 5 个重组断点,呈现出新的基因组重组模式。接种 HBap4-2018 的仔猪出现典型的临床症状,死亡率为 60%。仔猪血液中病毒载量高,肺部肉眼和组织病理学病变明显,表明 HBap4-2018 在仔猪中具有高致病性。