College of Veterinary Medicine, Northwest A&F University, No. 22 Xinong Road, Yangling, 712100, Shaanxi, China.
Teaching and Research Section of Biotechnology, Nanning University, Nanning, 530200, Guangxi, China.
Arch Virol. 2021 Feb;166(2):389-402. doi: 10.1007/s00705-020-04917-8. Epub 2021 Jan 1.
Recombination is an important phenomenon that accelerates evolution and enriches the genetic diversity of porcine reproductive and respiratory syndrome virus (PRRSV). Recombinant PRRSV isolates sometimes have different genetic backgrounds. In this study, we report a recombinant PRRSV (SD-YL1712) isolated from a pig farm. The genome of SD-YL1712 is 15,014 nucleotides in length, and its nucleotide and amino acid sequence conservation is higher than that of PRRSV strain JXA1 except within the NSP2 region. The NSP2 region of SDYL1712 shares the highest nucleotide (85.9%) and amino acid (84.1%) sequence identity with PRRSV strain NADC30. SD-YL1712 was found to contain a characteristic 131-amino-acid deletion in the NSP2 region. Two recombination breakpoints were detected at nt 2134 and nt 3958 within the NSP2 region, which revealed that SD-YL1712 originated from a recombination event between NADC30-like and HP-PRRSV-derived MLV-like strains. Interestingly, SD-YL1712 had an additional deletion at position 586, similar to that found in strain TJnh1501. Moreover, the pathogenicity of strain SD-YL1712 was found to be similar to that of HP-PRRSV JXA1, which was higher than that of the CH1a strain. Further analysis indicated that SD-YL1712 might be a transitional intermediate in the evolution of TJbd1401 to TJnh1501.
重组是加速进化和丰富猪繁殖与呼吸综合征病毒 (PRRSV) 遗传多样性的重要现象。重组 PRRSV 分离株有时具有不同的遗传背景。在本研究中,我们报告了一株从猪场分离的重组 PRRSV(SD-YL1712)。SD-YL1712 的基因组全长 15014 个核苷酸,其核苷酸和氨基酸序列保守性高于 PRRSV 毒株 JXA1,除 NSP2 区域外。SDYL1712 的 NSP2 区域与 PRRSV 毒株 NADC30 具有最高的核苷酸(85.9%)和氨基酸(84.1%)序列同一性。SD-YL1712 在 NSP2 区域发现含有一个特征性的 131 个氨基酸缺失。在 NSP2 区域的 nt 2134 和 nt 3958 检测到两个重组断点,表明 SD-YL1712 起源于 NADC30 样和 HP-PRRSV 衍生的 MLV 样株之间的重组事件。有趣的是,SD-YL1712 在位置 586 处有一个额外的缺失,与 TJnh1501 株相同。此外,SD-YL1712 株的致病性与 HP-PRRSV JXA1 相似,高于 CH1a 株。进一步分析表明,SD-YL1712 可能是 TJbd1401 向 TJnh1501 进化的过渡中间产物。