Li Junhui, Gong Wenjie, Mao Liping, Pan Xiaomei, Wu Qingqing, Guo Yidi, Jiang Jianfeng, Tang Huifen, Zhao Yi, Cheng Lanling, Tu Changchun, Yu Xinglong, He Sun, Zhang Wei
College of Veterinary Medicine, Hunan Agricultural University, Changsha, China.
Tecon Bio-Pharmaceuticals Co. Ltd., Urumqi, China.
Front Microbiol. 2024 Jun 26;15:1419499. doi: 10.3389/fmicb.2024.1419499. eCollection 2024.
Rapid evolution of (PRRSV) is the bottleneck for effective prevention and control of PRRS. Thus, understanding the prevalence and genetic background of PRRSV strains in swine-producing regions is important for disease prevention and control. However, there is only limited information about the epizootiological situation of PRRS in the Xinjiang Uygur Autonomous Region, China. In this study, blood or lung tissue samples were collected from 1,411 PRRS-suspected weaned pigs from 9 pig farms in Changji, Shihezi, and Wujiaqu cities between 2020 and 2022. The samples were first tested by RT-quantitative PCR, yielding a PRRSV-2 positive rate of 53.6%. Subsequently, 36 PRRSV strains were isolated through initial adaptation in bone marrow-derived macrophages followed by propagation in grivet monkey Marc-145 cells. Furthermore, 28 PRRSV-positive samples and 20 cell-adapted viruses were selected for high-throughput sequencing (HTS) to obtain the entire PRRSV genome sequences. Phylogenetic analysis based on the nucleotide sequences of the ORF5 gene of the PRRSV strains identified in this study grouped into sub-lineages 1.8 and 8.7 the former being the dominant strain currently circulating in Xinjiang. However, the NSP2 proteins of the Xinjiang PRRSV strains shared the same deletion patterns as sub-lineage 1.8 prototype strain NADC30 with the exception of 4 strains carrying 2-3 additional amino acid deletions. Further analysis confirmed that recombination events had occurred in 27 of 37 PRRSVs obtained here with the parental strains belonging to sub-lineages 1.8 and 8.7, lineages 3 and 5, with the recombination events having occurred most frequently in the 5' and 3' termini of ORF1a and 5' terminus of ORF1b.
猪繁殖与呼吸综合征病毒(PRRSV)的快速进化是有效防控猪繁殖与呼吸综合征(PRRS)的瓶颈。因此,了解猪繁殖与呼吸综合征病毒毒株在生猪产区的流行情况和遗传背景对于疾病防控至关重要。然而,关于中国新疆维吾尔自治区猪繁殖与呼吸综合征的流行病学情况,仅有有限的信息。在本研究中,于2020年至2022年间从昌吉、石河子和五家渠市的9个猪场的1411头疑似感染猪繁殖与呼吸综合征的断奶仔猪中采集血液或肺组织样本。样本首先通过逆转录定量PCR进行检测,猪繁殖与呼吸综合征病毒2型阳性率为53.6%。随后,通过在骨髓来源的巨噬细胞中初步适应,随后在猕猴Marc-145细胞中传代,分离出36株猪繁殖与呼吸综合征病毒毒株。此外,选择28份猪繁殖与呼吸综合征病毒阳性样本和20株细胞适应病毒进行高通量测序(HTS),以获得完整的猪繁殖与呼吸综合征病毒基因组序列。基于本研究中鉴定的猪繁殖与呼吸综合征病毒毒株的开放阅读框5(ORF5)基因核苷酸序列进行的系统发育分析表明,这些毒株分为亚系1.8和8.7,前者是目前在新疆流行的优势毒株。然而,新疆猪繁殖与呼吸综合征病毒毒株的非结构蛋白2(NSP2)蛋白与亚系1.8原型毒株NADC30具有相同的缺失模式,但有4株携带2 - 3个额外的氨基酸缺失。进一步分析证实,在此获得的37株猪繁殖与呼吸综合征病毒中有27株发生了重组事件,亲本毒株属于亚系1.8和8.7、谱系3和5,重组事件最常发生在开放阅读框1a的5'和3'末端以及开放阅读框1b的5'末端。