State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150069, China.
Institute of Animal Husbandry, Heilongjiang Academy of Agricultural Sciences, Harbin 150086, China.
Viruses. 2022 Jan 18;14(2):166. doi: 10.3390/v14020166.
Highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV) with enhanced replication capability emerged in China and has become dominant epidemic strain since 2006. Up to now, the replication-regulated genes of PRRSV have not been fully clarified. Here, by swapping the genes or elements between HP-PRRSV and classical PRRSV based on infectious clones, NSP1, NSP2, NSP7, NSP9 and 3'-UTR are found to contribute to the high replication efficiency of HP-PRRSV. Further study revealed that mutations at positions 117th or 119th in the 3'-UTR are significantly related to replication efficiency, and the nucleotide at position 120th is critical for viral rescue. The motif composed by 117-120th nucleotides was quite conservative within each lineage of PRRSV; mutations in the motif of HP-PRRSV and currently epidemic lineage 1 (L1) PRRSV showed higher synthesis ability of viral negative genomic RNA, suggesting that those mutations were beneficial for viral replication. RNA structure analysis revealed that this motif maybe involved into a pseudoknot in the 3'-UTR. The results discovered a novel motif, 117-120th nucleotide in the 3'-UTR, that is critical for replication of PRRSV-2, and mutations in the motif contribute to the enhanced replicative ability of HP-PRRSV or L1 PRRSV. Our findings will help to understand the molecular basis of PRRSV replication and find the potential factors resulting in an epidemic strain of PRRSV.
高致病性猪繁殖与呼吸综合征病毒(HP-PRRSV)在中国出现并具有增强的复制能力,自 2006 年以来已成为主要流行株。截至目前,PRRSV 的复制调控基因尚未完全阐明。在此,通过基于感染性克隆在 HP-PRRSV 和经典 PRRSV 之间交换基因或元件,发现 NSP1、NSP2、NSP7、NSP9 和 3'-UTR 有助于 HP-PRRSV 的高复制效率。进一步的研究表明,3'-UTR 中第 117 位或第 119 位的突变与复制效率显著相关,第 120 位的核苷酸对于病毒拯救至关重要。由 117-120 位核苷酸组成的基序在 PRRSV 的每个谱系内都非常保守;HP-PRRSV 和当前流行谱系 1(L1)PRRSV 中的基序突变显示出更高的病毒负基因组 RNA 合成能力,表明这些突变有利于病毒复制。RNA 结构分析表明,该基序可能涉及 3'-UTR 中的假结。该研究发现了一个新的基序,即 3'-UTR 中的 117-120 位核苷酸,对于 PRRSV-2 的复制至关重要,并且基序中的突变有助于增强 HP-PRRSV 或 L1 PRRSV 的复制能力。我们的研究结果将有助于理解 PRRSV 复制的分子基础,并发现导致 PRRSV 流行株的潜在因素。