Hodges Arabella L, Walker Lianna R, Everding Talia, Mote Benny E, Vu Hiep L X, Ciobanu Daniel C
Animal Science Department, University of Nebraska-Lincoln, Lincoln, NE 68583, USA.
J Anim Sci. 2025 Jan 4;103. doi: 10.1093/jas/skae395.
Porcine reproductive and respiratory syndrome virus (PRRSV) is the causative agent of a syndrome characterized by reproductive failure and respiratory complications (PRRS). Early detection and classification of PRRSV strains are vital for appropriate management strategies to minimize loss following outbreaks. The most widely used classification method for PRRSV is based on open reading frame 5 (ORF5) sequences. However, the effectiveness of the ORF5-based classification system in accurately representing genetic variation is under scrutiny because ORF5 constitutes less than 5% of the 15kb-long genome. In this study, a single Oxford Nanopore Flongle flow cell was used to identify and assemble the genome of a strain sampled in May of 2022 from a Midwest research farm. Based on comparisons with available PRRSV genomes, the assembled genome was determined to be a novel PRRSV-2 strain belonging to the 1-4-4 L1C.5 ORF5-based lineage. Phylogenetic analyses of ORF5 and whole-genome sequences demonstrated differences in clustering between PRRSV strains, supporting the inability of ORF5 to capture genome-wide variation. For example, high levels of variation were observed within ORF1a, which encodes the hypervariable nsp2 protein. Comparison of the newly assembled genome with the genome of a highly characterized strain (VR2332 PRRSV-2) identified a 100 amino acid deletion within nsp2 characteristic of NADC34-like PRRSV. Oxford Nanopore Technologies' Flongle flow cell has been proven in this study to provide a rapid, cost-effective and accessible approach for whole-genome sequencing of PRRSV strains present within clinical samples necessary for strain-specific genome-wide characterization.
猪繁殖与呼吸综合征病毒(PRRSV)是一种导致以繁殖失败和呼吸并发症为特征的综合征(PRRS)的病原体。PRRSV毒株的早期检测和分类对于采取适当的管理策略以尽量减少疫情爆发后的损失至关重要。PRRSV最广泛使用的分类方法是基于开放阅读框5(ORF5)序列。然而,基于ORF5的分类系统在准确反映基因变异方面的有效性正受到审视,因为ORF5在15kb长的基因组中所占比例不到5%。在本研究中,使用单个牛津纳米孔Flongle流动槽来鉴定和组装2022年5月从美国中西部一个研究农场采集的一株毒株的基因组。通过与现有PRRSV基因组进行比较,确定组装的基因组是一种新型PRRSV - 2毒株,属于基于ORF5的1 - 4 - 4 L1C.5谱系。对ORF5和全基因组序列的系统发育分析表明PRRSV毒株之间在聚类方面存在差异,这支持了ORF5无法捕捉全基因组变异的观点。例如,在编码高变nsp2蛋白的ORF1a内观察到高水平的变异。将新组装的基因组与一个高度特征化毒株(VR2332 PRRSV - 2)的基因组进行比较,发现在nsp2内有100个氨基酸缺失,这是类似NADC34的PRRSV的特征。本研究已证明牛津纳米孔技术公司的Flongle流动槽为临床样本中存在的PRRSV毒株的全基因组测序提供了一种快速、经济高效且可及性强的方法,这对于毒株特异性全基因组特征分析是必要的。