Munir A, Anjum A A, Altaf I, Awan A R
Ph.D. in Microbiology, Institute of Microbiology, Faculty of Veterinary Sciences, University of Veterinary and Animal Sciences, Lahore, Pakistan.
These authors contributed equally to this work and were considered as the first authors.
Iran J Vet Res. 2023;24(4):339-344. doi: 10.22099/IJVR.2023.47837.6940.
During past few years, the Ind-2001 lineage of the Middle East-South Asia topotype (ME-SA) of the foot-and-mouth disease (FMD) virus has been implicated in FMD outbreaks in Pakistan.
This work conducts a comprehensive evolutionary analysis of the Ind-2001 and Pan Asia II lineages, with a specific emphasis on their geographical distribution, lineage classification, and sub-lineage distribution within the region. Furthermore, it aims to expand our understanding of the conserved region of the VP1 protein.
Total samples (n=50) were subjected to antigen detection ELISA and RT-PCR for serotype determination. Confirmed serotype-O isolates (n=17) underwent sequencing for lineage comparison, mutation impact assessment on the VP1 protein GH loop, 3D structure prediction, and further comparative analysis.
Isolates collected from 2017 to 2020 were identified as serotypes O/ME-SA/Pan Asia II ANT10 and O/ME-SA/Pak14. Notably, isolates collected from 2020 to 2022 belonged to a novel FMDV serotype O/ME-SA/Ind-2001e lineage. Phylogenetic analyses indicated that these strains were distinct from dominant contemporaneous strains which may challenge Pakistan's FMD control measures. These isolates exhibited variance in the VP1 epitope, specifically in amino acid residues 135-155, known to influence neutralizing antibody generation.
Observed mutations suggest potential challenges to current vaccination efficacy against FMD. This emphasizes enhanced FMD surveillance and demonstrates that tracking the emergence of the O/ME-SA/Ind-2001e lineage is important for determining FMD control strategies in Asia.
在过去几年中,口蹄疫(FMD)病毒中东 - 南亚拓扑型(ME - SA)的Ind - 2001谱系与巴基斯坦的口蹄疫疫情有关。
这项工作对Ind - 2001和泛亚II谱系进行了全面的进化分析,特别强调它们在该地区的地理分布、谱系分类和亚谱系分布。此外,旨在扩展我们对口蹄疫病毒VP1蛋白保守区域的理解。
对总共50个样本进行抗原检测ELISA和RT - PCR以确定血清型。对确诊的O型分离株(n = 17)进行测序,用于谱系比较、评估VP1蛋白GH环上的突变影响、进行3D结构预测以及进一步的比较分析。
2017年至2020年收集的分离株被鉴定为O/ME - SA/泛亚II ANT10和O/ME - SA/巴基斯坦14血清型。值得注意的是,2020年至2022年收集的分离株属于一种新型口蹄疫病毒O/ME - SA/Ind - 2001e谱系。系统发育分析表明,这些毒株与同期的优势毒株不同,这可能对巴基斯坦的口蹄疫防控措施构成挑战。这些分离株在VP1表位上表现出差异,特别是在已知影响中和抗体产生的135 - 上的氨基酸残基处。
观察到的突变表明当前口蹄疫疫苗接种效果面临潜在挑战。这强调了加强口蹄疫监测,并表明追踪O/ME - SA/Ind - 2001e谱系的出现对于确定亚洲口蹄疫防控策略很重要。