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Epitope mapping and characterization of a novel Nsp10-specific monoclonal antibody that differentiates genotype 2 PRRSV from genotype 1 PRRSV

机译:新型Nsp10特异性单克隆抗体的抗原决定簇定位和表征,该抗体可区分基因型2 PRRSV和基因型1 PRRSV

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Background Porcine reproductive and respiratory syndrome virus (PRRSV), the causative agent of PRRS, has two distinct and highly diverse genotypes (genotype 1 and genotype 2) in the field. Accurate diagnosis and differentiation of the two genotypes of PRRSV are critical to the effective prevention and control of PRRS. The non-structural protein 10 (Nsp10) plays a vital role in viral replication and is one of the most conserved proteins of PRRSV, thus constituting a good candidate for PRRSV diagnosis. Results In this study, we generated a monoclonal antibody (mAb) 4D9 against Nsp10 by immunizing BALB/c mice with purified recombinant Nsp10 expressed by an Escherichia coli system. Through fine epitope mapping of mAb 4D9 using a panel of eukaryotic expressed polypeptides with GFP-tags, we identified the motif 286AIQPDYRDKL295 as the minimal unit of the linear B-cell epitope recognized by mAb 4D9. Protein sequence alignment indicated that 286AIQPDYRDKL295 was highly conserved in genotype 2 PRRSV strains, whereas genotype 1 PRRSV strains had variable amino acids in this motif. Furthermore, a mutant of the motif carrying two constant amino acids of genotype 1 PRRSV, Cys290 and Glu293, failed to react with mAb 4D9. More importantly, the mAb 4D9 could differentiate genotype 2 PRRSV strains from genotype 1 PRRSV strains using Western blotting and immunofluorescence analysis. Conclusion Our findings suggest that Nsp10-specific mAb generated in this study could be a useful tool for basic research and may facilitate the establishment of diagnostic methods to discriminate between genotype 1 and genotype 2 PRRSV infection.
机译:背景技术猪繁殖与呼吸综合征病毒(PRRSV)是PRRS的病原体,在该领域具有两种截然不同的基因型(基因型1和基因型2)。准确诊断和区分PRRSV的两种基因型对于有效预防和控制PRRS至关重要。非结构蛋白10(Nsp10)在病毒复制中起着至关重要的作用,并且是PRRSV最保守的蛋白之一,因此构成PRRSV诊断的良好候选者。结果在本研究中,我们通过用大肠杆菌系统表达的纯化重组Nsp10免疫BALB / c小鼠,从而产生了针对Nsp10的单克隆抗体(mAb)4D9。通过使用一组带有GFP标签的真核表达多肽对mAb 4D9进行精细表位作图,我们确定了基序 286 AIQPDYRDKL 295 是线性B细胞的最小单位被mAb 4D9识别的抗原决定簇。蛋白质序列比对表明, 286 AIQPDYRDKL 295 在基因型2 PRRSV菌株中高度保守,而基因型1 PRRSV菌株在该基序中具有可变氨基酸。此外,带有两个基因型1 PRRSV的恒定氨基酸Cys290和Glu293的基序突变体无法与mAb 4D9反应。更重要的是,使用Western印迹和免疫荧光分析,mAb 4D9可以将基因型2 PRRSV菌株与基因型1 PRRSV菌株区分开。结论我们的发现表明,本研究中产生的Nsp10特异性mAb可能是基础研究的有用工具,并且可能有助于建立区分基因型1和基因型2 PRRSV感染的诊断方法。

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