State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of Chinese Academy of Agricultural Sciences, Harbin, 150069, Heilongjiang, China.
Appl Microbiol Biotechnol. 2019 Mar;103(6):2689-2699. doi: 10.1007/s00253-019-09665-7. Epub 2019 Feb 7.
Porcine reproductive and respiratory syndrome virus (PRRSV) is leading to huge losses in the swine industry worldwide. Its nonstructural protein 2 (Nsp2), with a cysteine protease domain (PL2), is crucial for virus replication and as a trigger to host innate immune regulation. In this study, three monoclonal antibodies (mAbs) to Nsp2, designated 4A12, 4G8, and 8H11, were generated. Subsequently, a sequence of recombinant peptides with partial overlap was utilized to determine the epitopes using these mAbs. We found three novel minimal linear Nsp2 B cell epitopes, ELSDDSNRPV, HLKRYSPPAE, and CGWHCISA, which were identified by the antibodies 4A12, 4G8, and 8H11, respectively. Structure analysis indicates that HLKRYSPPAE and ELSDDSNRPV are located separately in hypervariable region 1 and hypervariable region 2 of Nsp2. Interestingly, CGWHCISA is located in the PL2 region, which is highly conserved in all arteriviruses, particularly at the expected conserved catalytic site at Cys54. Importantly, CGWHCISA is located in the inner region of the expected 3D structure of Nsp2, which reveals that the epitope is cryptic. These findings not only provide valuable insight for vaccine design and hold diagnostic potential for the identified epitopes, but also reveal a protective mechanism against variation under selective pressure in an important epitope.
猪繁殖与呼吸综合征病毒(PRRSV)在全球范围内给养猪业带来了巨大损失。其非结构蛋白 2(Nsp2)具有半胱氨酸蛋白酶结构域(PL2),对病毒复制和作为宿主先天免疫调节的触发因素至关重要。在本研究中,生成了针对 Nsp2 的三种单克隆抗体(mAb),分别命名为 4A12、4G8 和 8H11。随后,利用这些 mAb 用具有部分重叠的重组肽序列来确定表位。我们发现了三个新的 Nsp2 B 细胞线性表位,分别为 ELSDDSNRPV、HLKRYSPPAE 和 CGWHCISA,它们分别被抗体 4A12、4G8 和 8H11 识别。结构分析表明,HLKRYSPPAE 和 ELSDDSNRPV 分别位于 Nsp2 的高变区 1 和高变区 2 中。有趣的是,CGWHCISA 位于 PL2 区域,该区域在所有动脉炎病毒中高度保守,尤其是在预期的保守催化位点 Cys54 处。重要的是,CGWHCISA 位于 Nsp2 预期 3D 结构的内部区域,这表明该表位是隐蔽的。这些发现不仅为疫苗设计提供了有价值的见解,并为鉴定的表位提供了诊断潜力,而且还揭示了在重要表位下针对选择压力的变异的保护机制。