Division of Swine Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of the Chinese Academy of Agricultural Sciences, Harbin, PR China.
Intervirology. 2011;54(3):156-63. doi: 10.1159/000319838. Epub 2010 Nov 5.
Porcine circovirus type 2 (PCV2) is the causative agent of postweaning multisystemic syndrome in pigs. The capsid (Cap) protein encoded by ORF2 is the main structural protein involved in the host immune protective response to PCV2. It is therefore important to map the antigenic epitopes of the PCV2 Cap protein.
In this study, 5 monoclonal antibodies (mAbs) against the recombinant PCV2 Cap protein, expressed by the baculovirus system in Sf21 insect cells, were generated. The antigenic epitope recognized by these mAbs was located in the Cap A protein by Western blot analysis using 4 overlapping minifragments covering the Cap protein expressed in Escherichia coli. To locate the epitope more accurately, 3 sets of overlapping peptides were synthesized.
The results demonstrated that 4 of the 5 mAbs recognized the same core epitope ((26)RPWLVHPRHRY(36)) located in the nuclear localization signal (NLS) region at the N terminus of the Cap protein. The other mAb (1D2) reacted with the recombinant Cap protein only, indicating that it recognizes a potential conformational epitope. This mAb demonstrated a neutralizing effect on PCV2.
This is the first study to identify an antigenic epitope in the NLS region of the PCV2 Cap protein using mAbs. The results of this study will facilitate future investigations into the mechanism and function of nuclear localization of this protein.
猪圆环病毒 2 型(PCV2)是引起猪断奶后多系统衰弱综合征的病原体。ORF2 编码的衣壳(Cap)蛋白是宿主对 PCV2 免疫保护反应的主要结构蛋白。因此,绘制 PCV2 Cap 蛋白的抗原表位图谱非常重要。
本研究制备了针对杆状病毒表达系统在 Sf21 昆虫细胞中表达的重组 PCV2 Cap 蛋白的 5 株单克隆抗体(mAb)。通过 Western blot 分析,使用覆盖在大肠杆菌中表达的 Cap 蛋白的 4 个重叠的小片段,定位这些 mAb 识别的抗原表位。为了更准确地定位表位,合成了 3 组重叠肽。
结果表明,5 株 mAb 中的 4 株识别相同的核心表位((26)RPWLVHPRHRY(36)),该表位位于 Cap 蛋白 N 端核定位信号(NLS)区域。另 1 株 mAb(1D2)仅与重组 Cap 蛋白反应,表明它识别潜在的构象表位。该 mAb 对 PCV2 具有中和作用。
这是首次使用 mAb 鉴定 PCV2 Cap 蛋白 NLS 区域的抗原表位。本研究的结果将有助于进一步研究该蛋白的核定位机制和功能。