State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150069, China.
Department of Animal and Range Sciences, College of Agriculture and Natural Resources, Raya University, Maichew P.O. Box 92, Ethiopia.
Viruses. 2023 Feb 17;15(2):557. doi: 10.3390/v15020557.
African Swine Fever (ASF) is a highly contagious and lethal pig disease and poses a huge threat to the pig industry worldwide. ASF virus (ASFV) encodes more than 150 different proteins, but the biological properties of most viral proteins are still unknown. ASFV CP312R protein has been proven to be one of the most immunogenic proteins during ASFV infection in pigs; however, its specific epitopes have yet to be identified. In this study, we verified the immunogenicity of CP312R protein in the sera from attenuated ASFV-inoculated pigs. We generated seven anti-ASFV CP312R mouse monoclonal antibodies (mAbs) from mice immunized with recombinant CP312R protein (rCP312R). All seven mAbs are the IgG2b-Kappa isotype and specifically interacted with the CP312R protein expressed in various cells that were infected by ASFVs or transfected with plasmid CP312R. The epitope mapping was performed by using these characterized mAbs and the peptide scanning (Pepscan) method followed by Western blot. As a result, two antigenic determinant regions were identified: two of the seven mAbs recognized the KNEQGEEIYP amino acids, and the remaining five mAbs recognized the DEEVIRMNAE amino acids of the CP312R protein. These antigenic determinants of CP312R are conserved in different ASFV strains of seven genotypes. By using the characterized mAb, confocal microscopy observation revealed that the CP312R was mainly localized in the cytoplasm and, to some extent, in nuclei and on the nuclear membrane of infected host cells. In summary, our results benefit our understanding on the antigenic regions of ASFV CP312R and help to develop better serological diagnosis of ASF and vaccine research.
非洲猪瘟(ASF)是一种高度传染性和致命性的猪病,对全球养猪业构成巨大威胁。ASF 病毒(ASFV)编码超过 150 种不同的蛋白质,但大多数病毒蛋白的生物学特性仍不清楚。ASFV CP312R 蛋白已被证明是 ASFV 感染猪体内最具免疫原性的蛋白之一;然而,其特定的表位尚未确定。在本研究中,我们验证了 CP312R 蛋白在弱毒 ASFV 接种猪血清中的免疫原性。我们从用重组 CP312R 蛋白(rCP312R)免疫的小鼠中产生了 7 种抗 ASFV CP312R 单克隆抗体(mAb)。这 7 种 mAb 均为 IgG2b-Kappa 同种型,特异性与感染 ASFVs 或转染 CP312R 质粒的各种细胞中表达的 CP312R 蛋白相互作用。通过使用这些鉴定的 mAb 进行表位作图,并结合肽扫描(Pepscan)方法和 Western blot 进行检测。结果鉴定出两个抗原决定簇区域:这 7 种 mAb 中有两种识别 KNEQGEEIYP 氨基酸,其余 5 种 mAb 识别 CP312R 蛋白的 DEEVIRMNAE 氨基酸。CP312R 的这些抗原决定簇在七种基因型的不同 ASFV 毒株中是保守的。通过使用鉴定的 mAb,共聚焦显微镜观察显示 CP312R 主要定位于细胞质中,在一定程度上也定位于感染宿主细胞的核中和核膜上。总之,我们的研究结果有助于了解 ASFV CP312R 的抗原区域,并有助于开发更好的 ASF 血清学诊断和疫苗研究。