Xiao Bin, Hao Wenbo, Du Zhenglun, Liao Xiaoqing, Luo Shuhong
Bing Du Xue Bao. 2016 May;32(3):292-7.
This study was designed to prepare a monoclonal antibody against Orf virus 118 protein and explore the biological properties of ORFV118 using this antibody. We constructed a recombinant plasmid pET33b-ORFV118 that contained a full-length ORFV118 gene. The plasmid was transformed into E.coli BL21,and the expression of ORFV118 was induced by isopropyl-β-d-thiogalactoside (IPTG).Prokaryotic ORFV118 was purified via Ni-NTA affinity chromatography and was subsequently used as an antigen to immunize mice. An anti-ORFV118 antibody was prepared using hybridoma technology. The titer and specificity of this antibody were tested by an indirect ELISA and Western blot/immunohistochemistry, respectively. We successfully obtained three antibody-secreting hybridomas,1A2,3B5,and 5D10.The titers of the three hybridomas were 1:10000,1:6400,and 1:8000.The monoclonal antibody (mAb),1A2 and the highest titer was selected for further research. The mAb 1A2,an IgG1 type antibody was bonded to its immunizing antigen, both the eukaryotic and natural ORFV118 with high specificity. The immunohistochemical analysis showed that the focal specific staining was restricted to the epidermal layer and subcutaneous tissue, which conformed to the characteristics of an ORFV infection. The mAb 1A2 recognized ORFV118with high specificity. Further study of mAb 1A2 will facilitate our understanding of ORFV118 and provide potentially novel methods for the diagnosis, prevention, and treatment of Orf.
本研究旨在制备抗口疮病毒118蛋白的单克隆抗体,并利用该抗体探索口疮病毒ORFV118的生物学特性。我们构建了一个包含全长ORFV118基因的重组质粒pET33b-ORFV118。将该质粒转化到大肠杆菌BL21中,并用异丙基-β-D-硫代半乳糖苷(IPTG)诱导ORFV118的表达。通过镍-亚氨基二乙酸(Ni-NTA)亲和层析纯化原核ORFV118,随后将其用作抗原免疫小鼠。利用杂交瘤技术制备了抗ORFV118抗体。分别通过间接酶联免疫吸附测定(ELISA)和蛋白质免疫印迹法/免疫组织化学法检测该抗体的效价和特异性。我们成功获得了三个分泌抗体的杂交瘤细胞株,1A2、3B5和5D10。这三个杂交瘤细胞株的效价分别为1:10000、1:6400和1:8000。选择单克隆抗体(mAb)1A2及其最高效价进行进一步研究。单克隆抗体1A2是一种IgG1型抗体,与免疫抗原、真核和天然ORFV118具有高度特异性结合。免疫组织化学分析表明,局部特异性染色仅限于表皮层和皮下组织,这与口疮病毒感染的特征相符。单克隆抗体1A2对ORFV118具有高度特异性识别。对单克隆抗体1A2的进一步研究将有助于我们了解ORFV118,并为口疮的诊断、预防和治疗提供潜在的新方法。