Li Hong, Ning Zhangyong, Hao Wenbo, Zhang Shimeng, Liao Xiaoqing, Li Ming, Luo Shuhong
Institute of Antibody Engineering, School of Biotechnology, Southern Medical University, 1838 N. Guangzhou Avenue, Guangzhou, 510515, Guangdong, People's Republic of China.
Virus Genes. 2012 Jun;44(3):429-40. doi: 10.1007/s11262-011-0710-9. Epub 2012 Jan 12.
Recent outbreaks of orf in China have been attributed to a novel strain of Orf virus (ORFV) designated ORFV-Jilin. Currently, monoclonal antibodies (Mabs) have not yet been developed against this specific pathogen even though such entities could have potential applications regarding the diagnosis and characterization of ORFV-Jilin. Therefore, the current study was undertaken to generate Mab against the immunodominant ORFV059 protein of this virus. For this purpose, the ORFV-Jilin ORFV059 protein was expressed in Escherichia coli and subsequently used as an antigen to immunize mice and for the initial screening of hybridomas prepared from the mice for their ability to produce anti-ORFV059 protein Mabs via an indirect ELISA. Ten, positive hybridomas were identified in this manner and verified based on the ability of their released Mab to react specifically with both naturally and artificially expressed ORFV059 protein in Western blots. The two hybridomas with the greatest propensity to secrete Mab were subcloned three times before being introduced intraperitoneally into mice. Afterwards, both Mab were separately purified from the mice's ascetic fluids and found to successfully recognize the ORFV-Jilin ORFV059 protein in a variety of immunological assays. Thus, the widespread utility of these Mab as a diagnostic core reagent should prove invaluable for further investigations regarding the mechanisms of orf pathogenesis and the control of this disease. In this regard, it should be noted that Mab A3 was used to confirm the predicted late expression of the ORFV-Jilin ORFV059 protein during virus replication.
中国近期的羊口疮疫情归因于一种名为ORFV-吉林的新型羊口疮病毒(ORFV)毒株。目前,针对这种特定病原体的单克隆抗体(Mab)尚未研发出来,尽管这类抗体在ORFV-吉林的诊断和特性鉴定方面可能具有潜在应用价值。因此,本研究旨在制备针对该病毒免疫显性ORFV059蛋白的单克隆抗体。为此,将ORFV-吉林的ORFV059蛋白在大肠杆菌中表达,随后用作抗原免疫小鼠,并通过间接酶联免疫吸附测定法(ELISA)对从小鼠制备的杂交瘤进行初步筛选,以检测其产生抗ORFV059蛋白单克隆抗体的能力。通过这种方式鉴定出10个阳性杂交瘤,并根据其分泌的单克隆抗体在蛋白质免疫印迹法中与天然和人工表达的ORFV059蛋白特异性反应的能力进行验证。将分泌单克隆抗体倾向最大的两个杂交瘤进行三次亚克隆,然后腹腔注射到小鼠体内。之后,分别从小鼠腹水液中纯化出两种单克隆抗体,发现在各种免疫测定中均能成功识别ORFV-吉林的ORFV059蛋白。因此,这些单克隆抗体作为诊断核心试剂的广泛应用,对于进一步研究羊口疮发病机制和控制这种疾病应具有不可估量的价值。在这方面,应该注意到,单克隆抗体A3被用于证实ORFV-吉林的ORFV059蛋白在病毒复制过程中预测的晚期表达。