Huang Xueyong, Liu Guohua, Hu Xiaoning, Du Yanhua, Li Xingle, Xu Yuling, Chen Haomin, Xu Bianli
Institute for Infectious Disease Control and Prevention, Henan Provincial Center for Disease Prevention and Control, Zhengzhou 450016, China.
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Zhonghua Yu Fang Yi Xue Za Zhi. 2014 Apr;48(4):324-7.
To clone and express the recombinant capsid protein VP2 of enterovirus type 71 (EV71) and to identify the immune activity of expressed protein in order to build a basis for the investigation work of vaccine and diagnostic antigen.
VP2 gene of EV71 was amplified by PCR, and then was cut by restriction enzyme and inserted into expression vector pMAL-c2X. The positive recombinants were transferred into E.coli TB1, the genetically engineered bacteria including pMAL-c2X-VP2 plasmids were induced by isopropyl thiogalactoside ( IPTG) , and the expression products were analyzed by SDS-PAGE and western blotting method. EV71 IgM antibody detection method by ELISA was set up, and the sensitivity and specificity of this method was assessed; 60 neutralizing antibody positive serum samples from hand foot and mouth disease (HFMD) patients were determined, of which 52 samples were positive and 8 samples were negative; a total of 88 acute phase serum samples of HFMD patients diagnosed in clinical were also detected.
VP2 gene of 762 bp was obtained by PCR, the gene segment inserted into the recombinant vector was identified using restriction enzyme digestion. The recombinant vector could express a specific about 71 500 fusion protein in E.coli by SDS-PAGE. The purified recombinant protein of EV71-VP2 can react with the serum of HFMD patients to produce a specific band by western blotting. The sensitivity and specificity of ELISA was 87% and 83%, respectively. Of the 88 acute phase serum samples from children with HFMD, 48 samples (55%) were positive by the ELISA assay.
VP2 gene of EV71 has been cloned and a prokaryotic high expression system for VP2 gene was successfully constructed in the present study. The recombination EV71-VP2 has well antigenicity, which could be useful for developing diagnose reagent or vaccine of EV71.
克隆并表达肠道病毒71型(EV71)重组衣壳蛋白VP2,鉴定表达蛋白的免疫活性,为疫苗及诊断抗原的研究工作奠定基础。
采用PCR扩增EV71的VP2基因,经限制性内切酶酶切后插入表达载体pMAL-c2X。将阳性重组体转入大肠杆菌TB1,用异丙基硫代半乳糖苷(IPTG)诱导含pMAL-c2X-VP2质粒的基因工程菌,采用SDS-PAGE及western印迹法分析表达产物。建立ELISA法检测EV71 IgM抗体,评估该方法的敏感性和特异性;检测60份手足口病(HFMD)患者中和抗体阳性血清样本,其中52份阳性,8份阴性;同时检测88份临床诊断为HFMD患者的急性期血清样本。
PCR扩增获得762 bp的VP2基因,经限制性内切酶酶切鉴定基因片段已插入重组载体。重组载体在大肠杆菌中经SDS-PAGE可表达约71 500的特异性融合蛋白。纯化的EV71-VP2重组蛋白经western印迹法可与HFMD患者血清反应产生特异性条带。ELISA法的敏感性和特异性分别为87%和83%。88份HFMD患儿急性期血清样本中,ELISA法检测阳性48份(55%)。
本研究成功克隆了EV71的VP2基因,构建了VP2基因的原核高效表达系统。重组EV71-VP2具有良好的抗原性,可用于开发EV71诊断试剂或疫苗。