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作 者:陈静[1] 杨盼盼[1] 雷喜梅[1] 王晓梦[1] 高冬生[1] 常洪涛[1] 杨霞[1] 陈陆[1] 赵军[1] 王川庆[1]
机构地区:[1]河南农业大学禽病研究所,河南郑州450002
出 处:《中国兽医学报》2015年第10期1573-1577,共5页Chinese Journal of Veterinary Science
基 金:河南省高校科技创新团队支持计划资助项目(14IRTSTHN015);河南省郑州市重点科技攻关计划资助项目(121PZDGG314)
摘 要:为分析PEDV流行株和疫苗株S基因差异对疫苗免疫效果影响,分别在大肠杆菌中表达PEDV流行株CH/ZMDZY/11与疫苗株CV777S蛋白差异较大的N端(22~380aa)区域(SA),将纯化的SA蛋白免疫小鼠获得多克隆抗体,并以SA蛋白为抗原,通过Western Blot及间接ELISA的方法检测2种蛋白与多克隆抗体的反应性差异。结果表明,抗PEDV疫苗株SA蛋白(YSA)多抗与疫苗株SA蛋白的反应性明显高于与流行株SA蛋白(LSA)的反应性;与此相反,抗PEDV流行株SA蛋白多抗与流行株SA蛋白的反应性明显高于与疫苗株SA蛋白的反应性。研究结果提示,PEDV S蛋白22~380aa区域存在差异性抗原表位,PEDV流行株和疫苗株S基因的差异可能是导致基于CV777疫苗株的PED疫苗免疫效果不好的原因。本研究将为开发PEDV流行株亚单位疫苗用于预防临床PEDV流行株的感染提供理论依据。In order to analyze the effects of genetic differences of spike gene of porcine epidemic diarrhea virus(PEDV)on the efficacy of its vaccines,the spike gene N-terminal(22~380aa)domain of PEDV epidemic strain CH/ZMDZY/11 and CV777vaccine strain,which was designated as LSA and YSA,was expressed in E.coli respectively.Purified spike proteins were used to immunize Kunming mice to prepare anti-spike polyclonal antibodies.Cross-immunoreactivity between antiLSA and anti-YLA antibody was verified by ELISA and Western blot.In ELISA,anti-LSA antibody showed significant higher immunoreactivity with LSA than that of YSA,and anti-YSA antibody showed significant higher immunoreactivity with YSA than that of LSA.In Western blot,anti-LSA antibody couldnt recognize YSA and anti-YSA antibody couldnt recognize LSA.The results suggested that there were different epitopes in 22~380aa region of PEDV S protein.The less efficacy of CV777-based vaccine against epidemic PEDV strain could be due to these different epitopes.This study will provide a theoretical base for developing subunit vaccine for PED prevention.
关 键 词:PEDV流行株 CV777疫苗株 S蛋白 免疫反应性 ELISA
分 类 号:S852.65[农业科学—基础兽医学]
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