甲型流感病毒DNA疫苗双表达载体的构建及表达

doi:吉林省科技厅基金资助课题（200505184）

甲型流感病毒DNA疫苗双表达载体的构建及表达

彭丽萍¹,赵大鹏²,戚凤春²,汪春义²,张雪梅²,贾媛²,匡科伟²,陈云波²,宋泽民²，赵晓红³,徐建国¹

(1.吉林大学第一医院呼吸内科，吉林长春 130021；2.长春生物制品研究所,吉林长春 130062；3.吉林省长春市传染病医院，吉林长春 130123）

收稿日期:2007-03-13 修回日期:1900-01-01 出版日期:2008-01-28 发布日期:2008-01-28
通讯作者: 徐建国

Construction and expression of DNA vaccine coexpression vector of influenza A virus

PENG Li-ping¹,ZHAO Da-peng²,QI Feng-chun²,WANG Chun-yi²,ZHANG Xue-mei²,JIA Yuan²,KUANG Ke-wei²,CHEN Yun-bo²,SHONG Ze-min²,ZHAO Xiao-hong³,XU Jian-guo¹

(1.Department of Respiratory Diseases，First Hospital,Jilin University,Changchun 130021,China;2.Changchun Institute of Biological Products,Changchun 130062,China;3.Infectious Disease Hospital of Changchun City,Changchun 130123,China)

Received:2007-03-13 Revised:1900-01-01 Online:2008-01-28 Published:2008-01-28
Contact: XU Jian-guo

摘要/Abstract

摘要： 目的：构建含有甲型流感病毒M2基因与GM-CSF基因的DNA疫苗双表达载体，为研究甲型通用流感疫苗奠定基础。方法：将甲型流感病毒（H1N1）接种鸡胚后收获尿囊液，提取流感病毒总RNA，RT-PCR法扩增M2基因；将微小病毒内部核糖体进入位点（IRES）基因插入到质粒pVAXⅠ多克隆位点，再将M2基因和GM-CSF基因依次克隆到IRES的上、下游多克隆位点，构建出甲型流感病毒双表达载体pMIG，酶切鉴定后测序；脂质体法转染COS7细胞并检测目的蛋白的表达。结果：成功扩增出M2基因（约300 bp）、IRES基因(约580 bp)和GM-CSF基因(约400 bp)，酶切鉴定结果表明构建出甲型流感病毒双表达载体pMIG，Western blotting检测证明流感病毒M2蛋白的表达。结论：成功构建出流感病毒DNA疫苗双表达载体pMIG。

关键词: M2基因, DNA疫苗

Abstract: To construct the DNA vaccine coexpression vector containing M2 gene of influenza A virus and GM-CSF gene,which provides a basis for exploring broad-spectrum vaccine of influenza A virus.Methods Analogous　 strain of influenza A virus（H1N1） was inoculated by chicken and alantoic fluid was collected,the total RNA of influenza A virus was extracted,M2 gene was amplified by RT-PCR.Internal ribosome entry site(IRES) gene of minute virus was inserted into the multiple cloning sites(MCS) of the plasmid pVAXⅠ,then M2 gene and GM-CSF gene were in turns cloned into the MCS of the advanced and backward MCS of IRES for constructing pMIG-the coexpression vector of influenza A virus and sequencing after enzymetomy identification.Then the recombinant plasmid pMIG was transfected into COS7 cell by liposome method and the expression of the target protein was detected. Results M2 gene(300 bp),IRES gene(580 bp) and GM-CSF gene(400 bp) were successfully amplified,the result of enzymetomy identification indicated that the coexpression vector pMIG of influenza A virus was constructed,Western blotting testified that M2 protein of influenza A virus was expressed. Conclusion The coexpression vector pMIG of influenza A virus is successfully constructed.

Key words: M2 gene, DNA vaccine

中图分类号:

R373.1

彭丽萍,赵大鹏,戚凤春,汪春义,张雪梅,贾媛,匡科伟,陈云波,宋泽民，赵晓红,徐建国. 甲型流感病毒DNA疫苗双表达载体的构建及表达[J]. J4, 2008, 34(1): 65-68.

PENG Li-ping,ZHAO Da-peng,QI Feng-chun,WANG Chun-yi,ZHANG Xue-mei,JIA Yuan,KUANG Ke-wei,CHEN Yun-bo,SHONG Ze-min,ZHAO Xiao-hong,XU Jian-guo. Construction and expression of DNA vaccine coexpression vector of influenza A virus[J]. J4, 2008, 34(1): 65-68.

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