华西口腔医学杂志

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牙龈卟啉单胞菌FimA蛋白和IL-15真核共表达质粒的构建与鉴定

郭红梅1,杨丕山1,姜广水1,王喜军2   

  1. 山东大学口腔医院牙周科,山东大学口腔医院牙周科,山东大学口腔医院牙周科,口腔生物医学工程教育部重点实验室四川大学山东济南250012,山东济南250012,山东济南250012,四川成都610041
  • 收稿日期:2006-06-25 修回日期:2006-06-25 出版日期:2006-06-20 发布日期:2006-06-20
  • 通讯作者: 杨丕山,Tel:0531-88382368
  • 作者简介:郭红梅(1978-),女,山东人,博士研究生
  • 基金资助:

    国家自然科学基金资助项目(30371323);山东省自然科学基金资助项目(21350005200337)

Construction of Eukaryotic Co-expression Plasmid Harboring Genes Encoding Porphyromonas gingivalis Fim A and Human IL-15

 GUO Hong-mei1, YANG Pi-shan1, JIANG Guang-shui1, WANG Xi-jun2   

  1. 1. Dept. of  Periodontology, Stomatology Hospital of Shandong University, Jinan 250012, China; 2. Key. Laboratory of Oral Biomedical Engineering Ministry of Education, Sichuan University, Chengdu 610041, China
  • Received:2006-06-25 Revised:2006-06-25 Online:2006-06-20 Published:2006-06-20

摘要:

目的  构建含编码牙龈卟啉单胞菌FimA蛋白和IL-15基因的真核共表达质粒,并检测其在哺乳动物细胞中的表达。方法  应用基因重组技术,构建真核表达载体pIRES-fimA和真核共表达载体pIRES-fimA:IL15,通过酶切、PCR及DNA序列测定鉴定获得的质粒,用Lipofectamine 2000介导转染CHO细胞,用Western blot检测重组质粒在哺乳动物中的表达,酶联免疫吸附试验检测培养上清中的蛋白表达。结果  PCR扩增获得的fimA和IL-15目的基因与预计相同,定向插入真核表达质粒pIRES中,插入位相正确,未改变阅读框架。转染的CHO细胞能够检测到目的基因的表达,在培养上清中也可以检测到蛋白质的表达。结论  本实验成功构建了牙龈卟啉单胞菌FimA蛋白和IL-15的真核共表达质粒pIRES-fimA:IL15,为研制增强免疫应答的抗牙龈卟啉单胞菌DNA疫苗奠定了基础。

关键词: 牙龈卟啉单胞菌, 菌毛蛋白A, DNA疫苗, 转染

Abstract:

Objective  To construct a eukaryotic co-expression plasmid pIRES-fimA:IL15, which can be used as an immunoreaction-enhancing DNA vaccine against Porphyromonas gingivalis FimA, and investigate its expression in mammalian cells.  Methods  The eukaryotic co-expression plasmid pIRES-fimA:IL15 was constructed by molecular cloning methods and characterized by restricted endonuclease mapping, PCR and DNA sequencing. The plasmid was transfected into mammalian cell CHO using Lipofectamine 2000. Expression of fimA gene was detected by Western blot and the protein secretion in cultural medium was analyzed by ELISA. Results  Endonuclease mapping showed that the target genes fimA and IL-15 obtained by PCR had the same molecular size as predicted. The DNA sequencing data also indicated that inserted fimA gene and IL-15 gene had correct DNA sequence and orientation. The recombined plasmid could express FimA in mammalian cell CHO transfected. FimA and IL-15 could be secreted into cultural supernatant detected by ELISA.  Conclusion  A new eukaryotic co-expression plasmid pIRES-fimA:IL15 was constructed and it could be applied for further immunization in animal as an effective anti-Porphyromonas gingivalis vaccine.

Key words: Porphyromonas gingivalis, fimA, DNA vaccine, transfection