中国畜牧兽医 ›› 2019, Vol. 46 ›› Issue (11): 3387-3395.doi: 10.16431/j.cnki.1671-7236.2019.11.029

• 预防兽医 • 上一篇    下一篇

绵羊肺炎支原体pcDNA3.1-TBP30-Hsp70融合表达质粒的构建及对小鼠细胞免疫应答的影响

周怡1,2, 王柏林1,2, 杨美1,2, 何玲1,2, 覃岚1,2, 岳筠3, 张双翔3, 周碧君1,2, 王开功1,2, 程振涛1,2   

  1. 1. 贵州大学动物科学学院, 贵阳 550025;
    2. 贵州省动物疫病与兽医公共卫生重点实验室, 贵阳 550025;
    3. 贵州省动物疫病预防控制中心, 贵阳 550025
  • 收稿日期:2019-05-20 出版日期:2019-11-20 发布日期:2019-11-25
  • 通讯作者: 程振涛 E-mail:chengzhentao@sohu.com
  • 作者简介:周怡(1995-),女,贵州石阡人,硕士生,研究方向:预防兽医学,E-mail:1207234706@qq.com
  • 基金资助:
    国家自然科学基金项目(31660723);贵州省科技计划项目(黔科合基础[2019]1181号);贵州省研究生教育创新计划项目(GZZ2017002)

Construction of Mycoplasma ovipneumoniae pcDNA3.1-TBP30-Hsp70 Fusion Plasmid and Its Effect on Cellular Immune Response in Mice

ZHOU Yi1,2, WANG Bolin1,2, YANG Mei1,2, HE Ling1,2, QIN Lan1,2, YUE Jun3, ZHANG Shuangxiang3, ZHOU Bijun1,2, WANG Kaigong1,2, CHENG Zhentao1,2   

  1. 1. College of Animal Science, Guizhou University, Guiyang 550025, China;
    2. Key Laboratory of Animal Health and Veterinary Public Health, Guizhou Province, Guiyang 550025, China;
    3. Guizhou Provincial Animal Disease Prevention and Control Center, Guiyang 550025, China
  • Received:2019-05-20 Online:2019-11-20 Published:2019-11-25

摘要: 为探究绵羊肺炎支原体(Mycoplasma ovipneumoniae,Mo)pcDNA3.1-TBP30-Hsp70融合表达质粒对小鼠细胞免疫应答影响,本试验构建了绵羊肺炎支原体pcDNA3.1-TBP30-Hsp70融合表达质粒。用已构建的pMD19T-P30和pMD19-Hsp70质粒为模板,采用基因定点突变(SDM)原理设计引物,应用SOE-PCR扩增目的基因片段,并将其定向克隆至表达载体pcDNA3.1(+),构建重组质粒pcDNA 3.1(+)-TBP30和融合重组质pcDNA3.1(+)-TBP30-Hsp70。使用pcDNA3.1-TBP30、pcDNA3.1-TBP30-Hsp70、pcDNA3.1(+)和Elution Buffer对小鼠进行免疫,应用ELISA试剂盒检测小鼠血清中细胞因子白细胞介素-2(IL-2)、IL-4、干扰素-γ(INF-γ)分泌水平。结果显示,pcDNA3.1-TBP30-Hsp70酶切后可见大小分别约为1 413 bp的目的基因片段和5 400 bp的载体条带。与空白对照组和pcDNA3.1(+)组相比,免疫重组质粒组均可引起小鼠血清中细胞因子INF-γ、IL-2和IL-4分泌水平的增强,与空白对照组和pcDNA3.1(+)组相比差异显著或极显著(P<0.05;P<0.01);而空白对照组和空质粒组之间差异不显著(P>0.05);免疫pcDNA3.1-TBP30和pcDNA3.1-TBP30-Hsp70组小鼠血清IL-2、INF-γ和IL-4终分泌量增加,表明重组质粒组可刺激小鼠血清中IL-2、INF-γ和IL-4的变化,并且在时间上都呈现出先增多后减少的规律。本试验结果表明,重组质粒pcDNA3.1(+)-TBP30-Hsp70免疫小鼠后,IL-2和INF-γ分泌水平的升高,增强了机体的细胞免疫功能,进而调节机体细胞免疫影响T细胞和巨噬细胞的分泌,从而提高机体细胞免疫能力;IL-4分泌水平升高,促进机体Th2向Th1分化,维持Th1的优势状态,增强了机体的细胞免疫功能。本试验结果为绵羊肺炎支原体基因工程疫苗的研制提供了参考依据。

关键词: 绵羊肺炎支原体; SOE-PCR; 融合质粒; 细胞因子

Abstract: To investigate the effect of the fusion expression plasmid of Mycoplasma ovipneumoniae (Mo) pcDNA3.1-TBP30-Hsp70 on the cellular immune response in mice,a fusion expression plasmid of Mycoplasma ovipneumoniae pcDNA3.1-TBP30-Hsp70 was constructed.Using the constructed plasmids pMD19T-P30 and pMD19-Hsp70 as templates,primers were designed based on the principle of gene site-directed mutagenesis (SDM).The target gene fragments were amplified by SOE-PCR and directionally cloned into the expression vector pcDNA3.1(+) to construct pcDNA3.1(+)-TBP30 and the fusion plasmid pcDNA3.1(+)-TBP30-Hsp70.Mice were immunized with pcDNA3.1-TBP30,pcDNA3.1-TBP30-Hsp70,pcDNA3.1(+) and Elution Buffer.Serum levels of cytokines interleukin-2 (IL-2),IL-4 and interferon-γ (INF-γ) were detected by ELISA kit.The results showed that after digestion of pcDNA3.1-TBP30-Hsp70,the target gene fragments with the size of 1 413 bp and the vector bands with the size of 5 400 bp were visible.Compared with the blank control and the pcDNA3.1(+) groups,the immune recombinant plasmid groups could increase the secretion levels of cytokines INF-γ,IL-2 and IL-4 in the serum of mice.Compared with the blank control and the pcDNA3.1(+) groups,the difference was significant or extremely significant (P<0.05;P<0.01),but there was no significant difference between the blank control and blank plasmid groups (P>0.05).The final secretion of IL-2,INF-γ and IL-4 in serum of mice immunized with pcDNA3.1-TBP30 and pcDNA3.1-TBP30-Hsp70 increased,which indicated that the recombinant plasmids could stimulate the changes of IL-2,INF-γ and IL-4 in serum of mice,and showed the regularity of increasing and decreasing in time.The results showed that after immunizing mice with recombinant plasmid pcDNA3.1(+)-TBP30-Hsp70,the secretion levels of IL-2 and INF-γ increased,which enhanced the cellular immune function of the organism,and then regulated the cellular immunity of the organism to affect the secretion of T cells and macrophages,thereby improving the cellular immunity of the organism.Th2 differentiated into Th1,maintains the dominant state of Th1 and enhanced the cellular immune function of the body.The results provided a reference for the development of genetic engineering vaccine against Mycoplasma ovipneumoniae.

Key words: Mycoplasma ovipneumoniae; SOE-PCR; fusion plasmid; cytokine

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