Chin J Schisto Control ›› 2017, Vol. 29 ›› Issue (6): 780-783.

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Preliminary research on prokaryotic expression and immune protection of triosephosphate isomerase of Toxoplasma gondii

SHEN Shuang1|2| 3 | YIN Xu-ren4#| SONG Li-jun4| WANG Jie4| KE Xue-dan4| ZHOU Wei4| YU Chuan-xin4*   

  1. 1 Shanghai University of Medicine & Health Sciences Affiliated Sixth People’s Hospital East Campus| Shanghai 201306| China; 2 Shanghai Jiaotong University Affiliated Sixth People’s Hospital| China; 3 Public Health Research Center| Jiangnan University| China;4 Key Laboratory of National Health and Family Planning Commission on Parasitic Disease Control and Prevention| Jiangsu Provincial Key Laboratory on Parasite and Vector Control Technology| Jiangsu Institute of Parasitic Diseases|Wuxi| Jiangsu Province| People’s Republic of China
  • Online:2018-01-02 Published:2018-01-02
  • Contact: YU Chuan?xin

弓形虫磷酸丙糖异构酶原核表达及免疫保护的初步研究

沈双1|2|3|殷旭仁4#|宋丽君4|王玠4|柯雪丹4|周伟4|余传信4*   

  1. 1 上海健康医学院附属第六人民医院东院(上海 201306);2上海交通大学附属第六人民医院;3江南大学公共卫生研究中心;4国家卫生计生委寄生虫病预防与控制技术重点实验室|江苏省寄生虫与媒介控制技术重点实验室|江苏省血吸虫病防治研究所
  • 通讯作者: 余传信
  • 作者简介:沈双|男|助理研究员|硕士。研究方向:免疫诊断与免疫调节
  • 基金资助:
    2017年上海健康医学院师资人才百人库(其他类)项目;无锡市科技局科技创新与产业升级引导资金项目(CSE31N1518);江南大学公共卫生研究中心资助;江苏省公益类科研院所能力提升项目(BM2015024);江苏省“科教强卫工程”项目

Abstract: Objective To study the prokaryotic expression and immune protection of triosephosphate isomerase (TPI) of Toxoplasma gondii in mice. Methods Total RNA was extracted from toxoplasma tachyzoites, and TPI fragment was amplified by PCR and cloned into the prokaryotic expression vector pET?28a (+). The target protein was induced with IPTG and purified by Ni?NTA affinity chromatography. The mice were immunized 4 times by emulsified TPI with adjuvant, and the last time was the strengthen immunization. At the same time, an adjuvant group and a normal group were set as controls. The blood samples were got from the tail vein of the mice, and the serum antibody titres were detected. All the mice were challenged with 400 toxoplasma tachyzoites to observe the survival time. Results The TPI gene was amplified from T. gondii cDNA by PCR. The recombinant vector TPI/pET?28a (+) was usefully constructed, and the TPI protein was expressed and purified. The serum antibody titre could be more than 100 thousand. After infected with toxoplasma tachyzoites, the survival time of the mice in the experimental group was longer than that of the mice in the control groups. Conclusion The TPI protein of T. gondii could trigger the immunoprotection against T. gondii challenge in the mice.

Key words: Toxoplasma gondii; Triosephosphate isomerase; Prokaryotic expression; Immune protection

摘要: 目的 克隆刚地弓形虫磷酸丙糖异构酶(Triosephosphate isomerase,TPI)基因,原核表达和纯化蛋白,研究其对弓形虫感染小鼠的免疫保护作用。方法 抽提弓形虫速殖子总RNA,利用PCR技术扩增刚地弓形虫TPI基因,构建重组原核表达载体TPI/pET?28a(+),转化大肠杆菌BL21,IPTG诱导目的蛋白表达,镍亲和层析法纯化目的蛋白。将与佐剂乳化后的TPI蛋白对小鼠颈背部多点皮内免疫,间隔2周,连续免疫4次,最后一次为加强免疫,同时设置佐剂对照组与正常对照组。尾静脉采血检测小鼠血清抗体效价。以400个弓形虫速殖子/只接种小鼠腹腔,观察记录各组小鼠的生存率。结果 成功扩增到弓形虫TPI基因,构建原核表达载体TPI/pET?28a(+),获得纯化的TPI蛋白,TPI免疫4次后的小鼠血清抗体效价可达1:100 000以上,且生存期显著高于佐剂对照组与正常对照组。结论 弓形虫TPI蛋白对弓形虫感染小鼠具有一定的免疫保护作用,为研究弓形虫疫苗奠定了理论基础。

关键词: 刚地弓形虫;磷酸丙糖异构酶;原核表达;免疫保护

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