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日本血吸虫凋亡诱导因子SjAIF功能区片段的克隆及表达分析
引用本文:陆看,韩宏晓,洪炀,马茜茜,刘艳涛,韩倩,马帅,傅志强,林矫矫.日本血吸虫凋亡诱导因子SjAIF功能区片段的克隆及表达分析[J].中国人兽共患病杂志,2015,31(2):102-108.
作者姓名:陆看  韩宏晓  洪炀  马茜茜  刘艳涛  韩倩  马帅  傅志强  林矫矫
作者单位:1.上海师范大学生命与环境科学学院,上海 200234;2.中国农业科学院上海兽医研究所,农业部动物寄生虫学重点开放实验室,上海 200241;3.江苏省动物重要疫病与人兽共患病防控协同创新中心,扬州 225009
基金项目:国家自然科学基金(No.81271871)资助
摘    要:目的 克隆表达日本血吸虫凋亡诱导因子(SjAIF)功能区片段,并对其生物学特性进行初步分析。方法 应用PCR技术扩增日本血吸虫凋亡诱导因子的功能区片段,构建原核重组表达质粒并诱导其表达,实时定量PCR分析其在不同发育时期童虫和成虫的转录水平,通过Western-blot和间接ELISA法分析重组蛋白的抗原性和免疫原性,应用免疫组化分析该蛋白在虫体内的分布情况。结果 克隆了SjAIF功能区片段,大小为831 bp。成功构建了原核重组表达质粒pET-28a(+)-SjAIF,并在大肠杆菌中获得表达,重组蛋白分子量35 kD。实时定量PCR分析表明SjAIF基因在童虫和成虫的各个发育阶段均有转录,其中7 d~21 d虫体表达量较低,42 d和28 d虫体表达量较高,雌虫表达量高于雄虫。重组蛋白具有较好的抗原性和免疫原性,免疫小鼠后诱导产生了较高水平的特异性IgG抗体。该蛋白主要存在于日本血吸虫体被,少部分分布于实质组织中。结论 成功表达了SjAIF基因的功能区片段,对其生物学特性进行了初步分析,为进一步研究该基因生物学功能和作用提供了基础。

关 键 词:日本血吸虫  细胞凋亡  凋亡诱导因子  
收稿时间:2014-10-08

Cloning and expression analysis of a functional fragment of apoptosis-inducing factor (AIF) gene in Schistosoma japonicum
LU Kan,HAN Hong-xiao,HONG Yang,MA Qian-qian,LIU Yan-tao,HAN Qian,MA Shuai,FU Zhi-qiang,LIN Jiao-jiao.Cloning and expression analysis of a functional fragment of apoptosis-inducing factor (AIF) gene in Schistosoma japonicum[J].Chinese Journal of Zoonoses,2015,31(2):102-108.
Authors:LU Kan  HAN Hong-xiao  HONG Yang  MA Qian-qian  LIU Yan-tao  HAN Qian  MA Shuai  FU Zhi-qiang  LIN Jiao-jiao
Institution:1.College of Life and Environmental Sciences, Shanghai Normal University, Shanghai 200234, China;2.Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Science / Key Laboratory of Animal Parasitology, Ministry of Agriculture, Shanghai 200241, China;3.Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou 225009, China
Abstract:We cloned and expressed a functional fragment of apoptosis-inducing factor (AIF) gene in Schistosoma japonicum and further analyzed its biological characteristics. PCR technique was employed to amplify the functional fragment of SjAIF by employing a cDNA of 14 d (day) schistosomula as template. The fragment of AIF was subcloned into a pET28a(+) vector and the recombinant plasmid was transformed into competent E.coil/BL21 for producing recombinant protein. The expression level of SjAIF was determined at several different development stages of schistosomula and adult worms by using real-time RT-PCR. The recombinant protein was purified and then its antigenicity was accessed by Western blotting and ELISA. The distribution of the protein in Schistosoma japonicum was analyzed by immunolocalization. Real-time PCR analysis revealed that the expression of SjAIF was lower in 7 d, 14 d and 21 d than that in other stages. Western-blotting showed that the recombinant had good immunogenicity. The vaccinated group showed a good ability to induce IgG as examined by ELISA. Immunolocalization analysis revealed that the SjAIF was mainly distributed in tegument and parenchyma. The fragment of SjAIF was obtained and its molecular characterizations were preliminarily investigated. This study provided an important basis for further investigation of the biological characteristics and mechanism of the protein in Schistosoma japonicum
Keywords:Schistosoma japonicum  apoptosis  apoptosis-inducing factor
Supported by the National Natural Science Foundation of People’s Republic of China (No
  81271871)  
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