中国农业科学 ›› 2012, Vol. 45 ›› Issue (22): 4713-4719.doi: 10.3864/j.issn.0578-1752.2012.22.018

• 兽医 • 上一篇    下一篇

细粒棘球绦虫成虫表膜糖抗原的免疫性分析

 古努尔•吐尔逊, 米晓云, 张壮志, 石保新, 吐尔洪•依米提, 金映红, 张妹, 程小波, 张旭, 赵莉, 张文宝   

  1. 1.新疆畜牧科学院兽医研究所,乌鲁木齐 830000
    2.新疆农业大学,乌鲁木齐 830052
  • 收稿日期:2012-06-26 出版日期:2012-11-15 发布日期:2012-10-18
  • 通讯作者: 古努尔?吐尔逊,Tel:0991-4844713;E-mail:gulnural@126.com。米晓云与古努尔?吐尔逊为同等贡献作者。Tel:0991-4844713;E-mail:mixiaoyun1220@163.com
  • 作者简介:古努尔?吐尔逊,Tel:0991-4844713;E-mail:gulnural@126.com。米晓云与古努尔?吐尔逊为同等贡献作者。Tel:0991-4844713;E-mail:mixiaoyun1220@163.com
  • 基金资助:

    新疆少数民族科技人才特殊培养计划科研项目(201023108)

Analysis of Immunological Characteristics of Echinococcus Granulosus Adult Worm Surface Membrane -Associated Glycoantigen

 GU  Nu-尔•Tu-尔Xun, MI  Xiao-Yun, ZHANG  Zhuang-Zhi, SHI  Bao-Xin, TU  尔Hong-•Yi-Mi-Ti, JIN  Ying-Hong, ZHANG  Mei, CHENG  Xiao-Bo, ZHANG  Xu, ZHAO  Li, ZHANG  Wen-Bao   

  1. 1.Veterinary Research Institute of Animal Science Academy of Xinjiang Uygur Autonomous Region,Urumqi 830000
    2.Xinjiang Agricultural University, Urumqi 830052
  • Received:2012-06-26 Online:2012-11-15 Published:2012-10-18

摘要: 【目的】探索细粒棘球绦虫成虫表膜糖抗原的免疫性。【方法】细粒棘球绦虫成虫虫体冻融产物,经蛋白酶K消化,离心上清作为粗提表膜糖抗原,SDS-PAGE鉴定糖抗原成分,硫酸-蒽酮法测定多糖浓度,ELISA、Western- blot 和IFA法分别检测免疫小鼠抗血清抗体效价和特异性以及确定抗原在虫体组织中的位置。【结果】SDS-PAGE图谱显示无蛋白条带出现,表明成虫膜蛋白被蛋白酶K完全降解;制备的糖抗原浓度为2.54mg•mL-1,初步确定为糖抗原。ELISA结果显示,随着免疫次数增加,抗血清中特异性抗体(IgG 、IgM 和IgA)效价也随之升高。与阴性血清相比,IgG 、IgM 和IgA的P/N值分别为4.9、3.2和6.4。未检测到特异性IgE。Wenstern-blot检测结果显示,抗血清与原头蚴粗提虫体蛋白、细粒棘球绦虫成虫表膜蛋白、表膜糖抗原有效识别。IFA显色结果显示糖抗原在细粒棘球绦虫虫体表膜中有表达。【结论】经蛋白酶K消化后提取的细粒棘球绦虫表膜糖抗原具有良好的的免疫原性和免疫反应性,有望用于包虫病的诊断和免疫。

关键词: 细粒棘球绦虫 , 表膜糖抗原 , 抗血清

Abstract: 【Objective】 The immunological characteristics of the carbohydrate antigen (glycoprotein) of E. granulosus adult surface membrane were explored in this study . 【Method】 The freez-thaw E. granulosus adult worm lysis was digested by protease K, and centrifuged to collect supernatant as crude glycoantigen materials, which was identified by SDS-PAGE, quantified by sulfuric acid anthrone method. Then, the Balb/c mice were injected hypodermically by the material six times for anti-serum, which was collected to measure immunoglobulin (IgG, IgM and IgA) by ELISA, and to determine the specificity by western- blot method. To localize the site of the antigen composition in the E. granulosus adult worm by IFA. 【Result】 The SDS-PAGE showed that there was no visible band on the gel. This suggested that the proteins of the parasite surface membrane were degraded completely. The concentration of glycoantige was 2.54mg•mL-1 in the preparation. ELISA showed that the specific antibodies (IgG, IgM, and IgA) were rised gradually with the increase of the immunization times, and the positive/negative ration (P/N) of IgG, IgM and IgA equals to 4.9, 3.2 and 6.4, respectively. Comparatively, the specific IgE was not detected. Western blotting showed that the E. granulosus adult worm surface membrane glycoantigen and native proteins could be recognized by the anti-serum. IFA proved that the glycoantigen was located on the surface membrane of E. granulosus adult worm. 【Conclusion】 The glycoantigen of E. granulosus adult worms digested proteinase K has good immunogenicity and reactivity, and could be used to develop vaccine candidates and diagnosis material.

Key words: Echinococcus granulosus , surface membrane glycoantigen , antiserum