期刊文献+

阴道毛滴虫致病株可溶性抗原的电泳分析 被引量:5

ELECTROPHORETIC ANALYSIS OF SOLUBLE ANTIGENS OF A PATHOGENIC ISOLATE OF TRICHOMONAS VAGINALIS *
下载PDF
导出
摘要 目的:研究阴道毛滴虫一致病分离株的全虫可溶性抗原。方法:应用SDS-PAGE、激光光密度扫描、免疫印迹法等,对阴道毛滴虫一致病虫株的全虫可溶性抗原进行分析。结果:SDS-PAGE分离出14条蛋白带,在所分离的可溶性抗原中,分子量≤72kDa的占89.5%,分子量为48-51kDa的占19.2%,>100kDa的占7.4%,最低分子量为13kDa。免疫印迹试验显示免疫反应具有广泛性分子量范围,但在86kDa附近未显示出免疫反应。结论:在阴道毛滴虫一致病虫株全虫可溶性抗原中,分子量为48kDa蛋白质具有较高的蛋白含量和较强的免疫学反应。 AIM: To analyze the parasite soluble antigens of a pathogenic isolate of Trichomonas vaginalis. METHODS: The soluble antigens of a pathogenic isolate of T.vaginalis isolated from a patient suffered from trichomonad vaginitis was studied by means of SDS PAGE followed by densitometric analysis and immunoblotting. RESULTS: A total of 14 distinct protein bands was demonstrated using a 10% resolution gel concentration. Densitometrogram indicated that the soluble antigens with MWs of equal to and below 72 kDa accounted for 89 5% of the total volume with the dominant fractions of 48-51 kDa which accounted for 19 2%. Having MWs over 100 kDa accounted only for 7 4%, while the lowest M.W.fraction demonstrated was found to be at the site of 13 kDa. By immunoblotting, the specific anti T.vaginalis antibodies raised in mice recognized a broad spectrum of molecular size range of these antigenic fraction. However, no immunological reaction was seen at the 86 kDa site. CONCLUSION: The proteins of MWs 48-51 kDa possess a larger protein content and a higher immunological reactivity.
机构地区 扬州大学医学院
出处 《中国寄生虫学与寄生虫病杂志》 CAS CSCD 北大核心 1998年第4期296-299,共4页 Chinese Journal of Parasitology and Parasitic Diseases
基金 江苏省教委自然科学基金
关键词 阴道毛滴虫 抗原 电泳 Trichomonas vaginalis, antigen, SDS PAGE
  • 相关文献

参考文献2

  • 1诸葛健,工业微生物实验技术手册,1994年
  • 2张跃,中国寄生虫病防治杂志,1993年,6卷,65页

同被引文献22

  • 1郭步平,李宇飞.不同pH肝浸汤培养基培养阴道毛滴虫的观察[J].中国病原生物学杂志,2006,1(1):20-21. 被引量:6
  • 2闫艳,高兴政.白头翁体外抗阴道毛滴虫透射电镜观察[J].中国病原生物学杂志,2006,1(1):22-23. 被引量:20
  • 3van Der Schee C, van Belkum A, Zwijgers L, et al. Improved diagnosis of Trichomonas Vaginalis infection by PCR using vaginalswabs and urine specimens compared to diagnosis by wet mount microscopy, culture, and fluorescent staining [J]. J Clin MICrobiol, 1999,37(12):4127-4130.
  • 4Viikki M, Pukkala E, Nieminen P, et al. Gynaecological infections as risk determinants of subsequent cervical neoplasia[J]. Acta Oncologica,2000,39(1)-71-75.
  • 5Heine P, McGregor JA. Trichomonas vaginalis: a reemerging pathogen[J]. Clinical Obstetrics and Gynecology,1993, 36(1):137-144.
  • 6Petrin D, Delgaty K, Bhatt R, et al. Clinical and microbiological aspects of Trichomonas vaginalis[J]. Clinical Microbiology Reviews,1998,11(2):300-317.
  • 7Garcia AF, Chang TH, Benchimol M, et al. Iron and contact with host cells induce expression of adhesins on surface of Trichomonas vaginalis[J]. Mol Microbiol,2003 47(5): 1207- 1224.
  • 8Jose Batista De Jesus JB, Patricia Cuervo P, Magno Junqueira M, et al. Application of two- dimensional electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for proteomic analysis of the sexually ransmitted parasite Trichomonas vaginalis[J]. J Mass Soectrom,2007, 42(11 ): 1463-1473.
  • 9Kruger NJ. The Bradford method for Protein quantitation [J]. Methods Mol Bio1,1994,32(1):9-15.
  • 10Gorg A, Weiss W, Dunn MJ. Current two-dimensional electrophoresis technology for proteomics[J]. Proteomics,2004, 4 (12):3665-3685.

引证文献5

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部