Zhang Houshuang, Compaore Muller K A, Lee Eung-goo, Liao Min, Zhang Guohong, Sugimoto Chihiro, Fujisaki Kozo, Nishikawa Yoshifumi, Xuan Xuenan
National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido 080-8555, Japan.
Mol Biochem Parasitol. 2007 Feb;151(2):205-12. doi: 10.1016/j.molbiopara.2006.11.005. Epub 2006 Nov 30.
The cross-reactive antigens of Neospora caninum and Toxoplasma gondii are important in the exploration to determine the common mechanisms of parasite-host interaction. In this study, a gene encoding N. caninum apical membrane antigen 1 (NcAMA1) was identified by immunoscreening of a N. caninum tachyzoite cDNA expression library with antisera from mice immunized with recombinant T. gondii apical membrane antigen 1 (TgAMA1). NcAMA1 was encoded by an open reading frame of 1695 bp, which encoded a protein of 564 amino acids. The single-copy NcAMA1 gene was interrupted by seven introns. NcAMA1 showed 73.6% amino acid identity to TgAMA1. Mouse polyclonal antibodies raised against the recombinant NcAMA1 (rNcAMA1) recognized a 69-kDa native parasite protein by Western blotting. Immunofluorescence analysis showed that NcAMA1 was localized to the apical end of tachyzoites. Two-dimensional electrophoresis and Western blotting indicated that an approximately 57-kDa cleavage product was released into the excretory/secretory products of N. caninum. Preincubation of free tachyzoites with anti-rNcAMA1 IgG antibodies inhibited the invasion into host cells by N. caninum and T. gondii. These results indicated that AMA1 is a cross-reactive antigen between N. caninum and T. gondii and a potential common vaccine candidate to control two parasites.
犬新孢子虫和刚地弓形虫的交叉反应抗原在探索确定寄生虫与宿主相互作用的共同机制方面具有重要意义。在本研究中,通过用重组刚地弓形虫顶膜抗原1(TgAMA1)免疫的小鼠抗血清对犬新孢子虫速殖子cDNA表达文库进行免疫筛选,鉴定出一个编码犬新孢子虫顶膜抗原1(NcAMA1)的基因。NcAMA1由一个1695 bp的开放阅读框编码,该开放阅读框编码一个564个氨基酸的蛋白质。单拷贝的NcAMA1基因被7个内含子打断。NcAMA1与TgAMA1的氨基酸同一性为73.6%。用重组NcAMA1(rNcAMA1)制备的小鼠多克隆抗体通过蛋白质免疫印迹法识别出一种69 kDa的天然寄生虫蛋白。免疫荧光分析表明,NcAMA1定位于速殖子的顶端。二维电泳和蛋白质免疫印迹表明,一种约57 kDa的裂解产物被释放到犬新孢子虫的排泄/分泌产物中。用抗rNcAMA1 IgG抗体对游离速殖子进行预孵育可抑制犬新孢子虫和刚地弓形虫对宿主细胞的侵袭。这些结果表明,AMA1是犬新孢子虫和刚地弓形虫之间的交叉反应抗原,是控制这两种寄生虫的潜在共同疫苗候选物。