Petersen C, Gut J, Leech J H, Nelson R G
Parasitology Laboratory, San Francisco General Hospital, California.
Infect Immun. 1992 Jun;60(6):2343-8. doi: 10.1128/iai.60.6.2343-2348.1992.
Cryptosporidium parvum, an Apicomplexan parasite of gastrointestinal epithelial cells, causes severe disease in persons with AIDS and is a common cause of self-limited diarrhea in children, animal handlers, and residents of developing countries. No approved therapy exists; in research studies, however, hyperimmune bovine colostrum raised to Cryptosporidium oocysts and sporozoites has eradicated disease or decreased parasite burden in some AIDS patients. Although the protective antigens recognized by bovine hyperimmune colostrum have not been defined, protective antigens of other Apicomplexan parasites frequently have been associated with two unique structures of invasive forms, the trilaminar pellicle and the apical complex. In order to identify immunogenic Cryptosporidium proteins that may be protective antigens for use as recombinant immunogens in passive and/or active immunotherapy, we screened two genomic DNA expression libraries with polyspecific anti-Cryptosporidium antibodies. We used an approach to cloning apical complex and pellicle protein antigens that succeeded despite the lack of large numbers of organisms that would be necessitated for conventional biochemical approaches requiring organelle or membrane purification. We report here the molecular cloning of five C. parvum genes and the characterization of the cognate sporozoite proteins having molecular masses of greater than 500, 68/95, 45, 23, and 15/35 kDa. The light microscopic immunofluorescence pattern of antibodies recognizing these protein antigens suggest that they are located in the pellicle or apical complex of Cryptosporidium sporozoites.
微小隐孢子虫是一种寄生于胃肠道上皮细胞的顶复门寄生虫,可导致艾滋病患者患上严重疾病,也是儿童、动物饲养员和发展中国家居民自限性腹泻的常见病因。目前尚无获批的治疗方法;然而,在研究中,针对隐孢子虫卵囊和子孢子的超免疫牛初乳已使一些艾滋病患者的疾病得到根除或寄生虫负担减轻。虽然牛超免疫初乳识别的保护性抗原尚未明确,但其他顶复门寄生虫的保护性抗原通常与侵袭性形式的两种独特结构有关,即三层膜和顶复合体。为了鉴定可能作为重组免疫原用于被动和/或主动免疫治疗的保护性抗原的免疫原性隐孢子虫蛋白,我们用多特异性抗隐孢子虫抗体筛选了两个基因组DNA表达文库。我们采用了一种克隆顶复合体和膜蛋白抗原的方法,尽管缺乏大量用于需要细胞器或膜纯化的传统生化方法的生物体,但该方法仍取得了成功。我们在此报告了五个微小隐孢子虫基因的分子克隆以及分子量大于500、68/95、45、2