Facon B, Chamekh M, Dissous C, Capron A
Centre d'Immunologie et de Biologie Parasitaire, CNRS 624, Institut Pasteur, Lille, France.
Mol Biochem Parasitol. 1991 Apr;45(2):233-9. doi: 10.1016/0166-6851(91)90090-s.
cDNA was synthesized from RNA extracted from Echinococcus granulosus protoscoleces and cloned in the lambda gt11 expression vector. A pool of 5 E. granulosus patient sera was used to screen the library and allowed the selection of 13 clones. Ten of these were shown to be identical, among which clone 6 (Eg6) was chosen for further analysis. The nucleotide sequence (456-bp) presented an entire open reading frame coding for 152 amino acids. The fusion protein (FP6) was recognized by a mouse monoclonal antibody (EG 02 154/12) specific for E. granulosus antigen 5. Moreover, the presence of antibodies to FP6 seemed to be correlated to the ability of sera from hydatidosis patients to immunoprecipitate antigen 5. These results indicate that the cloned protein could be used as a standardized antigen for the diagnosis of hydatidosis.
从细粒棘球绦虫原头节提取的RNA合成cDNA,并克隆到λgt11表达载体中。使用一组5份细粒棘球绦虫患者血清筛选文库,选出13个克隆。其中10个显示相同,从中选择克隆6(Eg6)进行进一步分析。核苷酸序列(456bp)呈现一个完整的开放阅读框,编码152个氨基酸。融合蛋白(FP6)被细粒棘球绦虫抗原5特异性的小鼠单克隆抗体(EG 02 154/12)识别。此外,针对FP6的抗体的存在似乎与包虫病患者血清免疫沉淀抗原5的能力相关。这些结果表明,克隆的蛋白可作为包虫病诊断的标准化抗原。