首页> 外文期刊>Molecular and Biochemical Parasitology >Molecular cloning and characterization of a novel Schistosoma japonicum 'irradiated vaccine-specific' antigen, Sj14-3-3.
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Molecular cloning and characterization of a novel Schistosoma japonicum 'irradiated vaccine-specific' antigen, Sj14-3-3.

机译:新型日本血吸虫“辐射疫苗特异性”抗原Sj14-3-3的分子克隆和表征。

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A Schistosoma japonicum cDNA coding for a full length S. japonicum 14-3-3 protein was obtained by antibody screening of an adult worm cDNA library using sera taken from mice vaccinated with UV-attenuated cercariae, which are capable of transferring high levels of passive immunity to this parasite. The deduced amino acid sequence consists of 254 amino acids and is highly homologous with 14-3-3 family of proteins from a variety of species (55-69% identity). The recombinant S. japonicun 14-3-3 protein (rSj14-3-3) was expressed and purified in pGEX/E. coli, and in Western blotting was strongly recognised by sera from mice, rats and bovines vaccinated with irradiated S. japonicum cercariae. Analysis of mRNA showed that Sj14-3-3 is expressed in sporocysts and adult worms, but not in cercariae, however mouse antisera against rSj14-3-3 recognised a 29 kDa native antigen in antigen preparations made from eggs, cercariae, schistosomula and adult worms of S. japonicum indicating that this antigen is present in all life-cycle stages. The presence of the native antigen in detergent extracts of intact schistosomula suggests that it is also present in the schistosomular tegument which is the most vulnerable target for immune attack. However, antisera against rSj14-3-3 did not recognise a similar band in S. mansoni or S. haematobium antigens, indicating that, like the UV-attenuated vaccines, this protein induced species-specific immune responses. Southern blot analysis suggested that there may exist more than one gene copy and/or polymorphism for Sj14-3-3. Immunoelectron microscopy confirmed that the native antigen is present throughout the body of adult worms including the tegument, but is less abundant in the muscles. The potential of rSj14-3-3 as a vaccine is now under further investigation.
机译:日本血吸虫cDNA编码全长的日本血吸虫14-3-3蛋白,是通过使用成虫的cDNA抗体筛选抗体而获得的,该成虫cDNA文库的血清取自接种了紫外线衰减尾c的小鼠,该小鼠能够转移高水平的被动对这种寄生虫的免疫力。推导的氨基酸序列由254个氨基酸组成,与来自多种物种的14-3-3蛋白质家族高度同源(同一性为55-69%)。在pGEX / E中表达并纯化了重组日本血吸虫14-3-3蛋白(rSj14-3-3)。大肠埃希菌和西方印迹法在血清中被小鼠,大鼠和牛的免疫血清强烈识别。 mRNA分析表明,Sj14-3-3在孢子虫和成虫中表达,但在尾cer中不表达,但是针对rSj14-3-3的小鼠抗血清在由卵,尾eggs,血吸虫和成虫制成的抗原制剂中识别出29 kDa的天然抗原。日本血吸虫蠕虫表明此抗原存在于所有生命周期阶段。完整血吸虫去污剂提取物中天然抗原的存在表明它也存在于血吸虫皮中,这是免疫攻击的最易受攻击的目标。但是,针对rSj14-3-3的抗血清无法识别曼氏沙门氏菌或血红球菌抗原中的相似条带,表明该蛋白与紫外线衰减疫苗一样,可诱导物种特异性免疫反应。 Southern印迹分析表明,Sj14-3-3可能存在多个基因拷贝和/或多态性。免疫电子显微镜证实,天然抗原存在于成虫的整个身体中,包括外皮,但在肌肉中含量较低。 rSj14-3-3作为疫苗的潜力正在进一步研究中。

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