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Identification of common immunodominant antigens of Eimeria tenella Eimeria acervulina and Eimeria maxima by immunoproteomic analysis

机译:通过免疫蛋白质组学分析鉴定艾美尔球虫小叶艾美尔球虫和最大艾美尔球虫的常见免疫优势抗原

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摘要

Clinical chicken coccidiosis is mostly caused by simultaneous infection of several Eimeria species, and host immunity against Eimeria is species-specific. It is urgent to identify common immunodominant antigen of Eimeria for developing multivalent anticoccidial vaccines. In this study, sporozoite proteins of Eimeria tenella, Eimeria acervulina and Eimeria maxima were analyzed by two-dimensional electrophoresis (2DE). Western bot analysis was performed on the yielded 2DE gel using antisera of E. tenella E. acervulina and E. maxima respectively. Next, the detected immunodominant spots were identified by comparing the data from MALDI-TOF-MS/MS with available databases. Finally, Eimeria common antigens were identified by comparing amino acid sequence between the three Eimeria species. The results showed that analysis by 2DE of sporozoite proteins detected 629, 626 and 632 protein spots from E. tenella, E. acervulina and E. maxima respectively. Western bot analysis revealed 50 (E. tenella), 64 (E. acervulina) and 57 (E. maxima) immunodominant spots from the sporozoite 2DE gels of the three Eimeria species. The immunodominant spots were identified as 33, 27 and 25 immunodominant antigens of E. tenella, E. acervulina and E. maxima respectively. Fifty-four immunodominant proteins were identified as 18 ortholog proteins among the three Eimeria species. Finally, 5 of the 18 ortholog proteins were identified as common immunodominant antigens including elongation factor 2 (EF-2), 14-3-3 protein, ubiquitin-conjugating enzyme domain-containing protein (UCE) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH). In conclusion, our results not only provide Eimeria sporozoite immunodominant antigen map and additional immunodominant antigens, but also common immunodominant antigens for developing multivalent anticoccidial vaccines.
机译:临床鸡球虫病主要是由几种艾美球虫同时感染引起的,宿主针对艾美球虫的免疫是种特异性的。为开发多价抗球虫疫苗,迫切需要鉴定艾美尔球菌的常见免疫优势抗原。在这项研究中,通过二维电泳(2DE)分析了艾美尔球虫,小叶艾美球虫和最大艾美尔球虫的子孢子蛋白。 Western bot分析是分别使用大肠埃希氏菌和大肠埃希菌的抗血清对得到的2DE凝胶进行的。接下来,通过将MALDI-TOF-MS / MS的数据与可用数据库进行比较,鉴定出检测到的免疫显性斑点。最后,通过比较三种艾美球虫物种之间的氨基酸序列,鉴定了艾美球虫常见抗原。结果表明,通过2DE分析子孢子蛋白可分别检测到Tenella,E。acervulina和E. maxima的629、626和632个蛋白斑点。 Western bot分析显示,来自三个 Eimeria 物种的子孢子2DE凝胶的免疫优势斑点分别为50个(E. tenella),64个(E. acervulina)和57个(E. maxima)。免疫显性斑点被鉴定为 E的33、27和25个免疫显性抗原。 tenella,大肠埃希菌(E. acervulina) E。最大值。在这三个 Eimeria 物种中,有五十四种免疫优势蛋白被鉴定为18个直系同源蛋白。最后,在18种直向同源蛋白中,有5种被鉴定为常见的免疫优势抗原,包括延伸因子2(EF-2),14-3-3蛋白,包含泛素结合酶结构域的蛋白(UCE)和甘油醛-3-磷酸脱氢酶( GAPDH)。总之,我们的结果不仅提供了 Eimeria 子孢子的免疫优势抗原图谱和其他免疫优势抗原,而且还为开发多价抗球虫疫苗提供了常见的免疫优势抗原。

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