畜牧兽医学报 ›› 2020, Vol. 51 ›› Issue (12): 3111-3121.doi: 10.11843/j.issn.0366-6964.2020.12.020

• 预防兽医 • 上一篇    下一篇

柔嫩艾美耳球虫延伸因子1α特性与功能初步分析

梁珊珊1,2, 朱顺海2, 赵其平2, 黄兵2, 董辉2, 于钰1,2, 王青杰2, 余水兰2, 王海霞2, 韩红玉2*   

  1. 1. 上海师范大学生命科学学院, 上海 200234;
    2. 中国农业科学院上海兽医研究所, 农业农村部动物寄生虫学重点实验室, 上海 200241
  • 收稿日期:2020-06-22 出版日期:2020-12-25 发布日期:2020-12-23
  • 通讯作者: 韩红玉,主要从事球虫生物学与分子生物学研究,E-mail:hhysh@shvri.ac.cn
  • 作者简介:梁珊珊(1993-),女,河北唐山人,硕士生,主要从事动物细胞分子生物学研究
  • 基金资助:
    国家自然科学基金(31970420;31572266);国家寄生虫种质资源共享服务平台(TDRC-2019-194-30)

Preliminary Study on the Function of Elongation Factor 1α of Eimeria tenella

LIANG Shanshan1,2, ZHU Shunhai2, ZHAO Qiping2, HUANG Bing2, DONG Hui2, YU Yu1,2, WANG Qingjie2, YU Shuilan2, WANG Haixia2, HAN Hongyu2*   

  1. 1. College of Life Sciences, Shanghai Normal University, Shanghai 200234, China;
    2. Key Laboratory of Animal Parasitology of Ministry of Agriculture/Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai 200241, China
  • Received:2020-06-22 Online:2020-12-25 Published:2020-12-23

摘要: 鸡球虫病在世界范围内对家禽业具有重大的经济影响,导致高死亡率、低增长、低生产力和高防治成本。由于球虫耐药性问题严峻,球虫病的防治重点倾向于研究方便安全,并且与活疫苗相比更容易生产的亚单位疫苗。因此,迫切需要新的方法来有效地控制球虫病,包括寻找特定的分子靶标。本文以柔嫩艾美耳球虫孢子化卵囊cDNA第一链为模板,扩增了延伸因子1α(EtEF1α)的ORF序列,生物信息学分析显示,该基因编码450个氨基酸,预测相对分子质量为49.1 ku,等电点为4.7;编码的蛋白无信号肽和跨膜结构域,但都含有N-肉豆蔻酰化位点。qRT-PCR和Western blot分析EtEF1α在虫体不同发育阶段的mRNA转录水平和蛋白翻译水平,结果显示,EtEF1α在子孢子(Spz)和裂殖子(Mrz)的mRNA转录水平高于未孢子化卵囊(UO)和孢子化卵囊(SO),翻译水平在UO和Mrz高表达;间接免疫定位发现,EtEF1α主要定位于Spz一端和整个Mrz,随着虫体在细胞内发育,荧光强度逐渐增强。分泌试验显示该蛋白为分泌蛋白,但不是由微线体分泌的。入侵抑制试验结果表明,兔抗rEtEF1α多克隆抗体能抑制子孢子入侵DF-1细胞,抑制率约为22%。综上表明,该蛋白可能参与了虫体在宿主细胞内的生长发育和子孢子入侵宿主细胞的过程。

关键词: 柔嫩艾美耳球虫, 延伸因子1α, 特性分析, 入侵

Abstract: Coccidiosis infected by Eimeria spp. has a major economic impact on the poultry industry worldwide, resulting in high mortality, low growth, low productivity, and high control costs. Drug resistance of Eimeria spp. is a serious problem with the widespread use of anticoccidial drugs. The focus of coccidiosis prevention and control tends to research on subunit vaccines that are convenient, safe, and easier to produce than live vaccines. Therefore, new methods are urgently needed to effectively control coccidiosis, including the search for specific molecular targets. In this study, cDNA of E. tenella sporulated oocysts (SO) as a template, we amplified the ORF sequences of the elongation factor 1α of Eimeria tenella (EtEF1α). Bioinformatics analyses shows that the gene encodes 450 amino acids with a predicted molecular mass of 49.1 kDa. The isoelectric points were 4.7. Sequence analysis found that the proteins encoded by EtEF1α have no signal peptides and transmembrane domains, but contain N-myristoylation sites. The transcription and translation levels were analyzed using real-time quantitative PCR and Western blot. The results showed that the mRNA transcription levels of EtEF1α were higher in the sporozoite (Spz) and merozoite (Mrz) than unsporulated oocysts (UO) and SO, and the translation levels were high in UO and Mrz. Indirect immunofluorescence localization showed EtEF1α was mainly located at anterior of Spz and the whole cytoplasm of Mrz. As the parasites developed in the cell, the fluorescence intensity gradually brightens. The secretion assay indicated that EtEF1α was a secretion protein, but not secreted from micronemes. Invasion inhibition assay showed that rabbit anti-rEtEF1α polyclonal antibodies can inhibit sporozoite invasion of DF-1 cells. These results indicated that EtEF1α may play a role in the growth and development of the parasite in the host cell and participate in the process of sporozoite invasion into the host cell.

Key words: Eimeria tenella, elongation factor 1α, characteristic analyse, invasion

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