Wang Ziwen, Huang Bing, Dong Hui, Zhao Qiping, Zhu Shunhai, Xia Weili, Xu Shuaibin, Xie Yuxiang, Cui Xiaoxia, Tang Min, Men Qifei, Yang Zhiyuang, Li Cong, Zhu Xuelong, Han Hongyu
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Key Laboratory of Animal Parasitology of Ministry of Agriculture, Minhang, Shanghai, PR China.
Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, PR China.
PLoS One. 2016 Dec 15;11(12):e0168132. doi: 10.1371/journal.pone.0168132. eCollection 2016.
Eimeria tenella is an obligate intracellular parasite that actively invades cecal epithelial cells of chickens. The basis of cell invasion is not completely understood, but some key molecules of host cell invasion have been discovered. This paper investigated the characteristics of calcium-dependent protein kinase 4 (EtCDPK4), a critical molecule in E. tenella invasion of host cells. A full-length EtCDPK4 cDNA was identified from E. tenella using rapid amplification of cDNA ends. EtCDPK4 had an open reading frame of 1803 bp encoding a protein of 600 amino acids. Quantitative real-time PCR and western blotting were used to explore differences in EtCDPK4 transcription and translation in four developmental stages of E. tenella. EtCDPK4 was expressed at higher levels in sporozoites, but translation was higher in second-generation merozoites. In vitro invasion inhibition assays explored whether EtCDPK4 was involved in invasion of DF-1 cells by E. tenella sporozoites. Polyclonal antibodies against recombinant EtCDPK4 (rEtCDPK4) inhibited parasite invasion, decreasing it by approximately 52%. Indirect immunofluorescence assays explored EtCDPK4 distribution during parasite development after E. tenella sporozoite invasion of DF-1 cells in vitro. The results showed that EtCDPK4 might be important in sporozoite invasion and development. To analyze EtCDPK4 functional domains according to the structural characteristics of EtCDPK4 and study the kinase activity of rEtCDPK4, an in vitro phosphorylation system was established. We verified that rEtCDPK4 was a protein kinase that was completely dependent on Ca2+ for enzyme activity. Specific inhibitors of rEtCDPK4 activity were screened by kinase activity in vitro. Some specific inhibitors were applied to assays of DF-1 cell invasion by E. tenella sporozoites to confirm that the inhibitors functioned in vitro. W-7, H-7, H-89, and myristoylated peptide inhibited DF-1 invasion by E. tenella sporozoites. The experimental results showed that EtCDPK4 may be involved in E. tenella invasion of chicken cecal epithelial cells.
柔嫩艾美耳球虫是一种专性细胞内寄生虫,可主动侵入鸡的盲肠上皮细胞。细胞入侵的基础尚未完全了解,但已发现一些宿主细胞入侵的关键分子。本文研究了柔嫩艾美耳球虫入侵宿主细胞的关键分子——钙依赖性蛋白激酶4(EtCDPK4)的特性。利用cDNA末端快速扩增技术从柔嫩艾美耳球虫中鉴定出全长EtCDPK4 cDNA。EtCDPK4的开放阅读框为1803 bp,编码一个600个氨基酸的蛋白质。采用实时定量PCR和蛋白质免疫印迹法探讨EtCDPK4在柔嫩艾美耳球虫四个发育阶段转录和翻译的差异。EtCDPK4在子孢子中表达水平较高,但在第二代裂殖子中的翻译水平较高。体外入侵抑制试验探讨了EtCDPK4是否参与柔嫩艾美耳球虫子孢子对DF-1细胞的入侵。抗重组EtCDPK4(rEtCDPK4)的多克隆抗体抑制了寄生虫的入侵,使其减少了约52%。间接免疫荧光试验探讨了柔嫩艾美耳球虫子孢子体外入侵DF-1细胞后EtCDPK4在寄生虫发育过程中的分布。结果表明,EtCDPK4可能在子孢子入侵和发育中起重要作用。根据EtCDPK4的结构特征分析其功能结构域,并研究rEtCDPK4的激酶活性,建立了体外磷酸化系统。我们验证了rEtCDPK4是一种完全依赖Ca2+进行酶活性的蛋白激酶。通过体外激酶活性筛选rEtCDPK4活性的特异性抑制剂。将一些特异性抑制剂应用于柔嫩艾美耳球虫子孢子对DF-1细胞的入侵试验,以证实这些抑制剂在体外发挥作用。W-7、H-7、H-89和肉豆蔻酰化肽抑制了柔嫩艾美耳球虫子孢子对DF-1细胞的入侵。实验结果表明,EtCDPK4可能参与了柔嫩艾美耳球虫对鸡盲肠上皮细胞的入侵。