Molecular characterization and immune protection of an AN1-like zinc finger protein of Eimeria tenella

Coccidiosis is caused by multiple species of the apicomplexan protozoa Eimeria . Among them, Eimeria tenella is frequently considered to be the most pathogenic. Zinc finger proteins (ZnFPs) are a type of protein containing zinc finger domains. In the present study, a putative Eimeria tenella AN1-lik...

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Veröffentlicht in:Parasitology research (1987) 2020-02, Vol.119 (2), p.623-635
Hauptverfasser: Zhao, Huanzhi, Zhao, Qiping, Zhu, Shunhai, Huang, Bing, Lv, Ling, Liu, Guiling, Li, Zhihang, Wang, Lu, Dong, Hui, Han, Hongyu
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Sprache:eng
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Zusammenfassung:Coccidiosis is caused by multiple species of the apicomplexan protozoa Eimeria . Among them, Eimeria tenella is frequently considered to be the most pathogenic. Zinc finger proteins (ZnFPs) are a type of protein containing zinc finger domains. In the present study, a putative Eimeria tenella AN1-like ZnFP ( E. tenella AN1-like zinc finger domain-containing protein, putative partial mRNA, Et AN1-ZnFP) was cloned and characterized, and its immune protective effects were evaluated. The 798-bp ORF sequence of Et AN1-ZnFP that encoded a protein of approximately 27.0 kDa was obtained. The recombinant Et AN1-ZnFP protein (r Et AN1-ZnFP) was expressed in Escherichia coli . Western blot analysis showed that the recombinant protein was recognized by the anti-GST monoclonal antibody and anti-sporozoite protein rabbit serum. qPCR analysis revealed that Et AN1-ZnFP was highly expressed in unsporulated oocysts and sporozoites. Immunostaining with an anti-r Et AN1-ZnFP antibody indicated that Et AN1-ZnFP was uniformly distributed in the cytoplasm of sporozoites, except for the refractive body; furthermore, this protein was evenly distributed in the cytoplasm of immature schizonts but seldom distributed in mature schizonts. The results of the in vitro invasion inhibition assay indicated that the antibodies against r Et AN1-ZnFP efficiently reduced the ability of E. tenella sporozoites to invade host cells. Animal challenge experiments demonstrated that the chickens immunized with r Et AN1-ZnFP protein significantly decreased mean lesion scores and fecal oocyst output compared with challenged control group. The results suggest that Et AN1-ZnFP can induce partial immune protection against infection with E. tenella and could be an effective candidate for the development of new vaccines.
ISSN:0932-0113
1432-1955
DOI:10.1007/s00436-019-06545-x