Molecular characterization and functional analysis of Eimeria tenella citrate synthase

Chicken coccidiosis, caused by an obligate intracellular protozoan parasite of the genus Eimeria , is a major parasitic disease in the intensively reared poultry industry. Due to the widespread use of anticoccidial drugs, resistance has become an inevitable problem. In our previous study, Eimeria tenella citrate synthase ( Et CS) was found to be up-expressed in two drug-resistant strains (diclazuril-resistant and maduramycin-resistant strains) compared to drug-sensitive strain by RNA sequence. In this study, we cloned and expressed Et CS and obtain its polyclonal antibodies. Quantitative real-time polymerase chain (qPCR) reactions and Western blots were used to analyze the transcription and translation levels of Et CS in sensitive and three drug-resistant strains. Compared with the sensitive strain, the transcription of Et CS was both significantly upregulated in diclazuril-resistant and maduramycin-resistant strains, but was not significantly different in salinomycin-resistant strain. No significant difference was seen in translation level in the three drug-resistant strains. Indirect immunofluorescence indicated that Et CS was mainly located in the cytoplasm of sporozoites except for posterior refractile bodies and in the cytoplasm and surface of merozoites. Anti-r Et CS antibody has inhibitory effects on E. tenella sporozoite invasion of DF-1 cells and the inhibition rate is more than 83%. Binding of the protein to chicken macrophage (HD11) cells was confirmed by immunofluorescence assays. When macrophages were treated with r Et CS, secretion of nitric oxide and cell proliferation of the macrophages were substantially reduced. These results showed that Et CS may be related to host cell invasion of E. tenella and involve in the development of E.tenella resistance to some drugs.