Molecular cloning and characterization of Babesia orientalis rhoptry-associated protein 1
2014
Yu, Qian | He, Lan | Zhang, Wen-Jie | Cheng, Jian-Xi | Hu, Jin-Fang | Miao, Xiao-Yan | Huang, Yuan | Fan, Li-Zhe | Khan, Muhammad Kasib | Zhou, Yan-Qin | Hu, Min | Zhao, Jun-Long
The rhoptry-associated protein 1 (RAP-1) gene of Babesia orientalis was obtained from a cDNA expression library by immunoscreening with B. orientalis-infected water buffalo sera. The nucleotide sequence of the cDNA was 1732bp with an open reading frame (ORF) of 1434bp, encoding a polypeptide of 478 amino acid residues with a predicted size of 52.5kDa. The ORF was cloned into a pGEX-KG plasmid and subsequently expressed as a GST-fusion protein. The recombinant RAP-1 of B. orientalis (rBoRAP-1) was purified and evaluated as an antigen using Western blotting. The native BoRAP-1 was recognized by the antibodies raised in rabbits against rBoRAP-1. Strong immunofluorescence signals were observed in erythrocytes infected with B. orientalis. Phylogentic analysis revealed that B. orientalis fell into a Babesia clade and most closely related to Babesia bovis and Babesia ovis, which was similar to the previous reported trees based on 18S rRNA and HSP70 genes. The present study suggests that the BoRAP-1 might be a potential diagnostic antigen, and the RAP-1 genes can aid in the classification of Babesia and Theileria species.
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