Molecular cloning and characterization of a novel heat shock protein 20 of Babesia orientalis
2014
He, Lan | Yu, Qian | Zhang, Wen-Jie | Zhang, Qing-Li | Fan, Li-Zhe | Miao, Xiao-Yan | Khan, Muhammad Kasib | Hu, Min | Zhou, Yan-Qin | Zhao, Jun-Long
The heat shock protein 20 (HSP20) gene of Babesia orientalis (BoHSP20) was identified from both genomic DNA and cDNA. The full-length BoHSP20 gene was 690bp with one intron from position 88–243bp. The amplicon obtained from cDNA corresponded to a full-length open reading frame (ORF) with a length of 534bp, encoding a polypeptide of 178 amino acid residues with a predicted size of 20kDa. The ORF was cloned into a pET-28a plasmid and subsequently expressed as a His-fusion protein. The recombinant HSP20 of B. orientalis (rBoHSP20) was purified and evaluated as an antigen using Western blotting. Anti-B. orientalis water buffalo serum reacted with rBoHSP20, indicating that this protein was an immunodominant antigen and could be a useful diagnostic reagent to detect antibodies against B. orientalis in water buffalo. The native BoHSP20 was recognized by polyclonal antibody from the serum of rabbit immunized with rBoHSP20. Strong immunofluorescence signals were observed from B. orientalis in blood smears by fluorescence microscopy. Bacterial survival experiments indicated that HSP20 can significantly increase the viability of bacteria when the culture is exposed to thermal stress. The results suggest that BoHSP20 might play an important role during B. orientalis transmission from tick to host animal, given the sudden shifts in temperature involved. Phylogenetic analysis revealed that B. orientalis is in the Babesia clade and most closely related to Babesia bovis. Similar topologies were obtained from trees based on 18S rRNA and the HSP70 gene. The present study suggests that BoHSP20 might be a potential diagnostic antigen and that the HSP20 genes can aid in the classification of Babesia and Theileria species.
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