期刊
PROCESS BIOCHEMISTRY
卷 121, 期 -, 页码 170-177出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.procbio.2022.06.016
关键词
Epitope-based vaccine; Babesiosis; Immunoinformatics; Immunogenic protein
The current study aimed to design an epitope-based vaccine against bovine babesiosis. Four immunogenic proteins were selected and used for epitope prediction. The designed vaccine showed antigenicity, non-allergenicity, and stability. It could stably bind to TLR/MD-2. The DNA sequence of the vaccine was suitable for cloning in a vector. This vaccine can be considered as a potential candidate for preventing bovine babesiosis.
The current study was designed to introduce an efficient epitope-based vaccine against bovine babesiosis. Four immunogenic proteins of the Babesia. bovis including Trap, msa, bov57 and 12D3 were selected from VIOLION database, then the proteins were used for prediction of B cell and T cell epitopes. The predicted epitopes along with HBHA protein as a molecular adjuvant were used to design an epitope-based vaccine. Antigenicity, aller-genicity, physicochemical features, secondary structure and tertiary structure of the designed vaccine were evaluated by VaxiJen, AllerTOP, ProtParam, SOPMA and I-TASSER servers, respectively. A molecular docking strategy was conducted by ClusPro server to investigate interaction between the designed vaccine and TLR/MD-2. Intermolecular hydrogen bonds of the interaction were assessed by the LigPlot server and the stability of the protein-protein complex was evaluated by iMODs server. The results revealed that the designed vaccine was an antigen, non-allergen and stable protein with a molecular weight of 32 kDa which could stably bind to TLR/MD-2 through its HBHA domain. The results showed that the DNA sequence of the vaccine could be suitably cloned in the pET21a (+) vector. According to the results, the designed vaccine can be introduced as a proper candidate to prevent bovine babesiosis.
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