TY - JOUR ID - 105996 TI - In silico analysis of Omp25 and BLS Brucella melitensis antigens for designing subunit vaccine JO - Archives of Razi Institute JA - ARI LA - en SN - 0365-3439 AU - Tahmoorespur, M. AU - Sekhavati, M.H. AU - Yousefi, S. AU - Abbassi-Daloii, T. AU - Azghandi, M. AU - Akbari, R. AD - Department of Animal Science, Ferdowsi University of Mashhad, Mashhad, Iran Y1 - 2016 PY - 2016 VL - 71 IS - 1 SP - 35 EP - 42 KW - Brucella melitensis KW - Omp25 KW - BLS KW - Bioinformatics analysis KW - Recombinant vaccine DO - 10.22034/ari.2016.105996 N2 - Brucellosis is a well-known infection in domestic animals which caused by Brucella bacterium. Due toserious economic and medical consequences of this disease, various efforts have been made to prevent theinfection through the use of recombinant vaccines based on Brucella outer membrane protein (OMP)antigens. The objectives of the present study were cloning, sequencing and epitope prediction of Omp25and BLS genes as two major Brucella melitensis antigens. The full-length open reading frame (ORF) ofOmp25 and BLS genes were amplified and cloned into pTZ57R/T vector. Phylogenetic analysis ofsequenced genes showed that both genes were nearly similar in different Brucella species. Several onlineprediction softwares were used to predict B and T-cells epitopes, secondary and tertiary structures,antigenicity ability and enzymatic degradation sites. Bioinformatic tools used in the current study wereconfirmed by the results of three different experimental epitope predictions. Bioinformatic analysisidentified five and two B-cell and two and one T-cell epitopes for Omp25 and BLS antigens, respectively.Finally, according to the antigenicity ability and proteosomal recognition site common B and T-cell epitopewas predicted for Omp25 (154-162 amino acids) and BLS (37-48 and 119-139 amino acids). Results of thisstudy might be useful for recombinant vaccine development. UR - https://archrazi.areeo.ac.ir/article_105996.html L1 - https://archrazi.areeo.ac.ir/article_105996_98b6aa25c365c284280942f3bbc7d124.pdf ER -