In silico analysis of Omp25 and BLS Brucella melitensis antigens for designing subunit vaccine

Brucellosis is a well-known infection in domestic animals which caused by Brucella bacterium. Due to serious economic and medical consequences of this disease, various efforts have been made to prevent the infection through the use of recombinant vaccines based on Brucella outer membrane protein (OM...

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Main Authors: Tahmoorespur, M., Sekhavati, M.H., Yousefi, S., Abbassi-Daloii, T., Azghandi, M., Akbari, R.
Format: Article
Language:English
Published: Razi Vaccine and Serum Research Institute 2016-03-01
Series:Archives of Razi Institute
Subjects:
Online Access:http://www.archrazi.com/article_105996_10696.html
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author Tahmoorespur, M.
Sekhavati, M.H.
Yousefi, S.
Abbassi-Daloii, T.
Azghandi, M.
Akbari, R.
author_facet Tahmoorespur, M.
Sekhavati, M.H.
Yousefi, S.
Abbassi-Daloii, T.
Azghandi, M.
Akbari, R.
author_sort Tahmoorespur, M.
collection DOAJ
description Brucellosis is a well-known infection in domestic animals which caused by Brucella bacterium. Due to serious economic and medical consequences of this disease, various efforts have been made to prevent the infection 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 Omp25 and BLS genes as two major Brucella melitensis antigens. The full-length open reading frame (ORF) of Omp25 and BLS genes were amplified and cloned into pTZ57R/T vector. Phylogenetic analysis of sequenced genes showed that both genes were nearly similar in different Brucella species. Several online prediction 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 were confirmed by the results of three different experimental epitope predictions. Bioinformatic analysis identified 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 epitope was predicted for Omp25 (154-162 amino acids) and BLS (37-48 and 119-139 amino acids). Results of this study might be useful for recombinant vaccine development.
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spelling doaj.art-648c5a1651f2421ab5af01bab748ced82022-12-22T00:27:24ZengRazi Vaccine and Serum Research InstituteArchives of Razi Institute0365-34392008-98722016-03-017113542In silico analysis of Omp25 and BLS Brucella melitensis antigens for designing subunit vaccineTahmoorespur, M.0 Sekhavati, M.H.1Yousefi, S.2 Abbassi-Daloii, T.3 Azghandi, M.4Akbari, R.5Department of Animal Science, Ferdowsi University of Mashhad, Mashhad, IranDepartment of Animal Science, Ferdowsi University of Mashhad, Mashhad, IranDepartment of Animal Science, Ferdowsi University of Mashhad, Mashhad, IranDepartment of Animal Science, Ferdowsi University of Mashhad, Mashhad, IranDepartment of Animal Science, Ferdowsi University of Mashhad, Mashhad, IranDepartment of Animal Science, Ferdowsi University of Mashhad, Mashhad, IranBrucellosis is a well-known infection in domestic animals which caused by Brucella bacterium. Due to serious economic and medical consequences of this disease, various efforts have been made to prevent the infection 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 Omp25 and BLS genes as two major Brucella melitensis antigens. The full-length open reading frame (ORF) of Omp25 and BLS genes were amplified and cloned into pTZ57R/T vector. Phylogenetic analysis of sequenced genes showed that both genes were nearly similar in different Brucella species. Several online prediction 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 were confirmed by the results of three different experimental epitope predictions. Bioinformatic analysis identified 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 epitope was predicted for Omp25 (154-162 amino acids) and BLS (37-48 and 119-139 amino acids). Results of this study might be useful for recombinant vaccine development.http://www.archrazi.com/article_105996_10696.htmlBrucella melitensisOmp25BLSBioinformatics analysisRecombinant vaccine
spellingShingle Tahmoorespur, M.
Sekhavati, M.H.
Yousefi, S.
Abbassi-Daloii, T.
Azghandi, M.
Akbari, R.
In silico analysis of Omp25 and BLS Brucella melitensis antigens for designing subunit vaccine
Archives of Razi Institute
Brucella melitensis
Omp25
BLS
Bioinformatics analysis
Recombinant vaccine
title In silico analysis of Omp25 and BLS Brucella melitensis antigens for designing subunit vaccine
title_full In silico analysis of Omp25 and BLS Brucella melitensis antigens for designing subunit vaccine
title_fullStr In silico analysis of Omp25 and BLS Brucella melitensis antigens for designing subunit vaccine
title_full_unstemmed In silico analysis of Omp25 and BLS Brucella melitensis antigens for designing subunit vaccine
title_short In silico analysis of Omp25 and BLS Brucella melitensis antigens for designing subunit vaccine
title_sort in silico analysis of omp25 and bls brucella melitensis antigens for designing subunit vaccine
topic Brucella melitensis
Omp25
BLS
Bioinformatics analysis
Recombinant vaccine
url http://www.archrazi.com/article_105996_10696.html
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