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In silico analysis of epitope-based CadF vaccine design against Campylobacterjejuni

OBJECTIVE: Vaccination is an important strategy for the eradication of infectious diseases. CadF protein of Campylobacter jejuni is one of the important factors in the pathogenesis of this bacterium. The purpose of this work was to perform a bioinformatics study to identify an epitope-based CadF vac...

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Autores principales: Moballegh Naseri, Mona, Shams, Saeed, Moballegh Naseri, Mohammad, Bakhshi, Bita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652678/
https://www.ncbi.nlm.nih.gov/pubmed/33168057
http://dx.doi.org/10.1186/s13104-020-05364-z
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author Moballegh Naseri, Mona
Shams, Saeed
Moballegh Naseri, Mohammad
Bakhshi, Bita
author_facet Moballegh Naseri, Mona
Shams, Saeed
Moballegh Naseri, Mohammad
Bakhshi, Bita
author_sort Moballegh Naseri, Mona
collection PubMed
description OBJECTIVE: Vaccination is an important strategy for the eradication of infectious diseases. CadF protein of Campylobacter jejuni is one of the important factors in the pathogenesis of this bacterium. The purpose of this work was to perform a bioinformatics study to identify an epitope-based CadF vaccine, as a subunit vaccine. Full protein sequences of CadF were extracted from the NCBI and UniProt databases and subjected to in silico evaluations, including sequence analysis, allergenicity, antigenicity, epitope conservancy, and molecular docking assessments done by different servers. RESULTS: The results showed that CadF was a highly conserved protein belonging to the outer member proteins superfamily. Among the evaluated epitopes, LSDSLALRL was identified as an antigenic and non-allergenic peptide with a suitable structure for vaccine development. It was also able to stimulate both T and B cells. This 9-mer peptide was located in 136–144 segment of CadF protein and interacted with both HLA-A 0101 and HLA-DRB1 0101 alleles. Overall, the obtained theoretical results showed that CadF protein could be used for designing and evaluating a new effective vaccine against C. jejuni.
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spelling pubmed-76526782020-11-10 In silico analysis of epitope-based CadF vaccine design against Campylobacterjejuni Moballegh Naseri, Mona Shams, Saeed Moballegh Naseri, Mohammad Bakhshi, Bita BMC Res Notes Research Note OBJECTIVE: Vaccination is an important strategy for the eradication of infectious diseases. CadF protein of Campylobacter jejuni is one of the important factors in the pathogenesis of this bacterium. The purpose of this work was to perform a bioinformatics study to identify an epitope-based CadF vaccine, as a subunit vaccine. Full protein sequences of CadF were extracted from the NCBI and UniProt databases and subjected to in silico evaluations, including sequence analysis, allergenicity, antigenicity, epitope conservancy, and molecular docking assessments done by different servers. RESULTS: The results showed that CadF was a highly conserved protein belonging to the outer member proteins superfamily. Among the evaluated epitopes, LSDSLALRL was identified as an antigenic and non-allergenic peptide with a suitable structure for vaccine development. It was also able to stimulate both T and B cells. This 9-mer peptide was located in 136–144 segment of CadF protein and interacted with both HLA-A 0101 and HLA-DRB1 0101 alleles. Overall, the obtained theoretical results showed that CadF protein could be used for designing and evaluating a new effective vaccine against C. jejuni. BioMed Central 2020-11-10 /pmc/articles/PMC7652678/ /pubmed/33168057 http://dx.doi.org/10.1186/s13104-020-05364-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Note
Moballegh Naseri, Mona
Shams, Saeed
Moballegh Naseri, Mohammad
Bakhshi, Bita
In silico analysis of epitope-based CadF vaccine design against Campylobacterjejuni
title In silico analysis of epitope-based CadF vaccine design against Campylobacterjejuni
title_full In silico analysis of epitope-based CadF vaccine design against Campylobacterjejuni
title_fullStr In silico analysis of epitope-based CadF vaccine design against Campylobacterjejuni
title_full_unstemmed In silico analysis of epitope-based CadF vaccine design against Campylobacterjejuni
title_short In silico analysis of epitope-based CadF vaccine design against Campylobacterjejuni
title_sort in silico analysis of epitope-based cadf vaccine design against campylobacterjejuni
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652678/
https://www.ncbi.nlm.nih.gov/pubmed/33168057
http://dx.doi.org/10.1186/s13104-020-05364-z
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