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Design of a Multi-epitope Vaccine Against Acinetobacter baumannii Using Immunoinformatics Approach

Acinetobacter baumannii is one of the most successful pathogens causing nosocomial infections and has significantly multidrug-resistant. So far, there are no certain treatments to protect against infection with A. baumannii, therefore an effective A. baumannii vaccine needed. The purpose of this stu...

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Autores principales: Touhidinia, Maryam, Sefid, Fatemeh, Bidakhavidi, Mozhgan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397861/
https://www.ncbi.nlm.nih.gov/pubmed/34483787
http://dx.doi.org/10.1007/s10989-021-10262-4
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author Touhidinia, Maryam
Sefid, Fatemeh
Bidakhavidi, Mozhgan
author_facet Touhidinia, Maryam
Sefid, Fatemeh
Bidakhavidi, Mozhgan
author_sort Touhidinia, Maryam
collection PubMed
description Acinetobacter baumannii is one of the most successful pathogens causing nosocomial infections and has significantly multidrug-resistant. So far, there are no certain treatments to protect against infection with A. baumannii, therefore an effective A. baumannii vaccine needed. The purpose of this study was to predict antigenic epitopes of CarO protein for designing the A. baumannii vaccine using immunoinformatics analysis. CarO protein is one of the most important factors in the resistance against the antibiotic Carbapenem. In this study, T and B-cell epitopes of CarO protein were predicted and screened based on the antigenicity, toxicity, allergenicity features. The epitopes were linked by suitable linkers. Four different adjuvants were attached to the vaccine constructs which among them, vaccine construct 3 was chosen to predict the secondary and the 3D structure of the vaccine. The refinement process was performed to improve the quality of the 3D model structure; the validation process is performed using the Ramachandran plot and ProSA z-score. The designed vaccine's binding affinity to six various HLA molecules and TLR 2 and TLR4 were evaluated by molecular docking. Finally, in silico gene cloning was performed in the pET28a (+) vector. The findings suggest that the vaccine may be a promising vaccine to prevent A. baumannii infection.
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spelling pubmed-83978612021-08-30 Design of a Multi-epitope Vaccine Against Acinetobacter baumannii Using Immunoinformatics Approach Touhidinia, Maryam Sefid, Fatemeh Bidakhavidi, Mozhgan Int J Pept Res Ther Article Acinetobacter baumannii is one of the most successful pathogens causing nosocomial infections and has significantly multidrug-resistant. So far, there are no certain treatments to protect against infection with A. baumannii, therefore an effective A. baumannii vaccine needed. The purpose of this study was to predict antigenic epitopes of CarO protein for designing the A. baumannii vaccine using immunoinformatics analysis. CarO protein is one of the most important factors in the resistance against the antibiotic Carbapenem. In this study, T and B-cell epitopes of CarO protein were predicted and screened based on the antigenicity, toxicity, allergenicity features. The epitopes were linked by suitable linkers. Four different adjuvants were attached to the vaccine constructs which among them, vaccine construct 3 was chosen to predict the secondary and the 3D structure of the vaccine. The refinement process was performed to improve the quality of the 3D model structure; the validation process is performed using the Ramachandran plot and ProSA z-score. The designed vaccine's binding affinity to six various HLA molecules and TLR 2 and TLR4 were evaluated by molecular docking. Finally, in silico gene cloning was performed in the pET28a (+) vector. The findings suggest that the vaccine may be a promising vaccine to prevent A. baumannii infection. Springer Netherlands 2021-08-28 2021 /pmc/articles/PMC8397861/ /pubmed/34483787 http://dx.doi.org/10.1007/s10989-021-10262-4 Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Touhidinia, Maryam
Sefid, Fatemeh
Bidakhavidi, Mozhgan
Design of a Multi-epitope Vaccine Against Acinetobacter baumannii Using Immunoinformatics Approach
title Design of a Multi-epitope Vaccine Against Acinetobacter baumannii Using Immunoinformatics Approach
title_full Design of a Multi-epitope Vaccine Against Acinetobacter baumannii Using Immunoinformatics Approach
title_fullStr Design of a Multi-epitope Vaccine Against Acinetobacter baumannii Using Immunoinformatics Approach
title_full_unstemmed Design of a Multi-epitope Vaccine Against Acinetobacter baumannii Using Immunoinformatics Approach
title_short Design of a Multi-epitope Vaccine Against Acinetobacter baumannii Using Immunoinformatics Approach
title_sort design of a multi-epitope vaccine against acinetobacter baumannii using immunoinformatics approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397861/
https://www.ncbi.nlm.nih.gov/pubmed/34483787
http://dx.doi.org/10.1007/s10989-021-10262-4
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