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Novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach

While mankind is still dealing with the COVID-19 pandemic, a case of monkeypox virus (MPXV) has been reported to the WHO on May 7, 2022. Monkeypox is a viral zoonotic disease that has been a public health threat, particularly in Africa. However, it has recently expanded to other parts of the world,...

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Autores principales: Shantier, Shaza W., Mustafa, Mujahed I., Abdelmoneim, Abdelrahman H., Fadl, Hiba A., Elbager, Sahar G., Makhawi, Abdelrafie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510130/
https://www.ncbi.nlm.nih.gov/pubmed/36156077
http://dx.doi.org/10.1038/s41598-022-20397-z
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author Shantier, Shaza W.
Mustafa, Mujahed I.
Abdelmoneim, Abdelrahman H.
Fadl, Hiba A.
Elbager, Sahar G.
Makhawi, Abdelrafie M.
author_facet Shantier, Shaza W.
Mustafa, Mujahed I.
Abdelmoneim, Abdelrahman H.
Fadl, Hiba A.
Elbager, Sahar G.
Makhawi, Abdelrafie M.
author_sort Shantier, Shaza W.
collection PubMed
description While mankind is still dealing with the COVID-19 pandemic, a case of monkeypox virus (MPXV) has been reported to the WHO on May 7, 2022. Monkeypox is a viral zoonotic disease that has been a public health threat, particularly in Africa. However, it has recently expanded to other parts of the world, so it may soon become a global issue. Thus, the current work was planned and then designed a multi-epitope vaccine against MPXV utilizing the cell surface-binding protein as a target in order to develop a novel and safe vaccine that can evoke the desirable immunological response. The proposed MHC-I, MHC-II, and B-cell epitopes were selected to design multi-epitope vaccine constructs linked with suitable linkers in combination with different adjuvants to enhance the immune responses for the vaccine constructs. The proposed vaccine was composed of 275 amino acids and was shown to be antigenic in Vaxijen server (0.5311) and non-allergenic in AllerTop server. The 3D structure of the designed vaccine was predicted, refined and validated by various in silico tools to assess the stability of the vaccine. Moreover, the solubility of the vaccine construct was found greater than the average solubility provided by protein-Sol server which indicating the solubility of the vaccine construct. Additionally, the most promising epitopes bound to MHC I and MHC II alleles were found having good binding affinities with low energies ranging between − 7.0 and − 8.6 kcal/mol. According to the immunological simulation research, the vaccine was found to elicit a particular immune reaction against the monkeypox virus. Finally, the molecular dynamic study shows that the designed vaccine is stable with minimum RMSF against MHC I allele. We conclude from our research that the cell surface-binding protein is one of the primary proteins involved in MPXV pathogenesis. As a result, our study will aid in the development of appropriate therapeutics and prompt the development of future vaccines against MPXV.
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spelling pubmed-95101302022-09-26 Novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach Shantier, Shaza W. Mustafa, Mujahed I. Abdelmoneim, Abdelrahman H. Fadl, Hiba A. Elbager, Sahar G. Makhawi, Abdelrafie M. Sci Rep Article While mankind is still dealing with the COVID-19 pandemic, a case of monkeypox virus (MPXV) has been reported to the WHO on May 7, 2022. Monkeypox is a viral zoonotic disease that has been a public health threat, particularly in Africa. However, it has recently expanded to other parts of the world, so it may soon become a global issue. Thus, the current work was planned and then designed a multi-epitope vaccine against MPXV utilizing the cell surface-binding protein as a target in order to develop a novel and safe vaccine that can evoke the desirable immunological response. The proposed MHC-I, MHC-II, and B-cell epitopes were selected to design multi-epitope vaccine constructs linked with suitable linkers in combination with different adjuvants to enhance the immune responses for the vaccine constructs. The proposed vaccine was composed of 275 amino acids and was shown to be antigenic in Vaxijen server (0.5311) and non-allergenic in AllerTop server. The 3D structure of the designed vaccine was predicted, refined and validated by various in silico tools to assess the stability of the vaccine. Moreover, the solubility of the vaccine construct was found greater than the average solubility provided by protein-Sol server which indicating the solubility of the vaccine construct. Additionally, the most promising epitopes bound to MHC I and MHC II alleles were found having good binding affinities with low energies ranging between − 7.0 and − 8.6 kcal/mol. According to the immunological simulation research, the vaccine was found to elicit a particular immune reaction against the monkeypox virus. Finally, the molecular dynamic study shows that the designed vaccine is stable with minimum RMSF against MHC I allele. We conclude from our research that the cell surface-binding protein is one of the primary proteins involved in MPXV pathogenesis. As a result, our study will aid in the development of appropriate therapeutics and prompt the development of future vaccines against MPXV. Nature Publishing Group UK 2022-09-25 /pmc/articles/PMC9510130/ /pubmed/36156077 http://dx.doi.org/10.1038/s41598-022-20397-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shantier, Shaza W.
Mustafa, Mujahed I.
Abdelmoneim, Abdelrahman H.
Fadl, Hiba A.
Elbager, Sahar G.
Makhawi, Abdelrafie M.
Novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach
title Novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach
title_full Novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach
title_fullStr Novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach
title_full_unstemmed Novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach
title_short Novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach
title_sort novel multi epitope-based vaccine against monkeypox virus: vaccinomic approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510130/
https://www.ncbi.nlm.nih.gov/pubmed/36156077
http://dx.doi.org/10.1038/s41598-022-20397-z
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