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Detection of the peptidyl epitope for vaccine development against MPV

BACKGROUND: Monkeypox Virus (MPV) is the cause of zoonotic disease characterized by skin-eruption with pus cell formation and lymphadenopathy. This virus belongs to the Orthopoxvirus genus with DNA as its genetic material. Previously, this infection was reported from Africa and occasionally from USA...

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Autores principales: Sarkar, Indrani, Sen, Gargi, Ajmal Ali, Mohammd, Musaed Almutairi, Saeedah, Lee, Joongku, Sen, Arnab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier B.V. on behalf of King Saud University. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9683866/
https://www.ncbi.nlm.nih.gov/pubmed/36466790
http://dx.doi.org/10.1016/j.jksus.2022.102458
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author Sarkar, Indrani
Sen, Gargi
Ajmal Ali, Mohammd
Musaed Almutairi, Saeedah
Lee, Joongku
Sen, Arnab
author_facet Sarkar, Indrani
Sen, Gargi
Ajmal Ali, Mohammd
Musaed Almutairi, Saeedah
Lee, Joongku
Sen, Arnab
author_sort Sarkar, Indrani
collection PubMed
description BACKGROUND: Monkeypox Virus (MPV) is the cause of zoonotic disease characterized by skin-eruption with pus cell formation and lymphadenopathy. This virus belongs to the Orthopoxvirus genus with DNA as its genetic material. Previously, this infection was reported from Africa and occasionally from USA and UK. However, recently there is a sudden surge of infection in non-epidemic countries and a new strain of MPVhas been discovered. Therefore it is important to revisit the phylogeny of MPV with the addition of new strains. Recently WHO also stressed the need of developing vaccines for new strains. In this scenario we have two objectives for this study -first, to reveal the exact phylogenetic position of the 2022 strain and second, to identify specific peptides which may be used for vaccine development in the future. METHODS: The phylogenetic analysis was done with the help of Bayesian phylogeny. The dN/dS calculation was performed based on DNA polymerase genes of selected MPV strains. The peptidyl-epitope was searched in MPV2022/2 SLO strain with the help of several algorithms implemented in Allergen FP v.1.0, NetMHCII 2.3, MHCpred and Toxin Pred. The structure prediction of the proteins and peptides was performed through Hpepdock. The quality of the structures was validated through the Ramachandran plot. The molecular dynamics and simulation were performed through Gromacs software. The interaction between peptide and protein was assessed through Ligplot software. RESULTS: The phylogenetic analysis revealed that the considered 2022 MPVstrains were close to the USA strains. The evolutionary analysis showed the volatile nature of the genome. Moreover, 9-mer peptide sequence was identified as an epitope for vaccine development. CONCLUSIONS: The emergence of more virulent strains in near future may not be ruled out. Immunocompromised patients are more susceptible to this virus hence sub-unit vaccine is a better choice than a recombinant or attenuated vaccine against monkeypox. We have identified a small stretch of specific peptide which may be used for developing a subunit vaccine against this virus.
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spelling pubmed-96838662022-11-30 Detection of the peptidyl epitope for vaccine development against MPV Sarkar, Indrani Sen, Gargi Ajmal Ali, Mohammd Musaed Almutairi, Saeedah Lee, Joongku Sen, Arnab J King Saud Univ Sci Original Article BACKGROUND: Monkeypox Virus (MPV) is the cause of zoonotic disease characterized by skin-eruption with pus cell formation and lymphadenopathy. This virus belongs to the Orthopoxvirus genus with DNA as its genetic material. Previously, this infection was reported from Africa and occasionally from USA and UK. However, recently there is a sudden surge of infection in non-epidemic countries and a new strain of MPVhas been discovered. Therefore it is important to revisit the phylogeny of MPV with the addition of new strains. Recently WHO also stressed the need of developing vaccines for new strains. In this scenario we have two objectives for this study -first, to reveal the exact phylogenetic position of the 2022 strain and second, to identify specific peptides which may be used for vaccine development in the future. METHODS: The phylogenetic analysis was done with the help of Bayesian phylogeny. The dN/dS calculation was performed based on DNA polymerase genes of selected MPV strains. The peptidyl-epitope was searched in MPV2022/2 SLO strain with the help of several algorithms implemented in Allergen FP v.1.0, NetMHCII 2.3, MHCpred and Toxin Pred. The structure prediction of the proteins and peptides was performed through Hpepdock. The quality of the structures was validated through the Ramachandran plot. The molecular dynamics and simulation were performed through Gromacs software. The interaction between peptide and protein was assessed through Ligplot software. RESULTS: The phylogenetic analysis revealed that the considered 2022 MPVstrains were close to the USA strains. The evolutionary analysis showed the volatile nature of the genome. Moreover, 9-mer peptide sequence was identified as an epitope for vaccine development. CONCLUSIONS: The emergence of more virulent strains in near future may not be ruled out. Immunocompromised patients are more susceptible to this virus hence sub-unit vaccine is a better choice than a recombinant or attenuated vaccine against monkeypox. We have identified a small stretch of specific peptide which may be used for developing a subunit vaccine against this virus. The Authors. Published by Elsevier B.V. on behalf of King Saud University. 2023-01 2022-11-24 /pmc/articles/PMC9683866/ /pubmed/36466790 http://dx.doi.org/10.1016/j.jksus.2022.102458 Text en © 2022 The Authors Elsevier has created a Monkeypox Information Center (https://www.elsevier.com/connect/monkeypox-information-center) in response to the declared public health emergency of international concern, with free information in English on the monkeypox virus. The Monkeypox Information Center is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its monkeypox related research that is available on the Monkeypox Information Center - including this research content - immediately available in publicly funded repositories, with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the Monkeypox Information Center remains active.
spellingShingle Original Article
Sarkar, Indrani
Sen, Gargi
Ajmal Ali, Mohammd
Musaed Almutairi, Saeedah
Lee, Joongku
Sen, Arnab
Detection of the peptidyl epitope for vaccine development against MPV
title Detection of the peptidyl epitope for vaccine development against MPV
title_full Detection of the peptidyl epitope for vaccine development against MPV
title_fullStr Detection of the peptidyl epitope for vaccine development against MPV
title_full_unstemmed Detection of the peptidyl epitope for vaccine development against MPV
title_short Detection of the peptidyl epitope for vaccine development against MPV
title_sort detection of the peptidyl epitope for vaccine development against mpv
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9683866/
https://www.ncbi.nlm.nih.gov/pubmed/36466790
http://dx.doi.org/10.1016/j.jksus.2022.102458
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