Cargando…

Development of Multi-epitope Based Subunit Vaccine Against Crimean-Congo Hemorrhagic Fever Virus Using Reverse Vaccinology Approach

Crimean-Congo hemorrhagic fever (CCHF) is a viral disease caused by the Crimean-Congo hemorrhagic fever virus (CCHFV) of the Nairovirus genus. CCHF has occurred endemically in several regions of Africa, Southern Europe, and Central and Southeast Asia, with a case fatality rate of 5 to 80%. The World...

Descripción completa

Detalles Bibliográficos
Autores principales: Imran, Md. Ashik, Islam, Md. Rubiath, Saha, Akash, Ferdousee, Shahida, Mishu, Moshiul Alam, Ghosh, Ajit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9244561/
https://www.ncbi.nlm.nih.gov/pubmed/35789799
http://dx.doi.org/10.1007/s10989-022-10430-0
_version_ 1784738549363376128
author Imran, Md. Ashik
Islam, Md. Rubiath
Saha, Akash
Ferdousee, Shahida
Mishu, Moshiul Alam
Ghosh, Ajit
author_facet Imran, Md. Ashik
Islam, Md. Rubiath
Saha, Akash
Ferdousee, Shahida
Mishu, Moshiul Alam
Ghosh, Ajit
author_sort Imran, Md. Ashik
collection PubMed
description Crimean-Congo hemorrhagic fever (CCHF) is a viral disease caused by the Crimean-Congo hemorrhagic fever virus (CCHFV) of the Nairovirus genus. CCHF has occurred endemically in several regions of Africa, Southern Europe, and Central and Southeast Asia, with a case fatality rate of 5 to 80%. The World health organization enlisted CCHF as one of the top prioritized diseases for research and development in emergency contexts that making it a public health concern as no effective vaccine is available till date. Therefore, the present study aims to develop an effective multi-epitope subunit vaccine using immunoinformatics and reverse vaccinology approach against this virus. The B-cell and T-cell epitopes were predicted from structural and non-structural proteins, and filtered by immunogenicity, allergenicity, toxicity, conservancy, and cross-reactivity. The computational analysis revealed that the epitopes could induce an adequate immune response and had strong associations with their respective human leukocyte antigen (HLA) alleles with 98.94% of total world population coverage. Finally, the vaccine with 427 amino acids was constructed by connecting 8 cytotoxic T-lymphocytes, 4 helper T-lymphocytes, and 10 B-cell epitopes with appropriate linkers and β-defensin as an adjuvant. The antigenicity, allergenicity, solubility, and physiochemical properties of the vaccine were evaluated, followed by structural modelling, refinement, and validation. In addition, molecular docking and molecular dynamic simulations revealed a robust binding affinity and stability of the vaccine-immune receptor complex. Moreover, the codons were optimized for its higher expression in Escherichia coli (E. coli) K12 strain followed by in silico cloning. The proposed subunit vaccine developed in this study could be a potential candidate against CCHFV. However, further experimental validation is required to ensure the immunogenicity and safety profile of the proposed vaccine for combating and eradicating CCHFV. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10989-022-10430-0.
format Online
Article
Text
id pubmed-9244561
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Springer Netherlands
record_format MEDLINE/PubMed
spelling pubmed-92445612022-06-30 Development of Multi-epitope Based Subunit Vaccine Against Crimean-Congo Hemorrhagic Fever Virus Using Reverse Vaccinology Approach Imran, Md. Ashik Islam, Md. Rubiath Saha, Akash Ferdousee, Shahida Mishu, Moshiul Alam Ghosh, Ajit Int J Pept Res Ther Article Crimean-Congo hemorrhagic fever (CCHF) is a viral disease caused by the Crimean-Congo hemorrhagic fever virus (CCHFV) of the Nairovirus genus. CCHF has occurred endemically in several regions of Africa, Southern Europe, and Central and Southeast Asia, with a case fatality rate of 5 to 80%. The World health organization enlisted CCHF as one of the top prioritized diseases for research and development in emergency contexts that making it a public health concern as no effective vaccine is available till date. Therefore, the present study aims to develop an effective multi-epitope subunit vaccine using immunoinformatics and reverse vaccinology approach against this virus. The B-cell and T-cell epitopes were predicted from structural and non-structural proteins, and filtered by immunogenicity, allergenicity, toxicity, conservancy, and cross-reactivity. The computational analysis revealed that the epitopes could induce an adequate immune response and had strong associations with their respective human leukocyte antigen (HLA) alleles with 98.94% of total world population coverage. Finally, the vaccine with 427 amino acids was constructed by connecting 8 cytotoxic T-lymphocytes, 4 helper T-lymphocytes, and 10 B-cell epitopes with appropriate linkers and β-defensin as an adjuvant. The antigenicity, allergenicity, solubility, and physiochemical properties of the vaccine were evaluated, followed by structural modelling, refinement, and validation. In addition, molecular docking and molecular dynamic simulations revealed a robust binding affinity and stability of the vaccine-immune receptor complex. Moreover, the codons were optimized for its higher expression in Escherichia coli (E. coli) K12 strain followed by in silico cloning. The proposed subunit vaccine developed in this study could be a potential candidate against CCHFV. However, further experimental validation is required to ensure the immunogenicity and safety profile of the proposed vaccine for combating and eradicating CCHFV. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10989-022-10430-0. Springer Netherlands 2022-06-24 2022 /pmc/articles/PMC9244561/ /pubmed/35789799 http://dx.doi.org/10.1007/s10989-022-10430-0 Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2022 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
Imran, Md. Ashik
Islam, Md. Rubiath
Saha, Akash
Ferdousee, Shahida
Mishu, Moshiul Alam
Ghosh, Ajit
Development of Multi-epitope Based Subunit Vaccine Against Crimean-Congo Hemorrhagic Fever Virus Using Reverse Vaccinology Approach
title Development of Multi-epitope Based Subunit Vaccine Against Crimean-Congo Hemorrhagic Fever Virus Using Reverse Vaccinology Approach
title_full Development of Multi-epitope Based Subunit Vaccine Against Crimean-Congo Hemorrhagic Fever Virus Using Reverse Vaccinology Approach
title_fullStr Development of Multi-epitope Based Subunit Vaccine Against Crimean-Congo Hemorrhagic Fever Virus Using Reverse Vaccinology Approach
title_full_unstemmed Development of Multi-epitope Based Subunit Vaccine Against Crimean-Congo Hemorrhagic Fever Virus Using Reverse Vaccinology Approach
title_short Development of Multi-epitope Based Subunit Vaccine Against Crimean-Congo Hemorrhagic Fever Virus Using Reverse Vaccinology Approach
title_sort development of multi-epitope based subunit vaccine against crimean-congo hemorrhagic fever virus using reverse vaccinology approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9244561/
https://www.ncbi.nlm.nih.gov/pubmed/35789799
http://dx.doi.org/10.1007/s10989-022-10430-0
work_keys_str_mv AT imranmdashik developmentofmultiepitopebasedsubunitvaccineagainstcrimeancongohemorrhagicfevervirususingreversevaccinologyapproach
AT islammdrubiath developmentofmultiepitopebasedsubunitvaccineagainstcrimeancongohemorrhagicfevervirususingreversevaccinologyapproach
AT sahaakash developmentofmultiepitopebasedsubunitvaccineagainstcrimeancongohemorrhagicfevervirususingreversevaccinologyapproach
AT ferdouseeshahida developmentofmultiepitopebasedsubunitvaccineagainstcrimeancongohemorrhagicfevervirususingreversevaccinologyapproach
AT mishumoshiulalam developmentofmultiepitopebasedsubunitvaccineagainstcrimeancongohemorrhagicfevervirususingreversevaccinologyapproach
AT ghoshajit developmentofmultiepitopebasedsubunitvaccineagainstcrimeancongohemorrhagicfevervirususingreversevaccinologyapproach