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Highly conserved epitopes of DENV structural and non-structural proteins: Candidates for universal vaccine targets

Dengue is a severe emerging arthropod borne viral disease occurring globally. Around two fifths of the world's population, or up to 3.9 billion people, are at a risk of dengue infection. Infection induces a life-long protective immunity to the homologous serotype but confers only partial and tr...

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Autores principales: Verma, Mansi, Bhatnagar, Shradha, Kumari, Kavita, Mittal, Nidhi, Sukhralia, Shivani, Gopirajan AT, Shruthi, Dhanaraj, P.S., Lal, Rup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125761/
https://www.ncbi.nlm.nih.gov/pubmed/30738967
http://dx.doi.org/10.1016/j.gene.2019.02.001
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author Verma, Mansi
Bhatnagar, Shradha
Kumari, Kavita
Mittal, Nidhi
Sukhralia, Shivani
Gopirajan AT, Shruthi
Dhanaraj, P.S.
Lal, Rup
author_facet Verma, Mansi
Bhatnagar, Shradha
Kumari, Kavita
Mittal, Nidhi
Sukhralia, Shivani
Gopirajan AT, Shruthi
Dhanaraj, P.S.
Lal, Rup
author_sort Verma, Mansi
collection PubMed
description Dengue is a severe emerging arthropod borne viral disease occurring globally. Around two fifths of the world's population, or up to 3.9 billion people, are at a risk of dengue infection. Infection induces a life-long protective immunity to the homologous serotype but confers only partial and transient protection against subsequent infection caused by other serotypes. Thus, there is a need for a vaccine which is capable of providing a life- long protection against all the serotypes of dengue virus. In our study, comparative genomics of Dengue virus (DENV) was conducted to explore potential candidates for novel vaccine targets. From our analysis we successfully found 100% conserved epitopes in Envelope protein (RCPTQGE); NS3 (SAAQRRGR, PGTSGSPI); NS4A (QRTPQDNQL); NS4B (LQAKATREAQKRA) and NS5 proteins (QRGSGQV) in all DENV serotypes. Some serotype specific conserved motifs were also found in NS1, NS5, Capsid, PrM and Envelope proteins. Using comparative genomics and immunoinformatics approach, we could find conserved epitopes which can be explored as peptide vaccine candidates to combat dengue worldwide. Serotype specific epitopes can also be exploited for rapid diagnostics. All ten proteins are explored to find the conserved epitopes in DENV serotypes, thus making it the most extensively studied viral genome so far.
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spelling pubmed-71257612020-04-08 Highly conserved epitopes of DENV structural and non-structural proteins: Candidates for universal vaccine targets Verma, Mansi Bhatnagar, Shradha Kumari, Kavita Mittal, Nidhi Sukhralia, Shivani Gopirajan AT, Shruthi Dhanaraj, P.S. Lal, Rup Gene Article Dengue is a severe emerging arthropod borne viral disease occurring globally. Around two fifths of the world's population, or up to 3.9 billion people, are at a risk of dengue infection. Infection induces a life-long protective immunity to the homologous serotype but confers only partial and transient protection against subsequent infection caused by other serotypes. Thus, there is a need for a vaccine which is capable of providing a life- long protection against all the serotypes of dengue virus. In our study, comparative genomics of Dengue virus (DENV) was conducted to explore potential candidates for novel vaccine targets. From our analysis we successfully found 100% conserved epitopes in Envelope protein (RCPTQGE); NS3 (SAAQRRGR, PGTSGSPI); NS4A (QRTPQDNQL); NS4B (LQAKATREAQKRA) and NS5 proteins (QRGSGQV) in all DENV serotypes. Some serotype specific conserved motifs were also found in NS1, NS5, Capsid, PrM and Envelope proteins. Using comparative genomics and immunoinformatics approach, we could find conserved epitopes which can be explored as peptide vaccine candidates to combat dengue worldwide. Serotype specific epitopes can also be exploited for rapid diagnostics. All ten proteins are explored to find the conserved epitopes in DENV serotypes, thus making it the most extensively studied viral genome so far. Elsevier B.V. 2019-05-05 2019-02-08 /pmc/articles/PMC7125761/ /pubmed/30738967 http://dx.doi.org/10.1016/j.gene.2019.02.001 Text en © 2019 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database 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 COVID-19 resource centre remains active.
spellingShingle Article
Verma, Mansi
Bhatnagar, Shradha
Kumari, Kavita
Mittal, Nidhi
Sukhralia, Shivani
Gopirajan AT, Shruthi
Dhanaraj, P.S.
Lal, Rup
Highly conserved epitopes of DENV structural and non-structural proteins: Candidates for universal vaccine targets
title Highly conserved epitopes of DENV structural and non-structural proteins: Candidates for universal vaccine targets
title_full Highly conserved epitopes of DENV structural and non-structural proteins: Candidates for universal vaccine targets
title_fullStr Highly conserved epitopes of DENV structural and non-structural proteins: Candidates for universal vaccine targets
title_full_unstemmed Highly conserved epitopes of DENV structural and non-structural proteins: Candidates for universal vaccine targets
title_short Highly conserved epitopes of DENV structural and non-structural proteins: Candidates for universal vaccine targets
title_sort highly conserved epitopes of denv structural and non-structural proteins: candidates for universal vaccine targets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125761/
https://www.ncbi.nlm.nih.gov/pubmed/30738967
http://dx.doi.org/10.1016/j.gene.2019.02.001
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