Cargando…

Characterization of Chikungunya Virus-Like Particles

Chikungunya virus (CHIKV) is becoming a global concern due to the increasing number of outbreaks throughout the world and the absence of any CHIKV-specific vaccine or treatment. Virus-like particles (VLPs) are multistructured proteins that mimic the organization and conformation of native viruses bu...

Descripción completa

Detalles Bibliográficos
Autores principales: Noranate, Nitchakarn, Takeda, Naokazu, Chetanachan, Prukswan, Sittisaman, Pathompong, A-nuegoonpipat, Atchareeya, Anantapreecha, Surapee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180278/
https://www.ncbi.nlm.nih.gov/pubmed/25265335
http://dx.doi.org/10.1371/journal.pone.0108169
_version_ 1782337200845750272
author Noranate, Nitchakarn
Takeda, Naokazu
Chetanachan, Prukswan
Sittisaman, Pathompong
A-nuegoonpipat, Atchareeya
Anantapreecha, Surapee
author_facet Noranate, Nitchakarn
Takeda, Naokazu
Chetanachan, Prukswan
Sittisaman, Pathompong
A-nuegoonpipat, Atchareeya
Anantapreecha, Surapee
author_sort Noranate, Nitchakarn
collection PubMed
description Chikungunya virus (CHIKV) is becoming a global concern due to the increasing number of outbreaks throughout the world and the absence of any CHIKV-specific vaccine or treatment. Virus-like particles (VLPs) are multistructured proteins that mimic the organization and conformation of native viruses but lack the viral genome. They are noninfectious and potentially safer vaccine candidates. Recent studies demonstrated that the yield of CHIKV VLPs varies depending on the strains, despite the 95% amino acid similarity of the strains. This might be due to the codon usage, since protein expression is differently controlled by different organisms. We optimized the region encoding CHIKV structural proteins, C-E3-E2-6k-E1, inserted it into a mammalian expression vector, and used the resulting construct to transfect 293 cells. We detected 50-kDa proteins corresponding to E1 and/or E2 in the cell lysate and the supernatant. Transmission electron microscopy revealed spherical particles with a 50- to 60-nm diameter in the supernatant that resembled the native CHIKV virions. The buoyant density of the VLPs was 1.23 g/mL, and the yield was 20 µg purified VLPs per 10(8) cells. The VLPs aggregated when mixed with convalescent sera from chikungunya patients, indicating that their antigenicity is similar to that of native CHIKV. Antibodies elicited with the VLPs were capable of detecting native CHIKV, demonstrating that the VLPs retain immunogenicity similar to that of the native virion. These results indicated that CHIKV VLPs are morphologically, antigenically, and immunologically similar to the native CHIKV, suggesting that they have potential for use in chikungunya vaccines.
format Online
Article
Text
id pubmed-4180278
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-41802782014-10-07 Characterization of Chikungunya Virus-Like Particles Noranate, Nitchakarn Takeda, Naokazu Chetanachan, Prukswan Sittisaman, Pathompong A-nuegoonpipat, Atchareeya Anantapreecha, Surapee PLoS One Research Article Chikungunya virus (CHIKV) is becoming a global concern due to the increasing number of outbreaks throughout the world and the absence of any CHIKV-specific vaccine or treatment. Virus-like particles (VLPs) are multistructured proteins that mimic the organization and conformation of native viruses but lack the viral genome. They are noninfectious and potentially safer vaccine candidates. Recent studies demonstrated that the yield of CHIKV VLPs varies depending on the strains, despite the 95% amino acid similarity of the strains. This might be due to the codon usage, since protein expression is differently controlled by different organisms. We optimized the region encoding CHIKV structural proteins, C-E3-E2-6k-E1, inserted it into a mammalian expression vector, and used the resulting construct to transfect 293 cells. We detected 50-kDa proteins corresponding to E1 and/or E2 in the cell lysate and the supernatant. Transmission electron microscopy revealed spherical particles with a 50- to 60-nm diameter in the supernatant that resembled the native CHIKV virions. The buoyant density of the VLPs was 1.23 g/mL, and the yield was 20 µg purified VLPs per 10(8) cells. The VLPs aggregated when mixed with convalescent sera from chikungunya patients, indicating that their antigenicity is similar to that of native CHIKV. Antibodies elicited with the VLPs were capable of detecting native CHIKV, demonstrating that the VLPs retain immunogenicity similar to that of the native virion. These results indicated that CHIKV VLPs are morphologically, antigenically, and immunologically similar to the native CHIKV, suggesting that they have potential for use in chikungunya vaccines. Public Library of Science 2014-09-29 /pmc/articles/PMC4180278/ /pubmed/25265335 http://dx.doi.org/10.1371/journal.pone.0108169 Text en © 2014 Noranate et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Noranate, Nitchakarn
Takeda, Naokazu
Chetanachan, Prukswan
Sittisaman, Pathompong
A-nuegoonpipat, Atchareeya
Anantapreecha, Surapee
Characterization of Chikungunya Virus-Like Particles
title Characterization of Chikungunya Virus-Like Particles
title_full Characterization of Chikungunya Virus-Like Particles
title_fullStr Characterization of Chikungunya Virus-Like Particles
title_full_unstemmed Characterization of Chikungunya Virus-Like Particles
title_short Characterization of Chikungunya Virus-Like Particles
title_sort characterization of chikungunya virus-like particles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180278/
https://www.ncbi.nlm.nih.gov/pubmed/25265335
http://dx.doi.org/10.1371/journal.pone.0108169
work_keys_str_mv AT noranatenitchakarn characterizationofchikungunyaviruslikeparticles
AT takedanaokazu characterizationofchikungunyaviruslikeparticles
AT chetanachanprukswan characterizationofchikungunyaviruslikeparticles
AT sittisamanpathompong characterizationofchikungunyaviruslikeparticles
AT anuegoonpipatatchareeya characterizationofchikungunyaviruslikeparticles
AT anantapreechasurapee characterizationofchikungunyaviruslikeparticles