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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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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 |
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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 |
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