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Outer Membrane Vesicles from Neisseria Meningitidis (Proteossome) Used for Nanostructured Zika Virus Vaccine Production
The increase of Zika virus (ZIKV) infections in Brazil in the last two years leaves a prophylactic measures on alert for this new and emerging pathogen. Concerning of our positive experience, we developed a new prototype using Neisseria meningitidis outer membrane vesicles (OMV) on ZIKV cell growth...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974080/ https://www.ncbi.nlm.nih.gov/pubmed/29844457 http://dx.doi.org/10.1038/s41598-018-26508-z |
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author | Martins, Paula Machado, Daisy Theizen, Thais Holtz Guarnieri, João Paulo Oliveira Bernardes, Bruno Gaia Gomide, Gabriel Piccirillo Corat, Marcus Alexandre Finzi Abbehausen, Camilla Módena, José Luiz Proença Melo, Carlos Fernando Odir Rodrigues Morishita, Karen Noda Catharino, Rodrigo Ramos Arns, Clarice Weis Lancellotti, Marcelo |
author_facet | Martins, Paula Machado, Daisy Theizen, Thais Holtz Guarnieri, João Paulo Oliveira Bernardes, Bruno Gaia Gomide, Gabriel Piccirillo Corat, Marcus Alexandre Finzi Abbehausen, Camilla Módena, José Luiz Proença Melo, Carlos Fernando Odir Rodrigues Morishita, Karen Noda Catharino, Rodrigo Ramos Arns, Clarice Weis Lancellotti, Marcelo |
author_sort | Martins, Paula |
collection | PubMed |
description | The increase of Zika virus (ZIKV) infections in Brazil in the last two years leaves a prophylactic measures on alert for this new and emerging pathogen. Concerning of our positive experience, we developed a new prototype using Neisseria meningitidis outer membrane vesicles (OMV) on ZIKV cell growth in a fusion of OMV in the envelope of virus particles. The fusion of nanoparticles resulting from outer membrane vesicles of N. meningitidis with infected C6/36 cells line were analyzed by Nano tracking analysis (NTA), zeta potential, differential light scattering (DLS), scan and scanning transmission eletronic microscopy (SEM and STEM) and high resolution mass spectometry (HRMS) for nanostructure characterization. Also, the vaccination effects were viewed by immune response in mice protocols immunization (ELISA and inflammatory chemokines) confirmed by Zika virus soroneutralization test. The results of immunizations in mice showed that antibody production had a titer greater than 1:160 as compared to unvaccinated mice. The immune response of the adjuvant and non-adjuvant formulation activated the cellular immune response TH1 and TH2. In addition, the serum neutralization was able to prevent infection of virus particles in the glial tumor cell model (M059J). This research shows efficient strategies without recombinant technology or DNA vaccines. |
format | Online Article Text |
id | pubmed-5974080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59740802018-05-31 Outer Membrane Vesicles from Neisseria Meningitidis (Proteossome) Used for Nanostructured Zika Virus Vaccine Production Martins, Paula Machado, Daisy Theizen, Thais Holtz Guarnieri, João Paulo Oliveira Bernardes, Bruno Gaia Gomide, Gabriel Piccirillo Corat, Marcus Alexandre Finzi Abbehausen, Camilla Módena, José Luiz Proença Melo, Carlos Fernando Odir Rodrigues Morishita, Karen Noda Catharino, Rodrigo Ramos Arns, Clarice Weis Lancellotti, Marcelo Sci Rep Article The increase of Zika virus (ZIKV) infections in Brazil in the last two years leaves a prophylactic measures on alert for this new and emerging pathogen. Concerning of our positive experience, we developed a new prototype using Neisseria meningitidis outer membrane vesicles (OMV) on ZIKV cell growth in a fusion of OMV in the envelope of virus particles. The fusion of nanoparticles resulting from outer membrane vesicles of N. meningitidis with infected C6/36 cells line were analyzed by Nano tracking analysis (NTA), zeta potential, differential light scattering (DLS), scan and scanning transmission eletronic microscopy (SEM and STEM) and high resolution mass spectometry (HRMS) for nanostructure characterization. Also, the vaccination effects were viewed by immune response in mice protocols immunization (ELISA and inflammatory chemokines) confirmed by Zika virus soroneutralization test. The results of immunizations in mice showed that antibody production had a titer greater than 1:160 as compared to unvaccinated mice. The immune response of the adjuvant and non-adjuvant formulation activated the cellular immune response TH1 and TH2. In addition, the serum neutralization was able to prevent infection of virus particles in the glial tumor cell model (M059J). This research shows efficient strategies without recombinant technology or DNA vaccines. Nature Publishing Group UK 2018-05-29 /pmc/articles/PMC5974080/ /pubmed/29844457 http://dx.doi.org/10.1038/s41598-018-26508-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Martins, Paula Machado, Daisy Theizen, Thais Holtz Guarnieri, João Paulo Oliveira Bernardes, Bruno Gaia Gomide, Gabriel Piccirillo Corat, Marcus Alexandre Finzi Abbehausen, Camilla Módena, José Luiz Proença Melo, Carlos Fernando Odir Rodrigues Morishita, Karen Noda Catharino, Rodrigo Ramos Arns, Clarice Weis Lancellotti, Marcelo Outer Membrane Vesicles from Neisseria Meningitidis (Proteossome) Used for Nanostructured Zika Virus Vaccine Production |
title | Outer Membrane Vesicles from Neisseria Meningitidis (Proteossome) Used for Nanostructured Zika Virus Vaccine Production |
title_full | Outer Membrane Vesicles from Neisseria Meningitidis (Proteossome) Used for Nanostructured Zika Virus Vaccine Production |
title_fullStr | Outer Membrane Vesicles from Neisseria Meningitidis (Proteossome) Used for Nanostructured Zika Virus Vaccine Production |
title_full_unstemmed | Outer Membrane Vesicles from Neisseria Meningitidis (Proteossome) Used for Nanostructured Zika Virus Vaccine Production |
title_short | Outer Membrane Vesicles from Neisseria Meningitidis (Proteossome) Used for Nanostructured Zika Virus Vaccine Production |
title_sort | outer membrane vesicles from neisseria meningitidis (proteossome) used for nanostructured zika virus vaccine production |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974080/ https://www.ncbi.nlm.nih.gov/pubmed/29844457 http://dx.doi.org/10.1038/s41598-018-26508-z |
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