Cargando…

Complete Protection against Influenza Virus H1N1 Strain A/PR/8/34 Challenge in Mice Immunized with Non-Adjuvanted Novirhabdovirus Vaccines

Novirhabdoviruses like Viral Hemorrhagic Septicemia Virus (VHSV) and Infectious Hematopoietic Necrosis Virus (IHNV) are fish-infecting Rhabdoviruses belonging to the Mononegavirales order. By reverse genetics, we previously showed that a recombinant VHSV expressing the West Nile Virus (WNV) E glycop...

Descripción completa

Detalles Bibliográficos
Autores principales: Rouxel, Ronan N., Mérour, Emilie, Biacchesi, Stéphane, Brémont, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053517/
https://www.ncbi.nlm.nih.gov/pubmed/27711176
http://dx.doi.org/10.1371/journal.pone.0164245
_version_ 1782458432112033792
author Rouxel, Ronan N.
Mérour, Emilie
Biacchesi, Stéphane
Brémont, Michel
author_facet Rouxel, Ronan N.
Mérour, Emilie
Biacchesi, Stéphane
Brémont, Michel
author_sort Rouxel, Ronan N.
collection PubMed
description Novirhabdoviruses like Viral Hemorrhagic Septicemia Virus (VHSV) and Infectious Hematopoietic Necrosis Virus (IHNV) are fish-infecting Rhabdoviruses belonging to the Mononegavirales order. By reverse genetics, we previously showed that a recombinant VHSV expressing the West Nile Virus (WNV) E glycoprotein could serve as a vaccine platform against WNV. In the current study, we aimed to evaluate the potential of the Novirhabdovirus platform as a vaccine against influenza virus. Recombinant Novirhabdoviruses, rVHSV-HA and rIHNV-HA, expressing at the viral surface the hemagglutinin HA ectodomain were generated and used to immunized mice. We showed that mice immunized with either, rVHSV-HA or rIHNV-HA, elicited a strong neutralizing antibody response against influenza virus. A complete protection was conferred to the immunized mice when challenged with a lethal dose of influenza H1N1 A/PR/8/34 virus. Furthermore we showed that although acting as inert antigen in mice, since naturally inactivated over 20°C, mice immunized with rVHSV-HA or rIHNV-HA in the absence of adjuvant were also completely protected from a lethal challenge. Novirhabdoviruses platform are of particular interest as vaccines for mammals since they are cost effective to produce, relatively easy to generate and very effective to protect immunized animals.
format Online
Article
Text
id pubmed-5053517
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-50535172016-10-27 Complete Protection against Influenza Virus H1N1 Strain A/PR/8/34 Challenge in Mice Immunized with Non-Adjuvanted Novirhabdovirus Vaccines Rouxel, Ronan N. Mérour, Emilie Biacchesi, Stéphane Brémont, Michel PLoS One Research Article Novirhabdoviruses like Viral Hemorrhagic Septicemia Virus (VHSV) and Infectious Hematopoietic Necrosis Virus (IHNV) are fish-infecting Rhabdoviruses belonging to the Mononegavirales order. By reverse genetics, we previously showed that a recombinant VHSV expressing the West Nile Virus (WNV) E glycoprotein could serve as a vaccine platform against WNV. In the current study, we aimed to evaluate the potential of the Novirhabdovirus platform as a vaccine against influenza virus. Recombinant Novirhabdoviruses, rVHSV-HA and rIHNV-HA, expressing at the viral surface the hemagglutinin HA ectodomain were generated and used to immunized mice. We showed that mice immunized with either, rVHSV-HA or rIHNV-HA, elicited a strong neutralizing antibody response against influenza virus. A complete protection was conferred to the immunized mice when challenged with a lethal dose of influenza H1N1 A/PR/8/34 virus. Furthermore we showed that although acting as inert antigen in mice, since naturally inactivated over 20°C, mice immunized with rVHSV-HA or rIHNV-HA in the absence of adjuvant were also completely protected from a lethal challenge. Novirhabdoviruses platform are of particular interest as vaccines for mammals since they are cost effective to produce, relatively easy to generate and very effective to protect immunized animals. Public Library of Science 2016-10-06 /pmc/articles/PMC5053517/ /pubmed/27711176 http://dx.doi.org/10.1371/journal.pone.0164245 Text en © 2016 Rouxel 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rouxel, Ronan N.
Mérour, Emilie
Biacchesi, Stéphane
Brémont, Michel
Complete Protection against Influenza Virus H1N1 Strain A/PR/8/34 Challenge in Mice Immunized with Non-Adjuvanted Novirhabdovirus Vaccines
title Complete Protection against Influenza Virus H1N1 Strain A/PR/8/34 Challenge in Mice Immunized with Non-Adjuvanted Novirhabdovirus Vaccines
title_full Complete Protection against Influenza Virus H1N1 Strain A/PR/8/34 Challenge in Mice Immunized with Non-Adjuvanted Novirhabdovirus Vaccines
title_fullStr Complete Protection against Influenza Virus H1N1 Strain A/PR/8/34 Challenge in Mice Immunized with Non-Adjuvanted Novirhabdovirus Vaccines
title_full_unstemmed Complete Protection against Influenza Virus H1N1 Strain A/PR/8/34 Challenge in Mice Immunized with Non-Adjuvanted Novirhabdovirus Vaccines
title_short Complete Protection against Influenza Virus H1N1 Strain A/PR/8/34 Challenge in Mice Immunized with Non-Adjuvanted Novirhabdovirus Vaccines
title_sort complete protection against influenza virus h1n1 strain a/pr/8/34 challenge in mice immunized with non-adjuvanted novirhabdovirus vaccines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053517/
https://www.ncbi.nlm.nih.gov/pubmed/27711176
http://dx.doi.org/10.1371/journal.pone.0164245
work_keys_str_mv AT rouxelronann completeprotectionagainstinfluenzavirush1n1strainapr834challengeinmiceimmunizedwithnonadjuvantednovirhabdovirusvaccines
AT merouremilie completeprotectionagainstinfluenzavirush1n1strainapr834challengeinmiceimmunizedwithnonadjuvantednovirhabdovirusvaccines
AT biacchesistephane completeprotectionagainstinfluenzavirush1n1strainapr834challengeinmiceimmunizedwithnonadjuvantednovirhabdovirusvaccines
AT bremontmichel completeprotectionagainstinfluenzavirush1n1strainapr834challengeinmiceimmunizedwithnonadjuvantednovirhabdovirusvaccines