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

Autor: Rouxel RN; VIM, INRA, Université Paris-Saclay, 78350, Jouy-en-Josas, France., Mérour E; VIM, INRA, Université Paris-Saclay, 78350, Jouy-en-Josas, France., Biacchesi S; VIM, INRA, Université Paris-Saclay, 78350, Jouy-en-Josas, France., Brémont M; VIM, INRA, Université Paris-Saclay, 78350, Jouy-en-Josas, France.
Jazyk: angličtina
Zdroj: PloS one [PLoS One] 2016 Oct 06; Vol. 11 (10), pp. e0164245. Date of Electronic Publication: 2016 Oct 06 (Print Publication: 2016).
DOI: 10.1371/journal.pone.0164245
Abstrakt: 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.
Competing Interests: The authors have declared that no competing interests exist.
Databáze: MEDLINE