Attenuated infectious hematopoietic necrosis virus with rearranged gene order as potential vaccine

The genome of infectious hematopoietic necrosis virus (IHNV), a salmonid novirhabdovirus, has been engineered to modify the gene order and to evaluate the impact on a possible attenuation of the virus in vitro and in vivo. By reverse genetics, eight recombinant IHNVs (rIHNVs), termed NxGy according to the respective positions of the nucleoprotein (N) and glycoprotein (G) genes along the genome, have been recovered. All rIHNVs have been fully characterized in vitro for their cytopathic effects, kinetics of replication, and profiles of viral gene transcription. These rIHNVs are stable through up to 10 passages in cell culture. Following bath immersion administration of the various rIHNVs to juvenile trout, some of the rIHNVs were clearly attenuated (N2G3, N2G4, N3G4, and N4G1). The position of the N gene seems to be one of the most critical features correlated to the level of viral attenuation. The induced immune response potential in fish was evaluated by enzyme-linked immunosorbent spot assay (ELISPOT) and seroneutralization assays. The recombinant virus N2G3 induced a strong antibody response in immunized fish and conferred 86% of protection against wild-type IHNV challenge in trout, thus representing a promising starting point for the development of a live attenuated vaccine candidate. © 2016, American Society for Microbiology. All Rights Reserved.

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Main Authors: Rouxel, R. N., Tafalla, C., Mérour, E., Leal, E., Biacchesi, S., Brémont, M.
Format: journal article biblioteca
Language:eng
Published: 2016
Online Access:http://hdl.handle.net/20.500.12792/3894
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spelling dig-inia-es-20.500.12792-38942020-12-15T09:14:37Z Attenuated infectious hematopoietic necrosis virus with rearranged gene order as potential vaccine Rouxel, R. N. Tafalla, C. Mérour, E. Leal, E. Biacchesi, S. Brémont, M. The genome of infectious hematopoietic necrosis virus (IHNV), a salmonid novirhabdovirus, has been engineered to modify the gene order and to evaluate the impact on a possible attenuation of the virus in vitro and in vivo. By reverse genetics, eight recombinant IHNVs (rIHNVs), termed NxGy according to the respective positions of the nucleoprotein (N) and glycoprotein (G) genes along the genome, have been recovered. All rIHNVs have been fully characterized in vitro for their cytopathic effects, kinetics of replication, and profiles of viral gene transcription. These rIHNVs are stable through up to 10 passages in cell culture. Following bath immersion administration of the various rIHNVs to juvenile trout, some of the rIHNVs were clearly attenuated (N2G3, N2G4, N3G4, and N4G1). The position of the N gene seems to be one of the most critical features correlated to the level of viral attenuation. The induced immune response potential in fish was evaluated by enzyme-linked immunosorbent spot assay (ELISPOT) and seroneutralization assays. The recombinant virus N2G3 induced a strong antibody response in immunized fish and conferred 86% of protection against wild-type IHNV challenge in trout, thus representing a promising starting point for the development of a live attenuated vaccine candidate. © 2016, American Society for Microbiology. All Rights Reserved. 2020-10-22T15:42:13Z 2020-10-22T15:42:13Z 2016 journal article http://hdl.handle.net/20.500.12792/3894 10.1128/JVI.01024-16 eng Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ open access
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country España
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libraryname Biblioteca del INIA España
language eng
description The genome of infectious hematopoietic necrosis virus (IHNV), a salmonid novirhabdovirus, has been engineered to modify the gene order and to evaluate the impact on a possible attenuation of the virus in vitro and in vivo. By reverse genetics, eight recombinant IHNVs (rIHNVs), termed NxGy according to the respective positions of the nucleoprotein (N) and glycoprotein (G) genes along the genome, have been recovered. All rIHNVs have been fully characterized in vitro for their cytopathic effects, kinetics of replication, and profiles of viral gene transcription. These rIHNVs are stable through up to 10 passages in cell culture. Following bath immersion administration of the various rIHNVs to juvenile trout, some of the rIHNVs were clearly attenuated (N2G3, N2G4, N3G4, and N4G1). The position of the N gene seems to be one of the most critical features correlated to the level of viral attenuation. The induced immune response potential in fish was evaluated by enzyme-linked immunosorbent spot assay (ELISPOT) and seroneutralization assays. The recombinant virus N2G3 induced a strong antibody response in immunized fish and conferred 86% of protection against wild-type IHNV challenge in trout, thus representing a promising starting point for the development of a live attenuated vaccine candidate. © 2016, American Society for Microbiology. All Rights Reserved.
format journal article
author Rouxel, R. N.
Tafalla, C.
Mérour, E.
Leal, E.
Biacchesi, S.
Brémont, M.
spellingShingle Rouxel, R. N.
Tafalla, C.
Mérour, E.
Leal, E.
Biacchesi, S.
Brémont, M.
Attenuated infectious hematopoietic necrosis virus with rearranged gene order as potential vaccine
author_facet Rouxel, R. N.
Tafalla, C.
Mérour, E.
Leal, E.
Biacchesi, S.
Brémont, M.
author_sort Rouxel, R. N.
title Attenuated infectious hematopoietic necrosis virus with rearranged gene order as potential vaccine
title_short Attenuated infectious hematopoietic necrosis virus with rearranged gene order as potential vaccine
title_full Attenuated infectious hematopoietic necrosis virus with rearranged gene order as potential vaccine
title_fullStr Attenuated infectious hematopoietic necrosis virus with rearranged gene order as potential vaccine
title_full_unstemmed Attenuated infectious hematopoietic necrosis virus with rearranged gene order as potential vaccine
title_sort attenuated infectious hematopoietic necrosis virus with rearranged gene order as potential vaccine
publishDate 2016
url http://hdl.handle.net/20.500.12792/3894
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AT leale attenuatedinfectioushematopoieticnecrosisviruswithrearrangedgeneorderaspotentialvaccine
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