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The Viral Hemorrhagic Septicemia Virus (VHSV) Markers of Virulence in Rainbow Trout (Oncorhynchus mykiss)

Viral hemorrhagic septicemia virus (VHSV) is a highly contagious virus leading to high mortality in a large panel of freshwater and marine fish species. VHSV isolates originating from marine fish show low pathogenicity in rainbow trout. The analysis of several nearly complete genome sequences from m...

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Autores principales: Baillon, Laury, Mérour, Emilie, Cabon, Joëlle, Louboutin, Lénaïg, Vigouroux, Estelle, Alencar, Anna Luiza Farias, Cuenca, Argelia, Blanchard, Yannick, Olesen, Niels Jørgen, Panzarin, Valentina, Morin, Thierry, Brémont, Michel, Biacchesi, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606196/
https://www.ncbi.nlm.nih.gov/pubmed/33193184
http://dx.doi.org/10.3389/fmicb.2020.574231
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author Baillon, Laury
Mérour, Emilie
Cabon, Joëlle
Louboutin, Lénaïg
Vigouroux, Estelle
Alencar, Anna Luiza Farias
Cuenca, Argelia
Blanchard, Yannick
Olesen, Niels Jørgen
Panzarin, Valentina
Morin, Thierry
Brémont, Michel
Biacchesi, Stéphane
author_facet Baillon, Laury
Mérour, Emilie
Cabon, Joëlle
Louboutin, Lénaïg
Vigouroux, Estelle
Alencar, Anna Luiza Farias
Cuenca, Argelia
Blanchard, Yannick
Olesen, Niels Jørgen
Panzarin, Valentina
Morin, Thierry
Brémont, Michel
Biacchesi, Stéphane
author_sort Baillon, Laury
collection PubMed
description Viral hemorrhagic septicemia virus (VHSV) is a highly contagious virus leading to high mortality in a large panel of freshwater and marine fish species. VHSV isolates originating from marine fish show low pathogenicity in rainbow trout. The analysis of several nearly complete genome sequences from marine and freshwater isolates displaying varying levels of virulence in rainbow trout suggested that only a limited number of amino acid residues might be involved in regulating the level of virulence. Based on a recent analysis of 55 VHSV strains, which were entirely sequenced and phenotyped in vivo in rainbow trout, several amino acid changes putatively involved in virulence were identified. In the present study, these amino acid changes were introduced, alone or in combination, in a highly-virulent VHSV 23–75 genome backbone by reverse genetics. A total of 35 recombinant VHSV variants were recovered and characterized for virulence in trout by bath immersion. Results confirmed the important role of the NV protein (R116S) and highlighted a major contribution of the nucleoprotein N (K46G and A241E) in regulating virulence. Single amino acid changes in these two proteins drastically affect virus pathogenicity in rainbow trout. This is particularly intriguing for the N variant (K46G) which is unable to establish an active infection in the fins of infected trout, the main portal of entry of VHSV in this species, allowing further spread in its host. In addition, salmonid cell lines were selected to assess the kinetics of replication and cytopathic effect of recombinant VHSV and discriminate virulent and avirulent variants. In conclusion, three major virulence markers were identified in the NV and N proteins. These markers explain almost all phenotypes (92.7%) observed in trout for the 55 VHSV strains analyzed in the present study and herein used for the backward validation of virulence markers. The identification of VHSV specific virulence markers in this species is of importance both to predict the in vivo phenotype of viral isolates with targeted diagnostic tests and to improve prophylactic methods such as the development of safer live-attenuated vaccines.
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spelling pubmed-76061962020-11-13 The Viral Hemorrhagic Septicemia Virus (VHSV) Markers of Virulence in Rainbow Trout (Oncorhynchus mykiss) Baillon, Laury Mérour, Emilie Cabon, Joëlle Louboutin, Lénaïg Vigouroux, Estelle Alencar, Anna Luiza Farias Cuenca, Argelia Blanchard, Yannick Olesen, Niels Jørgen Panzarin, Valentina Morin, Thierry Brémont, Michel Biacchesi, Stéphane Front Microbiol Microbiology Viral hemorrhagic septicemia virus (VHSV) is a highly contagious virus leading to high mortality in a large panel of freshwater and marine fish species. VHSV isolates originating from marine fish show low pathogenicity in rainbow trout. The analysis of several nearly complete genome sequences from marine and freshwater isolates displaying varying levels of virulence in rainbow trout suggested that only a limited number of amino acid residues might be involved in regulating the level of virulence. Based on a recent analysis of 55 VHSV strains, which were entirely sequenced and phenotyped in vivo in rainbow trout, several amino acid changes putatively involved in virulence were identified. In the present study, these amino acid changes were introduced, alone or in combination, in a highly-virulent VHSV 23–75 genome backbone by reverse genetics. A total of 35 recombinant VHSV variants were recovered and characterized for virulence in trout by bath immersion. Results confirmed the important role of the NV protein (R116S) and highlighted a major contribution of the nucleoprotein N (K46G and A241E) in regulating virulence. Single amino acid changes in these two proteins drastically affect virus pathogenicity in rainbow trout. This is particularly intriguing for the N variant (K46G) which is unable to establish an active infection in the fins of infected trout, the main portal of entry of VHSV in this species, allowing further spread in its host. In addition, salmonid cell lines were selected to assess the kinetics of replication and cytopathic effect of recombinant VHSV and discriminate virulent and avirulent variants. In conclusion, three major virulence markers were identified in the NV and N proteins. These markers explain almost all phenotypes (92.7%) observed in trout for the 55 VHSV strains analyzed in the present study and herein used for the backward validation of virulence markers. The identification of VHSV specific virulence markers in this species is of importance both to predict the in vivo phenotype of viral isolates with targeted diagnostic tests and to improve prophylactic methods such as the development of safer live-attenuated vaccines. Frontiers Media S.A. 2020-10-20 /pmc/articles/PMC7606196/ /pubmed/33193184 http://dx.doi.org/10.3389/fmicb.2020.574231 Text en Copyright © 2020 Baillon, Mérour, Cabon, Louboutin, Vigouroux, Alencar, Cuenca, Blanchard, Olesen, Panzarin, Morin, Brémont and Biacchesi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Baillon, Laury
Mérour, Emilie
Cabon, Joëlle
Louboutin, Lénaïg
Vigouroux, Estelle
Alencar, Anna Luiza Farias
Cuenca, Argelia
Blanchard, Yannick
Olesen, Niels Jørgen
Panzarin, Valentina
Morin, Thierry
Brémont, Michel
Biacchesi, Stéphane
The Viral Hemorrhagic Septicemia Virus (VHSV) Markers of Virulence in Rainbow Trout (Oncorhynchus mykiss)
title The Viral Hemorrhagic Septicemia Virus (VHSV) Markers of Virulence in Rainbow Trout (Oncorhynchus mykiss)
title_full The Viral Hemorrhagic Septicemia Virus (VHSV) Markers of Virulence in Rainbow Trout (Oncorhynchus mykiss)
title_fullStr The Viral Hemorrhagic Septicemia Virus (VHSV) Markers of Virulence in Rainbow Trout (Oncorhynchus mykiss)
title_full_unstemmed The Viral Hemorrhagic Septicemia Virus (VHSV) Markers of Virulence in Rainbow Trout (Oncorhynchus mykiss)
title_short The Viral Hemorrhagic Septicemia Virus (VHSV) Markers of Virulence in Rainbow Trout (Oncorhynchus mykiss)
title_sort viral hemorrhagic septicemia virus (vhsv) markers of virulence in rainbow trout (oncorhynchus mykiss)
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606196/
https://www.ncbi.nlm.nih.gov/pubmed/33193184
http://dx.doi.org/10.3389/fmicb.2020.574231
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