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A single amino acid change in the non-structural NV protein impacts the virulence phenotype of Viral hemorrhagic septicemia virus in trout
Author(s) -
Laury Baillon,
Emilie Mérour,
Joëlle Cabon,
Lénaïg Louboutin,
Hélène Quenault,
Fabrice Touzain,
Thierry Morin,
Yannick Blanchard,
Stéphane Biacchesi,
Michel Brémont
Publication year - 2017
Publication title -
journal of general virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.55
H-Index - 167
eISSN - 1465-2099
pISSN - 0022-1317
DOI - 10.1099/jgv.0.000830
Subject(s) - virulence , biology , virology , reverse genetics , virus , infectious hematopoietic necrosis virus , asparagine , trout , mononegavirales , serine , amino acid , genome , microbiology and biotechnology , gene , genetics , rainbow trout , viral disease , fish <actinopterygii> , paramyxoviridae , phosphorylation , fishery
Novirhabdoviruses like the Viral hemorrhagic septicemia virus (VHSV) are rhabdoviruses infecting fish. In the current study, RNA genomes of different VHSV field isolates classified as high, medium or low virulent phenotypes have been sequenced by next-generation sequencing and compared. Various amino acid changes, depending on the VHSV phenotype, have been identified in all the VHSV proteins. As a starting point, we focused our study on the non-virion (NV) non-structural protein in which an arginine residue (R116) is present in all the virulent isolates and replaced by a serine/asparagine residue S/N116 in the attenuated isolates. A recombinant virus derived from a virulent VHSV strain in which the NV R116 residue has been replaced by a serine, rVHSVNVR116S, was generated by reverse genetics and used to infect juvenile trout. We showed that rVHSVNVR116S was highly attenuated and that surviving fish were almost completely protected from a challenge with the wild-type VHSV.

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