Characterization of gene deletion mutants of Cyprinid herpesvirus 3 (koi herpesvirus) lacking the immunogenic envelope glycoproteins pORF25, pORF65, pORF148 and pORF149.
Animals
Carps
Cell Nucleus
/ virology
Cells, Cultured
Cytoplasm
/ virology
Fish Diseases
/ pathology
Gene Deletion
Glycoproteins
/ genetics
Herpesviridae
/ genetics
Herpesviridae Infections
/ pathology
Microscopy, Electron
Viral Envelope Proteins
/ genetics
Viral Load
Viral Plaque Assay
Virion
/ ultrastructure
Virulence
Virus Replication
Cyprinid herpesvirus 3
Envelope glycoproteins
Gene deletion mutants
Koi herpesvirus
Virulence in carp
Virus replication in vitro
Journal
Virus research
ISSN: 1872-7492
Titre abrégé: Virus Res
Pays: Netherlands
ID NLM: 8410979
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
03
08
2018
revised:
07
12
2018
accepted:
08
12
2018
pubmed:
14
12
2018
medline:
26
2
2019
entrez:
14
12
2018
Statut:
ppublish
Résumé
Cyprinid herpesvirus 3 (CyHV-3) or koi herpesvirus is a global pathogen causing mass mortality in koi and common carp, against which improved vaccines are urgently needed. In this study we investigated the role of four nonessential, but immunogenic envelope glycoproteins encoded by members of the ORF25 gene family (ORF25, ORF65, ORF148 and ORF149) during CyHV-3 replication. Single deletion of ORF65 did not affect in vitro replication, and deletion of ORF148 even slightly enhanced virus growth on common carp brain (CCB) cells. Deletions of ORF25 or ORF149 led to reduced plaque sizes and virus titers, which was due to delayed entry into host cells. An ORF148/ORF149 double deletion mutant exhibited wild-type like growth indicating opposing functions of the two proteins. Electron microscopy of CCB cells infected with either mutant did not indicate any effects on virion formation and maturation in nucleus or cytoplasm, nor on release of enveloped particles. The ORF148, ORF149 and double deletion mutants were also tested in animal experiments using juvenile carp, and proved to be insufficiently attenuated for use as live virus vaccines. However, surviving fish were protected against challenge with wild-type CyHV-3, demonstrating that these antibody inducing proteins are dispensable for an efficient immune response in vivo.
Identifiants
pubmed: 30543872
pii: S0168-1702(18)30474-X
doi: 10.1016/j.virusres.2018.12.004
pii:
doi:
Substances chimiques
Glycoproteins
0
Viral Envelope Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
21-30Informations de copyright
Copyright © 2018 Elsevier B.V. All rights reserved.