<em>Cyprinid herpesvirus 3</em> Evolves In Vitro through an Assemblage of Haplotypes that Alternatively Become Dominant or Under-Represented
Sandro Klafack,
Anna-Sophie Fiston-Lavier,
Sven M. Bergmann,
Saliha Hammoumi,
Lars Schröder,
Walter Fuchs,
Angela Lusiastuti,
Pei-Yu Lee,
Sarahi Vega Heredia,
Master student consortium,
Anne-Sophie Gosselin-Grenet,
Jean-Christophe Avarre
Affiliations
Sandro Klafack
Institute of Infectology, Friedrich-Loeffer-Institut, Federal Research Institute for Animal Health, 17493 Greifswald-Insel Riems, Germany
Anna-Sophie Fiston-Lavier
ISEM, IRD, CNRS, EPHE, University of Montpellier, 34095 Montpellier, France
Sven M. Bergmann
Institute of Infectology, Friedrich-Loeffer-Institut, Federal Research Institute for Animal Health, 17493 Greifswald-Insel Riems, Germany
Saliha Hammoumi
ISEM, IRD, CNRS, EPHE, University of Montpellier, 34095 Montpellier, France
Lars Schröder
Institute of Molecular Virology and Cell Biology, Friedrich Loeffer Institut, Federal Research Institute for Animal Health, 17493 Greifswald-Insel Riems, Germany
Walter Fuchs
Institute of Molecular Virology and Cell Biology, Friedrich Loeffer Institut, Federal Research Institute for Animal Health, 17493 Greifswald-Insel Riems, Germany
Angela Lusiastuti
Research Institute for Freshwater Aquaculture and Fisheries Extension, Bogor 16129, Indonesia
Pei-Yu Lee
GenReach Biotechnology, Taichung City 407, Taiwan
Sarahi Vega Heredia
ISEM, IRD, CNRS, EPHE, University of Montpellier, 34095 Montpellier, France
Master student consortium
Faculty of Sciences, University of Montpellier, 34095 Montpellier, France
Anne-Sophie Gosselin-Grenet
DGIMI, University of Montpellier, INRA, 34095 Montpellier, France
Jean-Christophe Avarre
ISEM, IRD, CNRS, EPHE, University of Montpellier, 34095 Montpellier, France
Viruses are able to evolve in vitro by mutations after serial passages in cell cultures, which can lead to either a loss, or an increase, of virulence. Cyprinid herpesvirus 3 (CyHV-3), a 295-kb double-stranded DNA virus, is the etiological agent of the koi herpesvirus disease (KHVD). To assess the influence of serial passages, an isolate of CyHV-3 (KHV-T) was passaged 99 times onto common carp brain (CCB) cells, and virus virulence was evaluated during passages through the experimental infections of common carp. After 78 CCB passages, the isolate was much less virulent than the original form. A comparative genomic analysis of these three forms of KHV-T (P0, P78 and P99) revealed a limited number of variations. The largest one was a deletion of 1363 bp in the predicted ORF150, which was detected in P78, but not in P99. This unexpected finding was confirmed by conventional PCR and digital PCR. The results presented here primarily suggest that, CyHV-3 evolves, at least in vitro, through an assemblage of haplotypes that alternatively become dominant or under-represented.