PUBLICATION

Zebrafish (Danio rerio) larvae as a model for real-time studies of propagating VHS virus infection, tissue tropism and neutrophil activity

Authors
Marana, M.H., Schmidt, J.G., Biacchesi, S., Lorenzen, N., Jørgensen, L.V.G.
ID
ZDB-PUB-201120-83
Date
2020
Source
Journal of fish diseases   44(5): 563-571 (Journal)
Registered Authors
Keywords
in vivo visualization, infection kinetics, mortality, neutrophil response, tissue tropism, viral haemorrhagic septicaemia virus, zebrafish
MeSH Terms
  • Animals
  • Disease Models, Animal
  • Hemorrhagic Septicemia, Viral/virology*
  • Neutrophils/metabolism*
  • Novirhabdovirus/physiology*
  • Tropism/physiology*
  • Zebrafish*
PubMed
33170959 Full text @ J. Fish Dis.
Abstract
Viral haemorrhagic septicaemia virus (VHSV) is a negative-sense single-stranded RNA virus that infects more than 140 different fish species. In this study, zebrafish larvae were employed as in vivo model organisms to investigate progression of disease, the correlation between propagation of the infection and irreversibility of disease, cell tropism and in situ neutrophil activity towards the VHSV-infected cells. A recombinant VHSV strain, encoding "tomato" fluorescence (rVHSV-Tomato), was used in zebrafish to be able to follow the progress of the infection in the live host in real-time. Two-day-old zebrafish larvae were injected into the yolk sac with the recombinant virus. The virus titre peaked 96 hr post-infection in zebrafish larvae kept at 18°C, and correlated with 33% mortality and high morbidity among the larvae. By utilizing the transgenic zebrafish line Tg(fli1:GFP)y1 with fluorescently tagged endothelial cells, we were able to demonstrate that the virus initially infected endothelial cells lining the blood vessels. By observing the rVHSV-Tomato infection in the neutrophil reporter zebrafish line Tg(MPX:eGFP)i114 , we inferred that only a subpopulation of the neutrophils responded to the virus infection. We conclude that the zebrafish larvae are suitable for real-time studies of VHS virus infections, allowing in vivo dissection of host-virus interactions at the whole organism level.
Genes / Markers
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Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping