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Peer-reviewed veterinary case report

A method to measure an indicator of viraemia in Atlantic salmon using a reporter cell line.

Journal:
Journal of virological methods
Year:
2013
Authors:
Collet, Bertrand et al.
Affiliation:
Marine Scotland Science · United Kingdom

Plain-English summary

Researchers developed a new way to measure the presence of a virus in Atlantic salmon using a special fish cell line. This method focuses on Salmonid alphavirus (SAV), which causes a serious illness called Salmon Pancreas Disease (SPD) in farmed salmon. They tested two different virus samples and found that the cell line showed a significant increase in activity after being infected, indicating the virus was replicating. This new approach allows for monitoring the virus in salmon without harming the fish, making it easier to detect and study emerging diseases. Overall, the method appears to work well for tracking the virus in salmon.

Abstract

RTG-P1 is a transgenic fish cell line producing luciferase under the control of the IFN-induced Mx rainbow trout gene promoter. This cell line was used to measure viraemia of Salmonid alphavirus (SAV), the cause of Salmon Pancreas Disease (SPD), a serious disease in farmed Atlantic salmon. Two SAV genotype 1 (SAV1) isolates were used in this study, F93-125 (tissue-culture adapted, from Ireland) and 4640 (from a field case in Scotland). The kinetics and magnitude of luciferase activity were monitored versus the time of infection. During a direct infection experiment, the induction of luciferase significantly increased 16- and 4-fold after incubation for 6 days with F93-125 at 15 and 20°C, respectively. Filtration and heat treatment experiments demonstrated that the luciferase induction in RTG-P1 was dependent on viral replication. Unlike many cell lines used in fish viral diagnostic, RTG-P1 is not sensitive to salmonid serum, therefore, viraemia could be successfully monitored on serum collected from fish during a cohabitation challenge with 4640 isolate. A peak of viraemia could be detected 16 days post IP inoculation of the shedders. This novel cost-effective method to measure viraemia does not rely on development of cytopathic effect (CPE) in culture, is compatible with non-lethal blood collections in fish and can be used to assign emerging diseases to a viral aetiology.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/23602803/