Decreased water temperature enhance genotype 3 replication and severe heart pathology in experimentally infected rainbow trout.

Juliane Sørensen, Argelia Cuenca, Anne Berit Olsen, Kerstin Skovgaard, Tine Moesgaard Iburg, Niels Jørgen Olesen, Niccolò Vendramin
Author Information
  1. Juliane Sørensen: Section for Fish and Shellfish Diseases, National Institute for Aquatic Resources, Technical University of Denmark, Kgs. Lyngby, Denmark.
  2. Argelia Cuenca: Section for Fish and Shellfish Diseases, National Institute for Aquatic Resources, Technical University of Denmark, Kgs. Lyngby, Denmark.
  3. Anne Berit Olsen: Section of Aquatic Biosecurity Research, Norwegian Veterinary Institute, Bergen, Norway.
  4. Kerstin Skovgaard: Department of Biotechnology and Biomedicine, Technical University of Denmark, Kgs. Lyngby, Denmark.
  5. Tine Moesgaard Iburg: Section for Fish and Shellfish Diseases, National Institute for Aquatic Resources, Technical University of Denmark, Kgs. Lyngby, Denmark.
  6. Niels Jørgen Olesen: Section for Fish and Shellfish Diseases, National Institute for Aquatic Resources, Technical University of Denmark, Kgs. Lyngby, Denmark.
  7. Niccolò Vendramin: Section for Fish and Shellfish Diseases, National Institute for Aquatic Resources, Technical University of Denmark, Kgs. Lyngby, Denmark.

Abstract

genotype 3 (PRV-3) was first discovered in Denmark in 2017 in relation to disease outbreaks in rainbow trout (). While the virus appears to be widespread in farmed rainbow trout, disease outbreaks associated with detection of PRV-3 have only occurred in recirculating aquaculture systems, and has predominantly been observed during the winter months. To explore the possible effects of water temperature on PRV-3 infection in rainbow trout, an cohabitation trial was conducted at 5, 12, and 18°C. For each water temperature, a control tank containing mock-injected shedder fish and a tank with PRV-3 exposed fish were included. Samples were collected from all experimental groups every 2nd week post challenge (WPC) up until trial termination at 12 WPC. PRV-3 RNA load measured in heart tissue of cohabitants peaked at 6 WPC for animals maintained at 12 and 18°C, while it reached its peak at 12 WPC in fish maintained at 5°C. In addition to the time shift, significantly more virus was detected at the peak in fish maintained at 5°C compared to 12 and 18°C. In shedders, fish at 12 and 18°C cleared the infection considerably faster than the fish at 5°C: while shedders at 18 and 12°C had cleared most of the virus at 4 and 6 WPC, respectively, high virus load persisted in the shedders at 5°C until 12 WPC. Furthermore, a significant reduction in the hematocrit levels was observed in the cohabitants at 12°C in correlation with the peak in viremia at 6 WPC; no changes in hematocrit was observed at 18°C, while a non-significant reduction (due to large individual variation) trend was observed at cohabitants held at 5°C. Importantly, expression was positively correlated with PRV-3 virus load in all PRV-3 exposed groups. Immune gene expression analysis showed a distinct gene profile in PRV-3 exposed fish maintained at 5°C compared to 12 and 18°C. The immune markers mostly differentially expressed in the group at 5°C were important antiviral genes including and (viperin). In conclusion, these data show that low water temperature allow for significantly higher PRV-3 replication in rainbow trout, and a tendency for more severe heart pathology development in PRV-3 injected fish. Increased viral replication was mirrored by increased expression of important antiviral genes. Despite no mortality being observed in the experimental trial, the data comply with field observations of clinical disease outbreaks during winter and cold months.

Keywords

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Word Cloud

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