Discovery and surveillance of viruses from salmon in British Columbia using viral immune-response biomarkers, metatranscriptomics, and high-throughput RT-PCR. Issue 1 (1st September 2020)

• Record Type: Journal Article
• Authors: Mordecai, Gideon J; Di Cicco, Emiliano; Günther, Oliver P; Schulze, Angela D; Kaukinen, Karia H; Li, Shaorong; Tabata, Amy; Ming, Tobi J; Ferguson, Hugh W; Suttle, Curtis A; Miller, Kristina M
• Is Part Of: Virus evolution. Volume 7:Issue 1(2021)
• Publication Date: 2020-09-01
• Subjects: virus discovery -- viral ecology -- in situ hybridisation -- metatranscriptomics -- aquaculture -- fisheries; Viruses -- Evolution -- Periodicals; 579.2138
• DOI: 10.1093/ve/veaa069
• Languages: English
• ISSNs: 2057-1577

Abstract

Abstract: The emergence of infectious agents poses a continual economic and environmental challenge to aquaculture production, yet the diversity, abundance, and epidemiology of aquatic viruses are poorly characterised. In this study, we applied salmon host transcriptional biomarkers to identify and select fish in a viral disease state, but only those that were negative for known viruses based on RT-PCR screening. These fish were selected for metatranscriptomic sequencing to discover potential viral pathogens of dead and dying farmed Atlantic ( Salmo salar ) and Chinook ( Oncorhynchus tshawytscha ) salmon in British Columbia (BC). We found that the application of the biomarker panel increased the probability of discovering viruses in aquaculture populations. We discovered two viruses that have not previously been characterised in Atlantic salmon farms in BC (Atlantic salmon calicivirus and Cutthroat trout virus-2), as well as partially sequenced three putative novel viruses. To determine the epidemiology of the newly discovered or emerging viruses, we conducted high-throughput reverse transcription polymerase chain reaction (RT-PCR) and screened over 9, 000 farmed and wild salmon sampled over one decade. Atlantic salmon calicivirus and Cutthroat trout virus-2 were in more than half of the farmed Atlantic salmon we tested. Importantly we detected some of the viruses we first discovered in farmed Atlantic salmon in Chinook salmon, suggesting a broad host range. Finally, we applied in situ hybridisation to determine infection and found differing cell tropism for each virus tested. Our study demonstrates that continual discovery and surveillance of emerging viruses in these ecologically important salmon will be vital for management of both aquaculture and wild resources in the future.