Environmental DNA (eDNA) from multiple pathogens is elevated near active Atlantic salmon farms

The spread of infection from reservoir host populations is a key mechanism for disease emergence and extinction risk and is a management concern for salmon aquaculture and fisheries. Using a quantitative environmental DNA methodology, we assessed pathogen eDNA in relation to salmon farms in coastal...

Full description

Bibliographic Details
Main Author: Shea, Dylan
Format: Dataset
Language:unknown
Published: 2021
Subjects:
Online Access:https://zenodo.org/record/4069485
https://doi.org/10.5061/dryad.r7sqv9s98
Description
Summary:The spread of infection from reservoir host populations is a key mechanism for disease emergence and extinction risk and is a management concern for salmon aquaculture and fisheries. Using a quantitative environmental DNA methodology, we assessed pathogen eDNA in relation to salmon farms in coastal British Columbia, Canada, by testing for 39 species of salmon pathogens (viral, bacterial, and eukaryotic) in 134 marine environmental samples at 58 salmon farm sites (both active and inactive) over three years. Environmental DNA from twenty-two pathogen species was detected 496 times and species varied in their occurrence among years and sites, likely reflecting variation in environmental factors, other native host species, and strength of association with domesticated Atlantic salmon. Overall, we found that the probability of detecting pathogen eDNA was 2.72 (95% CI: 1.48, 5.02) times higher at active versus inactive salmon farm sites and 1.76 (95% CI: 1.28, 2.42) times higher per standard deviation increase in domesticated Atlantic salmon eDNA concentration at a site. If the distribution of pathogen eDNA accurately reflects the distribution of viable pathogens, our findings suggest that salmon farms serve as a potential reservoir for a number of infectious agents; thereby elevating the risk of exposure for wild salmon and other fish species that share the marine environment. Columns entitled "Year", "Site", "Active", "Atl_eDNA_Centered", "Microparasite_Spp", and "Binary_Microparasite_Detections" contain data that are fundamental to the analysis reported in this manuscript. The remaining columns in this table contain data that are supplementary to the analysis. Funding provided by: David Suzuki FoundationCrossref Funder Registry ID: http://dx.doi.org/10.13039/100014501Award Number: Funding provided by: Natural Sciences and Engineering Research Council of CanadaCrossref Funder Registry ID: http://dx.doi.org/10.13039/501100000038Award Number: Funding provided by: Ontario Graduate Scholarship*Crossref Funder Registry ...