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  • OPEN ACCESS
    Host–parasite transcriptomics during immunostimulant-enhanced rejection of salmon lice (Lepeophtheirus salmonis) by Atlantic salmon (Salmo salar)
    FACETS • Vol. 2 • pp. 477 - 495
    Salmon lice (Lepeophtheirus salmonis) are important ectoparasites of wild and farmed salmonids and cause major losses to the salmon farming industry throughout the Northern Hemisphere. With the emergence of resistance to several commonly used parasiticides, novel control strategies and integration of multiple treatment options are needed, including host immunostimulation. Here, we investigate the effects of a functional feed containing a peptidoglycan and nucleotide formulation on L. salmonis infection of Atlantic salmon (Salmo salar) by characterizing lice infection levels, the expression of several host immune genes, and the parasite transcriptomic response to the immunostimulated host. Although initial infection intensities were low, the low dose (LD) immunostimulant diet reduced the total lice burden by 50% relative to controls. Immunostimulant fed hosts up-regulated interleukin-1β in the skin and spleen. This gene has been implicated in successful responses of several salmonid species to salmon lice but is typically not observed in Atlantic salmon, suggesting a favorable influence on the immune response. Lice infecting LD immunostimulated salmon overexpressed genes putatively involved in parasite immunity, including carboxylesterases, and underexpressed genes putatively involved in feeding (e.g., proteases). These lice response genes further improve the characterization of the transcriptome of the non-model parasite by identifying genes potentially involved in evading host immunity.
  • OPEN ACCESS
    Comparing metabarcoding and morphological approaches to identify phytoplankton taxa associated with harmful algal blooms
    FACETS • Vol. 5 • No. 1 • pp. 784 - 811
    Molecular techniques are expected to be highly useful in detecting taxa causing harmful algal blooms (HABs). This is the first report in Canada evaluating HABs-related species identification using a combination of morphological and molecular approaches. Microscopy, quantitative polymerase chain reaction (qPCR), and metabarcoding with multiple markers (i.e., 16S, 18S-dinoflagellate and 18S-diatom, large subunit (28S) rDNA) were applied on samples (n = 54) containing suspected harmful algae (e.g., Alexandrium spp., Chattonella sp., Chrysochromulina spp., Dictyocha spp., Heterosigma akashiwo, Protoceratium reticulatum, Pseudochattonella verruculosa, Pseudo-nitzschia spp., Pseudopedinella sp.). Owing to methodology limitations, qPCR result interpretation was limited, although good detectability occurred using previously published assays for Alexandrium tamarense, H. akashiwo, and P. verruculosa. Overall, the multiple-marker metabarcoding results were superior to the morphology-based methods, with the exception of taxa from the silicoflagellate group. The combined results using both 18S markers and the 28S marker together closely corresponded with morphological identification of targeted species, providing the best overall taxonomic coverage and resolution. The most numerous unique taxa were identified using the 18S-dinoflagellate amplicon, and the best resolution to the species level occurred using the 28S amplicon. Molecular techniques are therefore promising for HABs taxa detection but currently depend on deploying multiple markers for metabarcoding.
  • OPEN ACCESS
    Marine ecozones represent a major gap in Canadian DNA barcoding efforts
    FACETS • Vol. 9 • pp. 1 - 11
    Because of Canada’s large size, it is impractical to obtain a comprehensive perspective on biotic change through morphological approaches. DNA metabarcoding offers a potential path, but its application requires access to a well-parameterized DNA barcode reference library. This study presents the current state of DNA barcode coverage for Canadian animals, highlighting progress, identifying gaps, and providing recommendations for future research. Our analysis indicates that many of the known species (100 000 terrestrial and 6000 marine) in the Canadian fauna possess DNA barcode coverage, but there are important gaps geographically and taxonomically. We summarize DNA barcode coverage for the species in freshwater, marine, and terrestrial environments by ecoregion, finding that 95.6% of the 2.3 million Canadian barcode records derive from terrestrial ecosystems. Although the density of barcode records per 100 km² is 13x higher for terrestrial than aquatic environments (22.4 vs. 1.7), coverage for 58% of marine species is available (54% for annelids, 52% for arthropods, 88% for chordates, 39% for echinoderms, and 46% for molluscs). By revealing data-deficient areas and taxonomic groups, this study offers a roadmap for expanding the DNA barcode library for the Canadian fauna as an essential foundation for the scalable biosurveillance initiatives that inform biodiversity conservation efforts.