| Rainbow trout (Oncorhynchus mykiss) |
In vivo disease resistance via antagonism/competition and immune readouts (e.g., phagocytic activity, lysozyme, cytokine gene expression), plus nutrition/growth responses |
Strain/efficacy depend on colonization ability and context; growth benefits are inconsistent across trials |
| Brown/sea trout (Salmo trutta) |
Immune-related humoral responses and protection against furunculosis; in vitro reduction of fungal pathogen adhesion (skin mucus context) |
Emphasis on adhesion/colonization and pathogen-specific interactions; studies are fewer than in rainbow trout |
| Atlantic salmon (Salmo salar) |
Mixed in vivo and ex vivo evidence; illustrates that strong in vitro inhibition may not translate to consistent in vivo protection |
Explicit mismatch between in vitro results and in vivo outcomes is described |
| Atlantic cod (Gadus morhua) |
Early larval/juvenile microbiota control, survival/growth improvements, and strain-specific mechanisms (e.g., production of antibacterial compound tropodithietic acid via Phaeobacter strains—discussed) |
Need for timing optimization (earlier introduction appears more efficient); some effects can be transient or stage-limited |
| Marine pleuronectiforms (e.g., halibut, turbot, haddock, pollack) |
Larviculture vector comparisons (rearing water, live feed), microbiota shifts, mucous cell proliferation, and variable survival/growth outcomes |
Dose and administration pathway may determine whether outcomes are positive; some trials report limited/unclear benefits |
| European perch (Perca fluviatilis) |
Administration-pathway dependent improvements in growth and immune indices (only via treated live feed reported in summary) |
Demonstrates route-specific efficacy rather than a universal effect |