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The effect of different intensities of the ectoparasitic salmon lice (Lepeophtheirus salmonis) on Atlantic salmon (Salmo salar)

https://doi.org/10.1111/jfd.13649
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Exocrine glands of L epeophtheirus salmonis ( C opepoda: C aligidae): Distribution, developmental appearance, and site of secretion
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Using observed load distributions with a simple model to analyse the epidemiology of sea lice (Lepeophtheirus salmonis) on sea trout (Salmo trutta)
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The complement system in teleosts
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The physiological effects of salmon lice infection on post-smolt of Atlantic salmon
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Host factors important in sea lice infections
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Stress responses and disease resistance in salmonid fish: Effects of chronic elevation of plasma cortisol
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Immune protection of Mozambique tilapia (Oreochromis mossambicus) exposed to different infectious doses of ectoparasite (Cryptocaryon irritans)
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Validation of Reference Genes for Real-Time Polymerase Chain Reaction Studies in Atlantic Salmon
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Understanding chronic nematode infections: Evolutionary considerations, current hypotheses and the way forward
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Production of nauplii of Lepeophtheirus salmonis (Krøyer) (Copepoda: Caligidae) from farmed and wild salmon and its relation to the infestation of wild sea trout (Salmo trutta L.) off the west coast of Ireland in 1991
inferredcites →https://doi.org/10.1016/0169-5347(96)10039-2openalex-snapshot
Ecological immunology: costly parasite defences and trade-offs in evolutionary ecology
inferredcites →https://doi.org/10.1016/j.cbd.2011.12.002openalex-snapshot
Comparative defense-associated responses in salmon skin elicited by the ectoparasite Lepeophtheirus salmonis
inferredcites →https://doi.org/10.1016/j.dci.2013.07.014openalex-snapshot
Antiviral functions of CD8+ cytotoxic T cells in teleost fish
inferredcites →https://doi.org/10.1016/j.dci.2014.09.015openalex-snapshot
Signatures of resistance to Lepeophtheirus salmonis include a TH2-type response at the louse-salmon interface
inferredcites →https://doi.org/10.1016/j.dci.2016.10.008openalex-snapshot
Contrasting expression of immune genes in scaled and scaleless skin of Atlantic salmon infected with young stages of Lepeophtheirus salmonis
inferredcites →https://doi.org/10.1016/j.dci.2018.04.023openalex-snapshot
Salmon louse rhabdoviruses: Impact on louse development and transcription of selected Atlantic salmon immune genes
inferredcites →https://doi.org/10.1016/j.exppara.2015.09.001openalex-snapshot
Molecular characterization and knock-down of salmon louse (Lepeophtheirus salmonis) prostaglandin E synthase
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Real-time gene expression analysis in carp (Cyprinus carpio L.) skin: Inflammatory responses caused by the ectoparasite Ichthyophthirius multifiliis
inferredcites →https://doi.org/10.1016/j.fsi.2007.01.002openalex-snapshot
The ontogeny and extrahepatic expression of complement factor C3 in Atlantic salmon (Salmo salar)
inferredcites →https://doi.org/10.1016/j.fsi.2009.03.012openalex-snapshot
Cloning and expression analysis of three striped trumpeter (Latris lineata) pro-inflammatory cytokines, TNF-α, IL-1β and IL-8, in response to infection by the ectoparasitic, Chondracanthus goldsmidi
inferredcites →https://doi.org/10.1016/j.fsi.2014.10.038openalex-snapshot
Difference in skin immune responses to infection with salmon louse (Lepeophtheirus salmonis) in Atlantic salmon (Salmo salar L.) of families selected for resistance and susceptibility
inferredcites →https://doi.org/10.1016/j.fsi.2018.04.016openalex-snapshot
Under control: The innate immunity of fish from the inhibitors' perspective
inferredcites →https://doi.org/10.1016/j.fsi.2020.05.014openalex-snapshot
Rainbow trout Oncorhynchus mykiss skin responses to salmon louse Lepeophtheirus salmonis: From copepodid to adult stage
inferredcites →https://doi.org/10.1016/j.fsi.2020.07.023openalex-snapshot
Immune gene expression and genome-wide association analysis in rainbow trout with different resistance to Yersinia ruckeri infection
inferredcites →https://doi.org/10.1016/j.fsi.2021.04.026openalex-snapshot
Dose-dependent co-infection of Argulus sp. and Aeromonas hydrophila in goldfish (Carassius auratus) modulates innate immune response and antioxidative stress enzymes
inferredcites →https://doi.org/10.1016/j.ijpara.2007.04.023openalex-snapshot
Density-dependent immune responses against the gastrointestinal nematode Strongyloides ratti
inferredcites →https://doi.org/10.1016/j.immuni.2011.03.018openalex-snapshot
Interleukin-10 Signaling in Regulatory T Cells Is Required for Suppression of Th17 Cell-Mediated Inflammation
inferredcites →https://doi.org/10.1016/j.molimm.2010.12.004openalex-snapshot
A role for specific collagen motifs during wound healing and inflammatory response of fibroblasts in the teleost fish gilthead seabream
inferredcites →https://doi.org/10.1016/j.molimm.2011.02.014openalex-snapshot
Constitutive high expression of interleukin-4/13A and GATA-3 in gill and skin of salmonid fishes suggests that these tissues form Th2-skewed immune environments
inferredcites →https://doi.org/10.1016/j.physbeh.2014.04.031openalex-snapshot
Ectoparasitic sea lice (Lepeophtheirus salmonis) affect behavior and brain serotonergic activity in Atlantic salmon (Salmo salar L.): Perspectives on animal welfare
inferredcites →https://doi.org/10.1016/j.pt.2006.08.006openalex-snapshot
Ecology of sea lice parasitic on farmed and wild fish
inferredcites →https://doi.org/10.1016/j.vetimm.2006.08.002openalex-snapshot
Quantitation of immune response gene expression and cellular localisation of interleukin-1β mRNA in Atlantic salmon, Salmo salar L., affected by amoebic gill disease (AGD)
inferredcites →https://doi.org/10.1016/s0065-308x(08)60233-xopenalex-snapshot
Sealice on Salmonids: Their Biology and Control
inferredcites →https://doi.org/10.1016/s0169-5347(02)00013-7openalex-snapshot
On the evolutionary ecology of specific immune defence
inferredcites →https://doi.org/10.1016/s1054-3139(97)80016-1openalex-snapshot
Open-ocean infestation by salmon lice (Lepeophtheirus salmonis): comparison of wild and escaped farmed Atlantic salmon (Salmo salar L.)
inferredcites →https://doi.org/10.1017/s0031182000055347openalex-snapshot
Processes influencing the distribution of parasite numbers within host populations with special emphasis on parasite-induced host mortalities
inferredcites →https://doi.org/10.1017/s0031182000075855openalex-snapshot
Patterns of macroparasite abundance and aggregation in wildlife populations: a quantitative review
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Host immune responses are necessary for density dependence in nematode infections
inferredcites →https://doi.org/10.1017/s0031182006002150openalex-snapshot
Are there general laws in parasite ecology?
inferredcites →https://doi.org/10.1017/s0031182098003448openalex-snapshot
Patterns of macroparasite aggregation in wildlife host populations
inferredcites →https://doi.org/10.1023/a:1004031318505openalex-snapshot
Infestations of wild adult Atlantic salmon (Salmo salar L.) by the ectoparasitic copepod sea louse Lepeophtheirus salmonis Krøyer: prevalence, intensity and the spatial distribution of males and [2pt] females on the host fish
inferredcites →https://doi.org/10.1073/pnas.0603525103openalex-snapshot
Epizootics of wild fish induced by farm fish
inferredcites →https://doi.org/10.1093/conphys/coaa023openalex-snapshot
Effects of laboratory salmon louse infection on osmoregulation, growth and survival in Atlantic salmon
inferredcites →https://doi.org/10.1093/icesjms/fsu132openalex-snapshot
Risk assessment of the environmental impact of Norwegian Atlantic salmon farming
inferredcites →https://doi.org/10.1093/oso/9780198506201.003.0002openalex-snapshot
Heterogeneities in macroparasite infections: patterns and processes
inferredcites →https://doi.org/10.1098/rspb.1998.0431openalex-snapshot
Host densities as determinants of abundance in parasite communities
inferredcites →https://doi.org/10.1098/rspb.2009.0771openalex-snapshot
How sea lice from salmon farms may cause wild salmonid declines in Europe and North America and be a threat to fishes elsewhere
inferredcites →https://doi.org/10.1098/rspb.2012.2359openalex-snapshot
Impact of parasites on salmon recruitment in the Northeast Atlantic Ocean
inferredcites →https://doi.org/10.1111/fme.12010openalex-snapshot
Relationship between sea lice levels on sea trout and fish farm activity in western Scotland
inferredcites →https://doi.org/10.1111/j.1365-3024.2007.00932.xopenalex-snapshot
Lepeophtheirus salmonis secretory/excretory products and their effects on Atlantic salmon immune gene regulation
inferredcites →https://doi.org/10.1111/jfd.12061openalex-snapshot
Salmon lice – impact on wild salmonids and salmon aquaculture
inferredcites →https://doi.org/10.1111/jfd.12514openalex-snapshot
Atlantic salmon infected with salmon lice are more susceptible to new lice infections
inferredcites →https://doi.org/10.1111/jfd.12547openalex-snapshot
Parasite fecundity decreases with increasing parasite load in the salmon louse Lepeophtheirus salmonis infecting Atlantic salmon Salmo salar
inferredcites →https://doi.org/10.1111/jfd.12770openalex-snapshot
RNA sequencing reveals distinct gene expression patterns during the development of parasitic larval stages of the salmon louse (Lepeophtheirus salmonis)
inferredcites →https://doi.org/10.1111/jfd.13167openalex-snapshot
Where art thou louse? A snapshot of attachment location preferences in salmon lice on Atlantic salmon hosts in sea cages
inferredcites →https://doi.org/10.1111/jfd.13649openalex-snapshot
The effect of different intensities of the ectoparasitic salmon lice (Lepeophtheirus salmonis) on Atlantic salmon (Salmo salar)
inferredcites →https://doi.org/10.1111/jzo.12498openalex-snapshot
Behaviour in Atlantic salmon confers protection against an ectoparasite
inferredcites →https://doi.org/10.1111/pim.12675openalex-snapshot
Immune response to Ichthyophthirius multifiliis and role of IgT
inferredcites →https://doi.org/10.1111/pim.12731openalex-snapshot
Salmon immunological defence and interplay with the modulatory capabilities of its ectoparasite Lepeophtheirus salmonis
inferredcites →https://doi.org/10.1139/f04-016openalex-snapshot
Sea lice (Lepeophtheirus salmonis) infection rates on juvenile pink (Oncorhynchus gorbuscha) and chum (Oncorhynchus keta) salmon in the nearshore marine environment of British Columbia, Canada
inferredcites →https://doi.org/10.1139/f99-021openalex-snapshot
Infection with low numbers of the sea louse Lepeophtheirus salmonis induces stress-related effects in postsmolt Atlantic salmon (Salmo salar)
inferredcites →https://doi.org/10.1155/2012/925135openalex-snapshot
CD4 + T Cells: Differentiation and Functions
inferredcites →https://doi.org/10.1186/1471-2164-15-200openalex-snapshot
Comparative transcriptomics of Atlantic Salmo salar, chum Oncorhynchus keta and pink salmon O. gorbuscha during infections with salmon lice Lepeophtheirus salmonis
inferredcites →https://doi.org/10.1186/1471-2164-9-498openalex-snapshot
Local and systemic gene expression responses of Atlantic salmon (Salmo salar L.) to infection with the salmon louse (Lepeophtheirus salmonis)
inferredcites →https://doi.org/10.1186/s13071-021-04690-wopenalex-snapshot
Roles of three putative salmon louse (Lepeophtheirus salmonis) prostaglandin E2 synthases in physiology and host–parasite interactions
inferredcites →https://doi.org/10.1242/jeb.01090openalex-snapshot
Immune response to fleas in a wild desert rodent: effect of parasite species, parasite burden, sex of host and host parasitological experience
inferredcites →https://doi.org/10.1371/journal.pbio.0060033openalex-snapshot
A Global Assessment of Salmon Aquaculture Impacts on Wild Salmonids
inferredcites →https://doi.org/10.1371/journal.pone.0073539openalex-snapshot
The Salmon Louse Lepeophtheirus salmonis (Copepoda: Caligidae) Life Cycle Has Only Two Chalimus Stages
inferredcites →https://doi.org/10.1371/journal.pone.0209178openalex-snapshot
Sea lice, Lepeophtheirus salmonis (Krøyer 1837), infected Atlantic salmon (Salmo salar L.) are more susceptible to infectious salmon anemia virus
inferredcites →https://doi.org/10.2307/3933openalex-snapshot
Regulation and Stability of Host-Parasite Population Interactions: I. Regulatory Processes
inferredcites →https://doi.org/10.3354/aei00090openalex-snapshot
Salmon lice infection on wild salmonids in marine protected areas: an evaluation of the Norwegian ‘National Salmon Fjords’
inferredcites →https://doi.org/10.3354/aei00142openalex-snapshot
Effects of salmon lice Lepeophtheirus salmonis on wild sea trout Salmo trutta—a literature review
inferredcites →https://doi.org/10.3354/dao014195openalex-snapshot
Effects of Cortisol implants on the susceptibility and the histopathology of the responses of naive coho salmon Oncorhynchus kisulch to experimental infection with Lepeophtheirus salmonis (Copepoda: Caligidae)
inferredcites →https://doi.org/10.3354/dao02397openalex-snapshot
Individual fish tank arrays in studies of Lepeophtheirus salmonis and lice loss variability
inferredcites →https://doi.org/10.3354/dao052057openalex-snapshot
Susceptibility of rainbow trout Oncorhynchus mykiss, Atlantic salmon Salmo salar and coho salmon Oncorhynchus kisutch to experimental infection with sea lice Lepeophtheirus salmonis
inferredcites →https://doi.org/10.3354/dao075229openalex-snapshot
Differential rejection of salmon lice by pink and chum salmon: disease consequences and expression of proinflammatory genes
inferredcites →https://doi.org/10.3389/fimmu.2018.01105openalex-snapshot
Mechanisms of Fish Macrophage Antimicrobial Immunity
inferredcites →https://doi.org/10.3389/fimmu.2018.01683openalex-snapshot
Interleukin (IL)-2 Is a Key Regulator of T Helper 1 and T Helper 2 Cytokine Expression in Fish: Functional Characterization of Two Divergent IL2 Paralogs in Salmonids
inferredcites →https://doi.org/10.3390/biology5020023openalex-snapshot
The Function of Fish Cytokines
inferredcites →https://doi.org/10.3390/biology5040045openalex-snapshot
Fish Immunoglobulins
inferredcites →https://doi.org/10.3390/biology9080233openalex-snapshot
Antimicrobial Peptides of Salmonid Fish: From Form to Function

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inferred← citeshttps://doi.org/10.2139/ssrn.4754205openalex-extracted
Population Dynamics of Ichthyophthirius Multifiliis in Goldfish (Carassius Auratus) Revealed a Negative Effect of Infection Density on the Parasite Growth
inferred← citeshttps://doi.org/10.1016/j.fsi.2023.108835openalex-snapshot
Transcriptomic and targeted immune transcript analyses confirm localized skin immune responses in Atlantic salmon towards the salmon louse
inferred← citeshttps://doi.org/10.1016/j.fsi.2024.109794openalex-snapshot
Daily crowding stress has limited, yet detectable effects on skin and head kidney gene expression in surgically tagged atlantic salmon (Salmo salar)
inferred← citeshttps://doi.org/10.1016/j.fsi.2024.109992openalex-snapshot
Cell death induced by Lepeophtheirus salmonis labial gland protein 3 in salmonid fish leukocytes: A mechanism for disabling host immune responses
inferred← citeshttps://doi.org/10.1017/s0031182023000847openalex-snapshot
Repeated exposure affects susceptibility and responses of Atlantic salmon (Salmo salar) towards the ectoparasitic salmon lice (Lepeophtheirus salmonis)
inferred← citeshttps://doi.org/10.1098/rspb.2025.1782openalex-snapshot
Parasites perform poorly at high host densities: an experimental test in the salmon louse Lepeophtheirus salmonis
inferred← citeshttps://doi.org/10.1111/csp2.13079openalex-snapshot
Louse‐induced mortality thresholds in Atlantic salmon of wild‐origin
inferred← citeshttps://doi.org/10.2139/ssrn.7038552openalex-snapshot
Too little, too late: Atlantic salmon responses to chalimus establishment and chronic adult stages of salmon louse in single and co-infested fish
inferred← citeshttps://doi.org/10.3354/aei00443openalex-snapshot
Modelling salmon lice-induced mortality of wild salmon post-smolts is highly sensitive to calibration data
inferred← citeshttps://doi.org/10.3389/fgene.2025.1633603openalex-snapshot
Sea lice (Lepeophtheirus salmonis) life stage impacts atlantic salmon transcriptomic responses under different thermal profiles
inferred← citeshttps://doi.org/10.3390/ijms26178315openalex-snapshot
Histological and Transcriptomic Characterization of Full-Thickness Skin Wound Healing in Maraena Whitefish (Coregonus maraena Bloch, 1779)
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