Histophagous ciliates caused high mortality among turbot in a commercial fish farm in southern Norway. The ciliates spread systemically in fry (< 0.3 g). In the early stages of infection the ciliates were found in connective tissue in skin and fins, as well as in nervous tissue. In terminal stages the whole organism was infected. In large turbot (500–1000 g), the ciliates were predominantly found in the central nervous system, causing liquefaction of the nervous tissue. The ciliates were not identified to species but resembled species in the genus Uronema (Scuticociliatida).
Combating and controlling sea lice causes large economic costs for the farmers, with estimated values of more than 305 million euros (€) per year. Increased resistance against traditional chemotherapeutants due to evolutionary drivers in the sea lice combined with the lack of an effective vaccine and few other chemical treatments available are expected to cause these costs to increase. Several possible methods for managing sea lice infestations have been investigated, but only cleaner fish has proven to have an effect on lice levels. Cleaning activity is well known in marine fish and has been observed in the wild as a form of symbiosis between two species: one species, the 'client' fish, seek out the other species, the 'cleaner' fish, to have ectoparasites and dead tissue cleared from its body. The Atlantic lumpfish is a relatively new aquaculture species, and wild-caught mature fish are used as brood stock for farmed production. This poses a biosecurity risk, as wild fish can carry pathogens, and the use of quarantine and health screening is recommended. Vaccine development is unfortunately lagging far behind relatively to the wide spread and high utilisation of the fish. This review contains description of the main pathogens and diseases that affect cleaner fish.
This is the first description of a persistent subclinical nodavirus infection in the Atlantic halibut Hippoglossus hippoglossus. Juvenile fish (1 to 5 g) were sampled at 4, 5 and 8 mo of age at a fish farm in Norway during and after weaning. None showed clinical signs of viral encephalopathy and retinopathy (VER) or other disease. Pathological changes and/or nodavirus were detected by light microscopy, immunohistochemistry, reverse transcriptase polymerase chain reaction (RT-PCR) and transmission electron microscopy in all fish examined. High numbers of virus particles were found in macrophage-like cells in the central nervous system, including brain and retina (CNS). The virus particles displayed the icosahedral shape and size (approximately 25 nm) characteristic of nodaviruses. The virus-infected cells formed focal cell aggregates and were seen in all regions of the brain and all nuclear cell layers of the retina. The cytoplasm of the infected cells was filled with membrane-enclosed inclusions packed with virus particles. Some virus particles lay along membranes and formed membrane-bound necklace-like arrangements. The virus-infected cells of the retina also contained pigment granula located generally inside virus inclusions and sometimes forming a coating around the virus particles. All frontal parts with the eyes and brain and 50% of the mid-parts, which included the abdominal organs, were found positive for nodavirus with RT-PCR. Pathological changes in these persistently nodavirus-infected fish differ from earlier descriptions in Atlantic halibut during outbreaks of VER. Vertical transmission from infected spawners is believed to be a major route for nodavirus infection. Detection of nodavirus in subclinical infected fish and a better understanding of its pathogenesis are important in order to prevent the spread of nodavirus in the fish-farming industry.
The aim of this study was to evaluate histologic post‐mortem autolytic changes in farmed Atlantic salmon. The fish were either stored at room temperature (RT, 21°C), refrigerated (4°C) or frozen (−20°C), while fish necropsy was performed at 0, 1, 4, 24 and 48 h post‐storage (hps). In addition, gills were sampled at 0, 5, 10, 15, 30 and 45 min post‐storage (mps) at room temperature (RT). The haematoxylin and eosin‐stained tissue slides were evaluated and scored by using a semi‐quantitative scoring system. Our findings demonstrated gills and pyloric caeca/pancreas as the most severely autolysed organs while heart and skeletal musculature were least affected. Generally, moderate to severe autolysis appeared first at 4 hps, while severe changes were seen at 24 hps. Gills demonstrated autolytic changes as early as 10 mps and pyloric caeca/pancreas at 1 hps. Freezing did not prevent the autolysis and even contributed to freezing artefacts, which may lead to misdiagnosis. Keeping organs refrigerated slowed the autolytic progress within the first 4 hps marginally. This study recommends gills and pyloric caeca/pancreas should be sampled as early as possible, at least within 10 min post‐necropsy.
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