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1.
J Helminthol ; 95: e22, 2021 Apr 20.
Article in English | MEDLINE | ID: mdl-33875029

ABSTRACT

Due to the increased prevalence of human infections with bird schistosome larvae (cercarial dermatitis) associated with bathing in Danish lakes, a nationwide survey of infected intermediate host snails was conducted in 2018-2020. Pulmonate snails (10,225 specimens) were collected from 39 freshwater lakes (in the four major geographic regions in Denmark) and subjected to shedding. Released schistosome cercariae were isolated and identified by polymerase chain reaction and sequencing whereby Trichobilharzia regenti, Trichobilharzia franki, Trichobilharzia szidati and Trichobilharzia anseri were recorded. Infections were primarily determined by biotic factors such as the presence of final host birds and intermediate host snails and water temperature was noted as an important abiotic parameter associated with the infection. No clear connection with other abiotic factors (conductivity, alkalinity, pH, nitrogen, phosphorous) was seen. The widespread occurrence of infected snails, when compared to previous investigations, suggests that climate changes at northern latitudes could be responsible for the increased risk of contracting cercarial dermatitis.


Subject(s)
Birds/parasitology , Schistosomatidae , Schistosomiasis , Animals , Bird Diseases/parasitology , Denmark , Lakes , Schistosomatidae/isolation & purification , Schistosomiasis/veterinary , Snails/parasitology
2.
J Fish Dis ; 41(7): 1147-1152, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29671884

ABSTRACT

A bacterial biosurfactant isolated from Pseudomonas (strain H6) has previously been shown to have a lethal effect on the oomycete Saprolegnia diclina infecting fish eggs. The present work demonstrates that the same biosurfactant has a strong in vitro antiparasitic effect on the fish pathogenic ciliate Ichthyophthirius multifiliis. Three life cycle stages (the infective theront stage, the tomont and the tomocyst containing tomites) were all susceptible to the surfactant. Theronts were the most sensitive showing 100% mortality in as low concentrations as 10 and 13 µg/ml within 30 min. Tomonts were the most resistant but were killed in concentrations of 100 µg/ml. Tomocysts, which generally are considered resistant to chemical and medical treatment, due to the surrounding protective cyst wall, were also sensitive. The surfactant, in concentrations of 10 and 13 µg/ml, penetrated the cyst wall and killed the enclosed tomites within 60 min. Rainbow trout fingerlings exposed to the biosurfactant showed no adverse immediate or late signs following several hours incubation in concentrations effective for killing the parasite. This bacterial surfactant may be further developed for application as an antiparasitic control agent in aquaculture.


Subject(s)
Antiprotozoal Agents/pharmacology , Ciliophora Infections/virology , Fish Diseases/drug therapy , Hymenostomatida/drug effects , Pseudomonas/chemistry , Surface-Active Agents/pharmacology , Animals , Ciliophora Infections/drug therapy , Ciliophora Infections/parasitology , Dose-Response Relationship, Drug , Fish Diseases/parasitology , In Vitro Techniques , Oncorhynchus mykiss
3.
J Fish Dis ; 41(1): 117-123, 2018 Jan.
Article in English | MEDLINE | ID: mdl-28707702

ABSTRACT

Teleosts are able to raise a protective immune response, comprising both innate and adaptive elements, against various pathogens. This is the basis for a widespread use of vaccines, administered as injection or immersion, in the aquaculture industry. It has been described that repeated injection vaccination of fish raises a secondary immune response, consisting of rapid, accelerated and increased antibody reaction. This study reports how rainbow trout responds to repeated immersion vaccination against yersiniosis (ERM) caused by the bacterial pathogen Yersinia ruckeri. It was found that rainbow trout does not raise a classical secondary response following repeated immersion vaccination. Serum antibody titres were merely slightly increased even after three immunizations, using 30-s immersion into a bacterin consisting of formalin-inactivated Y. ruckeri (serotype O1, biotypes 1 and 2), performed over a 3-month period. The densities of IgM-positive lymphocytes in spleen of fish immunized three times were increased compared to control fish, but no general trend for an increase with the number of immunizations was noted. The lack of a classical secondary response following repeated immersion vaccination may partly be explained by limited uptake of antigen by immersion compared to injection.


Subject(s)
Bacterial Vaccines/immunology , Oncorhynchus mykiss/immunology , Yersinia Infections/veterinary , Yersinia ruckeri/immunology , Animals , Antibodies/blood , Antibody Formation/immunology , Fish Diseases/immunology , Fish Diseases/microbiology , Fish Diseases/prevention & control , Immersion , Oncorhynchus mykiss/microbiology , Vaccination , Yersinia Infections/immunology , Yersinia Infections/prevention & control
4.
Parasitol Res ; 116(10): 2721-2726, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28795224

ABSTRACT

Baltic cod livers have during recent years been found increasingly and heavily infected with third-stage larvae of Contracaecum osculatum. The infections are associated with an increasing population of grey seals which are final hosts for the parasite. Heavy worm burdens challenge utilization and safety of the fish liver products, and technological solutions for removal of worms are highly needed. We investigated the attachment of the worm larvae in liver tissue by use of histochemical techniques and found that the cod host encapsulates the worm larvae in layers of host cells (macrophages, fibroblasts) supported by enclosures of collagen and calcium. A series of incubation techniques, applying compounds targeting molecules in the capsule, were then tested for their effect to induce worm escape/release reactions. Full digestion solutions comprising pepsin, NaCl, HCl and water induced a fast escape of more than 60% of the worm larvae within 20 min and gave full release within 65 min but the liver tissue became highly dispersed. HCl alone, in concentrations of 48 and 72 mM, triggered a corresponding release of worm larvae with minor effect on liver integrity. A lower HCl concentration of 24 mM resulted in 80% release within 35 min. Water and physiological saline had no effect on worm release, and 1% pepsin in water elicited merely a weak escape reaction. In addition to the direct effect of acid on worm behaviour it is hypothesised that the acid effect on calcium carbonate in the encapsulation, with subsequent release of reaction products, may contribute to activation of C. osculatum larvae and induce escape reactions. Short-term pretreatment of infected cod liver and possibly other infected fish products, using low acid concentrations is suggested as part of a technological solution for worm clearance as low acid concentrations had limited macroscopic effect on liver integrity within 35 min.


Subject(s)
Ascaridida Infections/veterinary , Ascaridoidea/isolation & purification , Fish Diseases/parasitology , Gadus morhua/parasitology , Liver/parasitology , Animals , Ascaridida Infections/parasitology , Ascaridoidea/physiology , Baltic States , Larva/physiology
5.
J Fish Dis ; 40(12): 1815-1821, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28548690

ABSTRACT

The protective effect in rainbow trout (Oncorhynchus mykiss) of an experimental subunit vaccine targeting antigens in the parasite Ichthyophthirius multifiliis has been evaluated and compared to effects elicited by a classical parasite homogenate vaccine. Three recombinant parasite proteins (two produced in E. coli and one in insect cells) were combined and injected i.p., and subsequently, protection and antibody responses were analysed. Both the experimental and the benchmark vaccine induced partial but significant protection against I. multifiliis when compared to control fish. Specific antibody responses of vaccinated trout (subunit vaccine) were raised against one neurohypophysial n-terminal domain protein #10 of three recombinant proteins, whereas the benchmark vaccine group showed specific antibody production against all three recombinant proteins. The immunogenic parasite protein #10 may be a potential vaccine candidate supplementing the protective I-antigen in future vaccine trials.


Subject(s)
Ciliophora Infections/veterinary , Fish Diseases/prevention & control , Fish Diseases/parasitology , Hymenostomatida/immunology , Oncorhynchus mykiss/immunology , Vaccines, Synthetic/immunology , Animals , Antibodies, Protozoan , Antibody Formation , Antigens, Protozoan/immunology , Cell Line , Ciliophora Infections/immunology , Ciliophora Infections/prevention & control , Escherichia coli , Fish Diseases/immunology , Oncorhynchus mykiss/parasitology , Protozoan Proteins/immunology , Vaccines, Synthetic/administration & dosage
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