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1.
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
2.
J Fish Dis ; 37(9): 771-83, 2014 Sep.
Article in English | MEDLINE | ID: mdl-23952070

ABSTRACT

Infections with the parasitic flagellate Ichthyobodo necator (Henneguy, 1883) cause severe skin and gill disease in rainbow trout Oncorhynchus mykiss (Walbaum, 1792) juveniles. The epidermal disturbances including hyperplasia and mucous cell exhaustion caused by parasitization are known, but no details on specific cellular and humoral reactions have been presented. By applying gene expression methods and immunohistochemical techniques, further details of immune processes in the affected skin can be presented. A population of I. necator was established in the laboratory and used to induce an experimental infection of juvenile rainbow trout. The course of infection was followed by sampling for parasite enumeration, immunohistochemistry (IHC) and quantitative PCR (qPCR) on days 0, 5, 9 and 14 post-infection. IHC showed a significant increase in the occurrence of IgM-positive cells in the skin of the infected fish, whereas IgT-positive cells were eliminated and the number of CD8-positive cells declined. qPCR studies supported the IHC findings showing a significant increase in IgM and a decrease in the CD8 gene expression. In addition, genes encoding innate immune genes such as lysozyme, SAA and cathelicidin 2 were up-regulated. Expression of cytokines (IL-1ß, IL-4/13A, IL-6, IL-8, IL-10), the cell marker CD4 and the transcription factor GATA3 showed a significant increase after infection. Cytokine profiling including up-regulation of IL-4/13A and IL-10 genes and transcription factor GATA3 connected to the proliferation of IgM producing lymphocytes suggests a partial shift towards a Th2 response associated with the I. necator infection.


Subject(s)
Cytokines/genetics , Euglenozoa Infections/veterinary , Fish Diseases/immunology , Gene Expression Regulation , Kinetoplastida/physiology , Oncorhynchus mykiss , Animals , CD8-Positive T-Lymphocytes , Cytokines/metabolism , Epidermis/immunology , Epidermis/parasitology , Euglenozoa Infections/genetics , Euglenozoa Infections/immunology , Euglenozoa Infections/parasitology , Fish Diseases/genetics , Fish Diseases/parasitology , Immunoglobulin M/genetics , Immunoglobulin M/metabolism , Immunohistochemistry/veterinary , Molecular Sequence Data , Polymerase Chain Reaction/veterinary , Sequence Analysis, DNA/veterinary
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