4.7 Article

Effect of two constant light regimens on antibody profiles and immune gene expression in Atlantic salmon following vaccination and experimental challenge with salmonid alphavirus

期刊

FISH & SHELLFISH IMMUNOLOGY
卷 118, 期 -, 页码 188-196

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2021.07.002

关键词

Atlantic salmon; Light stimulation; Smoltification; Vaccine; Antibody; Gene expression; Salmonid alphavirus

资金

  1. Research Council of Norway [267, 644]
  2. MSD Animal Health
  3. IEPHB [AAAA-A18-118012290427-7]

向作者/读者索取更多资源

The effects of light manipulation on antibody production and gene expression in farmed Atlantic salmon were examined in this study. Differences were observed in gene expression and antibody levels between fish exposed to constant light two weeks prior to vaccination and those exposed at the time of vaccination. However, these differences were eliminated by vaccination when the fish were challenged with salmonid alphavirus.
Before seawater transfer, farmed Atlantic salmon are subjected to treatments that may affect the immune system and susceptibility to pathogens. E.g., exposure to constant light (CL) stimulates smoltification, which prepares salmon to life in sea water, but endocrine changes in this period are associated with suppression of immune genes. Salmon are vaccinated towards end of the freshwater period to safeguard that adequate vaccine efficacy is achieved by the time the fish is transferred to sea. In the present study, we investigated how the responses to vaccination and viral infection varied depending on the time of CL onset relative to vaccination. The salmon were either exposed to CL two weeks prior to vaccination (2-PRI) or exposed to CL at the time of vaccination (0-PRI). A cohabitant challenge with salmonid alphavirus, the causative agent of pancreatic disease, was performed 9 weeks post vaccination. The immunological effects of the different light manipulation were examined at 0- and 6-weeks post vaccination, and 6 weeks post challenge. Antibody levels in serum were measured using a serological beadbased multiplex panel as well as ELISA, and 92 immune genes in heart and spleen were measured using an integrated fluidic circuit-based qPCR array for multiple gene expression. The 2-PRI group showed a moderate transcript down-regulation of genes in the heart at the time of vaccination, which were restored 6 weeks after vaccination (WPV). Conversely, at 6WPV a down-regulation was seen for the 0-PRI fish. Moreover, the 2-PRI group had significantly higher levels of antibodies binding to three of the vaccine components at 6WPV, compared to 0-PRI. In response to SAV challenge, transcription of immune genes between 2-PRI and 0-PRI was markedly dissimilar in the heart and spleen of control fish, but no difference was found between vaccinated salmon from the two CL regimens. Thus, by using labor-saving high throughput detection methods, we demonstrated that light regimens affected antibody production and transcription of immune genes in nonvaccinated and virus challenged salmon, but the differences between the light treatment groups appeared eliminated by vaccination.

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