Developmental oestrogen exposure differentially modulates IGF-I and TNF-α expression levels in immune organs of Yersinia ruckeri-challenged young adult rainbow trout (Oncorhynchus mykiss)

Gen Comp Endocrinol. 2014 Sep 1:205:168-75. doi: 10.1016/j.ygcen.2014.05.022. Epub 2014 May 27.

Abstract

Intensified aquaculture has strong impact on fish health by stress and infectious diseases and has stimulated the interest in the orchestration of cytokines and growth factors, particularly their influence by environmental factors, however, only scarce data are available on the GH/IGF-system, central physiological system for development and tissue shaping. Most recently, the capability of the host to cope with tissue damage has been postulated as critical for survival. Thus, the present study assessed the combined impacts of estrogens and bacterial infection on the insulin-like growth factors (IGF) and tumor-necrosis factor (TNF)-α. Juvenile rainbow trout were exposed to 2 different concentrations of 17β-estradiol (E2) and infected with Yersinia ruckeri. Gene expressions of IGF-I, IGF-II and TNF-α were measured in liver, head kidney and spleen and all 4 estrogen receptors (ERα1, ERα2, ERβ1 and ERβ2) known in rainbow trout were measured in liver. After 5 weeks of E2 treatment, hepatic up-regulation of ERα1 and ERα2, but down-regulation of ERß1 and ERß2 were observed in those groups receiving E2-enriched food. In liver, the results further indicate a suppressive effect of Yersinia-infection regardless of E2-treatment on day 3, but not of E2-treatment on IGF-I whilst TNF-α gene expression was not influenced by Yersinia-infection but was reduced after 5 weeks of E2-treatment. In spleen, the results show a stimulatory effect of Yersinia-infection, but not of E2-treatment on both, IGF-I and TNF-α gene expressions. In head kidney, E2 strongly suppressed both, IGF-I and TNF-α. To summarise, the treatment effects were tissue- and treatment-specific and point to a relevant role of IGF-I in infection.

Keywords: Bacteria; Fish infection; Head kidney; IGF-II; Liver; Spleen.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytokines / metabolism
  • Estradiol / pharmacology*
  • Gene Expression Regulation, Developmental / drug effects
  • Head Kidney / drug effects*
  • Head Kidney / metabolism
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism*
  • Insulin-Like Growth Factor II / genetics
  • Insulin-Like Growth Factor II / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Oncorhynchus mykiss / growth & development
  • Oncorhynchus mykiss / immunology*
  • Oncorhynchus mykiss / metabolism
  • Oncorhynchus mykiss / microbiology*
  • Organ Specificity / drug effects
  • Organ Specificity / genetics
  • Real-Time Polymerase Chain Reaction
  • Receptors, Estrogen / metabolism
  • Spleen / drug effects*
  • Spleen / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism*
  • Yersinia Infections / genetics
  • Yersinia Infections / immunology
  • Yersinia ruckeri / physiology*

Substances

  • Cytokines
  • Receptors, Estrogen
  • Tumor Necrosis Factor-alpha
  • Estradiol
  • Insulin-Like Growth Factor I
  • Insulin-Like Growth Factor II