Differential tissue immune stimulation through immersion in bacterial and viral agonists in the Antarctic Notothenia rossii

Fish Shellfish Immunol. 2024 May:148:109516. doi: 10.1016/j.fsi.2024.109516. Epub 2024 Mar 26.

Abstract

The genome evolution of Antarctic notothenioids has been modulated by their extreme environment over millennia and more recently by human-caused constraints such as overfishing and climate change. Here we investigated the characteristics of the immune system in Notothenia rossii and how it responds to 8 h immersion in viral (Poly I:C, polyinosinic: polycytidylic acid) and bacterial (LPS, lipopolysaccharide) proxies. Blood plasma antiprotease activity and haematocrit were reduced in Poly I:C-treated fish only, while plasma protein, lysozyme activity and cortisol were unchanged with both treatments. The skin and duodenum transcriptomes responded strongly to the treatments, unlike the liver and spleen which had a mild response. Furthermore, the skin transcriptome responded most to the bacterial proxy (cell adhesion, metabolism and immune response processes) and the duodenum (metabolism, response to stress, regulation of intracellular signal transduction, and immune system responses) to the viral proxy. The differential tissue response to the two proxy challenges is indicative of immune specialisation of the duodenum and the skin towards pathogens. NOD-like and C-type lectin receptors may be central in recognising LPS and Poly I:C. Other antimicrobial compounds such as iron and selenium-related genes are essential defence mechanisms to protect the host from sepsis. In conclusion, our study revealed a specific response of two immune barrier tissue, the skin and duodenum, in Notothenia rossii when exposed to pathogen proxies by immersion, and this may represent an adaptation to pathogen infective strategies.

Keywords: Endotoxin; Immune system; Nototheniidae; Transcriptome; Viral stimuli.

MeSH terms

  • Animals
  • Antarctic Regions
  • Conservation of Natural Resources*
  • Fisheries
  • Humans
  • Immersion
  • Lipopolysaccharides / metabolism
  • Lipopolysaccharides / pharmacology
  • Perciformes* / metabolism
  • Poly I / metabolism

Substances

  • Lipopolysaccharides
  • Poly I