Contrasting effects of acute and chronic stress on the transcriptome, epigenome, and immune response of Atlantic salmon. Issue 12 (2nd December 2018)

• Record Type: Journal Article
• Authors: Uren Webster, Tamsyn M.; Rodriguez-Barreto, Deiene; Martin, Samuel A.M.; Van Oosterhout, Cock; Orozco-terWengel, Pablo; Cable, Joanne; Hamilton, Alastair; Garcia De Leaniz, Carlos; Consuegra, Sofia
• Is Part Of: Epigenetics. Volume 13:Issue 12(2018)
• Page Start: 1191
• Page End: 1207
• Publication Date: 2018-12-02
• Subjects: DNA methylation -- RRBS -- transcriptomics -- rna-seq -- aquaculture -- stress -- early life -- immune response -- pathogen; Epigenesis -- Periodicals; Epigenetica; 572.86505
• DOI: 10.1080/15592294.2018.1554520
• Languages: English
• ISSNs: 1559-2294

Abstract

ABSTRACT: Stress experienced during early life may have lasting effects on the immune system, with impacts on health and disease dependent on the nature and duration of the stressor. The epigenome is especially sensitive to environmental stimuli during early life and represents a potential mechanism through which stress may cause long-lasting health effects. However, the extent to which the epigenome responds differently to chronic vs acute stressors is unclear, especially for non-mammalian species. We examined the effects of acute stress (cold-shock during embryogenesis) and chronic stress (absence of tank enrichment during larval-stage) on global gene expression (using RNA-seq) and DNA methylation (using RRBS) in the gills of Atlantic salmon ( Salmo salar ) four months after hatching. Chronic stress induced pronounced transcriptional differences, while acute stress caused few lasting transcriptional effects. However, both acute and chronic stress caused lasting and contrasting changes in the methylome. Crucially, we found that acute stress enhanced transcriptional immune response to a pathogenic challenge (bacterial lipopolysaccharide, LPS), while chronic stress suppressed it. We identified stress-induced changes in promoter and gene-body methylation that were associated with altered expression for a small proportion of immune-related genes, and evidence of wider epigenetic regulation within signalling pathways involved in immune response. Our results suggest that stress can affect immuno-competence through epigenetic mechanisms, and highlight the markedly different effects of chronic larval and acute embryonic stress. This knowledge could be used to harness the stimulatory effects of acute stress on immunity, paving the way for improved stress and disease management through epigenetic conditioning.