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Differential Expression of Immune Response Genes in Steller Sea Lions (Eumetopias jubatus): An Indicator of Ecosystem Health?

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Abstract

Characterization of the polygenic and polymorphic features of the Steller sea lion major histocompatibility complex (MHC) provides an ideal window for evaluating immunologic vigor of the population and identifying emergence of new genotypes that reflect ecosystem pressures. MHC genotyping can be used to measure the potential immunologic vigor of a population. However, since ecosystem-induced changes to MHC genotype can be slow to emerge, measurement of differential expression of these genes can potentially provide real-time evidence of immunologic perturbations. MHC DRB genes were cloned and sequenced using peripheral blood mononuclear leukocytes derived from 10 Steller sea lions from Southeast Alaska, Prince William Sound, and the Aleutian Islands. Nine unique DRB gene sequences were represented in each of 10 animals. MHC DRB gene expression was measured in a subset of six sea lions. Although DRB in genomic DNA was identical in all individuals, relative levels of expressed DRB mRNA was highly variable. Selective suppression of MHC DRB genes could be indicative of geographically disparate environmental pressures, thereby serving as an immediate and sensitive indicator of population and ecosystem health.

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References

  1. Andersen LC, Beaty JS, Nettles JW, Seyfried CE, Nepom GT, Nepom BS (1991) Allelic polymorphism in transcriptional regulatory regions of HLA-DQB genes. Journal of Experimental Medicine 173:181–192

    Article  CAS  Google Scholar 

  2. Berggren KT, Seddon JM (2005) MHC promoter polymorphism in grey wolves and domestic dogs. Immunogenetics [Online]

  3. Bowen L, Aldridge BM, Gulland FMD, et al. (2004) Class II multiformity generated by variable MHC-DRB region configurations in the California sea lion (Zalophus californianus) Immunogenetics 56:12–27

    Article  CAS  Google Scholar 

  4. Bowen L, Aldridge BM, DeLong R, Melin S, Buckles EL, Gulland F, et al. (2005) An immunogenetic basis for the high prevalence of urogenital cancer in a free-ranging population of California sea lions (Zalophus californianus). Immunogenetics 56:846–848

    Article  CAS  Google Scholar 

  5. Dong L, Ma Q, Whitlock JP Jr (1997) Down-regulation of major histocompatibility complex Q1b gene expression by 2,3,7,8-tetrachlorodibenzo-p-dioxin. Journal of Biological Chemistry 272:29614–29619

    Article  CAS  Google Scholar 

  6. Fox GA (2001) Wildlife as sentinels of human health effects in the Great Lakes—St. Lawrence basin. Environmental Health Perspectives 109(Suppl 6):853–861

    Article  Google Scholar 

  7. Hedrick PW (1994) Evolutionary genetics of the major histocompatibility complex. American Naturalist 143:945–964

    Article  Google Scholar 

  8. Hughes AL, Hughes MK (1995) Natural selection on the peptide-binding regions of major histocompatibility complex molecules. Immunogenetics 42:233–243

    Article  CAS  Google Scholar 

  9. Hughes DA, Pinder AC, Piper Z, Johnson IT, Lund EK (1996) Fish oil supplementation inhibits the expression of major histocompatibility complex class II molecules and adhesion molecules on human monocytes. American Journal of Clinical Nutrition 63:267–272

    CAS  Google Scholar 

  10. Klein J, Sato A (2000a) The HLA system: first of two parts. New England Journal of Medicine 343:702–709

    Article  CAS  Google Scholar 

  11. Klein J, Sato A (2000b) The HLA system: second of two parts. New England Journal of Medicine 343:782–786

    Article  CAS  Google Scholar 

  12. Leutenegger CM, Mislin CN, Sigrist B, Ehrengruber MU, Hofmann-Lehmann R, Lutz H (1999) Quantitative real-time PCR for the measurement of feline cytokine mRNA. Veterinary Immunology and Immunopathology 71:291–305

    Article  CAS  Google Scholar 

  13. Paul WE (1999) Fundamental Immunology, 4th ed., Philadelphia: Lippincott-Raven, xxi, 1589 pp

  14. Reizis B, Eisenstein M, Mor F, Cohen IR (1998) The peptide-binding strategy of the MHC class II I-A molecules. Immunology Today 19:212–216

    Article  CAS  Google Scholar 

  15. Rimsza LM, Roberts RA, Miller TP, Unger JM, LeBlanc M, Braziel RM, et al. (2004) Loss of MHC class II gene and protein expression in diffuse large B-cell lymphoma is related to decreased tumor immunosurveillance and poor patient survival regardless of other prognostic factors: a follow-up study from the Leukemia and Lymphoma Molecular Profiling Project. Blood 103:4251–4258

    Article  CAS  Google Scholar 

  16. Schwab CL, Fan R, Zheng Q, Myers P, Hebert P, Pruett SB (2005) Modeling and predicting stress-induced immunosuppression in mice using blood parameters. Toxicological Sciences 83:101–113

    Article  CAS  Google Scholar 

  17. Snyder DS, Unanue ER (1982) Corticosteroids inhibit murine macrophage 1a expression and interleukin 1 production. Journal of Immunology 129:1803–1805

    CAS  Google Scholar 

  18. Tabor GM, Aguirre AA (2004) Ecosystem health and sentinel species: adding an ecological element to the proverbial “canary in the mineshaft.” EcoHealth 1:226–228

    Article  Google Scholar 

  19. Trites AW, Larkin PA (1996) Changes in the abundance of Steller sea lions (Eumetopias jubatus) in Alaska from 1956 to 1992: how many were there? Aquatic Mammals 22:153–166

    Google Scholar 

  20. Venkatraman JT, Pendergast DR (2002) Effect of dietary intake on immune function in athletes. Sports Medicine 32:323–337

    Article  Google Scholar 

  21. Youn J, Lynes MA (1999) Metallothionein-induced suppression of cytotoxic T lymphocyte function is an important immunoregulatory control. Toxicological Sciences 52:199–208

    Article  CAS  Google Scholar 

  22. Yuhki N, O’Brien SJ (1990) DNA variation of the mammalian major histocompatibility complex reflects genomic diversity and population history. Proceedings of the National Academy of Sciences 87:836–840

    Article  CAS  Google Scholar 

  23. Zinkernagel RM (1979) Associations between major histocompatibility antigens and susceptibility to disease. Annual Review of Microbiology 33:201–213

    Article  CAS  Google Scholar 

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acknowledgments

We gratefully acknowledge the constructive suggestions offered by the editor. This research was funded in part by the Alaskan Department of Fish and Game (through NMFS co-operative agreement NA17FX1079) and a UC Davis Faculty Research Grant. Samples were collected under US Marine Mammal Protection Act and Endangered Species Act permits #965 and 358-1564.

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Correspondence to Lizabeth Bowen.

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Bowen, L., Aldridge, B., Beckmen, K. et al. Differential Expression of Immune Response Genes in Steller Sea Lions (Eumetopias jubatus): An Indicator of Ecosystem Health?. EcoHealth 3, 109–113 (2006). https://doi.org/10.1007/s10393-006-0021-0

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  • DOI: https://doi.org/10.1007/s10393-006-0021-0

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