Abstract
Eco-immunology recognises that immune systems and responses are an integrated part of an animal’s physiology, preventing harm that might be caused by pathogens. Laboratory-based immunology has given a tremendously strong understanding of the mechanisms by which this system functions, though this is focused on a few species. It is clear that immune responses are costly to make, such that animals have difficult decisions of resource allocation to make. For this reason alone, an eco-immunological approach is key to understanding the functional effect of immune responses. Animals live in antigenically complex environments. Because of the superb adaptiveness of the immune system (as well as its redundancy) the immune responses made by different individuals in a population may differ greatly, but the functional effect of this is unclear and ripe for investigation. The research challenges for eco-immunology are substantial, but achievable.
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Notes
- 1.
An antigen is a molecule to which an immune response is induced. Antigens are typically from pathogens, although experimentally any molecule introduced to an animal acts as an antigen. Auto-antigens are host-derived molecules to which, therefore, an auto-immune response is generated.
References
Abolins SR, Pocock MJO, Hafalla JCR, Riley EM, Viney ME (2011) Measures of immune function of wild mice, Mus musculus. Mol Ecol 20:881–892
Ardia DR, Schat KA, Winkler DW (2003) Reproductive effort reduces long-term immune function in breeding tree swallows (Tachycineta bicolor). Proc Roy Soc Lond B 270:1679–1683
Baracos VE, Whitmore WT, Gale R (1987) The metabolic cost of fever. Can J Physiol Pharmacol 65:1248–1254
Bhattarai KK, Xie Q-G, Mantelin S, Bishnoi U, Girke T, Navarre DA et al (2008) Tomato susceptibility to root-knot nematodes requires an intact jasmonic acid signaling pathway. Mol Plant Microbe Interact 9:1205–1214
Bleay C, Wilkes CP, Paterson S, Viney ME (2007) Density-dependent immune responses against the gastrointestinal nematode Strongyloides ratti. Int J Parasitol 37:1501–1509
Bonneaud C, Mazuc J, Gonzalez G, Haussy C, Chastel O, Faivre B et al (2003) Assessing the cost of mounting an immune response. Am Nat 3:367–379
Boysen P, Eide DM, Storset AK (2011) Natural killer cells in free-living Mus musculus have a primed phenotype. Mol Ecol 20:5103–5110
Brugman S, Nieuwenhuis EES (2010) Mucosal control of the intestinal microbial community. J Mol Med 88:881–888
Candela M, Maccaferria S, Turronia S, Carnevalib P, Brigidia P (2010) Functional intestinal microbiome, new frontiers in prebiotic design. Int J Food Micro 40:93–101
Cerf-Benussan N, Gaboriau-Routhiau V (2010) The immune system and the gut microbiota: friends or foe? Nat Rev Imm 10:735–744
Chaussabel D, Pascual V, Banchereau J (2010) Assessing the human immune system through blood transcriptomics. BMC Biol 8:84
Chung H, Kasper DL (2010) Microbiota-stimulated immune mechanisms to maintain gut homeostasis. Curr Opin Immun 22:455–460
Crimmins EM, Finch CE (2006) Infection, inflammation, height, and longevity. Proc Natl Acad Sci USA 103:498–503
Cunnington AJ, De Souze JB, Walther M, Riley EM (2012) Malaria impairs resistance to Salmonella through heme- and heme-oxygenase-dependent dysfunctional granulocyte mobilization. Nat Med. doi:10.1038/nm.2601
Davies SJ, Grogan JL, Blank RB, Lim KC, Locksley RM, McKerrow JH (2001) Modulation of blood fluke development in the liver by hepatic CD4+ lymphocytes. Science 294:1358–1361
Deerenberg C, Apanius V, Daan S, Bos N (1997) Reproductive effort decreases antibody responsiveness. Proc Roy Soc Lond B 264:1021–1029
Demas GE, Chefer V, Talan MI, Nelson RJ. (1997) Metabolic costs of mounting an antigen-stimulated immune response in adult and aged C57BL/6J mice. Am J Physiol Regul Integr Comp Physiol 273:R1631–R1637
Devalapalli AP, Lesher A, Shieh K, Solow JS, Everett ML, Edala AS et al (2006) Increased levels of IgE and autoreactive, polyreactive IgG in wild rodents: implications for the hygiene hypothesis. Scand J Immun 64:125–136
Diaz Heijtz R, Wangc S, Anuard F, Qiana Y, Björkholmd B, Samuelssond A et al (2011) Normal gut microbiota modulates brain development and behavior. Proc Natl Acad Sci U S A 108:3047–3052
Ding S, Chi MM, Scull BP, Rigby R, Schwerbrock NMJ, Magness S et al (2010) High-fat diet: bacteria interactions promote intestinal inflammation which precedes and correlates with obesity and insulin resistance in mouse. PLoS One 5:e12191
Dobzhansky T (1973) Nothing in biology makes sense except in the light of evolution. Am Bio Teach 35:125–129
Eckburg PB, Bik EM, Bernstein CN, Purdom E, Dethlefsen L, Sargent M et al (2005) Diversity of the human intestinal microbial flora. Science 308:1635–1638
Eraud C, Duriez O, Chastel O, Faivre B (2005) The energetic cost of humoral immunity in the Collared Dove, Streptopelia decaocto: is the magnitude sufficient to force energy-based trade-offs? Func Ecol 19:110–118
Ewenson E, Zann R, Flannery G (2003) PHA Immune response assay in captive zebra finches is modulated by activity prior to testing. Anim Behav 66:797–800
Good RA, Jose D, Cooper WC, Fernandes G, Krammer T, Yunis E (1977) Influence of nutrition on antibody production and cellular immune responses in man, rats, mice, and guinea pigs. In: Suskind RM (ed) Malnutrition and the immune response. Raven Press, New York, pp 169–183
Graham AL (2008) Ecological rules governing helminth-microparasite coinfection. Proc Natl Acad Sci USA 105:566–570
Graham AL, Allen JE, Read AF (2005) Evolutionary causes and consequences of immunopathology. Annu Rev Ecol Syst 36:373–397
Hasselquist D, Wasson MF, Winkler DW (2001) Humoral immunocompetence correlates with date of egg-laying and reflects work load in female tree swallows. Behav Ecol 12:93–97
Hanssen SA, Hasselquist D, Folstad I, Erikstad KE (2004) Costs of immunity: immune responsiveness reduces survival in a vertebrate. Proc Roy Soc Lond B 271:925–930
Hawkins AE, Jewell PA (1962) Food consumption and energy requirements of captive British shrews and the mole. Proc Zoo Soc Lond 138:137–155
Ing R, Su Z, Scott ME, Koski KG (2000) Suppressed T helper 2 immunity and prolonged survival of a nematode parasite in protein-malnourished mice. Proc Natl Acad Sci USA 97:7078–7083
Jackson JA, Begon M, Birtles R, Paterson S, Friberg IM, Hall A et al (2011) The analysis of immunological profiles in wild animals: a case study on immunodynamics in the field vole, Microtus agrestis. Mol Ecol 20:893–909
Jose DG, Good RA (1973) Quantitative effects of nutritional protein and calorie deficiency upon immune-responses to tumors in mice. Cancer Res 33:807–812
Kielmann XX (1977) Nutritional and immune responses of sub clinically malnourished Indian children. In: Suskind RM (ed) Malnutrition and the immune response. Raven Press, New York, pp 429–440
Koski KG, Scott ME (2001) Gastrointestinal nematodes, nutrition and immunity: breaking the negative spiral. Annu Rev Nutr 21:297–321
Koski KG, Su Z, Scott ME (1999) Energy deficits suppress both systemic and gut immunity during infection. Biochem Biophys Res Comm 264:796–801
Lee YK, Mazmanian SK (2010) Has the microbiota played a critical role in the evolution of the adaptive immune system? Science 330:1768–1773
Lello J, Boag B, Fenton A, Stevenson IR, Hudson PJ (2004) Competition and mutualism among the gut helminths of a mammalian host. Nature 428:840–844
Ley RE (2010) Obesity and the human microbiome. Curr Opin Gastro 26:5–11
Ley RE, Turnbaugh PJ, Klein S, Gfordon JI (2006) Microbial ecology: human gut microbes associated with obesity. Nature 444:1022–1023
Lochmiller RL, Deerenberg C (2000) Trade-offs in evolutionary immunology: just what is the cost of immunity? Oikos 88:87–98
Maizels RM (2005) Infections and allergy—helminths, hygiene and host immune regulation. Curr Opin Immunol 17:656–661
Martin LB, Scheuerlein A, Wikelski M (2003) Immune activity elevates energy expenditure of house sparrows: a link between direct and indirect costs? Proc Roy Soc Lond B 270:153–158
Martinez I, Merino S, Rodriguez-Caabeiro F (2004) Physiological responses to Trichinella spiralis infection in Wistar rats: Is immune response costly? Helminthologia 41:67–71
McDade TW (2003) Life history theory and the immune system: steps toward a human ecological immunology. Yearb Phys Anthropol 46:100–125
McDade TW, Reyes-Garcia V, Tanner S, Huanca T, Leonard WR (2008) Maintenance versus growth: investigating the costs of immune activation among children in lowland Bolivia. Am J Phys Athropol 136:478–484
Mclean JA, Speakman JR (1999) Energy budgets of lactating and non-reproductive brown long-eared bats (Plecotus auritus) suggest females use compensation in lactation. Funct Ecol 13:360–372
Neumann CG, Lawlor GJ, Stiehm ER, Swendseid ME, Newton C, Herbert J et al (1975) Immunologic responses in malnourished children. Am J Clin Nut 28:89–104
Neumann CG, Stiehm ER, Swenseid M, Ferguson AC, Lawlor G (1977) Cell-mediated immune response in Ghanaian children with protein-calorie malnutrition. In: Suskind RM (ed) Malnutrition and the immune response. Raven Press, New York, pp 77–89
Nunn CL, Gittleman JL, Antonovics J (2000) Promiscuity and the primate immune system. Science 290:1168–1170
Nussey DH, Watt K, Pilkington JG, Zamoyska R, McNeilly TN (2011) Age-related variation in immunity in a wild mammal population. Aging Cell 11:178–180
Palacios MG, Sparkman AM, Bronikowski AM (2010) Developmental plasticity of immune defence in two life-history ecotypes of the garter snake, Thamnophis elegans—a common-environment experiment. J Anim Ecol 80:431–437
Paterson S, Viney ME (2002) Host immune responses are necessary for density-dependence in nematode infections. Parasito 125:283–292
Pennisi E (2010) Body’s hardworking microbes get some overdue respect. Science 330:1619
Phelps RG, Turner AN, Rees AJ (1996) Direct identification of naturally processed autoantigen-derived peptides bound to HLA-DR15. J Biol Chem 271:18549–18553
Pocino M, Baute L, Malave I (1987) Calorie restriction modifies the delayed-type hypersensitivity response to the hapten trinitrobenzenesulfonic acid and to hapten-modified syngeneic spleen-cells. Cell Immun 109:261–271
Råberg L, Stjernman M (2003) Natural selection on immune responsiveness in blue tits Parus caeruleus. Evolution 57:1670–1678
Råberg L, Vestberg M, Hasselquist D, Holmdahl R, Svensson E, Nilsson J-A (2002) Basal metabolic rate and the evolution of the adaptive immune system. Proc Roy Soc Lond B 269:817–821
Rajilic-Stojanovic M, Smidt H, De Vos WM (2007) Diversity of the human gastrointestinal tract microbiota revisited. Env Micro 9:2125–2136
Read AF, Allen JE (2000) The economics of immunity. Science 290:1104–1105
Round JL, Mazanian SK (2009) The gut microbiota shapes intestinal immune responses during health and disease. Nat Rev Imm 9:313–323
Schulkin J (2003) Rethinking homeostasis: allostatic regulation in physiolgy and pathophysiology. MIT Press, London
Segura M, Mattea C, Thawania N, Su Z, Stevensona MM (2009) Modulation of malaria-induced immunopathology by concurrent gastrointestinal nematode infection in mice. Int J Parasitol 39:1525–1532
Sparkman AM, Palacios MG (2009) A test of life-history theories of immune defence in two ecotypes of the garter snake, Thamnophis elegans. J Anim Ecol 78:1242–1248
Speakman J (1997) Factors influencing the daily energy expenditure of small mammals. Proc Nutr Soc 56:1119–1136
Suri A, Walters JJ, Kanagawa O, Gross ML, Unanue ER (2003) Specificity of peptide selection by antigen-processing cells homozygous or heterozygous for expression of class II MHC molecules: the lack of competition. Proc Natl Acad Sci USA 100:5330–5335
Telfer S, Lambin X, Birtles R, Beldomenico P, Burthe S, Paterson S et al (2010) Species interactions in a parasite community drive infection risk in a wildlife population. Science 330:243–246
Turnbaugh PJ, Ley RE, Mahowald MA, Magrini V, Mardis ER, Gordon JI (2006) An obesity-associated gut microbiome with increased capacity for energy harvest. Nature 444:1027–1031
Turnbaugh PJ, Backhed F, Fulton L, Gordon JI (2008) Diet-induced obesity is linked to marked but reversible alterations in the mouse distal gut microbiome. Cell Host Micro 3:213–223
Turnbaugh PJ, Hamady M, Yatsunenko T, Cantarel BL, Duncan A, Ley RE et al (2009) A core gut microbiome in obese and lean twins. Nature 457:480–484
Turner AK, Begon M, Jackson JA, Bradley JE, Paterson S (2011) Genetic diversity in cytokines associated with immune variation and resistance to multiple pathogens in a natural rodent population. PLos Genet 7:e1002343
Viney ME, Cable J (2011) Macroparasite life-histories. Curr Biol 21:R767–R774
Viney ME, Lok JB (2007) Strongyloides spp. In WormBook, The C. elegans Research Community, eds. WormBook. doi/10.1895/wormbook.1.141.1. http://www.wormbook.org
Viney ME, Riley EM, Buchanan KL (2005) Optimal immune responses: immunocompetence revisited. Trend Ecol Evoln 20:665–669
Wagland BM, Steel JW, Windon RG, Dineen JK (1984) The response of lambs to vaccination and challenge with Trichostrongylus colubriformis: effect of plane of nutrition on, and the inter-relationship between, immunological responsiveness and resistance. Int J Parasitol 14:39–44
Westerterp K (1978) How rats economize—energy loss in starvation. Phsiol Zool 50:331–362
Williams TD, Christians JK, Aiken JJ, Evanson M (1999) Enhanced immune function does not depress reproductive output. Proc Roy Soc Lond B 266:753–757
Xiao W, Mindrinos MN, Seok J, Cuschieri J, Cuenca AG, Hong G et al (2011) A genomic storm in critically injured humans. J Exp Med 208:2581–2590
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Viney, M., Riley, E. (2014). From Immunology to Eco-Immunology: More than a New Name. In: Malagoli, D., Ottaviani, E. (eds) Eco-immunology. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-8712-3_1
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