Genotypic vs. condition effects on parasite-driven rare advantage

Journal of Evolutionary Biology

Volumn 17, Issue 5, 2004, Pages 967-973

  Dybdahl, M F ^a   Krist, A C ^b,c  

^a WASHINGTON STATE UNIVERSITY   (United States)

^b INDIANA UNIVERSITY   (United States)

^c UNIVERSITY OF WISCONSIN EAU CLAIRE   (United States)

Author keywords

Coevolution; Frequency dependent selection; Host parasite interactions; Parasite resistance; Red Queen hypothesis; Trade off

Indexed keywords

FRESH WATER; ISOENZYME;

COEVOLUTION; HOST SPECIFICITY; HOST-PARASITE INTERACTION; PARASITE RESISTANCE;

ANALYSIS OF VARIANCE; ANIMAL; ARTICLE; BIOLOGICAL MODEL; BODY CONSTITUTION; COMPARATIVE STUDY; EVOLUTION; FEMALE; GENETICS; GENOTYPE; HOST PARASITE INTERACTION; NEW ZEALAND; PARASITOLOGY; PHYSIOLOGY; SNAIL; TREMATODE;

ANALYSIS OF VARIANCE; ANIMALS; BODY CONSTITUTION; EVOLUTION; FEMALE; FRESH WATER; GENOTYPE; HOST-PARASITE RELATIONS; ISOENZYMES; MODELS, BIOLOGICAL; NEW ZEALAND; SNAILS; TREMATODA;

BASOMMATOPHORA; GASTROPODA; HYDROBIIDAE; MICROPHALLUS; POTAMOPYRGUS ANTIPODARUM; TREMATODA;

EID: 4444226490     PISSN: 1010061X     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1420-9101.2004.00759.x     Document Type: Article

References (35)

1. Ahmed, A.M., Baggott, S.L., Maingon, R. & Kurd, H. 2002. The costs of mounting an immune response are reflected in the reproductive fitness of the mosquito Anopheles gambiae. Oikos 97: 371-377.
2. Clarke, B. 1976. The ecological genetics of host-parasite relationships. In: Genetic Aspects of Host-parasite Relationships, Vol. 14 (A. E. R. Taylor & R. Muller, eds), pp. 87-103. Blackwell Scientific, Oxford.
3. Cooper, L.A., Richards, C.S., Lewis, F.A. & Minchella, D.J. 1994. Schistosoma mansoni: relationship between low fecundity and reduced susceptibility to parasite infection in the snail Biomphalaria glabrata. Exp. Parasitol. 79: 21-28.
4. Cousin, C., Ofori, K., Acholonu, S., Miller, A., Richards, C., Lewis, F. & Knight, M. 1995. Schistosoma mansoni: changes in the albumen gland of Biomphalaria glabrata snails selected for nonsusceptibility to the parasite. J. Parasitol. 81: 905-911.
5. Dybdahl, M.F. & Lively, C.M. 1995. Diverse, endemic, and polyphyletic clones in mixed populations of a freshwater snail Potamopyrgus antipodarum. J. Evol. Biol. 8: 385-398
6. Dybdahl, M.F. & Lively, C.M. 1996. The geography of coevolution: comparative population structures for a snail and its trematode parasite. Evolution 50: 2264-2275.
7. Dybdahl, M.F. & Lively, C.M. 1998. Host-parasite coevolution: evidence for rare advantage and time-lagged selection in a natural population. Evolution 52: 1057-1066.
8. Dybdahl, M.F. & Storfer, A. 2003. Parasite local adaptation: Red Queen vs. Suicide King. Trends in Ecology and Evolution 18: 523-530.
9. Fair, J.M., Hansen, E.S. & Ricklefs, R.E. 1999. Growth, developmental stability and immune response in juvenile Japanese quails (Coturnix coturnix japonica). Proc. R. Soc. Lond. B 266: 1735-1742.
10. Hamilton, W.D., Axelrod, R. & Tanese, R. 1990. Sexual reproduction as an adaptation to resist parasites: a review. Proc. Natl. Acad. Sci. USA 87: 3566-3573.
11. Howard, R.S. & Lively, C.M. 1994. Parasitism, mutation accumulation and the maintenance of sex. Nature 367: 554-557.
12. Jaenike, J. 1978. A hypothesis to account for the maintenance of sex in populations. Evolutionary Theory 3: 191-194.
13. Jokela, J. 1997. Optimal energy allocation tactics and indeterminate growth: life-history evolution of long-lived bivalves. In: Evolutionary Ecology of Freshwater Animals (B. Streit, T. Stadler & C. M. Lively, eds), pp. 179-196. Birkhauser Verlag, Basel.
14. Jokela, J. & Lively, C.M. 1995. Spatial variation for infection by digenetic trematodes in a population of freshwater snails (Potamopyrgus antipodarum). Oecologia 103: 509-517.
15. Jokela, J., Uotila, L. & Taskinen, J. 1993. Effect of trematode parasite Rhipidocotyle fennica on energy allocation of freshwater clam Anodonta piscinalis. Functional Ecology 7: 332-338.
16. Klasing, K.C., Laurin, D.E., Peng, R.K. & Fry, D.M. 1987. Immunologically mediated growth depression in chicks: influence of feed intake, corticosterone, and interleukin-1. J. Nutrition. 117: 1629-1637.
17. Krist, A.C., Jokela, J., Wiehn, J. & Lively, C.M. 2004. Effects of host condition on susceptibility to infection, parasite development rate, and parasite transmission in a snail-trematode interaction. J. Evol. Biol 17: 33-40.
18. Levri, E.P. & Lively, C.M. 1996. The effects of size, reproductive condition, and parasitism on the foraging behaviour in a freshwater snail, Potamopyrgus antipodarum. Animal Behaviour 51: 891-901.
19. Little, T.J. & Ebert, D. 2000. The cause of parasitic infection in natural populations of Daphnia (Crustacea: Cladocera): the role of host genetics. Proc. R. Soc. Lond. B 267: 2037-2042.
20. Lively, C.M. 1987. Evidence from a New Zealand snail for the maintenance of sex by parasitism. Nature 328: 519-521.
21. Lively, C.M. 1996. Host-parasite coevolution and sex - do interactions between biological enemies maintain genetic variation and cross-fertilization? BioScience 46: 107-114.
22. Lively, C.M. & Dybdahl, M.F. 2000. Parasite adaptation to locally common host genotypes. Nature 405: 679-681.
23. Lively, C.M. & McKenzie, J. 1991. Experimental infection of a freshwater snail, Potamopyrgus antipodarum with a digenetic trematode, Microphallus sp. New Zealand Nat. Sci. 18: 59-62.
24. Minchella, D.J. 1985. Host life-history variation in response to parasitism. Parasitology 90: 205-216.
25. Norusis, M.J. 1990. SPSS Advanced Statistics User's Guide. SPSS Inc., Chicago.
26. Rigby, M.C. & Jokela, J. 2000. Predator avoidance and immune defense: costs and trade-offs in snails. Proc. R. Soc. Lond. B 267: 171-176.
27. Rigby, M.C. & Moret, Y. 2000. Life-history trade-offs with immune defenses. In: Evolutionary Biology of Host-parasite Relationships: Theory Meets Reality (R. Poulin, S. Morand & A. Skorping, eds), pp. 129-141. Elsevier Science, New York.
28. Rigby, M.C., Hechinger, R.F. & Stevens, L. 2002. Why should parasite resistance be costly? Trends in Parasitol. 18: 116-120
29. Rothschild, M. 1941. The effect of trematode parasites on the growth of Littorina neritoides (L.). J. Mar. Biol. Assoc. UK 25: 69-80.
30. Seger, J. & Hamilton, W.D. 1988. Parasites and sex. In: The Evolution of Sex (R. E. Michod & B. R. Levin, eds), pp. 176-193. Sinauer, Sunderland, MA, USA.
31. Sheldon, B.C. & Verhulst, S. 1996. Ecological immunology: costly parasite defenses and trade-offs in evolutionary ecology. Trends Ecol. Evol. 11: 317-321.
32. Sokal, R.R. & Rohlf, F.J. 1995. Biometry, 3rd edn. W.H. Freeman and Company, New York.
33. Webster, J.P. & Woolhouse, M.E.J 1999. Cost of resistance: relationship between reduced fertility and increased resistance in a snail-schistosome host-parasite system. Proc. R. Soc. Lond. B. 266: 391-396.
34. Winterbourn, M. 1970. The New Zealand species of Potamopyrgus (Gastropoda: Hydrobiidae). Malacologia 10: 283-321.
35. Winterbourn, M.J. 1973. Larval Trematoda parasitizing the New Zealand species of Potamopyrgus (Gastropoda: Hydrobiidae). Mauri Ora 2: 17-30.