Reciprocal effects between host phenotype and pathogens: new insights from an old problem

Trends in Parasitology

Volumn 25, Issue 8, 2009, Pages 364-369

  Blanchet, Simon ^a,b   Thomas, Frédéric ^c,d   Loot, Géraldine ^a  

^a CNRS   (France)

^b Centre National de la Recherche Scientifique and Paul Sabatier University   (France)

^c INSTITUT DE RECHERCHE POUR LE DÉVELOPPEMENT   (France)

^d UNIVERSITÉ DE MONTRÉAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; GENETIC TRAIT; HOST PARASITE INTERACTION; NONHUMAN; PARASITE TRANSMISSION; PATHOGENESIS; PHENOTYPE;

ANIMALS; CESTODA; FEMALE; GALLIFORMES; HOST-PARASITE INTERACTIONS; MALE; ONCORHYNCHUS MYKISS; PARASITIC DISEASES, ANIMAL; PHENOTYPE; SEX CHARACTERISTICS; SMEGMAMORPHA; TRICHOSTRONGYLUS;

EID: 67949112793     PISSN: 14714922     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pt.2009.05.005     Document Type: Article

References (49)

1. Combes C. Parasitism, The Ecology and Evolution of Intimate Interactions (2001), The University of Chicago Press Ltd
2. Poulin R. Evolutionary Ecology of Parasites: From Individuals to Communities (2007), Chapman & Hall
3. Moore J. Parasites and the behaviour of animals (2002), Oxford University Press
4. Ostfeld R.S., et al. Spatial epidemiology: an emerging (or re-emerging) discipline. Trends Ecol. Evol. 20 (2005) 328-336
5. Lefevre T., et al. The ecological significance of manipulative parasites. Trends Ecol. Evol. 24 (2009) 41-48
6. Poulin R., et al. Size, behaviour, and acquisition of ectoparasitic copepods by brook trout, Salvelinus fontinalis. Oikos 61 (1991) 169-174
7. Beldomenico P.M., et al. Poor condition and infection: a vicious circle in natural populations. P. Roy. Soc. B 275 (2008) 1753-1759
8. Flint P.L., and Franson J.C. Does influenza A affect body condition of wild mallard ducks, or vice versa?. P. Roy. Soc. B (2009) 10.1098/rspb.2008.1962
9. Bourque J.F., et al. Cestode parasitism as a regulator of early life-history survival in an estuarine population of rainbow smelt Osmerus mordax. Mar. Ecol. Prog. Ser. 314 (2006) 295-307
10. Blanchet S., et al. Why parasitized hosts look different? Resolving the 'chicken-egg' dilemma. Oecologia 160 (2009) 37-47
11. Hamilton W.D., and Zuk M. Heritable true fitness and bright birds - a role for parasites. Science 218 (1982) 384-387
12. Collins S. Is there only one type of male handicap. P. Roy. Soc. B 252 (1993) 193-197
13. Folstad I., et al. Sexually selected color in male sticklebacks: a signal of both parasite exposure and parasite resistance?. Oikos 69 (1994) 511-515
14. Sanchez M.I., et al. Sandpipers select red brine shrimps rich in both carotenoids and parasites. Ethology 115 (2009) 196-200
15. Milinski M., and Bakker T. Female sticklebacks use male coloration in mate choice and hence avoid parasitized males. Nature 344 (1990) 330-333
16. Redpath S.M., et al. Testing the role of parasites in driving the cyclic population dynamics of a gamebird. Ecol. Lett. 9 (2006) 410-418
17. Mougeot F., et al. The effect of aggressiveness on the population dynamics of a territorial bird. Nature 421 (2003) 737-739
18. Mougeot F., et al. Testosterone, immunocompetence, and honest sexual signaling in male red grouse. Behav. Ecol. 15 (2004) 930-937
19. Mougeot F., et al. Interactions between population processes in a cyclic species: parasites reduce autumn territorial behaviour of male red grouse. Oecologia 144 (2005) 289-298
20. Seivwright L.J., et al. Interactions between intrinsic and extrinsic mechanisms in a cyclic species: testosterone increases parasite infection in red grouse. P. Roy. Soc. B 272 (2005) 2299-2304
21. Fox A., and Hudson P.J. Parasites reduce territorial behaviour in red grouse (Lagopus lagopus scoticus). Ecol. Lett. 4 (2001) 139-143
22. Safran R.J., et al. Sexual signal exaggeration affects physiological state in male barn swallows. Curr. Biol. 18 (2008) R461-R462
23. Rubenstein D.R., and Hauber M.E. Dynamic feedback between phenotype and physiology in sexually selected traits. Trends Ecol. Evol. 23 (2008) 655-658
24. Royce R.A., et al. Current concepts - sexual transmission of HIV. N. Engl. J. Med. 336 (1997) 1072-1078
25. Liljeros F., et al. The web of human sexual contacts. Nature 411 (2001) 907-908
26. Knell R.J., and Webberley K.M. Sexually transmitted diseases of insects: distribution, evolution, ecology and host behaviour. Biol. Rev. Camb. Philos. Soc. 79 (2004) 557-581
27. May R.M., and Anderson R.M. Transmission dynamics of HIV-infection. Nature 326 (1987) 137-142
28. Fleming D.T., and Wasserheit J.N. From epidemiological synergy to public health policy and practice: the contribution of other sexually transmitted diseases to sexual transmission of HIV infection. Sex. Transm. Infect. 75 (1999) 3-17
29. Galvin S.R., and Cohen M.S. The role of sexually transmitted diseases in HIV transmission. Nat. Rev. Microbiol. 2 (2004) 33-42
30. Møller A.P. A fungus infecting domestic flies manipulates sexual-behavior of its host. Behav. Ecol. Sociobiol. 33 (1993) 403-407
31. Boots M., and Knell R.J. The evolution of risky behaviour in the presence of a sexually transmitted disease. P. Roy. Soc. B 269 (2002) 585-589
32. Aral S. Sexual risk behaviour and infection: epidemiological considerations. Sex. Transm. Infect. 80 (2004) 8-12
33. McCoy K.D., et al. Local adaptation of the ectoparasite Ixodes uriae to its seabird host. Evol. Ecol. Res. 4 (2002) 441-456
34. Arnott S.A., et al. Parasite-associated growth enhancement in a fish-cestode system. P. Roy. Soc. B 267 (2000) 657-663
35. Barber I. Parasites grow larger in faster growing fish hosts. Int. J. Parasitol. 35 (2005) 137-143
36. Blair L., and Webster J.P. Dose-dependent schistosome-induced mortality and morbidity risk elevates host reproductive effort. J. Evol. Biol. 20 (2007) 54-61 10.1111/j.1420-9101.2006.01230.x
37. Poulin R., et al. Infection of brook trout fry, Salvelinus fontinalis, by ectoparasitic copepods: the role of host behaviour and initial parasite load. Anim. Behav. 41 (1991) 467-476
38. Lebreton J.D., et al. Modeling survival and testing biological hypotheses using marked animals - a unified approach with case-studies. Ecol. Monogr. 62 (1992) 67-118
39. Mills L.S., et al. Estimating animal abundance using noninvasive DNA sampling: promise and pitfalls. Ecol. Appl. 10 (2000) 283-294
40. Bonfil R., et al. Transoceanic migration, spatial dynamics, and population linkages of white sharks. Science 310 (2005) 100-103
41. van Gils J.A., et al. Hampered foraging and migratory performance in swans infected with low-pathogenic avian influenza A virus. PLoS One 2 (2007) e184
42. Latorre-Margalef N., et al. Effects of influenza A virus infection on migrating mallard ducks. P. Roy. Soc. B B 276 (2009) 10.1098/rspb.2008.1501
43. Haugen T.O., et al. Density dependence and density independence in the demography and dispersal of pike over four decades. Ecol. Monogr. 77 (2007) 483-502
44. Lambrechts L., et al. Coevolutionary interactions between host and parasite genotypes. Trends Parasitol. 22 (2006) 12-16
45. Poulin R., and Morand S. The diversity of parasites. Q. Rev. Biol. 75 (2000) 277-293
46. Kuris A.M., et al. Ecosystem energetic implications of parasite and free-living biomass in three estuaries. Nature 454 (2008) 515-518
47. Pedersen A.B., and Greives T.J. The interaction of parasites and resources cause crashes in a wild mouse population. J. Anim. Ecol. 77 (2008) 370-377
48. Cochran G.M., et al. Infectious causation of disease: an evolutionary perspective. Perspect. Biol. Med. 43 (2000) 406-448
49. Franceschi N., et al. The effects of parasite age and intensity on variability in acanthocephalan-induced behavioural manipulation. Int. J. Parasitol. 38 (2008) 1161-1170