Higher resources decrease fluctuating selection during host-parasite coevolution

Ecology Letters

Volumn 17, Issue 11, 2014, Pages 1380-1388

  Lopez Pascua, Laura ^a   Hall, Alex R ^b   Best, Alex ^c   Morgan, Andrew D ^d   Boots, Mike ^e   Buckling, Angus ^e  

^a OXFORD UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^b ETH ZURICH   (Switzerland)

^c UNIVERSITY OF SHEFFIELD   (United Kingdom)

^d UNIVERSITY OF EDINBURGH   (United Kingdom)

^e UNIVERSITY OF EXETER   (United Kingdom)

Author keywords

Adaptive dynamics; Bacteria; Experimental evolution; Virus

Indexed keywords

BIOLOGICAL MODEL; EVOLUTION; GENETIC SELECTION; GENETICS; PATHOGENICITY; POPULATION DYNAMICS; PSEUDOMONAS FLUORESCENS; PSEUDOMONAS PHAGE; VIROLOGY;

BIOLOGICAL EVOLUTION; MODELS, BIOLOGICAL; POPULATION DYNAMICS; PSEUDOMONAS FLUORESCENS; PSEUDOMONAS PHAGES; SELECTION, GENETIC;

EID: 84907818034     PISSN: 1461023X     EISSN: 14610248     Source Type: Journal    
DOI: 10.1111/ele.12337     Document Type: Article

References (41)

1. Agrawal, A. & Lively, C.M. (2002). Infection genetics: gene-for-gene versus matching-alleles models and all points in between. Evol. Ecol. Res., 4, 79-90.
2. Anderson, R.M. & May, R.M. (1981). The population dynamics of microparasites and their invertebrate hosts. Philos. Trans. R. Soc. Lond. B Biol. Sci., 291, 451-524.
3. Anderson, R.M. & May, R.M. (1982). Coevolution of hosts and parasites. Parasitology, 85, 411-426.
4. Bell, G. (1990). The ecology and genetics of fitness in chlamydomonas.1. Genotype-by-environment interaction among pure strains. Proc. R. Soc. Lond. B, 240, 295-321.
5. Bell, G. (2010). Fluctuating selection: the perpetual renewal of adaptation in variable environments. Philos. Trans. R. Soc. Lond. B Biol. Sci., 365, 87-97.
6. Best, A., White, A., Kisdi, E., Antonovics, J., Brockhurst, M.A. & Boots, M. (2010). The evolution of host-parasite range. Am. Nat., 176, 63-71.
7. Black, A.J. & McKane, A.J. (2012). Stochastic formulation of ecological models and their applications. Trends Ecol. Evol., 27, 337-345.
8. Blanquart, F. & Gandon, S. (2013). Time-shift experiments and patterns of adaptation across time and space. Ecol. Lett., 16, 31-38.
9. Bohannan, B.J.M. & Lenski, R.E. (2000a). Linking genetic change to community evolution: insights from studies of bacteria and bacteriophage. Ecol. Lett., 3, 362-377.
10. Bohannan, B.J.M. & Lenski, R.E. (2000b). The relative importance of competition and predation varies with productivity in a model community. Am. Nat., 156, 329-340.
11. Boots, M. (2011). The evolution of resistance to a parasite is determined by resources. Am. Nat., 178, 214-220.
12. Boots, M., White, A., Best, A. & Bowers, R. (2014). How specificity and epidemiology drive the coevolution of static trait diversity in hosts and parasites. Evolution, doi:10.1111/evo.12393.
13. Buckling, A. & Hodgson, D.J. (2007). Short-term rates of parasite evolution predict the evolution of host diversity. J. Evol. Biol., 20, 1682-1688.
14. Dieckmann, U. & Law, R. (1996). The dynamical theory of coevolution: a derivation from stochastic ecological processes. J. Math. Biol., 34, 579-612.
15. Doedel, E.J., Champneys, A.R., Dercole, F. (2008) AUTO-07P: Continuation and Bifurcation Software for Ordinary Differential Equations. Available at: http://sourceforge.net/projects/auto-07p/. Last accessed 23 March 2014.
16. Flor, H.H. (1956). The complementary genetic system in flax and flax rust. Adv. Genet., 8, 29-54.
17. Flores, C.O., Meyer, J.R., Valverde, S., Farr, L. & Weitz, J.S. (2011) Statistical structure of host-phage interactions. Proc. Natl. Acad. Sci. USA, 108, E288-E297
18. Forde, S.E., Thompson, J.N. & Bohannan, B.J.M. (2004). Adaptation varies through space and time in a coevolving host-parasitoid interaction. Nature, 431, 841-844.
19. Forde, S.E., Thompson, J.N. & Bohannan, B.J.M. (2007). Gene flow reverses an adaptive cline in a coevolving host-parasitoid interaction. Am. Nat., 169, 794-801.
20. Forde, S.E., Thompson, J.N., Holt, R.D. & Bohannan, B.J.M. (2008). Coevolution drives temporal changes in fitness and diversity across environments in a bacteria-bacteriophage interaction. Evolution, 62, 1830-1839.
21. Frank, S.A. (1993). Specificity versus detectable polymorphism in host-parasite genetics. Proc. R. Soc. Lond. B, 254, 191-197.
22. Geritz, S.A.H., Kisdi, E., Meszéna, G. & Metz, J.A.J. (1998). Evolutionarily singular strategies and the adaptive growth and branching of the evolutionary tree. Evol. Ecol., 12, 35-57
23. Gomez, P. & Buckling, A. (2011). Bacteria-phage antagonistic coevolution in soil. Science, 332, 106-109.
24. Hall, A., Scanlan, P.D., Morgan, A.D. & Buckling, A. (2011). Host-parasite coevolutionary arms races give way to flcutuating selection. Ecol. Lett., 14, 635-642.
25. 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.
26. Harrison, E., Laine, A.L., Hietala, M. & Brockhurst, M.A. (2013). Rapidly fluctuating environments constrain coevolutionary arms races by impeding selective sweeps. Proc. Biol. Sci., 280, 20130937.
27. Hochberg, M.E. & van Baalen, M. (1998). Antagonistic coevolution over productivity gradients. Am. Nat., 152, 620-634.
28. Lopez-Pascua, L.D.C. & Buckling, A. (2008). Increasing productivity accelerates host-parasite coevolution. J. Evol. Biol., 21, 853-860.
29. Lopez-Pascua, L.D.C., Brockhurst, M.A. & Buckling, A. (2010). Antagonistic coevolution across productivity gradients: an experimental test of the effects of dispersal. J. Evol. Biol., 23, 207-211.
30. Marston, M.F., Pierciey, F.J. Jr, Shepard, A., Gearin, G., Qi, J., Yandava, C. et al. (2012). Rapid diversification of coevolving marine Synechococcus and a virus. Proc. Natl. Acad. Sci. USA, 109, 4544-4549.
31. Pal, C., Macia, M.D., Oliver, A., Schachar, I. & Buckling, A. (2007). Coevolution with viruses drives the evolution of bacterial mutation rates. Nature, 450, 1079-1081.
32. Parker, M.A. (1994). Pathogens and sex in plants. Evol. Ecol., 8, 560-584.
33. Poullain, V. & Nuismer, S.L. (2012). Infection genetics and the likelihood of host shifts in coevolving host-parasite interactions. Am. Nat., 180, 618-628.
34. Rode, N.O., Charmantier, A. & Lenormand, T. (2011). Male-female coevolution in the wild: evidence from a time series in Artemia franciscana. Evolution, 65, 2881-2892.
35. Rosenzweig, M.L. (1995). Species Diversity in Space and Time. Cambridge University Press, Cambridge.
36. Sasaki, A. (2000). Host-parasite coevolution in a multilocus gene-for-gene system. Proc. R. Soc. Lond. B, 267, 2183-2188.
37. Scanlan, P.D., Hall, A.R., Burlinson, P., Preston, G. & Buckling, A. (2013). No effect of host-parasite co-evolution on host range expansion. J. Evol. Biol., 26, 205-209.
38. Thompson, J.N. (2005). The Geographic Mosaic of Coevolution. University of Chicago Press, Chicago.
39. Thompson, J.N. & Burdon, J.J. (1992). Gene-for-gene coevolution between plants and parasites. Nature, 360, 121-125.
40. Thrall, P.H. & Burdon, J.J. (2003). Evolution of virulence in a plant host-pathogen metapopulation. Science, 299, 1735-1737.
41. Venail, P.A., MacLean, R.C., Bouvier, T., Brockhurst, M.A., Hochberg, M.E. & Mouquet, N. (2008). Diversity and productivity peak at intermediate dispersal rate in evolving metacommunities. Nature, 452, 210-214.