Skip to main content
Proceedings of the Royal Society B: Biological Sciences logoLink to Proceedings of the Royal Society B: Biological Sciences
. 2004 Oct 22;271(1553):2187–2194. doi: 10.1098/rspb.2004.2837

Transmission rates and adaptive evolution of pathogens in sympatric heterogeneous plant populations.

I Gudelj 1, F van den Bosch 1, C A Gilligan 1
PMCID: PMC1691847  PMID: 15475340

Abstract

Diversification in agricultural cropping patterns is widely practised to delay the build-up of virulent races that can overcome host resistance in pathogen populations. This can lead to balanced polymorphism, but the long-term consequences of this strategy for the evolution of crop pathogen populations are still unclear. The widespread occurrence of sibling species and reproductively isolated sub-species among fungal and oomycete plant pathogens suggests that evolutionary divergence is common. This paper develops a mathematical model of host-pathogen interactions using a simple framework of two hosts to analyse the influences of sympatric host heterogeneity on the long-term evolutionary behaviour of plant pathogens. Using adaptive dynamics, which assumes that sequential mutations induce small changes in pathogen fitness, we show that evolutionary outcomes strongly depend on the shape of the trade-off curve between pathogen transmission on sympatric hosts. In particular, we determine the conditions under which the evolutionary branching of a monomorphic into a dimorphic population occurs, as well as the conditions that lead to the evolution of specialist (single host range) or generalist (multiple host range) pathogen populations.

Full Text

The Full Text of this article is available as a PDF (152.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Anderson R. M., May R. M. Coevolution of hosts and parasites. Parasitology. 1982 Oct;85(Pt 2):411–426. doi: 10.1017/s0031182000055360. [DOI] [PubMed] [Google Scholar]
  2. Anderson R. M., May R. M. Population biology of infectious diseases: Part I. Nature. 1979 Aug 2;280(5721):361–367. doi: 10.1038/280361a0. [DOI] [PubMed] [Google Scholar]
  3. Bowers R. G., Hodgkinson D. E. Community dynamics, trade-offs, invasion criteria and the evolution of host resistance to microparasites. J Theor Biol. 2001 Oct 7;212(3):315–331. doi: 10.1006/jtbi.2001.2378. [DOI] [PubMed] [Google Scholar]
  4. Gupta S., Hill A. V. Dynamic interactions in malaria: host heterogeneity meets parasite polymorphism. Proc Biol Sci. 1995 Sep 22;261(1362):271–277. doi: 10.1098/rspb.1995.0147. [DOI] [PubMed] [Google Scholar]
  5. Nowak Martin A., Sigmund Karl. Evolutionary dynamics of biological games. Science. 2004 Feb 6;303(5659):793–799. doi: 10.1126/science.1093411. [DOI] [PubMed] [Google Scholar]
  6. doi: 10.1098/rstb.1997.0026. [DOI] [PMC free article] [Google Scholar]
  7. doi: 10.1098/rstb.1997.0180. [DOI] [PMC free article] [Google Scholar]
  8. Rand D. A., Wilson H. B., McGlade J. M. Dynamics and evolution: evolutionarily stable attractors, invasion exponents and phenotype dynamics. Philos Trans R Soc Lond B Biol Sci. 1994 Feb 28;343(1035):261–283. doi: 10.1098/rstb.1994.0025. [DOI] [PubMed] [Google Scholar]
  9. Regoes R. R., Nowak M. A., Bonhoeffer S. Evolution of virulence in a heterogeneous host population. Evolution. 2000 Feb;54(1):64–71. doi: 10.1111/j.0014-3820.2000.tb00008.x. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the Royal Society B: Biological Sciences are provided here courtesy of The Royal Society

RESOURCES