Literature DB >> 20002253

Antagonistic coevolution across productivity gradients: an experimental test of the effects of dispersal.

L D C Lopez-Pascua1, M A Brockhurst, A Buckling.   

Abstract

Coevolution commonly occurs in spatially heterogeneous environments, resulting in variable selection pressures acting on coevolving species. Dispersal across such environments is predicted to have a major impact on local coevolutionary dynamics. Here, we address how co-dispersal of coevolving populations of host and parasite across an environmental productivity gradient affected coevolution in experimental populations of bacteria and their parasitic viruses (phages). The rate of coevolution between bacteria and phages was greater in high-productivity environments. High-productivity immigrants ( approximately 2% of the recipient population) caused coevolutionary dynamics (rates of coevolution and degree of generalist evolution) in low-productivity environments to be largely indistinguishable from high-productivity environments, whereas immigration from low-productivity environments ( approximately 0.5% of the population) had no discernable impact. These results could not be explained by demography alone, but rather high-productivity immigrants had a selective advantage in low-productivity environments, but not vice versa. Coevolutionary interactions in high-productivity environments are therefore likely to have a disproportionate impact on coevolution across the landscape as a whole.

Mesh:

Year:  2009        PMID: 20002253     DOI: 10.1111/j.1420-9101.2009.01877.x

Source DB:  PubMed          Journal:  J Evol Biol        ISSN: 1010-061X            Impact factor:   2.411


  12 in total

1.  Resource availability affects the structure of a natural bacteria-bacteriophage community.

Authors:  Timothée Poisot; Gildas Lepennetier; Esteban Martinez; Johan Ramsayer; Michael E Hochberg
Journal:  Biol Lett       Date:  2010-10-20       Impact factor: 3.703

2.  Resource use of soilborne Streptomyces varies with location, phylogeny, and nitrogen amendment.

Authors:  Daniel C Schlatter; Anita L DavelosBaines; Kun Xiao; Linda L Kinkel
Journal:  Microb Ecol       Date:  2013-11       Impact factor: 4.552

3.  Trophic network structure emerges through antagonistic coevolution in temporally varying environments.

Authors:  Timothée Poisot; Peter H Thrall; Michael E Hochberg
Journal:  Proc Biol Sci       Date:  2011-06-08       Impact factor: 5.349

4.  Phages limit the evolution of bacterial antibiotic resistance in experimental microcosms.

Authors:  Quan-Guo Zhang; Angus Buckling
Journal:  Evol Appl       Date:  2012-01-13       Impact factor: 5.183

5.  Spatial heterogeneity, frequency-dependent selection and polymorphism in host-parasite interactions.

Authors:  Aurélien Tellier; James K M Brown
Journal:  BMC Evol Biol       Date:  2011-11-01       Impact factor: 3.260

6.  The impact of resource availability on bacterial resistance to phages in soil.

Authors:  Pedro Gómez; Jonathan Bennie; Kevin J Gaston; Angus Buckling
Journal:  PLoS One       Date:  2015-04-09       Impact factor: 3.240

Review 7.  Bacteria-phage coevolution as a driver of ecological and evolutionary processes in microbial communities.

Authors:  Britt Koskella; Michael A Brockhurst
Journal:  FEMS Microbiol Rev       Date:  2014-03-27       Impact factor: 16.408

8.  What Can Phages Tell Us about Host-Pathogen Coevolution?

Authors:  John J Dennehy
Journal:  Int J Evol Biol       Date:  2012-11-18

9.  Rapidly fluctuating environments constrain coevolutionary arms races by impeding selective sweeps.

Authors:  Ellie Harrison; Anna-Liisa Laine; Mikael Hietala; Michael A Brockhurst
Journal:  Proc Biol Sci       Date:  2013-06-12       Impact factor: 5.349

10.  Higher resources decrease fluctuating selection during host-parasite coevolution.

Authors:  Laura Lopez Pascua; Alex R Hall; Alex Best; Andrew D Morgan; Mike Boots; Angus Buckling
Journal:  Ecol Lett       Date:  2014-08-28       Impact factor: 9.492

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