Literature DB >> 19272015

Source populations act as coevolutionary pacemakers in experimental selection mosaics containing hotspots and coldspots.

Tom Vogwill1, Andy Fenton, Angus Buckling, Michael E Hochberg, Michael A Brockhurst.   

Abstract

Natural populations of hosts and their enemies are often spatially structured, with patches that vary in the strength of reciprocal selection, so-called coevolutionary hotspots and coldspots with strong or weak reciprocal selection, respectively. Theory predicts that dispersal from hotspots should intensify coevolution in coldspots, whereas dispersal from coldspots should weaken coevolution in hotspots; however, there have been few empirical tests. We addressed this using paired populations of the bacterium Pseudomonas fluorescens and the phage SBW25Phi2 linked by one-way dispersal. Within each population, the strength of reciprocal selection was manipulated by altering the bacteria-phage encounter rate, which changes the rate of coevolution without affecting environmental productivity. We observed that dispersal from hotspots accelerated coevolution in coldspots, while dispersal from coldspots decelerated coevolution in hotspots. These results confirm theoretical predictions and suggest that source populations can act as coevolutionary "pacemakers" for recipient populations, overriding local conditions.

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Year:  2009        PMID: 19272015     DOI: 10.1086/597374

Source DB:  PubMed          Journal:  Am Nat        ISSN: 0003-0147            Impact factor:   3.926


  12 in total

1.  The costs of evolving resistance in heterogeneous parasite environments.

Authors:  Britt Koskella; Derek M Lin; Angus Buckling; John N Thompson
Journal:  Proc Biol Sci       Date:  2011-12-14       Impact factor: 5.349

2.  Below-ground abiotic and biotic heterogeneity shapes above-ground infection outcomes and spatial divergence in a host-parasite interaction.

Authors:  Ayco J M Tack; Anna-Liisa Laine; Jeremy J Burdon; Andrew Bissett; Peter H Thrall
Journal:  New Phytol       Date:  2015-04-13       Impact factor: 10.151

3.  The geographic mosaic of coevolution in mutualistic networks.

Authors:  Lucas P Medeiros; Guilherme Garcia; John N Thompson; Paulo R Guimarães
Journal:  Proc Natl Acad Sci U S A       Date:  2018-11-07       Impact factor: 11.205

4.  Dispersal network structure and infection mechanism shape diversity in a coevolutionary bacteria-phage system.

Authors:  Michael Sieber; Matthew Robb; Samantha E Forde; Ivana Gudelj
Journal:  ISME J       Date:  2013-10-03       Impact factor: 10.302

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

Review 6.  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

Review 7.  Understanding the ecology and evolution of host-parasite interactions across scales.

Authors:  Rachel M Penczykowski; Anna-Liisa Laine; Britt Koskella
Journal:  Evol Appl       Date:  2015-08-20       Impact factor: 5.183

8.  Spatial heterogeneity lowers rather than increases host-parasite specialization.

Authors:  E Hesse; A Best; M Boots; A R Hall; A Buckling
Journal:  J Evol Biol       Date:  2015-07-22       Impact factor: 2.411

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

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

10.  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

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