Cargando…

Higher resources decrease fluctuating selection during host–parasite coevolution

We still know very little about how the environment influences coevolutionary dynamics. Here, we investigated both theoretically and empirically how nutrient availability affects the relative extent of escalation of resistance and infectivity (arms race dynamic; ARD) and fluctuating selection (fluct...

Descripción completa

Detalles Bibliográficos
Autores principales: Lopez Pascua, Laura, Hall, Alex R, Best, Alex, Morgan, Andrew D, Boots, Mike, Buckling, Angus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257576/
https://www.ncbi.nlm.nih.gov/pubmed/25167763
http://dx.doi.org/10.1111/ele.12337
_version_ 1782347773040918528
author Lopez Pascua, Laura
Hall, Alex R
Best, Alex
Morgan, Andrew D
Boots, Mike
Buckling, Angus
author_facet Lopez Pascua, Laura
Hall, Alex R
Best, Alex
Morgan, Andrew D
Boots, Mike
Buckling, Angus
author_sort Lopez Pascua, Laura
collection PubMed
description We still know very little about how the environment influences coevolutionary dynamics. Here, we investigated both theoretically and empirically how nutrient availability affects the relative extent of escalation of resistance and infectivity (arms race dynamic; ARD) and fluctuating selection (fluctuating selection dynamic; FSD) in experimentally coevolving populations of bacteria and viruses. By comparing interactions between clones of bacteria and viruses both within- and between-time points, we show that increasing nutrient availability resulted in coevolution shifting from FSD, with fluctuations in average infectivity and resistance ranges over time, to ARD. Our model shows that range fluctuations with lower nutrient availability can be explained both by elevated costs of resistance (a direct effect of nutrient availability), and reduced benefits of resistance when population sizes of hosts and parasites are lower (an indirect effect). Nutrient availability can therefore predictably and generally affect qualitative coevolutionary dynamics by both direct and indirect (mediated through ecological feedbacks) effects on costs of resistance.
format Online
Article
Text
id pubmed-4257576
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BlackWell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-42575762014-12-12 Higher resources decrease fluctuating selection during host–parasite coevolution Lopez Pascua, Laura Hall, Alex R Best, Alex Morgan, Andrew D Boots, Mike Buckling, Angus Ecol Lett Letters We still know very little about how the environment influences coevolutionary dynamics. Here, we investigated both theoretically and empirically how nutrient availability affects the relative extent of escalation of resistance and infectivity (arms race dynamic; ARD) and fluctuating selection (fluctuating selection dynamic; FSD) in experimentally coevolving populations of bacteria and viruses. By comparing interactions between clones of bacteria and viruses both within- and between-time points, we show that increasing nutrient availability resulted in coevolution shifting from FSD, with fluctuations in average infectivity and resistance ranges over time, to ARD. Our model shows that range fluctuations with lower nutrient availability can be explained both by elevated costs of resistance (a direct effect of nutrient availability), and reduced benefits of resistance when population sizes of hosts and parasites are lower (an indirect effect). Nutrient availability can therefore predictably and generally affect qualitative coevolutionary dynamics by both direct and indirect (mediated through ecological feedbacks) effects on costs of resistance. BlackWell Publishing Ltd 2014-11 2014-08-28 /pmc/articles/PMC4257576/ /pubmed/25167763 http://dx.doi.org/10.1111/ele.12337 Text en © 2014 The Authors. Ecology Letters published by John Wiley & Sons Ltd and CNRS. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Lopez Pascua, Laura
Hall, Alex R
Best, Alex
Morgan, Andrew D
Boots, Mike
Buckling, Angus
Higher resources decrease fluctuating selection during host–parasite coevolution
title Higher resources decrease fluctuating selection during host–parasite coevolution
title_full Higher resources decrease fluctuating selection during host–parasite coevolution
title_fullStr Higher resources decrease fluctuating selection during host–parasite coevolution
title_full_unstemmed Higher resources decrease fluctuating selection during host–parasite coevolution
title_short Higher resources decrease fluctuating selection during host–parasite coevolution
title_sort higher resources decrease fluctuating selection during host–parasite coevolution
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257576/
https://www.ncbi.nlm.nih.gov/pubmed/25167763
http://dx.doi.org/10.1111/ele.12337
work_keys_str_mv AT lopezpascualaura higherresourcesdecreasefluctuatingselectionduringhostparasitecoevolution
AT hallalexr higherresourcesdecreasefluctuatingselectionduringhostparasitecoevolution
AT bestalex higherresourcesdecreasefluctuatingselectionduringhostparasitecoevolution
AT morganandrewd higherresourcesdecreasefluctuatingselectionduringhostparasitecoevolution
AT bootsmike higherresourcesdecreasefluctuatingselectionduringhostparasitecoevolution
AT bucklingangus higherresourcesdecreasefluctuatingselectionduringhostparasitecoevolution