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Dynamical trade-offs arise from antagonistic coevolution and decrease intraspecific diversity

Trade-offs play an important role in evolution. Without trade-offs, evolution would maximize fitness of all traits leading to a “master of all traits”. The shape of trade-offs has been shown to determine evolutionary trajectories and is often assumed to be static and independent of the actual evolut...

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Autores principales: Huang, Weini, Traulsen, Arne, Werner, Benjamin, Hiltunen, Teppo, Becks, Lutz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727225/
https://www.ncbi.nlm.nih.gov/pubmed/29233970
http://dx.doi.org/10.1038/s41467-017-01957-8
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author Huang, Weini
Traulsen, Arne
Werner, Benjamin
Hiltunen, Teppo
Becks, Lutz
author_facet Huang, Weini
Traulsen, Arne
Werner, Benjamin
Hiltunen, Teppo
Becks, Lutz
author_sort Huang, Weini
collection PubMed
description Trade-offs play an important role in evolution. Without trade-offs, evolution would maximize fitness of all traits leading to a “master of all traits”. The shape of trade-offs has been shown to determine evolutionary trajectories and is often assumed to be static and independent of the actual evolutionary process. Here we propose that coevolution leads to a dynamical trade-off. We test this hypothesis in a microbial predator–prey system and show that the bacterial growth-defense trade-off changes from concave to convex, i.e., defense is effective and cheap initially, but gets costly when predators coevolve. We further explore the impact of such dynamical trade-offs by a novel mathematical model incorporating de novo mutations for both species. Predator and prey populations diversify rapidly leading to higher prey diversity when the trade-off is concave (cheap). Coevolution results in more convex (costly) trade-offs and lower prey diversity compared to the scenario where only the prey evolves.
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spelling pubmed-57272252017-12-14 Dynamical trade-offs arise from antagonistic coevolution and decrease intraspecific diversity Huang, Weini Traulsen, Arne Werner, Benjamin Hiltunen, Teppo Becks, Lutz Nat Commun Article Trade-offs play an important role in evolution. Without trade-offs, evolution would maximize fitness of all traits leading to a “master of all traits”. The shape of trade-offs has been shown to determine evolutionary trajectories and is often assumed to be static and independent of the actual evolutionary process. Here we propose that coevolution leads to a dynamical trade-off. We test this hypothesis in a microbial predator–prey system and show that the bacterial growth-defense trade-off changes from concave to convex, i.e., defense is effective and cheap initially, but gets costly when predators coevolve. We further explore the impact of such dynamical trade-offs by a novel mathematical model incorporating de novo mutations for both species. Predator and prey populations diversify rapidly leading to higher prey diversity when the trade-off is concave (cheap). Coevolution results in more convex (costly) trade-offs and lower prey diversity compared to the scenario where only the prey evolves. Nature Publishing Group UK 2017-12-12 /pmc/articles/PMC5727225/ /pubmed/29233970 http://dx.doi.org/10.1038/s41467-017-01957-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Huang, Weini
Traulsen, Arne
Werner, Benjamin
Hiltunen, Teppo
Becks, Lutz
Dynamical trade-offs arise from antagonistic coevolution and decrease intraspecific diversity
title Dynamical trade-offs arise from antagonistic coevolution and decrease intraspecific diversity
title_full Dynamical trade-offs arise from antagonistic coevolution and decrease intraspecific diversity
title_fullStr Dynamical trade-offs arise from antagonistic coevolution and decrease intraspecific diversity
title_full_unstemmed Dynamical trade-offs arise from antagonistic coevolution and decrease intraspecific diversity
title_short Dynamical trade-offs arise from antagonistic coevolution and decrease intraspecific diversity
title_sort dynamical trade-offs arise from antagonistic coevolution and decrease intraspecific diversity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727225/
https://www.ncbi.nlm.nih.gov/pubmed/29233970
http://dx.doi.org/10.1038/s41467-017-01957-8
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