Cargando…

Host–parasite fluctuating selection in the absence of specificity

Fluctuating selection driven by coevolution between hosts and parasites is important for the generation of host and parasite diversity across space and time. Theory has focused primarily on infection genetics, with highly specific ‘matching-allele’ frameworks more likely to generate fluctuating sele...

Descripción completa

Detalles Bibliográficos
Autores principales: Best, Alex, Ashby, Ben, White, Andy, Bowers, Roger, Buckling, Angus, Koskella, Britt, Boots, Mike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698645/
https://www.ncbi.nlm.nih.gov/pubmed/29093222
http://dx.doi.org/10.1098/rspb.2017.1615
_version_ 1783280799070552064
author Best, Alex
Ashby, Ben
White, Andy
Bowers, Roger
Buckling, Angus
Koskella, Britt
Boots, Mike
author_facet Best, Alex
Ashby, Ben
White, Andy
Bowers, Roger
Buckling, Angus
Koskella, Britt
Boots, Mike
author_sort Best, Alex
collection PubMed
description Fluctuating selection driven by coevolution between hosts and parasites is important for the generation of host and parasite diversity across space and time. Theory has focused primarily on infection genetics, with highly specific ‘matching-allele’ frameworks more likely to generate fluctuating selection dynamics (FSD) than ‘gene-for-gene’ (generalist–specialist) frameworks. However, the environment, ecological feedbacks and life-history characteristics may all play a role in determining when FSD occurs. Here, we develop eco-evolutionary models with explicit ecological dynamics to explore the ecological, epidemiological and host life-history drivers of FSD. Our key result is to demonstrate for the first time, to our knowledge, that specificity between hosts and parasites is not required to generate FSD. Furthermore, highly specific host–parasite interactions produce unstable, less robust stochastic fluctuations in contrast to interactions that lack specificity altogether or those that vary from generalist to specialist, which produce predictable limit cycles. Given the ubiquity of ecological feedbacks and the variation in the nature of specificity in host–parasite interactions, our work emphasizes the underestimated potential for host–parasite coevolution to generate fluctuating selection.
format Online
Article
Text
id pubmed-5698645
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-56986452017-12-16 Host–parasite fluctuating selection in the absence of specificity Best, Alex Ashby, Ben White, Andy Bowers, Roger Buckling, Angus Koskella, Britt Boots, Mike Proc Biol Sci Evolution Fluctuating selection driven by coevolution between hosts and parasites is important for the generation of host and parasite diversity across space and time. Theory has focused primarily on infection genetics, with highly specific ‘matching-allele’ frameworks more likely to generate fluctuating selection dynamics (FSD) than ‘gene-for-gene’ (generalist–specialist) frameworks. However, the environment, ecological feedbacks and life-history characteristics may all play a role in determining when FSD occurs. Here, we develop eco-evolutionary models with explicit ecological dynamics to explore the ecological, epidemiological and host life-history drivers of FSD. Our key result is to demonstrate for the first time, to our knowledge, that specificity between hosts and parasites is not required to generate FSD. Furthermore, highly specific host–parasite interactions produce unstable, less robust stochastic fluctuations in contrast to interactions that lack specificity altogether or those that vary from generalist to specialist, which produce predictable limit cycles. Given the ubiquity of ecological feedbacks and the variation in the nature of specificity in host–parasite interactions, our work emphasizes the underestimated potential for host–parasite coevolution to generate fluctuating selection. The Royal Society 2017-11-15 2017-11-01 /pmc/articles/PMC5698645/ /pubmed/29093222 http://dx.doi.org/10.1098/rspb.2017.1615 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Best, Alex
Ashby, Ben
White, Andy
Bowers, Roger
Buckling, Angus
Koskella, Britt
Boots, Mike
Host–parasite fluctuating selection in the absence of specificity
title Host–parasite fluctuating selection in the absence of specificity
title_full Host–parasite fluctuating selection in the absence of specificity
title_fullStr Host–parasite fluctuating selection in the absence of specificity
title_full_unstemmed Host–parasite fluctuating selection in the absence of specificity
title_short Host–parasite fluctuating selection in the absence of specificity
title_sort host–parasite fluctuating selection in the absence of specificity
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698645/
https://www.ncbi.nlm.nih.gov/pubmed/29093222
http://dx.doi.org/10.1098/rspb.2017.1615
work_keys_str_mv AT bestalex hostparasitefluctuatingselectionintheabsenceofspecificity
AT ashbyben hostparasitefluctuatingselectionintheabsenceofspecificity
AT whiteandy hostparasitefluctuatingselectionintheabsenceofspecificity
AT bowersroger hostparasitefluctuatingselectionintheabsenceofspecificity
AT bucklingangus hostparasitefluctuatingselectionintheabsenceofspecificity
AT koskellabritt hostparasitefluctuatingselectionintheabsenceofspecificity
AT bootsmike hostparasitefluctuatingselectionintheabsenceofspecificity