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Friendly foes: The evolution of host protection by a parasite
Hosts are often infected by multiple parasite species, yet the ecological and evolutionary implications of the interactions between hosts and coinfecting parasites are largely unknown. Most theoretical models of evolution among coinfecting parasites focus on the evolution of virulence, but parasites...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121858/ https://www.ncbi.nlm.nih.gov/pubmed/30283650 http://dx.doi.org/10.1002/evl3.19 |
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author | Ashby, Ben King, Kayla C. |
author_facet | Ashby, Ben King, Kayla C. |
author_sort | Ashby, Ben |
collection | PubMed |
description | Hosts are often infected by multiple parasite species, yet the ecological and evolutionary implications of the interactions between hosts and coinfecting parasites are largely unknown. Most theoretical models of evolution among coinfecting parasites focus on the evolution of virulence, but parasites may also evolve to protect their hosts by reducing susceptibility (i.e., conferring resistance) to other parasites or reducing the virulence of coinfecting parasites (i.e., conferring tolerance). Here, we analyze the eco‐evolutionary dynamics of parasite‐conferred resistance and tolerance using coinfection models. We show that both parasite‐conferred resistance and tolerance can evolve for a wide range of underlying trade‐offs. The shape and strength of the trade‐off qualitatively affects the outcome causing shifts between the minimisation or maximization of protection, intermediate stable strategies, evolutionary branching, and bistability. Furthermore, we find that a protected dimorphism can readily evolve for parasite‐conferred resistance, but find no evidence of evolutionary branching for parasite‐conferred tolerance, in general agreement with previous work on host evolution. These results provide novel insights into the evolution of parasite‐conferred resistance and tolerance, and suggest clues to the underlying trade‐offs in recent experimental work on microbe‐mediated protection. More generally, our results highlight the context dependence of host‐parasite relationships in complex communities. |
format | Online Article Text |
id | pubmed-6121858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61218582018-10-03 Friendly foes: The evolution of host protection by a parasite Ashby, Ben King, Kayla C. Evol Lett Letters Hosts are often infected by multiple parasite species, yet the ecological and evolutionary implications of the interactions between hosts and coinfecting parasites are largely unknown. Most theoretical models of evolution among coinfecting parasites focus on the evolution of virulence, but parasites may also evolve to protect their hosts by reducing susceptibility (i.e., conferring resistance) to other parasites or reducing the virulence of coinfecting parasites (i.e., conferring tolerance). Here, we analyze the eco‐evolutionary dynamics of parasite‐conferred resistance and tolerance using coinfection models. We show that both parasite‐conferred resistance and tolerance can evolve for a wide range of underlying trade‐offs. The shape and strength of the trade‐off qualitatively affects the outcome causing shifts between the minimisation or maximization of protection, intermediate stable strategies, evolutionary branching, and bistability. Furthermore, we find that a protected dimorphism can readily evolve for parasite‐conferred resistance, but find no evidence of evolutionary branching for parasite‐conferred tolerance, in general agreement with previous work on host evolution. These results provide novel insights into the evolution of parasite‐conferred resistance and tolerance, and suggest clues to the underlying trade‐offs in recent experimental work on microbe‐mediated protection. More generally, our results highlight the context dependence of host‐parasite relationships in complex communities. John Wiley and Sons Inc. 2017-08-31 /pmc/articles/PMC6121858/ /pubmed/30283650 http://dx.doi.org/10.1002/evl3.19 Text en © 2017 The Author(s). Evolution Letters published by Wiley Periodicals, Inc. on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letters Ashby, Ben King, Kayla C. Friendly foes: The evolution of host protection by a parasite |
title | Friendly foes: The evolution of host protection by a parasite |
title_full | Friendly foes: The evolution of host protection by a parasite |
title_fullStr | Friendly foes: The evolution of host protection by a parasite |
title_full_unstemmed | Friendly foes: The evolution of host protection by a parasite |
title_short | Friendly foes: The evolution of host protection by a parasite |
title_sort | friendly foes: the evolution of host protection by a parasite |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121858/ https://www.ncbi.nlm.nih.gov/pubmed/30283650 http://dx.doi.org/10.1002/evl3.19 |
work_keys_str_mv | AT ashbyben friendlyfoestheevolutionofhostprotectionbyaparasite AT kingkaylac friendlyfoestheevolutionofhostprotectionbyaparasite |