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...

Full description

Bibliographic Details
Main Authors: Ashby, B, King, K
Format: Journal article
Published: Wiley 2017
_version_ 1826259482583236608
author Ashby, B
King, K
author_facet Ashby, B
King, K
author_sort Ashby, B
collection OXFORD
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.
first_indexed 2024-03-06T18:50:35Z
format Journal article
id oxford-uuid:101442c7-45ad-46ce-9426-b490289a12a1
institution University of Oxford
last_indexed 2024-03-06T18:50:35Z
publishDate 2017
publisher Wiley
record_format dspace
spelling oxford-uuid:101442c7-45ad-46ce-9426-b490289a12a12022-03-26T09:54:34ZFriendly foes: the evolution of host protection by a parasiteJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:101442c7-45ad-46ce-9426-b490289a12a1Symplectic Elements at OxfordWiley2017Ashby, BKing, KHosts 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.
spellingShingle Ashby, B
King, K
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
work_keys_str_mv AT ashbyb friendlyfoestheevolutionofhostprotectionbyaparasite
AT kingk friendlyfoestheevolutionofhostprotectionbyaparasite