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The evolution of juvenile susceptibility to infectious disease

Infection prior to reproduction usually carries greater fitness costs for hosts than infection later in life, suggesting selection should tend to favour juvenile resistance. Yet, juveniles are generally more susceptible than adults across a wide spectrum of host taxa. While physiological constraints...

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Detalles Bibliográficos
Autores principales: Ashby, Ben, Bruns, Emily
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030539/
https://www.ncbi.nlm.nih.gov/pubmed/29925619
http://dx.doi.org/10.1098/rspb.2018.0844
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author Ashby, Ben
Bruns, Emily
author_facet Ashby, Ben
Bruns, Emily
author_sort Ashby, Ben
collection PubMed
description Infection prior to reproduction usually carries greater fitness costs for hosts than infection later in life, suggesting selection should tend to favour juvenile resistance. Yet, juveniles are generally more susceptible than adults across a wide spectrum of host taxa. While physiological constraints and a lack of prior exposure can explain some of this pattern, studies in plants and insects suggest that hosts may trade off juvenile susceptibility against other life-history traits. However, it is unclear precisely how trade-offs shape the evolution of juvenile susceptibility. Here, we theoretically explore the evolution of juvenile susceptibility subject to trade-offs with maturation or reproduction, which could realistically occur due to resource allocation during development (e.g. prioritizing growth over immune defence). We show how host lifespan, the probability of maturation (i.e. of reaching the adult stage) and transmission mode affect the results. Our key finding is that elevated juvenile susceptibility is expected to evolve over a wide range of conditions, but should be lowest when hosts have moderate lifespans and an intermediate probability of reaching the adult stage. Our results elucidate how interactions between trade-offs and the epidemiological-demographic structure of the population can lead to the evolution of elevated juvenile susceptibility.
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spelling pubmed-60305392018-07-22 The evolution of juvenile susceptibility to infectious disease Ashby, Ben Bruns, Emily Proc Biol Sci Evolution Infection prior to reproduction usually carries greater fitness costs for hosts than infection later in life, suggesting selection should tend to favour juvenile resistance. Yet, juveniles are generally more susceptible than adults across a wide spectrum of host taxa. While physiological constraints and a lack of prior exposure can explain some of this pattern, studies in plants and insects suggest that hosts may trade off juvenile susceptibility against other life-history traits. However, it is unclear precisely how trade-offs shape the evolution of juvenile susceptibility. Here, we theoretically explore the evolution of juvenile susceptibility subject to trade-offs with maturation or reproduction, which could realistically occur due to resource allocation during development (e.g. prioritizing growth over immune defence). We show how host lifespan, the probability of maturation (i.e. of reaching the adult stage) and transmission mode affect the results. Our key finding is that elevated juvenile susceptibility is expected to evolve over a wide range of conditions, but should be lowest when hosts have moderate lifespans and an intermediate probability of reaching the adult stage. Our results elucidate how interactions between trade-offs and the epidemiological-demographic structure of the population can lead to the evolution of elevated juvenile susceptibility. The Royal Society 2018-06-27 2018-06-20 /pmc/articles/PMC6030539/ /pubmed/29925619 http://dx.doi.org/10.1098/rspb.2018.0844 Text en © 2018 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
Ashby, Ben
Bruns, Emily
The evolution of juvenile susceptibility to infectious disease
title The evolution of juvenile susceptibility to infectious disease
title_full The evolution of juvenile susceptibility to infectious disease
title_fullStr The evolution of juvenile susceptibility to infectious disease
title_full_unstemmed The evolution of juvenile susceptibility to infectious disease
title_short The evolution of juvenile susceptibility to infectious disease
title_sort evolution of juvenile susceptibility to infectious disease
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030539/
https://www.ncbi.nlm.nih.gov/pubmed/29925619
http://dx.doi.org/10.1098/rspb.2018.0844
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