Cargando…
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...
Autores principales: | , |
---|---|
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 |
_version_ | 1783337156162355200 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6030539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ashbyben theevolutionofjuvenilesusceptibilitytoinfectiousdisease AT brunsemily theevolutionofjuvenilesusceptibilitytoinfectiousdisease AT ashbyben evolutionofjuvenilesusceptibilitytoinfectiousdisease AT brunsemily evolutionofjuvenilesusceptibilitytoinfectiousdisease |