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The evolution of age-specific resistance to infectious disease

Innate, infection-preventing resistance often varies between host life stages. Juveniles are more resistant than adults in some species, whereas the opposite pattern is true in others. This variation cannot always be explained by prior exposure or physiological constraints and so it has been hypothe...

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Detalles Bibliográficos
Autores principales: Buckingham, Lydia J., Bruns, Emily L., Ashby, Ben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874267/
https://www.ncbi.nlm.nih.gov/pubmed/36695037
http://dx.doi.org/10.1098/rspb.2022.2000
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author Buckingham, Lydia J.
Bruns, Emily L.
Ashby, Ben
author_facet Buckingham, Lydia J.
Bruns, Emily L.
Ashby, Ben
author_sort Buckingham, Lydia J.
collection PubMed
description Innate, infection-preventing resistance often varies between host life stages. Juveniles are more resistant than adults in some species, whereas the opposite pattern is true in others. This variation cannot always be explained by prior exposure or physiological constraints and so it has been hypothesized that trade-offs with other life-history traits may be involved. However, little is known about how trade-offs between various life-history traits and resistance at different life stages affect the evolution of age-specific resistance. Here, we use a mathematical model to explore how trade-offs with natural mortality, reproduction and maturation combine to affect the evolution of resistance at different life stages. Our results show that certain combinations of trade-offs have substantial effects on whether adults or juveniles are more resistant, with trade-offs between juvenile resistance and adult reproduction inherently more costly than trade-offs involving maturation or mortality (all else being equal), resulting in consistent evolution of lower resistance at the juvenile stage even when infection causes a lifelong fecundity reduction. Our model demonstrates how the differences between patterns of age-structured resistance seen in nature may be explained by variation in the trade-offs involved and our results suggest conditions under which trade-offs tend to select for lower resistance in juveniles than adults.
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spelling pubmed-98742672023-01-25 The evolution of age-specific resistance to infectious disease Buckingham, Lydia J. Bruns, Emily L. Ashby, Ben Proc Biol Sci Evolution Innate, infection-preventing resistance often varies between host life stages. Juveniles are more resistant than adults in some species, whereas the opposite pattern is true in others. This variation cannot always be explained by prior exposure or physiological constraints and so it has been hypothesized that trade-offs with other life-history traits may be involved. However, little is known about how trade-offs between various life-history traits and resistance at different life stages affect the evolution of age-specific resistance. Here, we use a mathematical model to explore how trade-offs with natural mortality, reproduction and maturation combine to affect the evolution of resistance at different life stages. Our results show that certain combinations of trade-offs have substantial effects on whether adults or juveniles are more resistant, with trade-offs between juvenile resistance and adult reproduction inherently more costly than trade-offs involving maturation or mortality (all else being equal), resulting in consistent evolution of lower resistance at the juvenile stage even when infection causes a lifelong fecundity reduction. Our model demonstrates how the differences between patterns of age-structured resistance seen in nature may be explained by variation in the trade-offs involved and our results suggest conditions under which trade-offs tend to select for lower resistance in juveniles than adults. The Royal Society 2023-01-25 2023-01-25 /pmc/articles/PMC9874267/ /pubmed/36695037 http://dx.doi.org/10.1098/rspb.2022.2000 Text en © 2023 The Authors. https://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/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Buckingham, Lydia J.
Bruns, Emily L.
Ashby, Ben
The evolution of age-specific resistance to infectious disease
title The evolution of age-specific resistance to infectious disease
title_full The evolution of age-specific resistance to infectious disease
title_fullStr The evolution of age-specific resistance to infectious disease
title_full_unstemmed The evolution of age-specific resistance to infectious disease
title_short The evolution of age-specific resistance to infectious disease
title_sort evolution of age-specific resistance to infectious disease
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874267/
https://www.ncbi.nlm.nih.gov/pubmed/36695037
http://dx.doi.org/10.1098/rspb.2022.2000
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