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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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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. |
format | Online Article Text |
id | pubmed-9874267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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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