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Life-history strategy defends against disease and may select against physiological resistance

Host ecological traits may limit exposure to infectious disease, thereby generating the wide variation in disease incidence observed between host populations or species. The exclusion of disease by ecological traits may then allow selection to act against physiological defenses when they are costly...

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Detalles Bibliográficos
Autores principales: Gibson, Amanda K, Petit, Elsa, Mena-Ali, Jorge, Oxelman, Bengt, Hood, Michael E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3686206/
https://www.ncbi.nlm.nih.gov/pubmed/23789082
http://dx.doi.org/10.1002/ece3.583
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author Gibson, Amanda K
Petit, Elsa
Mena-Ali, Jorge
Oxelman, Bengt
Hood, Michael E
author_facet Gibson, Amanda K
Petit, Elsa
Mena-Ali, Jorge
Oxelman, Bengt
Hood, Michael E
author_sort Gibson, Amanda K
collection PubMed
description Host ecological traits may limit exposure to infectious disease, thereby generating the wide variation in disease incidence observed between host populations or species. The exclusion of disease by ecological traits may then allow selection to act against physiological defenses when they are costly to maintain in the absence of disease. This study investigates ecological resistance in the Silene-Microbotryum pathosystem. An estimated 80% of perennial Silene species host the anther-smut disease while no annuals harbor the disease in nature. Artificial inoculations of annual and perennial Silene plants, obtained from both natural and horticultural populations, demonstrate that the absence of disease in annuals is not explained by elevated physiological resistance. The annual habit is thus a powerful form of ecological defense against anther smut. Moreover, the higher susceptibility of annual species to anther smut relative to perennials supports the hypothesis of a loss of costly physiological resistance under ecological protection. The observation in annuals that physiological susceptibility is correlated with lower rates of flowering (i.e., lower fitness) suggests that variation in physiological resistance is costly in the absence of disease, even in a naїve Silene species. The absence of disease in natural populations of annuals combined with their high physiological susceptibility attest to the strength of host ecology in shaping the distribution of disease and to the dynamic nature of disease resistance.
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spelling pubmed-36862062013-06-20 Life-history strategy defends against disease and may select against physiological resistance Gibson, Amanda K Petit, Elsa Mena-Ali, Jorge Oxelman, Bengt Hood, Michael E Ecol Evol Original Research Host ecological traits may limit exposure to infectious disease, thereby generating the wide variation in disease incidence observed between host populations or species. The exclusion of disease by ecological traits may then allow selection to act against physiological defenses when they are costly to maintain in the absence of disease. This study investigates ecological resistance in the Silene-Microbotryum pathosystem. An estimated 80% of perennial Silene species host the anther-smut disease while no annuals harbor the disease in nature. Artificial inoculations of annual and perennial Silene plants, obtained from both natural and horticultural populations, demonstrate that the absence of disease in annuals is not explained by elevated physiological resistance. The annual habit is thus a powerful form of ecological defense against anther smut. Moreover, the higher susceptibility of annual species to anther smut relative to perennials supports the hypothesis of a loss of costly physiological resistance under ecological protection. The observation in annuals that physiological susceptibility is correlated with lower rates of flowering (i.e., lower fitness) suggests that variation in physiological resistance is costly in the absence of disease, even in a naїve Silene species. The absence of disease in natural populations of annuals combined with their high physiological susceptibility attest to the strength of host ecology in shaping the distribution of disease and to the dynamic nature of disease resistance. Blackwell Publishing Ltd 2013-06 2013-05-08 /pmc/articles/PMC3686206/ /pubmed/23789082 http://dx.doi.org/10.1002/ece3.583 Text en © 2013 Published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Research
Gibson, Amanda K
Petit, Elsa
Mena-Ali, Jorge
Oxelman, Bengt
Hood, Michael E
Life-history strategy defends against disease and may select against physiological resistance
title Life-history strategy defends against disease and may select against physiological resistance
title_full Life-history strategy defends against disease and may select against physiological resistance
title_fullStr Life-history strategy defends against disease and may select against physiological resistance
title_full_unstemmed Life-history strategy defends against disease and may select against physiological resistance
title_short Life-history strategy defends against disease and may select against physiological resistance
title_sort life-history strategy defends against disease and may select against physiological resistance
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3686206/
https://www.ncbi.nlm.nih.gov/pubmed/23789082
http://dx.doi.org/10.1002/ece3.583
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