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Carbon Costs of Constitutive and Expressed Resistance to a Non-Native Pathogen in Limber Pine

Increasing the frequency of resistance to the non-native fungus Cronartium ribicola (causative agent of white pine blister rust, WPBR) in limber pine populations is a primary management objective to sustain high-elevation forest communities. However, it is not known to what extent genetic disease re...

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Autores principales: Vogan, Patrick J., Schoettle, Anna W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5051957/
https://www.ncbi.nlm.nih.gov/pubmed/27706249
http://dx.doi.org/10.1371/journal.pone.0162913
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author Vogan, Patrick J.
Schoettle, Anna W.
author_facet Vogan, Patrick J.
Schoettle, Anna W.
author_sort Vogan, Patrick J.
collection PubMed
description Increasing the frequency of resistance to the non-native fungus Cronartium ribicola (causative agent of white pine blister rust, WPBR) in limber pine populations is a primary management objective to sustain high-elevation forest communities. However, it is not known to what extent genetic disease resistance is costly to plant growth or carbon economy. In this study, we measured growth and leaf-level physiology in (1) seedling families from seed trees that have previously been inferred to carry or not carry Cr4, the dominant R gene allele conferring complete, gene-for-gene resistance to WPBR in limber pine, and (2) populations that were and were not infected with C. ribicola. We found that, in the absence of C. ribicola exposure, there was no significant difference in carbon relations between families born from seed trees that harbor the resistance allele compared to those that lack it, either to plant growth and phenology or leaf-level photosynthetic traits. However, post-infection with C. ribicola, growth was significantly reduced in inoculation survivors expressing complete resistance compared to uninoculated seedlings. Furthermore, inoculation survivors exhibited significant increases in a suite of traits including photosynthetic rate, respiration rate, leaf N, and stomatal conductance and a decrease in photosynthetic water-use efficiency. The lack of constitutive carbon costs associated with Cr4 resistance in non-stressed limber pine is consistent with a previous report that the R gene allele is not under selection in the absence of C. ribicola and suggests that host resistance may not bear a constitutive cost in pathosystems that have not coevolved. However, under challenge by C. ribicola, complete resistance to WPBR in limber pine has a significant cost to plant growth, though enhanced carbon acquisition post-infection may offset this somewhat. These costs and effects on performance further complicate predictions of this species’ response in warmer future climates in the presence of WPBR.
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spelling pubmed-50519572016-10-27 Carbon Costs of Constitutive and Expressed Resistance to a Non-Native Pathogen in Limber Pine Vogan, Patrick J. Schoettle, Anna W. PLoS One Research Article Increasing the frequency of resistance to the non-native fungus Cronartium ribicola (causative agent of white pine blister rust, WPBR) in limber pine populations is a primary management objective to sustain high-elevation forest communities. However, it is not known to what extent genetic disease resistance is costly to plant growth or carbon economy. In this study, we measured growth and leaf-level physiology in (1) seedling families from seed trees that have previously been inferred to carry or not carry Cr4, the dominant R gene allele conferring complete, gene-for-gene resistance to WPBR in limber pine, and (2) populations that were and were not infected with C. ribicola. We found that, in the absence of C. ribicola exposure, there was no significant difference in carbon relations between families born from seed trees that harbor the resistance allele compared to those that lack it, either to plant growth and phenology or leaf-level photosynthetic traits. However, post-infection with C. ribicola, growth was significantly reduced in inoculation survivors expressing complete resistance compared to uninoculated seedlings. Furthermore, inoculation survivors exhibited significant increases in a suite of traits including photosynthetic rate, respiration rate, leaf N, and stomatal conductance and a decrease in photosynthetic water-use efficiency. The lack of constitutive carbon costs associated with Cr4 resistance in non-stressed limber pine is consistent with a previous report that the R gene allele is not under selection in the absence of C. ribicola and suggests that host resistance may not bear a constitutive cost in pathosystems that have not coevolved. However, under challenge by C. ribicola, complete resistance to WPBR in limber pine has a significant cost to plant growth, though enhanced carbon acquisition post-infection may offset this somewhat. These costs and effects on performance further complicate predictions of this species’ response in warmer future climates in the presence of WPBR. Public Library of Science 2016-10-05 /pmc/articles/PMC5051957/ /pubmed/27706249 http://dx.doi.org/10.1371/journal.pone.0162913 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Vogan, Patrick J.
Schoettle, Anna W.
Carbon Costs of Constitutive and Expressed Resistance to a Non-Native Pathogen in Limber Pine
title Carbon Costs of Constitutive and Expressed Resistance to a Non-Native Pathogen in Limber Pine
title_full Carbon Costs of Constitutive and Expressed Resistance to a Non-Native Pathogen in Limber Pine
title_fullStr Carbon Costs of Constitutive and Expressed Resistance to a Non-Native Pathogen in Limber Pine
title_full_unstemmed Carbon Costs of Constitutive and Expressed Resistance to a Non-Native Pathogen in Limber Pine
title_short Carbon Costs of Constitutive and Expressed Resistance to a Non-Native Pathogen in Limber Pine
title_sort carbon costs of constitutive and expressed resistance to a non-native pathogen in limber pine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5051957/
https://www.ncbi.nlm.nih.gov/pubmed/27706249
http://dx.doi.org/10.1371/journal.pone.0162913
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