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Differences in ascorbate and glutathione levels as indicators of resistance and susceptibility in Eucalyptus trees infected with Phytophthora cinnamomi.

Identifieur interne : 001556 ( Main/Exploration ); précédent : 001555; suivant : 001557

Differences in ascorbate and glutathione levels as indicators of resistance and susceptibility in Eucalyptus trees infected with Phytophthora cinnamomi.

Auteurs : Raymond W. Dempsey [Australie] ; Andrew Merchant ; Michael Tausz

Source :

RBID : pubmed:22977205

Descripteurs français

English descriptors

Abstract

In this study we investigated the role that ascorbate (AA) and glutathione (GSH) play in the plant pathogen interaction of susceptible Eucalyptus sieberi L. A. Johnson and resistant Eucalyptus sideroxylon Woolls with Phytophthora cinnamomi Rands root infection. In a glasshouse study, seedlings were grown in soil-free plant boxes to facilitate the inoculation of the root systems by a P. cinnamomi zoospore solution. Ascorbate and GSH concentrations were measured in infected roots and leaves, along with leaf gas exchange, chlorophyll fluorescence and carbohydrate concentrations over a time course up to 312 h (13 days) post-inoculation (pi). At the early stages of infection (from 24 h pi), significant decreases in AA and GSH concentrations were observed in the infected roots and leaves of the susceptible E. sieberi seedlings. At the later stage of infection (312 h pi), the earlier AA decreases in the leaves of infected plants had become significant increases. In contrast, late, significant AA increases in the absence of any GSH changes were observed in the infected roots of the resistant E. sideroxylon seedlings. In E. sideroxylon leaves, a significant GSH increase occurred at 24 h pi; however, by 312 h pi the earlier increase had become a significant decrease, while no changes occurred in AA. In E. sieberi, photosynthesis (A), stomatal conductance (g(s)) and PSII quantum efficiency (Φ(PSII)) were reduced by ~60, 80 and 30%, respectively, in infected plants and remained significantly lower than uninfected controls for the duration of the experiment. Significant reductions in these parameters did not occur until later (120 h pi for g(s) and 312 h pi for A and Φ(PSII)), and to a lesser extent in the resistant species. Non-structural carbohydrate analysis of roots and leaves indicate that carbohydrate metabolism and resource flow between shoots and roots may have been altered at later infection stages. This study suggests that reduced antioxidant capacity, leaf physiological function and carbohydrate metabolism are associated with susceptibility in E. sieberi to P. cinnamomi infection, while AA increases and new root formation were associated with resistance in E. sideroxylon.

DOI: 10.1093/treephys/tps076
PubMed: 22977205


Affiliations:


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Le document en format XML

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<term>Antioxidants (metabolism)</term>
<term>Ascorbic Acid (analysis)</term>
<term>Ascorbic Acid (metabolism)</term>
<term>Carbohydrate Metabolism (MeSH)</term>
<term>Carbohydrates (MeSH)</term>
<term>Chlorophyll (metabolism)</term>
<term>Disease Resistance (MeSH)</term>
<term>Disease Susceptibility (MeSH)</term>
<term>Eucalyptus (chemistry)</term>
<term>Eucalyptus (immunology)</term>
<term>Eucalyptus (parasitology)</term>
<term>Eucalyptus (physiology)</term>
<term>Glutathione (analysis)</term>
<term>Glutathione (metabolism)</term>
<term>Host-Pathogen Interactions (MeSH)</term>
<term>Photosynthesis (physiology)</term>
<term>Photosystem II Protein Complex (physiology)</term>
<term>Phytophthora (physiology)</term>
<term>Plant Leaves (chemistry)</term>
<term>Plant Leaves (immunology)</term>
<term>Plant Leaves (parasitology)</term>
<term>Plant Leaves (physiology)</term>
<term>Plant Roots (chemistry)</term>
<term>Plant Roots (immunology)</term>
<term>Plant Roots (parasitology)</term>
<term>Plant Roots (physiology)</term>
<term>Plant Shoots (chemistry)</term>
<term>Plant Shoots (immunology)</term>
<term>Plant Shoots (parasitology)</term>
<term>Plant Shoots (physiology)</term>
<term>Plant Transpiration (physiology)</term>
<term>Seedlings (chemistry)</term>
<term>Seedlings (immunology)</term>
<term>Seedlings (parasitology)</term>
<term>Seedlings (physiology)</term>
<term>Time Factors (MeSH)</term>
<term>Trees (MeSH)</term>
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<term>Acide ascorbique (analyse)</term>
<term>Acide ascorbique (métabolisme)</term>
<term>Antioxydants (analyse)</term>
<term>Antioxydants (métabolisme)</term>
<term>Arbres (MeSH)</term>
<term>Chlorophylle (métabolisme)</term>
<term>Complexe protéique du photosystème II (physiologie)</term>
<term>Eucalyptus (composition chimique)</term>
<term>Eucalyptus (immunologie)</term>
<term>Eucalyptus (parasitologie)</term>
<term>Eucalyptus (physiologie)</term>
<term>Facteurs temps (MeSH)</term>
<term>Feuilles de plante (composition chimique)</term>
<term>Feuilles de plante (immunologie)</term>
<term>Feuilles de plante (parasitologie)</term>
<term>Feuilles de plante (physiologie)</term>
<term>Glucides (MeSH)</term>
<term>Glutathion (analyse)</term>
<term>Glutathion (métabolisme)</term>
<term>Interactions hôte-pathogène (MeSH)</term>
<term>Métabolisme glucidique (MeSH)</term>
<term>Photosynthèse (physiologie)</term>
<term>Phytophthora (physiologie)</term>
<term>Plant (composition chimique)</term>
<term>Plant (immunologie)</term>
<term>Plant (parasitologie)</term>
<term>Plant (physiologie)</term>
<term>Pousses de plante (composition chimique)</term>
<term>Pousses de plante (immunologie)</term>
<term>Pousses de plante (parasitologie)</term>
<term>Pousses de plante (physiologie)</term>
<term>Prédisposition aux maladies (MeSH)</term>
<term>Racines de plante (composition chimique)</term>
<term>Racines de plante (immunologie)</term>
<term>Racines de plante (parasitologie)</term>
<term>Racines de plante (physiologie)</term>
<term>Résistance à la maladie (MeSH)</term>
<term>Transpiration des plantes (physiologie)</term>
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<term>Antioxidants</term>
<term>Ascorbic Acid</term>
<term>Glutathione</term>
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<term>Antioxidants</term>
<term>Ascorbic Acid</term>
<term>Chlorophyll</term>
<term>Glutathione</term>
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<keywords scheme="MESH" qualifier="analyse" xml:lang="fr">
<term>Acide ascorbique</term>
<term>Antioxydants</term>
<term>Glutathion</term>
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<keywords scheme="MESH" qualifier="chemistry" xml:lang="en">
<term>Eucalyptus</term>
<term>Plant Leaves</term>
<term>Plant Roots</term>
<term>Plant Shoots</term>
<term>Seedlings</term>
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<keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr">
<term>Eucalyptus</term>
<term>Feuilles de plante</term>
<term>Plant</term>
<term>Pousses de plante</term>
<term>Racines de plante</term>
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<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr">
<term>Eucalyptus</term>
<term>Feuilles de plante</term>
<term>Plant</term>
<term>Pousses de plante</term>
<term>Racines de plante</term>
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<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>Eucalyptus</term>
<term>Plant Leaves</term>
<term>Plant Roots</term>
<term>Plant Shoots</term>
<term>Seedlings</term>
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<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Acide ascorbique</term>
<term>Antioxydants</term>
<term>Chlorophylle</term>
<term>Glutathion</term>
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<term>Eucalyptus</term>
<term>Feuilles de plante</term>
<term>Plant</term>
<term>Pousses de plante</term>
<term>Racines de plante</term>
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<keywords scheme="MESH" qualifier="parasitology" xml:lang="en">
<term>Eucalyptus</term>
<term>Plant Leaves</term>
<term>Plant Roots</term>
<term>Plant Shoots</term>
<term>Seedlings</term>
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<term>Complexe protéique du photosystème II</term>
<term>Eucalyptus</term>
<term>Feuilles de plante</term>
<term>Photosynthèse</term>
<term>Phytophthora</term>
<term>Plant</term>
<term>Pousses de plante</term>
<term>Racines de plante</term>
<term>Transpiration des plantes</term>
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<term>Eucalyptus</term>
<term>Photosynthesis</term>
<term>Photosystem II Protein Complex</term>
<term>Phytophthora</term>
<term>Plant Leaves</term>
<term>Plant Roots</term>
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<term>Seedlings</term>
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<term>Carbohydrates</term>
<term>Disease Resistance</term>
<term>Disease Susceptibility</term>
<term>Host-Pathogen Interactions</term>
<term>Time Factors</term>
<term>Trees</term>
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<term>Arbres</term>
<term>Facteurs temps</term>
<term>Glucides</term>
<term>Interactions hôte-pathogène</term>
<term>Métabolisme glucidique</term>
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<div type="abstract" xml:lang="en">In this study we investigated the role that ascorbate (AA) and glutathione (GSH) play in the plant pathogen interaction of susceptible Eucalyptus sieberi L. A. Johnson and resistant Eucalyptus sideroxylon Woolls with Phytophthora cinnamomi Rands root infection. In a glasshouse study, seedlings were grown in soil-free plant boxes to facilitate the inoculation of the root systems by a P. cinnamomi zoospore solution. Ascorbate and GSH concentrations were measured in infected roots and leaves, along with leaf gas exchange, chlorophyll fluorescence and carbohydrate concentrations over a time course up to 312 h (13 days) post-inoculation (pi). At the early stages of infection (from 24 h pi), significant decreases in AA and GSH concentrations were observed in the infected roots and leaves of the susceptible E. sieberi seedlings. At the later stage of infection (312 h pi), the earlier AA decreases in the leaves of infected plants had become significant increases. In contrast, late, significant AA increases in the absence of any GSH changes were observed in the infected roots of the resistant E. sideroxylon seedlings. In E. sideroxylon leaves, a significant GSH increase occurred at 24 h pi; however, by 312 h pi the earlier increase had become a significant decrease, while no changes occurred in AA. In E. sieberi, photosynthesis (A), stomatal conductance (g(s)) and PSII quantum efficiency (Φ(PSII)) were reduced by ~60, 80 and 30%, respectively, in infected plants and remained significantly lower than uninfected controls for the duration of the experiment. Significant reductions in these parameters did not occur until later (120 h pi for g(s) and 312 h pi for A and Φ(PSII)), and to a lesser extent in the resistant species. Non-structural carbohydrate analysis of roots and leaves indicate that carbohydrate metabolism and resource flow between shoots and roots may have been altered at later infection stages. This study suggests that reduced antioxidant capacity, leaf physiological function and carbohydrate metabolism are associated with susceptibility in E. sieberi to P. cinnamomi infection, while AA increases and new root formation were associated with resistance in E. sideroxylon.</div>
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<AbstractText>In this study we investigated the role that ascorbate (AA) and glutathione (GSH) play in the plant pathogen interaction of susceptible Eucalyptus sieberi L. A. Johnson and resistant Eucalyptus sideroxylon Woolls with Phytophthora cinnamomi Rands root infection. In a glasshouse study, seedlings were grown in soil-free plant boxes to facilitate the inoculation of the root systems by a P. cinnamomi zoospore solution. Ascorbate and GSH concentrations were measured in infected roots and leaves, along with leaf gas exchange, chlorophyll fluorescence and carbohydrate concentrations over a time course up to 312 h (13 days) post-inoculation (pi). At the early stages of infection (from 24 h pi), significant decreases in AA and GSH concentrations were observed in the infected roots and leaves of the susceptible E. sieberi seedlings. At the later stage of infection (312 h pi), the earlier AA decreases in the leaves of infected plants had become significant increases. In contrast, late, significant AA increases in the absence of any GSH changes were observed in the infected roots of the resistant E. sideroxylon seedlings. In E. sideroxylon leaves, a significant GSH increase occurred at 24 h pi; however, by 312 h pi the earlier increase had become a significant decrease, while no changes occurred in AA. In E. sieberi, photosynthesis (A), stomatal conductance (g(s)) and PSII quantum efficiency (Φ(PSII)) were reduced by ~60, 80 and 30%, respectively, in infected plants and remained significantly lower than uninfected controls for the duration of the experiment. Significant reductions in these parameters did not occur until later (120 h pi for g(s) and 312 h pi for A and Φ(PSII)), and to a lesser extent in the resistant species. Non-structural carbohydrate analysis of roots and leaves indicate that carbohydrate metabolism and resource flow between shoots and roots may have been altered at later infection stages. This study suggests that reduced antioxidant capacity, leaf physiological function and carbohydrate metabolism are associated with susceptibility in E. sieberi to P. cinnamomi infection, while AA increases and new root formation were associated with resistance in E. sideroxylon.</AbstractText>
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