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16 results on '"Zimmermann, Sabine"'

1. Ectomycorrhizal symbiosis helps plants to challenge salt stress conditions.

Author

Guerrero-Galán C, Calvo-Polanco M, and Zimmermann SD

Subjects
Plant Roots growth & development, Sodium metabolism, Water metabolism, Fungi physiology, Mycorrhizae physiology, Plant Roots microbiology, Plant Roots physiology, Salt Stress, Symbiosis
Abstract

Soil salinity is an environmental condition that is currently increasing worldwide. Plant growth under salinity induces osmotic stress and ion toxicity impairing root water and nutrient absorption, but the association with beneficial soil microorganisms has been linked to an improved adaptation to this constraint. The ectomycorrhizal (ECM) symbiosis has been proposed as a key factor for a better tolerance of woody species to salt stress, thanks to the reduction of sodium (Na + ) uptake towards photosynthetic organs. Although no precise mechanisms for this enhanced plant salt tolerance have been described yet, in this review, we summarize the knowledge accumulated so far on the role of ECM symbiosis. Moreover, we propose several strategies by which ECM fungi might help plants, including restriction of Na + entrance into plant tissues and improvement of mineral nutrition and water balances. This positive effect of ECM fungi has been proven in field assays and the results obtained point to a promising application in forestry cultures and reforestation.

Published
2019
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2. Biotrophic transportome in mutualistic plant-fungal interactions.

Author

Casieri L, Ait Lahmidi N, Doidy J, Veneault-Fourrey C, Migeon A, Bonneau L, Courty PE, Garcia K, Charbonnier M, Delteil A, Brun A, Zimmermann S, Plassard C, and Wipf D

Subjects
Biomass, Fungi growth & development, Plant Development, Plants metabolism, Fungi physiology, Plant Physiological Phenomena, Plants microbiology, Symbiosis
Abstract

Understanding the mechanisms that underlie nutrient use efficiency and carbon allocation along with mycorrhizal interactions is critical for managing croplands and forests soundly. Indeed, nutrient availability, uptake and exchange in biotrophic interactions drive plant growth and modulate biomass allocation. These parameters are crucial for plant yield, a major issue in the context of high biomass production. Transport processes across the polarized membrane interfaces are of major importance in the functioning of the established mycorrhizal association as the symbiotic relationship is based on a 'fair trade' between the fungus and the host plant. Nutrient and/or metabolite uptake and exchanges, at biotrophic interfaces, are controlled by membrane transporters whose regulation patterns are essential for determining the outcome of plant-fungus interactions and adapting to changes in soil nutrient quantity and/or quality. In the present review, we summarize the current state of the art regarding transport systems in the two major forms of mycorrhiza, namely ecto- and arbuscular mycorrhiza.

Published
2013
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6. Potasium nutrition in rice under salt stress: role of arbuscular mycorrhizal symbiosis?

Author

Doan, T. Luu, Courty, Pierre-Emmanuel, Zimmermann, Sabine, Seck, Maguette, Robert, Marine, Corratgé-Faillie, Claire, Very, Anne-Alliénor, ProdInra, Migration, Centre National de la Recherche Scientifique (CNRS), Agroécologie [Dijon], and Université de Bourgogne (UB)-Institut National de la Recherche Agronomique (INRA)-Université Bourgogne Franche-Comté [COMUE] (UBFC)-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement

Subjects
[SDV] Life Sciences [q-bio], [SDE] Environmental Sciences, [SDV]Life Sciences [q-bio], fungi, [SDE]Environmental Sciences, food and beverages, [SDV.BV]Life Sciences [q-bio]/Vegetal Biology, [SDV.BV] Life Sciences [q-bio]/Vegetal Biology
Abstract

Arbuscular mycorrhizal fungi (AMF) establish a symbiotic association with the roots of 80% of terrestrial plants and form complex tree-shaped feeding structures called arbuscules in colonized root cells. This association with AMF not only provides more efficient uptake of nutrients for the plant, but also confers protection against pathogens and increased tolerance to environmental stress such as salt stress [1]. Rice (Oryza sativa), the most salt-sensitive crop species amongst cereals, has a productivity strongly reduced around the world due to soil salinity/salinization and increased sea level (in deltas). High Na+ concentrations (salt stress conditions) impairs K+ uptake and inhibits many K+-activated enzymes. Rice exhibits molecular mechanisms to alleviate salt stress such as maintaining a high cellular K+/Na+ ratio, e.g. by a more efficient K+ uptake, which was recently shown to occur upon root/AMF interaction [2]. Knowledge on the role of root/AMF interaction on K+/Na+ transport upon salt stress is sparse [2, 3]. The aim of the research is to understand the mechanisms by which AMF improve plant K+ nutrition upon salt stress, taking Rhizophagus irregularis (model AMF)-rice interaction as a model. We will investigate the mechanisms by which AMF mediate K+ uptake and translocation towards root cells. Rice loss-of-function mutants for each of the three major K+ uptake systems of the plant, OsAKT1, OsHAK5 and OsHAK1, were inoculated with R. irregularis and submitted to salt stress, and their K+ contents and K+/Na+ ratios were monitored to identify key player(s) for AMF-mediated improved rice K+ nutrition and salt tolerance.

Published
2019

7. The Hebeloma cylindrosporum phosphate transporter HcPT2 was involved in phosphate efflux at the fungus-plant interface

Author

Becquer, Adeline, Garcia, K., Amenc, Laurie, Russet, Sylvie, BAEZA, Yoan, Zimmermann, Sabine, Plassard, Claude, Ecologie fonctionnelle et biogéochimie des sols et des agro-écosystèmes (UMR Eco&Sols), Institut National de la Recherche Agronomique (INRA)-Institut de Recherche pour le Développement (IRD)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Department of Agronomy, University of El-Tarf, Biochimie et Physiologie Moléculaire des Plantes (BPMP), Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS), Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut de Recherche pour le Développement (IRD)-Institut National de la Recherche Agronomique (INRA), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), and Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)

Subjects
hebeloma cylindrosporum, Vegetal Biology, pinus pinaster, système racinaire, symbiose ectomycorhizienne, transporteur de phosphate, fungi, root systems, [SDV.BV]Life Sciences [q-bio]/Vegetal Biology, maritime pine, immunolocalisation, Biologie végétale
Abstract

Ectomycorrhizal (ECM) symbiosis is defined as a mutual association between fungal symbionts and roots of woody plants. This symbiosis is strongly represented in temperate and boreal forests and is considered to be the most widespread means of increasing P acquisition by trees. Despite the importance of the ECM association, current knowledge about molecular mechanisms involved in membrane transport between the two partners is still limited. Therefore, the identification of the mechanisms essential for the symbiosis is a major issue. To better understand these mechanisms, we used a model association between the ECM basidiomycete Hebeloma cylindrosporum and the maritime pine Pinus pinaster. The fungal genome contains three transporters of Pi (HcPT1.1, HcPT1.2, and HcPT2), which have been already characterized as H+ Pi carriers. We hypothesized that one of these carriers could be responsible for both influx and efflux of Pi from the soil to the fungus and from the fungus to the plant. Our results suggest that HcPT2 would be the best candidate to fill both roles. An in vitro ectomycorrhizal system was used to investigate phosphate flux from H. cylindrosporum toward a liquid compartment containing pine roots. Interestingly, the expression pattern of HcPT2 was correlated to fungal phosphate efflux. Moreover, immuno-localization experiments showed that the protein is located (i) in the extraradical hyphae and the fungal sheath, compatible with Pi uptake, and (ii) within the Hartig net, which is the place of exchange between fungal and host cells. In order to study more specifically the role of HcPT2 at the fungus-plant interface, overexpressing and knock-down transgenic H. cylindrosporum strains were produced. Fungal strains with up regulated expression of HcPT2 increased phosphate efflux within the interaction medium, supporting a role of HcPT2 in phosphate transfer to the plant. In addition, the modification of HcPT2 expression strongly affects Pi nutrition of P. pinaster.

Published
2015

8. Comparative genomics, proteomics and transcriptomics give new insight into the exoproteome of the basidiomycete Hebeloma cylindrosporum and its involvement in ectomycorrhizal symbiosis

Author

DORE, Jeanne, PERRAUD, Marie, Dieryckx, Cindy, Kohler, Annegret, Morin, Emmanuelle, Henrissat, Bernard, Lindquist, Erika, Zimmermann, Sabine D., Girard, Vincent, Kuo, Alan, Grigoriev, Igor V, Martin, Francis, Marmeisse, Roland, Gay, Gilles, Laboratoire d'Ecologie Microbienne - UMR 5557 (LEM), Institut National de la Recherche Agronomique (INRA)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Ecole Nationale Vétérinaire de Lyon (ENVL)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS), Génomique fonctionnelle des champignons pathogènes des plantes (FungiPath), Microbiologie, adaptation et pathogénie (MAP), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS), Interactions Arbres-Microorganismes (IAM), Institut National de la Recherche Agronomique (INRA)-Université de Lorraine (UL), Architecture et fonction des macromolécules biologiques (AFMB), Institut National de la Recherche Agronomique (INRA)-Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Department of Energy / Joint Genome Institute (DOE), Los Alamos National Laboratory (LANL), Biochimie et Physiologie Moléculaire des Plantes (BPMP), Institut National de la Recherche Agronomique (INRA)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), U.S. Department of Energy (DE-AC02-05CH11231), ANR (ANR-11-607 LABX-0002-01), Centre National de la Recherche Scientifique (CNRS)-Ecole Nationale Vétérinaire de Lyon (ENVL)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Recherche Agronomique (INRA)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS), Université de Lorraine (UL)-Institut National de la Recherche Agronomique (INRA), Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS), Ecologie microbienne ( EM ), Centre National de la Recherche Scientifique ( CNRS ) -Ecole Nationale Vétérinaire de Lyon ( ENVL ) -Université Claude Bernard Lyon 1 ( UCBL ), Université de Lyon-Université de Lyon-Institut National de la Recherche Agronomique ( INRA ) -VetAgro Sup ( VAS ), Microbiologie, adaptation et pathogénie ( MAP ), Université Claude Bernard Lyon 1 ( UCBL ), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon ( INSA Lyon ), Université de Lyon-Institut National des Sciences Appliquées ( INSA ) -Institut National des Sciences Appliquées ( INSA ) -Centre National de la Recherche Scientifique ( CNRS ), Interactions Arbres-Microorganismes ( IAM ), Institut National de la Recherche Agronomique ( INRA ) -Université de Lorraine ( UL ), Architecture et fonction des macromolécules biologiques ( AFMB ), Centre National de la Recherche Scientifique ( CNRS ) -Aix Marseille Université ( AMU ) -Institut National de la Recherche Agronomique ( INRA ), DOE Joint Genome Institute, Biochimie et Physiologie Moléculaire des Plantes ( BPMP ), Centre international d'études supérieures en sciences agronomiques ( Montpellier SupAgro ) -Institut national de la recherche agronomique [Montpellier] ( INRA Montpellier ) -Université de Montpellier ( UM ) -Centre National de la Recherche Scientifique ( CNRS ) -Institut national d’études supérieures agronomiques de Montpellier ( Montpellier SupAgro ), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Ecole Nationale Vétérinaire de Lyon (ENVL), Centre National de la Recherche Scientifique (CNRS)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon, Centre National de la Recherche Scientifique (CNRS)-Aix Marseille Université (AMU)-Institut National de la Recherche Agronomique (INRA), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro), Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), and Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)

Subjects
Proteomics, [SDV.OT]Life Sciences [q-bio]/Other [q-bio.OT], Hebeloma cylindrosporum, Proteome, Genes, Fungal, fungi, Genomics, exoproteome, shotgun protein quantification, ectomycorrhiza, Fungal Proteins, Mycorrhizae, soil organic matter, Hebeloma, [ SDV.OT ] Life Sciences [q-bio]/Other [q-bio.OT], Symbiosis, transcriptome
Abstract

Extracellular proteins play crucial roles in the interaction between mycorrhizal fungi and their environment. Computational prediction and experimental detection allowed identification of 869 proteins constituting the exoproteome of Hebeloma cylindrosporum. Small secreted proteins (SSPs) and carbohydrate-active enzymes (CAZymes) were the two major classes of extracellular proteins. Twenty-eight per cent of the SSPs were secreted by free-living mycelia and five of the 10 most abundant extracellular proteins were SSPs. By contrast, 63-75% of enzymes involved in nutrient acquisition were secreted. A total of 150 extracellular protein-coding genes were differentially expressed between mycorrhizas and free-living mycelia. SSPs were the most affected. External environmental conditions also affected expression of 199 exoproteome genes in mycorrhizas. SSPs displayed different patterns of regulation in response to presence of a host plant or other environmental signals. Several of the genes most overexpressed in the presence of organic matter encoded oxidoreductases. Hebeloma cylindrosporum has not fully lost its ancestral saprotrophic capacities but rather adapted them not to harm its hosts and to use soil organic nitrogen. The complex and divergent patterns of regulation of SSPs in response to a symbiotic partner and/or organic matter suggest various roles in the biology of mycorrhizal fungi.

Published
2015

9. The phosphate transporter HcPT2, first candidate for phosphate efflux in ectomycorhizal symbiosis?

Author

Becquer, Adeline, Amenc, Laurie, Garcia, Kevin, Russet, Sylvie, BAEZA, Yoan, Zimmermann, Sabine, Plassard, Claude, Ecologie fonctionnelle et biogéochimie des sols et des agro-écosystèmes (UMR Eco&Sols), Institut National de la Recherche Agronomique (INRA)-Institut de Recherche pour le Développement (IRD)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Department of Agronomy, University of Wisconsin-Madison, Biochimie et Physiologie Moléculaire des Plantes (BPMP), Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS), Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut de Recherche pour le Développement (IRD)-Institut National de la Recherche Agronomique (INRA), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), and Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)

Subjects
[SDV.SA]Life Sciences [q-bio]/Agricultural sciences, fungi, [SDV.BV]Life Sciences [q-bio]/Vegetal Biology
Abstract

In forest ecosystems, the availability of phosphorus as inorganic P (Pi) limits tree growth. To overcome this deficiency, trees are associated with fungi through new organs called ectomycorrhizae (ECM). Despite the importance of phosphate nutrition, the mechanisms involved in the unidirectional transfer of P between the fungus and the plant are still unknown. Therefore, the identification of these mechanisms essential for symbiosis is a major issue. To understand better these mechanisms, we used a model association between the ECM basidiomycete Hebeloma cylindrosporum and the maritime Pine, Pinus pinaster. The fungal genome contains three transporters of Pi (HcPT1.1, HcPT1.2 and HcPT2) which have been already characterized as H+:Pi carriers.We hypothesized that one of these carriers could be responsible for both influx and efflux of Pi respectively from the soil to the fungus and from the fungus to the plant. Our first results suggest that HcPT2 would be the best candidate to fill both roles. Immunolocalization showed that the protein is located in (i) the extraradical hyphae and the fungal sheath involved in Pi uptake and (ii) the Hartig net, ie the interface between fungal and host cells. We also produced overexpressing and knock-down transgenic H. cylindrosporum strains to study specifically the role of HcPT2 in (i) the P efflux from the fungus measured in vitro and (ii) the P nutrition of the host plant grown at low and high P levels. Finally, if our hypothesis is confirmed, the main question will be to define how this transporter is regulated to provide both influx and efflux of phosphate in ECM symbiosis.

Published
2014

10. Potassium nutrition of ectomycorrhizal Pinus pinaster: overexpression of the Hebeloma cylindrosporum HcTrk1 transporter affects the translocation of both K(+) and phosphorus in the host plant

Author

Garcia, Kevin, Delteil, Amandine, Conéjéro, Geneviève, Becquer, Adeline, Plassard, Claude, Sentenac, Hervé, Zimmermann, Sabine, Biochimie et Physiologie Moléculaire des Plantes (BPMP), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro), Plateforme d'histocytologie et d'imagerie cellulaire végétale (PHIV), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Amélioration génétique et adaptation des plantes méditerranéennes et tropicales (UMR AGAP), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut National de la Recherche Agronomique (INRA)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut National de la Recherche Agronomique (INRA)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro), Ecologie fonctionnelle et biogéochimie des sols et des agro-écosystèmes (UMR Eco&Sols), Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut de Recherche pour le Développement (IRD)-Institut National de la Recherche Agronomique (INRA), Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS), Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)-Amélioration génétique et adaptation des plantes méditerranéennes et tropicales (UMR AGAP), Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro), and Institut National de la Recherche Agronomique (INRA)-Institut de Recherche pour le Développement (IRD)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)

Subjects
Hebeloma cylindrosporum, plant potassium nutrition, fungi, protein-EGFP fusion, phosphate transporter HcPT1.1, [SDV.BV]Life Sciences [q-bio]/Vegetal Biology, ectomycorrhizal symbiosis, in situ hybridization, potassium-sodium transporter HcTrk1, overexpression
Abstract

International audience; Mycorrhizal associations are known to improve the hydro-mineral nutrition of their host plants. However, the importance of mycorrhizal symbiosis for plant potassium nutrition has so far been poorly studied. We therefore investigated the impact of the ectomycorrhizal fungus Hebeloma cylindrosporum on the potassium nutrition of Pinus pinaster and examined the involvement of the fungal potassium transporter HcTrk1. HcTrk1 transcripts and proteins were localized in ectomycorrhizas using in situ hybridization and EGFP translational fusion constructs. Importantly, an overexpression strategy was performed on a H. cylindrosporum endogenous gene in order to dissect the role of this transporter. The potassium nutrition of mycorrhizal pine plants was significantly improved under potassium-limiting conditions. Fungal strains overexpressing HcTrk1 reduced the translocation of potassium and phosphorus from the roots to the shoots of inoculated plants in mycorrhizal experiments. Furthermore, expression of HcTrk1 and the phosphate transporter HcPT1.1 were reciprocally linked to the external inorganic phosphate and potassium availability. The development of these approaches provides a deeper insight into the role of ectomycorrhizal symbiosis on host plant K(+) nutrition and in particular, the K(+) transporter HcTrk1. The work augments our knowledge of the link between potassium and phosphorus nutrition via the mycorrhizal pathway.

Published
2014

11. The disregarded mycorrhizal contribution to plant potassium nutrition

Author

Garcia, Kevin, Zimmermann, Sabine, Biochimie et Physiologie Moléculaire des Plantes (BPMP), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro), and Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)

Subjects
K+ nutrition, fungi, Potassium, food and beverages, [SDV.BV]Life Sciences [q-bio]/Vegetal Biology, transfer from the soil to the plant, root, symbiosis, K+transport
Abstract

International audience; Potassium (K+) is one of the most abundant element of soil composition but its very low availability limits plant growth and productivity of ecosystems. Because this cation participates in many biological processes, its constitutive uptake from soil solution is crucial for the plant cell machinery. Thus, the understanding of strategies responsible of K+ nutrition is a major issue in plant science. Mycorrhizal associations occurring between roots and hyphae of underground fungi improve hydro-mineral nutrition of the majority of terrestrial plants. The contribution of this mutualistic symbiosis to the enhancement of plant K+ nutrition is still underestimated and poorly studied so far. This mini-review examines the current knowledge about the impact of both arbuscular mycorrhizal and ectomycorrhizal symbioses on the transfer of K+ from the soil to the plants. A model summarizing plant and fungal transport systems identified and hypothetically involved in K+ transport is proposed. In addition, some data related to benefits for plants provided by the improvement of K+ nutrition thanks to mycorrhizal symbioses are presented.

Published
2014

12. The role of mycorrhizal contribution to plant potassium nutrition

Author

Garcia, Kevin and Zimmermann, Sabine

Subjects
Vegetal Biology, symbiose ectomycorhizienne, fungi, food and beverages, Potassium, K+transport, root, K+ nutrition, symbiosis, transfer from the soil to the plant, canaux potassiques shaker, absorption du potassium, mycorrhizae, Biologie végétale
Abstract

Potassium (K+) is one of the most abundant element of soil composition but its very low availability limits plant growth and productivity of ecosystems. Because this cation participates in many biological processes, its constitutive uptake from soil solution is crucial for the plant cell machinery. Thus, the understanding of strategies responsible of K+ nutrition is a major issue in plant science. Mycorrhizal associations occurring between roots and hyphae of underground fungi improve hydro-mineral nutrition of the majority of terrestrial plants. The contribution of this mutualistic symbiosis to the enhancement of plant K+ nutrition is still underestimated and poorly studied so far. This mini-review examines the current knowledge about the impact of both arbuscular mycorrhizal and ectomycorrhizal symbioses on the transfer of K+ from the soil to the plants. A model summarizing plant and fungal transport systems identified and hypothetically involved in K+ transport is proposed. In addition, some data related to benefits for plants provided by the improvement of K+ nutrition thanks to mycorrhizal symbioses are presented.

Published
2014

13. Plant potassium nutrition in ectomycorrhizal symbiosis: properties and roles of the three fungal TOK potassium channels in <italic>Hebeloma cylindrosporum</italic>.

Author

Guerrero‐Galán, Carmen, Delteil, Amandine, Garcia, Kevin, Houdinet, Gabriella, Conéjéro, Geneviève, Gaillard, Isabelle, Sentenac, Hervé, and Zimmermann, Sabine Dagmar

Subjects
PLANT potassium metabolism, ECTOMYCORRHIZAL fungi, HEBELOMA, FUNGI, PINE seedlings
Abstract

Summary: Ectomycorrhizal fungi play an essential role in the ecology of boreal and temperate forests through the improvement of tree mineral nutrition. Potassium (K+) is an essential nutrient for plants and is needed in high amounts. We recently demonstrated that the ectomycorrhizal fungus Hebeloma cylindrosporum improves the K+ nutrition of Pinus pinaster under shortage conditions. Part of the transport systems involved in K+ uptake by the fungus has been deciphered, while the molecular players responsible for the transfer of this cation towards the plant remain totally unknown. Analysis of the genome of H. cylindrosporum revealed the presence of three putative tandem‐pore outward‐rectifying K+ (TOK) channels that could contribute to this transfer. Here, we report the functional characterization of these three channels through two‐electrode voltage‐clamp experiments in oocytes and yeast complementation assays. The expression pattern and physiological role of these channels were analysed in symbiotic interaction with P. pinaster. Pine seedlings colonized by fungal transformants overexpressing two of them displayed a larger accumulation of K+ in shoots. This study revealed that TOK channels have distinctive properties and functions in axenic and symbiotic conditions and suggested that HcTOK2.2 is implicated in the symbiotic transfer of K+ from the fungus towards the plant. [ABSTRACT FROM AUTHOR]

Published
2018
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14. Control of K+ channel activity and transport in plants: the C-linker of Arabidopsis Shaker inward channels plays a crucial role in both surface expression and channel activity

Author

NIEVES CORDONES, Manuel, Chavanieu, Alain, Jeanguenin, Linda, Alcon, Carine, Estaran, Sebastien, Chérel, Isabelle, Zimmermann, Sabine, Sentenac, Herve, Gaillard, Isabelle, Biochimie et Physiologie Moléculaire des Plantes (BPMP), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro), Université de Montpellier (UM), ProdInra, Archive Ouverte, and Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)

Subjects
transport de potassium, water stress, arabidopsis, shaker potassium channel, fungi, stress salin, food and beverages, [SDV.BV]Life Sciences [q-bio]/Vegetal Biology, [SDV.BV] Life Sciences [q-bio]/Vegetal Biology, canaux potassiques shaker, stress hydrique
Abstract

Control of K+ channel activity and transport in plants: the C-linker of Arabidopsis Shaker inward channels plays a crucial role in both surface expression and channel activity. Gordon Research Conferences - Salt & Water Stress in Plants

Published
2012

15. Secrets of the fungus-specific potassium channel TOK family.

Author

Houdinet, Gabriella, Guerrero-Galán, Carmen, Rose, Benjamin D., Garcia, Kevin, and Zimmermann, Sabine D.

Subjects
*POTASSIUM channels, *TRANSMEMBRANE domains, *FILAMENTOUS fungi, *YEAST fungi, *BINDING sites
Abstract

The tandem-pore outward-rectifying potassium (K+) channel family (TOK) is found only in fungi. Therefore, a specific role in fungus physiology can be assumed. ScTOK1 was the first TOK channel characterized in Saccharomyces cerevisiae that displayed a unique structure: two pore domains and eight transmembrane domains per subunit. ScTOK1 induces mainly outward K+ currents upon membrane depolarization, and is highly regulated. The gating model of TOK channels has evolved over the years and involves external and internal K+ concentration, potential binding sites, and membrane potential. TOK channels have also been found recently in filamentous fungi, and light has been shed on their potential role in beneficial and pathogenic interactions with host organisms. Several families of potassium (K+) channels are found in membranes of all eukaryotes, underlining the importance of K+ uptake and redistribution within and between cells and organs. Among them, TOK (tandem-pore outward-rectifying K+) channels consist of eight transmembrane domains and two pore domains per subunit organized in dimers. These channels were originally studied in yeast, but recent identifications and characterizations in filamentous fungi shed new light on this fungus-specific K+ channel family. Although their actual function in vivo is often puzzling, recent works indicate a role in cellular K+ homeostasis and even suggest a role in plant–fungus symbioses. This review aims at synthesizing the current knowledge on fungal TOK channels and discussing their potential role in yeasts and filamentous fungi. [ABSTRACT FROM AUTHOR]

Published
2023
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16. Plant potassium nutrition in ectomycorrhizal symbiosis: properties and roles of the three fungal TOK potassium channels in Hebeloma cylindrosporum

Author

Geneviève Conejero, Gabriella Houdinet, Isabelle Gaillard, Hervé Sentenac, Carmen Guerrero-Galán, Sabine Zimmermann, Kevin Garcia, Amandine Delteil, Biochimie et Physiologie Moléculaire des Plantes (BPMP), Université de Montpellier (UM)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de biochimie et physiologie des plantes, Institut National de la Recherche Agronomique (INRA), Biology and Microbiology Department, South Dakota State University (SDSTATE), Plateforme Histocytologie et Imagerie Cellulaire Végétale, Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad), Zimmermann, Sabine, Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut National de la Recherche Agronomique (INRA)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), and Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)

Subjects
0106 biological sciences, 0301 basic medicine, Potassium Channels, Saccharomyces cerevisiae, Fungus, maritime pine, absorption du potassium, champignon mycorhizien, 01 natural sciences, Microbiology, nutrition minérale, Ectosymbiosis, 03 medical and health sciences, Symbiosis, Mycorrhizae, Botany, Hebeloma, ion potassium, [SDV.BV]Life Sciences [q-bio]/Vegetal Biology, Axenic, Ecology, Evolution, Behavior and Systematics, Minerals, Vegetal Biology, pinus pinaster, shaker potassium channel, biology, fungi, Biological Transport, 15. Life on land, Pinus, biology.organism_classification, Yeast, Complementation, hebeloma cylindrosporum, 030104 developmental biology, Seedlings, Potassium, Pinus pinaster, canaux potassiques shaker, Plant nutrition, Biologie végétale, 010606 plant biology & botany
Abstract

Ectomycorrhizal fungi play an essential role in the ecology of boreal and temperate forests through the improvement of tree mineral nutrition. Potassium (K+ ) is an essential nutrient for plants and is needed in high amounts. We recently demonstrated that the ectomycorrhizal fungus Hebeloma cylindrosporum improves the K+ nutrition of Pinus pinaster under shortage conditions. Part of the transport systems involved in K+ uptake by the fungus has been deciphered, while the molecular players responsible for the transfer of this cation towards the plant remain totally unknown. Analysis of the genome of H. cylindrosporum revealed the presence of three putative tandem-pore outward-rectifying K+ (TOK) channels that could contribute to this transfer. Here, we report the functional characterization of these three channels through two-electrode voltage-clamp experiments in oocytes and yeast complementation assays. The expression pattern and physiological role of these channels were analysed in symbiotic interaction with P. pinaster. Pine seedlings colonized by fungal transformants overexpressing two of them displayed a larger accumulation of K+ in shoots. This study revealed that TOK channels have distinctive properties and functions in axenic and symbiotic conditions and suggested that HcTOK2.2 is implicated in the symbiotic transfer of K+ from the fungus towards the plant.

Published
2018

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