Arbuscular cell invasion coincides with extracellular vesicles and membrane tubules.
Identifieur interne : 000575 ( Main/Curation ); précédent : 000574; suivant : 000576Arbuscular cell invasion coincides with extracellular vesicles and membrane tubules.
Auteurs : Ronelle Roth [Royaume-Uni] ; Stefan Hillmer [Allemagne] ; Charlotta Funaya [Allemagne] ; Marco Chiapello [Royaume-Uni] ; Karin Schumacher [Allemagne] ; Libera Lo Presti [Allemagne] ; Regine Kahmann [Allemagne] ; Uta Paszkowski [Royaume-Uni]Source :
- Nature plants [ 2055-0278 ] ; 2019.
Descripteurs français
- KwdFr :
- Cellules végétales (microbiologie), Feuilles de plante (cytologie), Feuilles de plante (microbiologie), Feuilles de plante (ultrastructure), Glomeromycota (physiologie), Hyphae (physiologie), Membrane cellulaire (microbiologie), Membrane cellulaire (ultrastructure), Mycorhizes (cytologie), Mycorhizes (physiologie), Oryza (cytologie), Oryza (génétique), Oryza (microbiologie), Racines de plante (cytologie), Racines de plante (microbiologie), Racines de plante (ultrastructure), Symbiose (MeSH), Tomographie en microscopie électronique (MeSH), Ustilago (pathogénicité), Végétaux génétiquement modifiés (MeSH), Vésicules extracellulaires (métabolisme), Zea mays (microbiologie).
- MESH :
- cytologie : Feuilles de plante, Mycorhizes, Oryza, Racines de plante.
- génétique : Oryza.
- microbiologie : Cellules végétales, Feuilles de plante, Membrane cellulaire, Oryza, Racines de plante, Zea mays.
- métabolisme : Vésicules extracellulaires.
- pathogénicité : Ustilago.
- physiologie : Glomeromycota, Hyphae, Mycorhizes.
- ultrastructure : Feuilles de plante, Membrane cellulaire, Racines de plante, Symbiose, Tomographie en microscopie électronique, Végétaux génétiquement modifiés.
English descriptors
- KwdEn :
- Cell Membrane (microbiology), Cell Membrane (ultrastructure), Electron Microscope Tomography (MeSH), Extracellular Vesicles (metabolism), Glomeromycota (physiology), Hyphae (physiology), Mycorrhizae (cytology), Mycorrhizae (physiology), Oryza (cytology), Oryza (genetics), Oryza (microbiology), Plant Cells (microbiology), Plant Leaves (cytology), Plant Leaves (microbiology), Plant Leaves (ultrastructure), Plant Roots (cytology), Plant Roots (microbiology), Plant Roots (ultrastructure), Plants, Genetically Modified (MeSH), Symbiosis (MeSH), Ustilago (pathogenicity), Zea mays (microbiology).
- MESH :
- cytology : Mycorrhizae, Oryza, Plant Leaves, Plant Roots.
- genetics : Oryza.
- metabolism : Extracellular Vesicles.
- microbiology : Cell Membrane, Oryza, Plant Cells, Plant Leaves, Plant Roots, Zea mays.
- pathogenicity : Ustilago.
- physiology : Glomeromycota, Hyphae, Mycorrhizae.
- ultrastructure : Cell Membrane, Plant Leaves, Plant Roots.
- Electron Microscope Tomography, Plants, Genetically Modified, Symbiosis.
Abstract
During establishment of arbuscular mycorrhizal symbioses, fungal hyphae invade root cells producing transient tree-like structures, the arbuscules, where exchange of photosynthates for soil minerals occurs. Arbuscule formation and collapse lead to rapid production and degradation of plant and fungal membranes, their spatiotemporal dynamics directly influencing nutrient exchange. We determined the ultra-structural details of both membrane surfaces and the interstitial apoplastic matrix by transmission electron microscopy tomography during growth and senescence of Rhizophagus irregularis arbuscules in rice. Invasive growth of arbuscular hyphae was associated with abundant fungal membrane tubules (memtubs) and plant peri-arbuscular membrane evaginations. Similarly, the phylogenetically distant arbuscular mycorrhizal fungus, Gigaspora rosea, and the fungal maize pathogen, Ustilago maydis, developed memtubs while invading host cells, revealing structural commonalities independent of the mutualistic or parasitic outcome of the interaction. Additionally, extracellular vesicles formed continuously in the peri-arbuscular interface from arbuscule biogenesis to senescence, suggesting an involvement in inter-organismic signal and nutrient exchange throughout the arbuscule lifespan.
DOI: 10.1038/s41477-019-0365-4
PubMed: 30737514
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<term>Extracellular Vesicles (metabolism)</term>
<term>Glomeromycota (physiology)</term>
<term>Hyphae (physiology)</term>
<term>Mycorrhizae (cytology)</term>
<term>Mycorrhizae (physiology)</term>
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<term>Plant Roots (cytology)</term>
<term>Plant Roots (microbiology)</term>
<term>Plant Roots (ultrastructure)</term>
<term>Plants, Genetically Modified (MeSH)</term>
<term>Symbiosis (MeSH)</term>
<term>Ustilago (pathogenicity)</term>
<term>Zea mays (microbiology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Cellules végétales (microbiologie)</term>
<term>Feuilles de plante (cytologie)</term>
<term>Feuilles de plante (microbiologie)</term>
<term>Feuilles de plante (ultrastructure)</term>
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<term>Membrane cellulaire (microbiologie)</term>
<term>Membrane cellulaire (ultrastructure)</term>
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<term>Mycorhizes (physiologie)</term>
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<term>Tomographie en microscopie électronique (MeSH)</term>
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<term>Végétaux génétiquement modifiés (MeSH)</term>
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<term>Racines de plante</term>
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<term>Oryza</term>
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<term>Feuilles de plante</term>
<term>Membrane cellulaire</term>
<term>Oryza</term>
<term>Racines de plante</term>
<term>Zea mays</term>
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<term>Oryza</term>
<term>Plant Cells</term>
<term>Plant Leaves</term>
<term>Plant Roots</term>
<term>Zea mays</term>
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<term>Racines de plante</term>
<term>Symbiose</term>
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<front><div type="abstract" xml:lang="en">During establishment of arbuscular mycorrhizal symbioses, fungal hyphae invade root cells producing transient tree-like structures, the arbuscules, where exchange of photosynthates for soil minerals occurs. Arbuscule formation and collapse lead to rapid production and degradation of plant and fungal membranes, their spatiotemporal dynamics directly influencing nutrient exchange. We determined the ultra-structural details of both membrane surfaces and the interstitial apoplastic matrix by transmission electron microscopy tomography during growth and senescence of Rhizophagus irregularis arbuscules in rice. Invasive growth of arbuscular hyphae was associated with abundant fungal membrane tubules (memtubs) and plant peri-arbuscular membrane evaginations. Similarly, the phylogenetically distant arbuscular mycorrhizal fungus, Gigaspora rosea, and the fungal maize pathogen, Ustilago maydis, developed memtubs while invading host cells, revealing structural commonalities independent of the mutualistic or parasitic outcome of the interaction. Additionally, extracellular vesicles formed continuously in the peri-arbuscular interface from arbuscule biogenesis to senescence, suggesting an involvement in inter-organismic signal and nutrient exchange throughout the arbuscule lifespan.</div>
</front>
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<Abstract><AbstractText>During establishment of arbuscular mycorrhizal symbioses, fungal hyphae invade root cells producing transient tree-like structures, the arbuscules, where exchange of photosynthates for soil minerals occurs. Arbuscule formation and collapse lead to rapid production and degradation of plant and fungal membranes, their spatiotemporal dynamics directly influencing nutrient exchange. We determined the ultra-structural details of both membrane surfaces and the interstitial apoplastic matrix by transmission electron microscopy tomography during growth and senescence of Rhizophagus irregularis arbuscules in rice. Invasive growth of arbuscular hyphae was associated with abundant fungal membrane tubules (memtubs) and plant peri-arbuscular membrane evaginations. Similarly, the phylogenetically distant arbuscular mycorrhizal fungus, Gigaspora rosea, and the fungal maize pathogen, Ustilago maydis, developed memtubs while invading host cells, revealing structural commonalities independent of the mutualistic or parasitic outcome of the interaction. Additionally, extracellular vesicles formed continuously in the peri-arbuscular interface from arbuscule biogenesis to senescence, suggesting an involvement in inter-organismic signal and nutrient exchange throughout the arbuscule lifespan.</AbstractText>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Roth</LastName>
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<ForeName>Charlotta</ForeName>
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<Author ValidYN="Y"><LastName>Paszkowski</LastName>
<ForeName>Uta</ForeName>
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<AffiliationInfo><Affiliation>Department of Plant Sciences, University of Cambridge, Cambridge, UK. up220@cam.ac.uk.</Affiliation>
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<CommentsCorrectionsList><CommentsCorrections RefType="CommentIn"><RefSource>Nat Plants. 2019 Feb;5(2):131-132</RefSource>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D002462" MajorTopicYN="N">Cell Membrane</DescriptorName>
<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
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<MeshHeading><DescriptorName UI="D000067128" MajorTopicYN="N">Extracellular Vesicles</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
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