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Des fossiles d’arbuscules ont été trouvés dans des terrains
du Dévonien (-400 MA) et des spores typiques du phylum dans des roches de l’Ordovicien
(-460 MA) ; les Glomeromycota étaient donc présents lors des premiers stades de colonisation
des terres émergées par les plantes.

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association des mycologues francophones de belgique

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Le rôle vital des mycorhizes. Marc-André Sélosse

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Des associations de champignons utiles aux plantes cultivées. Exposé de Marc-André Sélosse. Paysages in Marciac, 29 juillet 2014, dans le cadre de la journée "Agroécologie".

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Au microscope, une mycorhize de truffe ressemble à une sorte de manchon qui recouvre les radicelles. Des filaments (le mycelium) se développent en surface lui donnant un aspect plus ou moins chevelu en fonction de l'espèce de truffe. A partir d'avril, des petites sphères, les primordia (des "embryons" de truffes), se forment sur le mycelium.

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Un protocole de coloration et d'observation réalisable durant une séance 

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Un protocole de coloration et d'observation réalisable durant une séance 

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association des mycologues francophones de belgique

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Mise en évidence des endomycorhizes et coloration d'une exomycorhize (M. Lecomte)

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Page de mise en évidence des endomycorhizes et coloration d'une exomycorhize (M. Lecomte)

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Plant fungal interactions(extrait de STRUCTURE OF PLANTS AND FUNGIEdited by: Zoltán Kristóf)

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Plant fungal interactions(extrait de STRUCTURE OF PLANTS AND FUNGIEdited by: Zoltán Kristóf)

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Most land plants live in mutualistic symbiosis with fungi in their roots: this structural, functional unit is called mycorrhiza. Mycorrhizae are "dual organs of absorption formed when symbiotic fungi inhabit healthy absorbing organs (roots, rhizomes or thalli) of most terrestrial plants and many aquatics and epiphytes." (Trappe). Different types of mycorrhizae can be distinguished according to the plant and fungal partners and structural characteristics. Important distinctions are whether the hyphae colonizing the plant grow intracellularly (endomycorrhizae) or only intercellularly in the plant tissue (ectomycorrhizae) or both (ectendomycorrhizae). The most common types are arbuscular mycorrhizae (AM) and ectomycorrhizae (ECM).

ECM are formed with fungi belonging to Asco- and Basidiomycota or a few zygomycetes, many of which produce macroscopic sporocarps. ECM plants are mostly woody plants, trees and shrubs. ECM have three main functional-anatomical parts: (i) special intraradical hyphal structures termed the Hartig-net formed in the intercellular spaces, (ii) the fungal mantle covering the root surface and (iii) the hyphal structures emanating from the mantle surface (e.g. cystidia, hyphae, rhizomorphs).

Two types of Hartig-net are distinguished. The cortical Hartig-net surrounds some layers of cortical cells and occurs in most gymnosperm and many angiosperm ECM plants. The epidermal Hartig-net surrounds radially elongated epidermal cells and occurs in most angiosperm ECM plant. As discussed above, two main types are distinguished based on the anatomy of the hyphal mantle. The hyphal organization can be detected in plectenchymatic mantles, whereas the cellular organization is characteristic of pseudoparenchymatic mantles. The main function of emanating hyphae is nutrient uptake from the soil. The hyphae can form rhizomophs, some can have differentiated anatomy, i.e. they have central hyphae with a big lumen and partially or completely disappeared septa which features make the nutrient transport more effective.

The most prevalent mycorrhiza type is the arbuscular mycorrhiza (AM). There are AM forming plants in all main terrestrial plant groups, on the other hand, all AM fungi exclusively belong to the phylum Glomeromycota. These fungi are obligate biotrophic endocellular symbionts. Their name refers to the special, multi-branched intracellular structure, the arbusculum resembling a small tree. Because of the high density of fine branches on the arbuscules, the surface of the plant cell membrane is multiplied, owing to a special membrane (periarbuscular membrane, PAM) that surrouns the arbuscules and contains special transporters and aquaporins etc. Arbuscules are ephemeral structures, they function for a couple of days,collapse and new arbuscules arise.

Prior to the colonization of the roots, the plant and fungal partners stimulate each other and their mutual recognition plays a crucial role in the success of the establishment of the interaction. The roots excrete strigolactons which stimulate the growth and branching of AMF hyphae and also the germination of AMF chlamydospores. The fungi produce "myc-factors" (lipochitooligosaccharides) which initiate processes necessary for the successful colonization in the plants. The hyphae run on the surface of the roots and develop a swollen structure (appressorium or hyphopodium) from which a hypha grows into the root. The plant cells undergo a complete reorganization when the AMF hypha enters and grows through the cell, this special organization is called the pre-penetration apparatus (PPA). The endoplasmic reticulum (ER) forms a tube like structure which assigns the direction of the hyphal growth. The plant cell nucleus also moves to the penetration site and migrates in front of the growing hyphae through the cell. The intracellular growth of the hyphae needs continuous membrane development, so there is an intensive production of vesicules fusing into the plant cell membrane surrounding the hyphae. This process is controlled by the exocytosis regulation.

The arbuscules, albeit different, show several similarities with the intracellular haustoria of endocellular biotrophic pathogens. The AMF could also develop structures named vesicles in the roots, mainly in the intercellular spaces. The main function of these vesicles is storage. Their appearance could be seasonal and some AMF species do not form vesicles at all. Two main types of AM anatomy can be distinguished, of course, with several intermediate forms as well.

In the Arum-type the fungal hyphae grow intercellularly and well-developed arbuscules are formed on branches entering the neighboring cells. In the Paris-type the hyphae grow intracellularly, develop hyphal coils in some cortical cells and smaller arbuscules develop on these coils. Both the fungal and the plant partner influence the type developed.

Endophytic fungi spend at least one phase of their life cycle colonizing plant tissues inter- or intracellularly causing no symptoms of tissue damage. This definition is not a phylogenetic term, endophytic fungi can thus be found in several fungal groups. The best known endophytes (C-endophytes) belong to the family Clavicipitaceae (ergot family, Pezizomycotina, Ascomycota) and colonize aboveground tissues of grasses. The rare intercalar growing of hyphae was found in these endophytes. Fungal endophytes can be grouped according to several aspects, e.g. plant tissues colonized, systemic, non-systemic spread in plant. A form-group of root-colonizing endophytic fungi is the so called dark septate endophytes (DSE) that belong to a few orders of the phylum Ascomycota. DSE fungi are septate and generally have melanized hyphae that colonize the cortical cells and intercellular regions of roots and form a densely septated intracellular structure called microsclerotia. Although C-endophytes have been intensively studied, our general knowledge on the function and diversity of endophytes is limited especially if compared to some types of mycorrhizae.

Plant pathogenic fungi are spread through all fungal groups and their interaction with plants is diverse, with few common structural characteristics. Biotrophic pathogens need living host cells/tissues to exhaust while nectrotrophic pathogens first kill the host tissues to be able to take the nutrients from the host. Accordingly, there are fundamental differences between the molecular mechanisms, possible defense reactions of those two types. E.g. programmed cell death (PCD), which helps necrotrophic fungi, could protect the spread of biotrophic pathogens.

The fungal binding on the host surface is a fundamental step of the successful infection. The chemical and physical characteristics of this surface have fundamental effects on the adhesion and germination of fungal propagules on the plant, e.g. hydrophobic surfaces, like the outermost cuticle layer of the plants, could induce spore germination. Similarly to AMF, several plant pathogenic fungi develop appressoria at the entry points. Plant pathogenic fungi can have different mechanisms to enter the plant. Pressure is the main driving force of the entry of the rice pathogen Magnaporthe grisea. The changes of the wall and chemical content of the appressorium of the fungus induce osmotic water influx which produces enormous pressure pushing the hypha across the plant cell wall. Other pathogens use enzymes or enzymes and pressure together to enter the host plants. In stem rust, the hyphae grow on the leaf surface till they reach a guard cell of a stoma and the growing on the guard cell induces the turning downwards of the hyphae which therefore grows through the stoma and colonize the plant. Biotrophic endocellular parasites can develop special intracellular structures called haustoria through which they take the nutrients up from host cells.

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Most land plants live in mutualistic symbiosis with fungi in their roots: this structural, functional unit is called mycorrhiza. Mycorrhizae are "dual organs of absorption formed when symbiotic fungi inhabit healthy absorbing organs (roots, rhizomes or thalli) of most terrestrial plants and many aquatics and epiphytes." (Trappe).

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Alix Helme-Guizon et Marc-André Selosse

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Ectomycorhize formée de l'association entre une racine de Pinus radiata et de Suillus brevipes -Brundrett MC. 2008. Mycorrhizal Associations: The Web Resource. http://mycorrhizas.info/ecm.html

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Rôle des mycorhizes dans la nutrition hydrominérale des plantes -sujet de BAC 2015-

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Rôle des mycorhizes dans la nutrition hydrominérale des plantes -sujet de BAC 2015-

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Permaculture- Hervé Coves nous parle des mycorhizes 

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Permaculture- Hervé Coves nous parle des mycorhizes 