The arbuscular mycorrhizal symbiosis: a molecular review of the fungal dimension
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Abstract:
Mycorrhizal associations vary widely in structure and function, but the most common interaction is the arbuscular mycorrhizal (AM) symbiosis. This interaction is formed between the roots of over 80% of all terrestrial plant species and Zygomycete fungi from the Order Glomales. These fungi are termed AM fungi and are obligate symbionts which form endomycorrhizal symbioses. This symbiosis confers benefits directly to the host plant's growth and development through the acquisition of P and other mineral nutrients from the soil by the fungus. In addition, they may also enhance the plant's resistance to biotic and abiotic stresses. These beneficial effects of the AM symbiosis occur as a result of a complex molecular dialogue between the two symbiotic partners. Identifying the molecules involved in the dialogue is a prerequisite for a greater understanding of the symbiosis. Ongoing research attempts to understand the underlying dialogue and concomitant molecular changes occurring in the plant and the fungus during the establishment of a functioning AM symbiosis. This paper focuses on the molecular approaches being used to study AM fungal genes being expressed in the symbiotic and asymbiotic stages of its lifecycle. In addition, the importance of studying these fungi, in relation to understanding plant processes, is discussed briefly.Keywords:
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The well-known fig–fig wasp and yucca–yucca moth mutualisms are classic examples of obligate mutualisms that have been shaped by millions of years of coevolution. Pollination systems involving obligate seed parasites are only expected to evolve under rare circumstances where their positive effects are not swamped by abundant co-pollinators and heavy costs resulting from seed destruction. Here, we show that, in Phyllantheae, specialization to pollination by Epicephala moths evolved at least five times, involving more than 500 Phyllantheae species in this obligate association. Active pollination behaviour evolved once in Epicephala , 10–20 Myr after the initial divergence of their host plants. The pollinating Epicephala moths thus radiated on an already-diverged host lineage and successively colonized new Phyllantheae hosts, thereby giving rise to repeated independent evolution of the specialized pollination system in Phyllantheae. The present evolutionary success of this association rests entirely upon active pollination by Epicephala , making this a distinct example of an evolutionary key innovation. Overall, our findings provide a clear empirical demonstration of how a combination of evolutionary innovation and partner shifts facilitates the spread of mutualism in a coevolving species interaction.
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Rhizophagus irregularis
Manihot esculenta
Glomeromycota
Arbuscular mycorrhizal fungi
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Summary Recent years have seen fascinating contributions to our understanding of the molecular dialogue between fungi and plants entering into arbuscular mycorrhizal (AM) symbioses. Attention has shifted from descriptions of physiological and cellular events to molecular genetics and modern chemical diagnostics. Genes, signal transduction pathways and the chemical structures of components relevant to the symbiosis have been defined. This review examines our current knowledge of signals and mechanisms involved in the establishment of AM symbioses. Contents Summary 35 I. Introduction 35 II. Presymbiotic dialogue – recognition and anticipation 36 III. Early symbiotic phase – contact and penetration 39 IV. Mature symbiotic phase – haustoria and mineral nutrition 41 V. Concluding remarks 43 Acknowledgements 43 References 43
Glomeromycota
Arbuscular mycorrhizal fungi
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Glomeromycota
Arbuscular mycorrhizal fungi
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Glomeromycota
Mutualism
Arbuscular mycorrhiza
Arbuscular mycorrhizal fungi
Plant Roots
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Mycorrhizal Fungi
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Arbuscular mycorrhizal fungi
Glomeromycota
Mycorrhizal Fungi
Terrestrial plant
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Mutualism is a fundamental building block of ecological communities and an important driver of biotic evolution. Classic theory suggests that a pairwise two‐species obligate mutualism is fragile, with a large perturbation potentially driving both mutualist populations into extinction. In nature, however, there are many cases of pairwise obligate mutualism. Such pairwise obligate mutualisms are occasionally associated with additional interactions with facultative mutualists. Here, we use a mathematical model to show that when a two‐species obligate mutualism has a single additional link to a third facultative mutualist, the obligate mutualism can become permanently persistent. In the model, a facultative mutualist interacts with one of two inter‐dependent obligate mutualists, and the facultative mutualist enhances the persistence not only of its directly interacting obligate mutualist, but also that of the other obligate mutualist indirectly, enabling the permanent coexistence of the three mutualist species. The effect of the facultative mutualist is strong; it can allow a three‐species permanent coexistence even when two obligate mutualists by themselves are not sustainable (i.e. not locally stable). These results suggest that facultative mutualists can play a pivotal role for the persistence of obligate mutualisms, and contribute to a better understanding on the mechanisms maintaining more complex mutualistic networks of multiple species.
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See also the Commentary by Rosendahl
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