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Mycorrhiza-induced resistance: more than the sum of its parts?

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TLDR
This opinion article proposes that MIR is a cumulative effect of direct plant responses to mycorrhizal infection and indirect immune responses to ISR-eliciting rhizobacteria in the myCorrhizosphere.
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This article is published in Trends in Plant Science.The article was published on 2013-10-01 and is currently open access. It has received 359 citations till now. The article focuses on the topics: Systemic acquired resistance & Mycorrhizosphere.

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Induced systemic resistance by beneficial microbes

TL;DR: This review focuses on molecular processes at the interface between plant roots and ISR-eliciting mutualists, and on the progress in the understanding of ISR signaling and systemic defense priming.
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Priming for Enhanced Defense

TL;DR: This review covers recent advances in disclosing molecular mechanisms of priming, which include elevated levels of pattern-recognition receptors and dormant signaling enzymes, transcription factor HsfB1 activity, and alterations in chromatin state.
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Defense Priming: An Adaptive Part of Induced Resistance.

TL;DR: Priming is an adaptive strategy that improves the defensive capacity of plants and can be durable and maintained throughout the plant's life cycle and can even be transmitted to subsequent generations, therefore representing a type of plant immunological memory.
Journal ArticleDOI

Plant root-microbe communication in shaping root microbiomes.

TL;DR: Current knowledge on the formation and maintenance of root-associated microbial communities and plant– microbe interactions with a particular emphasis on the effect of microbe–microbe interactions on the shape of microbial communities at the root surface are discussed.
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Signaling in the Rhizosphere

TL;DR: The shaping of the rhizomicrobiome is discussed and which aspects can be considered signaling are defined and divided into three categories: between microbes, from plants to microorganisms, and from microorganisms to plants.
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Journal ArticleDOI

Plant-growth-promoting rhizobacteria.

TL;DR: This review restricts itself to bacteria that are derived from and exert this effect on the root and generally designated as PGPR (plant-growth-promoting rhizobacteria), which can be direct or indirect in their effects on plant growth.
Journal ArticleDOI

The Role of Root Exudates in Rhizosphere Interactions with Plants and Other Organisms

TL;DR: Recent advances in elucidating the role of root exudates in interactions between plant roots and other plants, microbes, and nematodes present in the rhizosphere are described.
Journal ArticleDOI

QUORUM SENSING: Cell-to-Cell Communication in Bacteria

TL;DR: This review focuses on the architectures of bacterial chemical communication networks; how chemical information is integrated, processed, and transduced to control gene expression; how intra- and interspecies cell-cell communication is accomplished; and the intriguing possibility of prokaryote-eukaryote cross-communication.
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The rhizosphere microbiome and plant health

TL;DR: In this article, the authors discuss evidence that upon pathogen or insect attack, plants are able to recruit protective microorganisms, and enhance microbial activity to suppress pathogens in the rhizosphere.
Journal ArticleDOI

A Renaissance of Elicitors: Perception of Microbe-Associated Molecular Patterns and Danger Signals by Pattern-Recognition Receptors

TL;DR: Current evidence indicates that MAMPs, DAMPs, and effectors are all perceived as danger signals and induce a stereotypic defense response, and the importance of MAMP/PRR signaling for plant immunity is highlighted.
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Frequently Asked Questions (18)
Q1. What contributions have the authors mentioned in the paper "Mycorrhiza-induced resistance: more than the sum of its parts?" ?

This ‘ mycorrhiza-induced resistance ’ ( MIR ) provides systemic protection against a wide range of attackers and shares characteristics with systemic acquired resistance ( SAR ) after pathogen infection and induced systemic resistance ( ISR ) following root colonisation by non-pathogenic rhizobacteria. In this opinion article, the authors present a novel model of MIR that integrates different aspects of the induced resistance phenomenon. The authors propose that MIR is a cumulative effect of direct plant responses to mycorrhizal infection and indirect immune responses to ISR-eliciting rhizobacteria in the mycorrhizosphere. 

The consequences of the mycorrhizosphere effect, including recruitment of PGPRs, may not only boost nutrient mobilisation by AMF but could also provide non-nutritional benefits, such as disease suppression via antibiosis and/or competitive exclusion. 

Well-known examples of defenceeliciting MAMPs from bacteria are rhamnolipids, the elongation factor Tu, flagellin, and cell-wall lipopolysaccharides [53]. 

Recognition of MAMPs by pattern-recognition receptors elicits a series of signalling cascades resulting in enhanced production of the plant defence hormone SA and expression of MAMP-triggered immunity [21]. 

Estimates suggest plants can exude up to 40% of their photosynthates from roots, representing a rich source of energy for soil microbes [15]. 

increased densities of selected rhizobacteria in the mycorrhizosphere have the potential to suppress pests and diseases in systemic plant tissues through priming of inducible defences. 

The spatially confined structure of the mycorrhizosphere allows rhizobacterial strains to reach exceptionally high cell densities [5]. 

A global inventory of microbial diversity through 16S RNA gene sequence analysis, coupled to temporal profiling of metabolites in mycorrhizal root exudates would be an alternative strategy to decipher the contribution of mycorrhizosphere bacteria in MIR. 

Involvement of candidate plant metabolites as regulators of resistance-inducing activities by mycorrhizosphere bacteria can be verified by genetic manipulation of the corresponding biosynthetic pathways in the host plant. 

Because ABA can suppress SA-dependent defences against biotrophic pathogens [36,37], it is plausible that AMF stimulate ABA production in the roots to promote theirTable 1. 

The enhanced microbial activity surrounding mycorrhizal roots compared with non-mycorrhizal roots is called the ‘mycorrhizosphere effect’ [5]. 

Rothamsted Research receives grant aid from the Biotechnology and Biological Science Research Council of the U.K. S.C.M.W.’s research is supported by the Dutch Technology Foundation STW (VIDI grant no. 

the potential for mycorrhizosphere bacteria to elicit ISR is not only determined by their presence, but also depends on their metabolic activity in relation to chemical signals from mycorrhizal root exudates, their cell density, and the presence of competing microbes. 

Research on plant–mycorrhiza interactions has mostly focussed on the physiology of nutrient-for-carbon exchange and plant signal-transduction pathways controlling the interaction. 

It has been estimated that 80% of plant species retain these ancient arbuscular mycorrhizal associations [1], illustrating the importance of this mutualism to both partners. 

In non-mycorrhizal Arabidopsis, mutation in the malate transporter gene ALMT1 affects recruitment of ISR-eliciting Bacillus subtilis FB17 after treatment of the leaves with MAMPs [48], indicating thatlittle was known about their additional beneficial role in the rhizosphere, despite the fact that non-hosts for parasitic Orobanchaceae produce strigolactones profusely. 

This autoinduction process, known as quorum sensing (QS), allows bacteria to adjust community gene expression in accordance with their environment [54]. 

It is thus possible that jasmonates function as complementary long-distance signals of MIR, which may be the result of systemic signalling processes similar to autoregulation of nodulation during rhizobia–legume interactions [65].