Long-distance signalling in plant defence.

By Martin Heil, J. Ton. Trends in Plant Science, 2008

622 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Insect Science, Plant Science

View Paper: https://www.semanticscholar.org/paper/a094048733cd02fa00fcfc81d9a480f3d1db3b7f

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In Ecology, Evolution, Behavior and Systematics

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Citations in the corpus

Whitefly infestation of pepper plants elicits defence responses against bacterial pathogens in leaves and roots and changes the below‐ground microflora (2011, background): “This long-distance signalling can be mediated by classical hormones such as JA, SA and their derivatives, whichmove through the vascular system of the plant, but plants may also use volatile signals to achieve a faster signalling or to circumvent vascular restrictions (Heil & Ton 2008).”
Rhizobacteria-induced systemic resistance (2009, background): “It is likely that MeSA can travel by both air and vascular transport to mediate long-distance induction of resistance in distal leaves that lack a direct vascular connection to the attacked leaf and in neighbouring plants (Heil and Ton, 2008).”
The ecology of herbivore‐induced silicon defences in grasses (2016, background): “…a signalling cascade which triggers a defence response, including the production of the so-called wound hormones [jasmonic acid (JA) and salicylic acid], changes in gene expression and increases in secondary metabolites (Heil & Ton 2008; Bonaventure, VanDoorn & Baldwin 2011; Stam et al. 2014).”
Costs and benefits of induced resistance to herbivores and pathogens in plants (2010, background): “VOCs even serve as systemic signals within plants and hence function as plant hormones [43, 69–71, 153], which may benefit plants in ways unrelated to plant defence.”
Plastic defence expression in plants (2010, background): “These observations suggests a two-step regulatory system in which self-priming by airborne signals prepares the systemic tissues for a rapid response, whereas full activation of resistance requires confirmation by a vascular long-distance signal or arrival of the plant enemy (Heil and Ton 2008).”
Deciphering Chemical Language of Plant Communication (2016, background): “2013), recruit predators and parasitoids (Heil 2008) and mediate plant–plant communication (Heil and Ton 2008).”
Insect attraction to synthetic herbivore‐induced plant volatile‐treated field crops (2011, positive): “Tel: +61 2 6365 7697; fax: +61 2 6365 57590; e-mail: mrsimpson@csu.edu.au use these volatile cues for locating hosts or prey (Dicke et al., 1990; Pare & Tumlinson, 1999; Hilker & Meiners, 2006; Heil & Ton, 2008; Dicke, 2009).”
Variation in natural plant products and the attraction of bodyguards involved in indirect plant defense (2010, background): “In addition, MeSA acts as a long-distance signal within a plant, leading to systemic acquired resistance (SAR) (Shulaev et al. 1997; Ryu et al. 2004; Park et al. 2007; Heil and Ton 2008).”
Root-emitted volatile organic compounds: can they mediate belowground plant-plant interactions? (2016, background): “…Arimura et al. 2000a; Sugimoto et al. 2014) or can prime their defences against pests (Engelberth et al. 2004; Ton et al. 2006; Heil and Kost 2006), suggesting that VOCs play key roles in mediating within- and between-plant signalling aboveground (Heil and Ton 2008; Heil and Karban 2010) (Fig.”
Attraction of the stink bug egg parasitoid Telenomus podisi to defence signals from soybean activated by treatment with cis‐jasmone (2009, background): “…blend for the attraction of the natural enemy, and to understand how T. podisi achieves this specific response to soybean HIPVs from different varieties in the context of a complex volatile blend (D’Alessandro et al., 2006; Maffei et al., 2007; Heil & Ton, 2008; Heil, 2008; van Dam & Poppy, 2008).”
Multitrophic interactions below and above ground: en route to the next level (2011, background): “…DEFENCES Herbivore-induced responses can trigger the production of several signalling molecules that are transported throughout the plant and then cause increases in the content of defensive compounds sensu strictu in as yet undamaged parts of the plant (Staswick & Tiryaki 2004; Heil & Ton 2008).”
Plant volatiles cause direct, induced and associational resistance in common bean to the fungal pathogen Colletotrichum lindemuthianum (2015, background): “Indeed, the systemic induction of resistance after a local attack has been discussed as a main ‘raison d0être’ of the induced VOCs because this effect benefits the emitter plant (Farmer 2001; Heil & Ton 2008; Heil & Karban 2010).”
Priming of induced plant defense responses (2009, background): “The identity of the long-distance signal(s) that travel(s) from the site of primary infection to the remote parts of the plant to inducePR gene expression and SAR, however, is still unclear (Conrath, 2006; Durrant and Dong, 2004, Grant and Lamb, 2006; Heil and Ton, 2008; Ryals et al., 1996).”
Defensive plant responses induced by Nesidiocoris tenuis (Hemiptera: Miridae) on tomato plants (2015, background): “…volatiles (so-called herbivore-induced plant volatiles or HIPVs) that play a double role in defense by priming both distal parts of the same plant and its neighbors (Frost et al. 2008) and attracting secondary consumers such as parasitoids and predators (Heil and Ton 2008) or repelling herbivores.”