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35 results for “plant induced defense”
Data from: Species-specific plant–soil feedbacks alter herbivore-induced gene expression and defense chemistry in Plantago lanceolata
Plants actively interact with antagonists and beneficial organisms occurring in the above- and belowground domains of terrestrial ecosystems. In the past decade, studies have focused on the role of plant–soil feedbacks (PSF) in a broad range of ecological processes. However, PSF and its legacy effects on plant defense traits, such as induction of defense-related genes and production of defensive secondary metabolites, have not received much attention. Here, we study soil legacy effects created by twelve common grassland plant species on the induction of four defense-related genes, involved in jasmonic acid signaling, related to chewing herbivore defense (LOX2, PPO7), and in salicylic acid signaling, related to pathogen defense (PR1 and PR2) in Plantago lanceolata in response to aboveground herbivory by Mamestra brassicae. We also assessed soil legacy and herbivory effects on the production of terpenoid defense compounds (the iridoid glycosides aucubin and catalpol) in P. lanceolata. Our results show that both soil legacy and herbivory influence phenotypes of P. lanceolata in terms of induction of Pl PPO7 and Pl LOX2, whereas the expression of Pl PR1 and Pl PR2-1 is not affected by soil legacies, nor by herbivory. We also find species-specific soil legacy effects on the production of aucubin. Moreover, P. lanceolata accumulates more catalpol when they are grown in soils conditioned by grass species. Our study highlights that PSF can influence aboveground plant–insect interactions through the impacts on plant defense traits and suggests that aboveground plant defense responses can be determined, at least partly, by plant-specific legacy effects induced by belowground organisms.
Data from: Constitutive and herbivore-induced plant defenses regulate herbivore population growth
1. Induced plant defenses regulated by the phytohormones jasmonic acid and salicylic acid are predicted to influence herbivore population dynamics, in part because they can operate in a density-dependent manner. While there is ample evidence that induced plant responses affect individual performance and growth of herbivores, whether they scale-up to regulate herbivore population dynamics is still unclear. 2. We evaluated the consequences of variation in plant defenses and herbivore density on herbivore development, reproduction and density-dependent population growth. We investigated potential mechanisms affecting the strength of herbivore density-dependent processes by manipulating jasmonate expression, quantifying plant defensive traits (phytohormones jasmonic acid and salicylic acid and serine proteinase inhibitors) and adding aphids (Macrosiphum euphorbiae) at different densities to plants to simulate different initial population density and herbivore load. We manipulated jasmonate defenses by using genetically modified lines of tomato plants (Solanum lycopersicum) with elevated or suppressed jasmonate-dependent defenses. Jasmonate-insensitive plants cannot induce the jasmonic acid pathway, while jasmonate-overexpressing plants constitutively express jasmonate-dependent defenses. 3. We found that jasmonate defenses provided resistance against aphids and influenced density-dependent processes. Jasmonate-overexpressing plants reduced aphid reproduction, prolonged developmental time, dampened aphid populations across all aphid densities, and caused density-independent aphid population growth. Aphid feeding on jasmonate-overexpressing plants did not activate the salicylic acid pathway, thus on this plant line jasmonate defenses affected aphid responses. In contrast, jasmonate-insensitive plants increased aphid reproduction, shortened the developmental time, reduced population growth only at high initial densities, and promoted strong negative density-dependent population growth. Aphid feeding on jasmonate-insensitive plants did not induce jasmonate-dependent defenses, but induced the salicylic acid pathway in a density-dependent manner, which resulted in negative density-dependent aphid population growth. 4. Aphid feeding on jasmonate-insensitive and overexpressing plant differentially activated the salicylate pathway, revealing a negative crosstalk between the defensive phytohormones jasmonic acid and salicylic acid. By muting or enhancing jasmonate-mediated responses and quantifying salicylic acid phytohormone induction, we demonstrated that plant defenses are a key factor driving not only the performance, but also the density dependence processes of herbivore populations.
Data from: Integration of two herbivore-induced plant volatiles results in synergistic effects on plant defense and resistance
Plants can use induced volatiles to detect herbivore‐ and pathogen‐attacked neighbors and prime their defenses. Several individual volatile priming cues have been identified, but whether plants are able to integrate multiple cues from stress‐related volatile blends remains poorly understood. Here, we investigated how maize plants respond to two herbivore‐induced volatile priming cues with complementary information content, the green leaf volatile (Z)‐3‐hexenyl acetate (HAC) and the aromatic volatile indole. In the absence of herbivory, HAC directly induced defense gene expression, while indole had no effect. Upon induction by simulated herbivory, both volatiles increased jasmonate signaling, defense gene expression and defensive secondary metabolite production and increased plant resistance. Defenses and resistance in dual‐volatile exposed plants were more strongly induced than in plants exposed to single volatiles. Induced defense levels in dual volatile‐exposed plants were significantly higher than predicted from the added effects of the individual volatiles, with the exception of induced plant volatile production, which showed no increase upon dual‐exposure relative to single exposure. Thus, plants can integrate different volatile cues into strong and specific responses that promote herbivore defense induction and resistance. Integrating multiple volatiles may be beneficial, as volatile blends are more reliable indicators of future stress than single cues.
Temperature differentially influences the capacity of Trichoderma species to induce plant defense responses in tomato against insect pests
<p>Species of the ecological opportunistic, avirulent fungus, <em>Trichoderma</em> are widely used in agriculture for their ability to protect crops from the attack of pathogenic fungi and for plant growth promotion activity. Recently, it has been shown that they may also have complementary properties that enhance plant defense barriers against insects. However, the use of these fungi is somewhat undermined by their variable level of biocontrol activity, which is influenced by environmental conditions. Understanding the source of this variability is essential for its profitable and wide use in plant protection. Here, we focus on the impact of temperature on <em>Trichoderma afroharzianum</em> T22, <em>Trichoderma atroviride</em> P1, and the defense response induced in tomato by insects. The <em>in vitro</em> development of these two strains was differentially influenced by temperature, and the observed pattern was consistent with temperature-dependent levels of resistance induced by them in tomato plants against the aphid, <em>Macrosiphum euphorbiae</em>, and the noctuid moth, <em>Spodoptera littoralis</em>. Tomato plants treated with <em>T. afroharzianum</em> T22 exhibited enhanced resistance toward both insect pests at 25°C, while <em>T. atroviride</em> P1 proved to be more effective at 20°C. The comparison of plant transcriptomic profiles generated by the two <em>Trichoderma</em> species allowed the identification of specific defense genes involved in the observed response, and a selected group was used to assess, by real-time quantitative reverse transcription PCR (qRT-PCR), the differential gene expression in <em>Trichoderma</em>-treated tomato plants subjected to the two temperature regimens that significantly affected fungal biological performance. These results will help pave the way toward a rational selection of the most suitable <em>Trichoderma</em> isolates for field applications, in order to best face the challenges imposed by local environmental conditions and by extreme climatic shifts due to global warming.</p>
Phenotypic plasticity in plant defense across life stages: inducibility, transgenerational induction, and transgenerational priming in wild radish
As they develop, many plants deploy shifts in anti-herbivore defense allocation due to changing costs and benefits of their defensive traits. Plant defenses are known to be primed or directly induced by herbivore damage within generations, and across generations by long-lasting epigenetic mechanisms. However, little is known about the ontogenetic trajectories of epigenetically inducible defensive traits across generations and their consequences. To help fill this knowledge gap, we conducted a multigenerational experiment to determine whether defense induction in wild radish plants was reflected in chromatin modifications (DNA methylation); we then examined ontogenetic trajectories (seedlings to reproductive plants) of current and transgenerational plasticity in anti-herbivore chemical (glucosinolates) and physical (trichomes) defenses in this species. Herbivory triggered genome methylation both in targeted plants and their offspring. Within one generation, both defenses were highly inducible at the seedling stage but only marginally or non-inducible in reproductive plants. Across generations, herbivory experienced by mother plants caused strong direct induction of physical defenses in their progeny, with effects lasting from seedling to reproductive stages. For chemical defenses, however, this transgenerational induction was evident only in adults. Transgenerational priming was observed in physical defenses both for seedlings and adult plants. Our results show that transgenerational induction and priming in response to herbivore offense differ for physical and chemical defense and change across plant life stages.
Data from: Constitutive and herbivore-induced plant defenses regulate herbivore population growth
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Olfactory perception of herbivore‐induced plant volatiles elicits counter‐defenses in larvae of the tobacco cutworm
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Data from: Integration of two herbivore-induced plant volatiles results in synergistic effects on plant defense and resistance
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Phenotypic plasticity in plant defense across life stages: inducibility, transgenerational induction, and transgenerational priming in wild radish
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Data from: Combined effects of mutualistic rhizobacteria counteract virus-induced suppression of indirect plant defenses in soybean
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Data from: Species-specific plant–soil feedbacks alter herbivore-induced gene expression and defense chemistry in Plantago lanceolata
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Allyl-isothiocyanate treatment induces a complex transcriptional reprogramming including heat stress, oxidative stress and plant defense responses in Arabidopsis thaliana
GEO Series GSE81634. Arabidopsis thaliana. 12 samples. Type: Expression profiling by array.
DEX Induced effector RiNLE1 expression inhibited plant defense genes expression
GEO Series GSE155682. Medicago truncatula. 6 samples. Type: Expression profiling by high throughput sequencing.
Exogenous bacterial cellulose induces plant tissue regeneration through the regulation of cytokinin and defense networks
GEO Series GSE270487. Arabidopsis thaliana. 24 samples. Type: Expression profiling by high throughput sequencing.
Non-self induced AIG2A and AIG2B genes repress two chemical defense pathways to modulate plant immunity
GEO Series GSE196599. Arabidopsis thaliana. 12 samples. Type: Expression profiling by high throughput sequencing.
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