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An untargeted global metabolomic analysis reveals the biochemical changes underlying basal resistance and priming in Solanum lycopersicum, and identifies 1‐methyltryptophan as a metabolite involved in plant responses to Botrytis cinerea and Pseudomonas syringae

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Metabolomics — the link between genotypes and phenotypes
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Accumulation of gentisic acid as associated with systemic infections but not with the hypersensitive response in plant-pathogen interactions
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Quercetin-induced H2O2 mediates the pathogen resistance against Pseudomonas syringae pv. Tomato DC3000 in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.biocontrol.2010.05.012openalex-snapshot
Chitosan-induced ethylene-independent resistance does not reduce crop yield in bean
inferredcites →https://doi.org/10.1016/j.biotechadv.2011.01.003openalex-snapshot
Polyamines: Natural and engineered abiotic and biotic stress tolerance in plants
inferredcites →https://doi.org/10.1016/j.celrep.2013.03.030openalex-snapshot
A Feedback Regulatory Loop between G3P and Lipid Transfer Proteins DIR1 and AZI1 Mediates Azelaic-Acid-Induced Systemic Immunity
inferredcites →https://doi.org/10.1016/j.chroma.2012.08.047openalex-snapshot
Ultra-high performance liquid chromatography coupled to high resolution Orbitrap mass spectrometry for metabolomic profiling of the endogenous phytohormonal status of the tomato plant
inferredcites →https://doi.org/10.1016/j.envexpbot.2011.06.003openalex-snapshot
Identification of defence metabolites in tomato plants infected by the bacterial pathogen Pseudomonas syringae
inferredcites →https://doi.org/10.1016/j.jplph.2010.07.028openalex-snapshot
Priming for JA-dependent defenses using hexanoic acid is an effective mechanism to protect Arabidopsis against B. cinerea
inferredcites →https://doi.org/10.1016/j.jplph.2014.11.004openalex-snapshot
Role of dioxygenase α-DOX2 and SA in basal response and in hexanoic acid-induced resistance of tomato (Solanum lycopersicum) plants against Botrytis cinerea
inferredcites →https://doi.org/10.1016/j.pbi.2007.06.002openalex-snapshot
Priming for stress resistance: from the lab to the field
inferredcites →https://doi.org/10.1016/j.pbi.2009.05.011openalex-snapshot
Plants under attack: systemic signals in defence
inferredcites →https://doi.org/10.1016/j.pbi.2013.06.011openalex-snapshot
Fatty acids and early detection of pathogens
inferredcites →https://doi.org/10.1016/j.plaphy.2012.10.004openalex-snapshot
Identification of indole-3-carboxylic acid as mediator of priming against Plectosphaerella cucumerina
inferredcites →https://doi.org/10.1016/j.tplants.2006.03.005openalex-snapshot
Licensed to kill: the lifestyle of a necrotrophic plant pathogen
inferredcites →https://doi.org/10.1016/s0065-2296(09)51009-9openalex-snapshot
Chapter 9 Priming of Induced Plant Defense Responses
inferredcites →https://doi.org/10.1016/s1360-1385(02)02244-6openalex-snapshot
Priming in plant–pathogen interactions
inferredcites →https://doi.org/10.1016/s1360-1385(97)01176-xopenalex-snapshot
A new view of lignification
inferredcites →https://doi.org/10.1023/a:1008760518772openalex-snapshot
Induced Disease Resistance in Plants by Chemicals
inferredcites →https://doi.org/10.1023/a:1013713905833openalex-snapshot
Metabolomics – the link between genotypes and phenotypes
inferredcites →https://doi.org/10.1038/35081178openalex-snapshot
Natural products and plant disease resistance
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Constitutive expression of ETHYLENE‐RESPONSE‐FACTOR1 in Arabidopsis confers resistance to several necrotrophic fungi
inferredcites →https://doi.org/10.1073/pnas.0802332105openalex-snapshot
COI1 is a critical component of a receptor for jasmonate and the bacterial virulence factor coronatine
inferredcites →https://doi.org/10.1073/pnas.1218872110openalex-snapshot
Cyclophilin 20-3 relays a 12-oxo-phytodienoic acid signal during stress responsive regulation of cellular redox homeostasis
inferredcites →https://doi.org/10.1073/pnas.1305745110openalex-snapshot
Glutathione and tryptophan metabolism are required for Arabidopsis immunity during the hypersensitive response to hemibiotrophs
inferredcites →https://doi.org/10.1073/pnas.1530509100openalex-snapshot
Statistical significance for genomewide studies
inferredcites →https://doi.org/10.1093/aob/mcp259openalex-snapshot
Polyamines: ubiquitous polycations with unique roles in growth and stress responses
inferredcites →https://doi.org/10.1093/aob/mct049openalex-snapshot
The folate precursor para-aminobenzoic acid elicits induced resistance against Cucumber mosaic virus and Xanthomonas axonopodis
inferredcites →https://doi.org/10.1093/mp/ssp104openalex-snapshot
Recent Progress in Deciphering the Biosynthesis of Aspartate-Derived Amino Acids in Plants
inferredcites →https://doi.org/10.1094/mpmi-22-11-1455openalex-snapshot
Hexanoic Acid-Induced Resistance Against Botrytis cinerea in Tomato Plants
inferredcites →https://doi.org/10.1104/pp.010605openalex-snapshot
Abscisic Acid Determines Basal Susceptibility of Tomato to Botrytis cinerea and Suppresses Salicylic Acid-Dependent Signaling Mechanisms
inferredcites →https://doi.org/10.1104/pp.104.051839openalex-snapshot
Possible Roles for Mannitol and Mannitol Dehydrogenase in the Biotrophic Plant PathogenUromyces fabae
inferredcites →https://doi.org/10.1104/pp.106.092627openalex-snapshot
Vitamin B1-Induced Priming Is Dependent on Hydrogen Peroxide and theNPR1Gene in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.099226openalex-snapshot
Resistance to Botrytis cinerea in sitiens, an Abscisic Acid-Deficient Tomato Mutant, Involves Timely Production of Hydrogen Peroxide and Cell Wall Modifications in the Epidermis
inferredcites →https://doi.org/10.1104/pp.107.103374openalex-snapshot
AtNUDT7, a Negative Regulator of Basal Immunity in Arabidopsis, Modulates Two Distinct Defense Response Pathways and Is Involved in Maintaining Redox Homeostasis
inferredcites →https://doi.org/10.1104/pp.111.180224openalex-snapshot
Benzoxazinoid Metabolites Regulate Innate Immunity against Aphids and Fungi in Maize
inferredcites →https://doi.org/10.1104/pp.112.199810openalex-snapshot
ASPARTATE OXIDASE Plays an Important Role in Arabidopsis Stomatal Immunity
inferredcites →https://doi.org/10.1104/pp.112.202846openalex-snapshot
Lipid Profiling of the Arabidopsis Hypersensitive Response Reveals Specific Lipid Peroxidation and Fragmentation Processes: Biogenesis of Pimelic and Azelaic Acid
inferredcites →https://doi.org/10.1104/pp.112.207514openalex-snapshot
Defense Activated by 9-Lipoxygenase-Derived Oxylipins Requires Specific Mitochondrial Proteins
inferredcites →https://doi.org/10.1104/pp.113.4.1177openalex-snapshot
Increased Resistance to Oxidative Stress in Transgenic Plants by Targeting Mannitol Biosynthesis to Chloroplasts
inferredcites →https://doi.org/10.1104/pp.125.2.652openalex-snapshot
The Arabidopsis ISR1 Locus Controlling Rhizobacteria-Mediated Induced Systemic Resistance Is Involved in Ethylene Signaling
inferredcites →https://doi.org/10.1105/tpc.110.082800openalex-snapshot
A Sister Group Contrast Using Untargeted Global Metabolomic Analysis Delineates the Biochemical Regulation Underlying Desiccation Tolerance in Sporobolus stapfianus
inferredcites →https://doi.org/10.1105/tpc.112.098343openalex-snapshot
Novel Plant Immune-Priming Compounds Identified via High-Throughput Chemical Screening Target Salicylic Acid Glucosyltransferases in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.103564openalex-snapshot
Pipecolic Acid, an Endogenous Mediator of Defense Amplification and Priming, Is a Critical Regulator of Inducible Plant Immunity
inferredcites →https://doi.org/10.1105/tpc.113.112839openalex-snapshot
Constitutively Elevated Salicylic Acid Levels Alter Photosynthesis and Oxidative State but Not Growth in Transgenic Populus
inferredcites →https://doi.org/10.1111/j.1364-3703.2005.00311.xopenalex-snapshot
The Pseudomonas syringae phytotoxin coronatine promotes virulence by overcoming salicylic acid‐dependent defences in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-3040.2012.02505.xopenalex-snapshot
Nitric oxide production mediates oligogalacturonide‐triggered immunity and resistance to Botrytis cinerea in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-3059.2008.01891.xopenalex-snapshot
Preventive and post‐infection control of Botrytis cinerea in tomato plants by hexanoic acid
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03299.xopenalex-snapshot
Absence of the endo‐β‐1,4‐glucanases Cel1 and Cel2 reduces susceptibility to Botrytis cinerea in tomato
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03687.xopenalex-snapshot
Extracellular pyridine nucleotides induce PR gene expression and disease resistance in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03912.xopenalex-snapshot
Metabolomic analysis reveals a common pattern of metabolic re‐programming during invasion of three host plant species by Magnaporthe grisea
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04224.xopenalex-snapshot
Tryptophan-derived secondary metabolites in Arabidopsis thaliana confer non-host resistance to necrotrophic Plectosphaerella cucumerina fungi
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04254.xopenalex-snapshot
The metabolic transition during disease following infection of Arabidopsis thaliana by Pseudomonas syringae pv. tomato
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04639.xopenalex-snapshot
Metabolomic approaches reveal that cell wall modifications play a major role in ethylene‐mediated resistance against Botrytis cinerea
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.04920.xopenalex-snapshot
Inducible NAD overproduction in Arabidopsis alters metabolic pools and gene expression correlated with increased salicylate content and resistance to Pst‐AvrRpm1
inferredcites →https://doi.org/10.1111/j.1399-3054.2007.01001.xopenalex-snapshot
Metabolomic technologies and their application to the study of plants and plant–host interactions
inferredcites →https://doi.org/10.1111/j.1467-7652.2009.00439.xopenalex-snapshot
Molecular analysis of menadione‐induced resistance against biotic stress in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1574-6968.2007.00930.xopenalex-snapshot
Botrytis cinerea virulence factors: new insights into a necrotrophic and polyphageous pathogen
inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00763.xopenalex-snapshot
Riboflavin‐induced Priming for Pathogen Defense in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/mpp.12010openalex-snapshot
Hexanoic acid is a resistance inducer that protects tomato plants against P seudomonas syringae by priming the jasmonic acid and salicylic acid pathways
inferredcites →https://doi.org/10.1111/mpp.12112openalex-snapshot
Hexanoic acid protects tomato plants against B otrytis cinerea by priming defence responses and reducing oxidative stress
inferredcites →https://doi.org/10.1111/nph.13032openalex-snapshot
Linking phytochrome to plant immunity: low red : far‐red ratios increase A rabidopsis susceptibility to B otrytis cinerea by reducing the biosynthesis of indolic glucosinolates and camalexin
inferredcites →https://doi.org/10.1111/pce.12122openalex-snapshot
New insights into the regulation of plant immunity by amino acid metabolic pathways
inferredcites →https://doi.org/10.1111/tpj.12027openalex-snapshot
Arabidopsis wat1 ( walls are thin1 )‐mediated resistance to the bacterial vascular pathogen, Ralstonia solanacearum , is accompanied by cross‐regulation of salicylic acid and tryptophan metabolism
inferredcites →https://doi.org/10.1126/science.1170025openalex-snapshot
Priming in Systemic Plant Immunity
inferredcites →https://doi.org/10.1146/annurev-phyto-072910-095355openalex-snapshot
Reactive Oxygen Species in Phytopathogenic Fungi: Signaling, Development, and Disease
inferredcites →https://doi.org/10.1146/annurev-phyto-082712-102321openalex-snapshot
Pseudomonas syringae pv. tomato DC3000: A Model Pathogen for Probing Disease Susceptibility and Hormone Signaling in Plants
inferredcites →https://doi.org/10.1146/annurev.phyto.36.1.453openalex-snapshot
SYSTEMIC RESISTANCE INDUCED BY RHIZOSPHERE BACTERIA
inferredcites →https://doi.org/10.1146/annurev.phyto.42.040803.140421openalex-snapshot
SYSTEMIC ACQUIRED RESISTANCE
inferredcites →https://doi.org/10.1146/annurev.phyto.43.040204.135923openalex-snapshot
Contrasting Mechanisms of Defense Against Biotrophic and Necrotrophic Pathogens
inferredcites →https://doi.org/10.1199/tab.0039openalex-snapshot
The Arabidopsis Thaliana-Pseudomonas Syringae Interaction
inferredcites →https://doi.org/10.1371/journal.pone.0019823openalex-snapshot
The Indoleamine-2,3-Dioxygenase (IDO) Inhibitor 1-Methyl-D-tryptophan Upregulates IDO1 in Human Cancer Cells
inferredcites →https://doi.org/10.1556/aphyt.44.2009.1.5openalex-snapshot
Effects of rutin on the growth ofBotrytis cinerea, Alternaria alternataandFusarium solani
inferredcites →https://doi.org/10.3389/fpls.2014.00488openalex-snapshot
Priming of plant resistance by natural compounds. Hexanoic acid as a model
inferredcites →https://doi.org/10.3389/fpls.2015.00170openalex-snapshot
How salicylic acid takes transcriptional control over jasmonic acid signaling
inferredcites →https://doi.org/10.3390/md8040968openalex-snapshot
Chitosan in Plant Protection
inferredcites →https://doi.org/10.4049/jimmunol.181.8.5396openalex-snapshot
The Indoleamine 2,3-Dioxygenase Pathway Is Essential for Human Plasmacytoid Dendritic Cell-Induced Adaptive T Regulatory Cell Generation
inferredcites →https://doi.org/10.5511/plantbiotechnology.24.135openalex-snapshot
Tomato as a model plant for plant-pathogen interactions

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1016/j.btre.2020.e00425openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.12.028openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jplph.2019.05.009openalex-snapshot
Ammonium mediated changes in carbon and nitrogen metabolisms induce resistance against Pseudomonas syringae in tomato plants
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inferred← citeshttps://doi.org/10.3389/fmicb.2020.00732openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2016.01658openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2016.01964openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2023.1114172openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/app10228152openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/horticulturae9020130openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms17101673openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms19061759openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms232012418openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms24033025openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/metabo10050210openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/metabo10110466openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/metabo9040060openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microorganisms10102013openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants14121876openalex-snapshot
Physiological, Chemical and Metabolite Profiling of Pectobacterium carotovorum-Inoculated Tomato Plants Grown in Nutrient-Amended Soils
inferred← citeshttps://doi.org/10.3390/plants15040567openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants9030300openalex-snapshot
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inferred← citeshttps://doi.org/10.5772/66485openalex-snapshot
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inferred← citeshttps://doi.org/10.6035/14104.2023.791364openalex-snapshot
Endophytic communities in S. lycopersicum genotypes: Isolation of a novel fungal strain and its application to plant
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