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Trehalose Biosynthesis Promotes Pseudomonas aeruginosa Pathogenicity in Plants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Combining Genomic Tools to Dissect Multifactorial Virulence in Pseudomonas aeruginosa
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Physiological roles of trehalose in bacteria and yeasts: a comparative analysis
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In vitro insertional mutagenesis with a selectable DNA fragment
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Construction of improved Escherichia-Pseudomonas shuttle vectors derived from pUC18/19 and sequence of the region required for their replication in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1016/j.carres.2011.01.018openalex-snapshot
Inhibition of trehalose breakdown increases new carbon partitioning into cellulosic biomass in Nicotiana tabacum
inferredcites →https://doi.org/10.1016/j.cell.2006.02.047openalex-snapshot
Specific Bacterial Suppressors of MAMP Signaling Upstream of MAPKKK in Arabidopsis Innate Immunity
inferredcites →https://doi.org/10.1016/j.cub.2011.06.064openalex-snapshot
Trehalose Renders the Dauer Larva of Caenorhabditis elegans Resistant to Extreme Desiccation
inferredcites →https://doi.org/10.1016/j.tplants.2007.03.007openalex-snapshot
Plant development: introducing trehalose metabolism
inferredcites →https://doi.org/10.1016/s0021-9258(18)84465-9openalex-snapshot
NOTES ON SUGAR DETERMINATION
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NOTES ON SUGAR DETERMINATION
inferredcites →https://doi.org/10.1016/s0076-6879(57)03350-9openalex-snapshot
[12] Colorimetric analysis of sugars
inferredcites →https://doi.org/10.1016/s0092-8674(00)80958-7openalex-snapshot
Molecular Mechanisms of Bacterial Virulence Elucidated Using a Pseudomonas aeruginosa– Caenorhabditis elegans Pathogenesis Model
inferredcites →https://doi.org/10.1016/s0304-4165(96)00082-7openalex-snapshot
Cloning and sequencing of a cluster of genes encoding novel enzymes of trehalose biosynthesis from thermophilic archaebacterium Sulfolobus acidocaldarius
inferredcites →https://doi.org/10.1038/nature02485openalex-snapshot
Bacterial disease resistance in Arabidopsis through flagellin perception
inferredcites →https://doi.org/10.1038/nature09606openalex-snapshot
Sugar transporters for intercellular exchange and nutrition of pathogens
inferredcites →https://doi.org/10.1039/b918710copenalex-snapshot
Metabolic profiling of Pseudomonas aeruginosa demonstrates that the anti-sigma factor MucA modulates osmotic stress tolerance
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Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways: a genetic analysis
inferredcites →https://doi.org/10.1073/pnas.0437901100openalex-snapshot
Hypersusceptibility of cystic fibrosis mice to chronic Pseudomonas aeruginosa oropharyngeal colonization and lung infection
inferredcites →https://doi.org/10.1073/pnas.0502425102openalex-snapshot
Flagellin induces innate immunity in nonhost interactions that is suppressed by Pseudomonas syringae effectors
inferredcites →https://doi.org/10.1073/pnas.0511100103openalex-snapshot
An ordered, nonredundant library of Pseudomonas aeruginosa strain PA14 transposon insertion mutants
inferredcites →https://doi.org/10.1073/pnas.052450699openalex-snapshot
The mur2 mutant of Arabidopsis thaliana lacks fucosylated xyloglucan because of a lesion in fucosyltransferase AtFUT1
inferredcites →https://doi.org/10.1073/pnas.0711982105openalex-snapshot
Dynamics of Pseudomonas aeruginosa genome evolution
inferredcites →https://doi.org/10.1073/pnas.1114907108openalex-snapshot
Pseudomonas aeruginosa RhlR is required to neutralize the cellular immune response in a Drosophila melanogaster oral infection model
inferredcites →https://doi.org/10.1073/pnas.142314099openalex-snapshot
Trehalose synthesis is induced upon exposure of Escherichia coli to cold and is essential for viability at low temperatures
inferredcites →https://doi.org/10.1073/pnas.94.24.13245openalex-snapshot
Use of model plant hosts to identify Pseudomonas aeruginosa virulence factors
inferredcites →https://doi.org/10.1073/pnas.96.2.715openalex-snapshot
Killing of Caenorhabditis elegans by Pseudomonas aeruginosa used to model mammalian bacterial pathogenesis
inferredcites →https://doi.org/10.1093/glycob/cwg047openalex-snapshot
New insights on trehalose: a multifunctional molecule
inferredcites →https://doi.org/10.1104/pp.103.021253openalex-snapshot
Microarray Analysis of the Nitrate Response in Arabidopsis Roots and Shoots Reveals over 1,000 Rapidly Responding Genes and New Linkages to Glucose, Trehalose-6-Phosphate, Iron, and Sulfate Metabolism
inferredcites →https://doi.org/10.1104/pp.104.039503openalex-snapshot
Trehalose Mediated Growth Inhibition of Arabidopsis Seedlings Is Due to Trehalose-6-Phosphate Accumulation
inferredcites →https://doi.org/10.1104/pp.106.087700openalex-snapshot
Interactions between MUR10/CesA7-Dependent Secondary Cellulose Biosynthesis and Primary Cell Wall Structure
inferredcites →https://doi.org/10.1104/pp.121.2.383openalex-snapshot
The mur4 Mutant of Arabidopsis Is Partially Defective in the de Novo Synthesis of Uridine Diphospho l -Arabinose
inferredcites →https://doi.org/10.1104/pp.124.1.105openalex-snapshot
Trehalose Induces the ADP-Glucose Pyrophosphorylase Gene,ApL3, and Starch Synthesis in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.124.4.1766openalex-snapshot
Pathogenesis of the Human Opportunistic PathogenPseudomonas aeruginosa PA14 in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.009837openalex-snapshot
The MUR3 Gene of Arabidopsis Encodes a Xyloglucan Galactosyltransferase That Is Evolutionarily Related to Animal Exostosins
inferredcites →https://doi.org/10.1105/tpc.108.059873openalex-snapshot
Disrupting Two Arabidopsis thaliana Xylosyltransferase Genes Results in Plants Deficient in Xyloglucan, a Major Primary Cell Wall Component
inferredcites →https://doi.org/10.1105/tpc.3.1.49openalex-snapshot
Identification of Pseudomonas syringae pathogens of Arabidopsis and a bacterial locus determining avirulence on both Arabidopsis and soybean.
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04448.xopenalex-snapshot
The contribution of MvfR to Pseudomonas aeruginosa pathogenesis and quorum sensing circuitry regulation: multiple quorum sensing‐regulated genes are modulated without affecting lasRI, rhlRI or the production of N‐acyl‐ l ‐homoserine lactones
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02662.xopenalex-snapshot
Delayed embryo development in the ARABIDOPSIS TREHALOSE‐6‐PHOSPHATE SYNTHASE 1 mutant is associated with altered cell wall structure, decreased cell division and starch accumulation
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00537.xopenalex-snapshot
Exogenous trehalose alters Arabidopsis transcripts involved in cell wall modification, abiotic stress, nitrogen metabolism, and plant defense
inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02171.xopenalex-snapshot
Identification of the trehalose biosynthetic loci of Pseudomonas syringae and their contribution to fitness in the phyllosphere
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03751.xopenalex-snapshot
Genetic and physiological analysis of the relationship between partial resistance to clubroot and tolerance to trehalose in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1474-9726.2010.00582.xopenalex-snapshot
Trehalose extends longevity in the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1126/science.7527588openalex-snapshot
Correction of Lethal Intestinal Defect in a Mouse Model of Cystic Fibrosis by Human CFTR
inferredcites →https://doi.org/10.1126/science.7604262openalex-snapshot
Common Virulence Factors for Bacterial Pathogenicity in Plants and Animals
inferredcites →https://doi.org/10.1128/aem.00860-08openalex-snapshot
Global Gene Expression Profiles Suggest an Important Role for Nutrient Acquisition in Early Pathogenesis in a Plant Model ofPseudomonas aeruginosaInfection
inferredcites →https://doi.org/10.1128/aem.59.2.473-478.1993openalex-snapshot
Roles of N-acetylglutaminylglutamine amide and glycine betaine in adaptation of Pseudomonas aeruginosa to osmotic stress
inferredcites →https://doi.org/10.1128/aem.63.11.4543-4551.1997openalex-snapshot
Green fluorescent protein as a marker for Pseudomonas spp
inferredcites →https://doi.org/10.1128/aem.72.1.802-810.2006openalex-snapshot
New rfp - and pES213-Derived Tools for Analyzing Symbiotic Vibrio fischeri Reveal Patterns of Infection and lux Expression In Situ
inferredcites →https://doi.org/10.1128/iai.59.12.4310-4317.1991openalex-snapshot
Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector
inferredcites →https://doi.org/10.1128/iai.68.7.3998-4004.2000openalex-snapshot
Acquisition of Expression of the Pseudomonas aeruginosa ExoU Cytotoxin Leads to Increased Bacterial Virulence in a Murine Model of Acute Pneumonia and Systemic Spread
inferredcites →https://doi.org/10.1128/iai.71.5.2404-2413.2003openalex-snapshot
Use of the Galleria mellonella Caterpillar as a Model Host To Study the Role of the Type III Secretion System in Pseudomonas aeruginosa Pathogenesis
inferredcites →https://doi.org/10.1128/jb.01231-09openalex-snapshot
Pseudomonas aeruginosaIncreases Formation of Multidrug-Tolerant Persister Cells in Response to Quorum-Sensing Signaling Molecules
inferredcites →https://doi.org/10.1128/jb.168.2.512-522.1986openalex-snapshot
Gene cluster of Pseudomonas syringae pv. "phaseolicola" controls pathogenicity of bean plants and hypersensitivity of nonhost plants
inferredcites →https://doi.org/10.1128/jb.175.18.5934-5944.1993openalex-snapshot
The pilG gene product, required for Pseudomonas aeruginosa pilus production and twitching motility, is homologous to the enteric, single-domain response regulator CheY
inferredcites →https://doi.org/10.1128/jb.180.7.1741-1749.1998openalex-snapshot
Cloning and Characterization of the Pseudomonas aeruginosa zwf Gene Encoding Glucose-6-Phosphate Dehydrogenase, an Enzyme Important in Resistance to Methyl Viologen (Paraquat)
inferredcites →https://doi.org/10.1128/jb.182.13.3843-3845.2000openalex-snapshot
Positive Correlation between Virulence of Pseudomonas aeruginosa Mutants in Mice and Insects
inferredcites →https://doi.org/10.1128/jb.188.7.2721-2725.2006openalex-snapshot
Microarray Analysis of the Osmotic Stress Response inPseudomonas aeruginosa
inferredcites →https://doi.org/10.1186/1471-2164-7-162openalex-snapshot
Clustering of Pseudomonas aeruginosa transcriptomes from planktonic cultures, developing and mature biofilms reveals distinct expression profiles
inferredcites →https://doi.org/10.1186/gb-2006-7-10-r90openalex-snapshot
Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial
inferredcites →https://doi.org/10.1271/bbb.60.640openalex-snapshot
Purification and Properties of a Novel Enzyme, Trehalose Synthase, fromPimelobactersp. R48
inferredcites →https://doi.org/10.1371/journal.pone.0024235openalex-snapshot
In-Vivo Expression Profiling of Pseudomonas aeruginosa Infections Reveals Niche-Specific and Strain-Independent Transcriptional Programs
inferredcites →https://doi.org/10.1371/journal.ppat.1002813openalex-snapshot
Genome-Wide Identification of Pseudomonas aeruginosa Virulence-Related Genes Using a Caenorhabditis elegans Infection Model
inferredcites →https://doi.org/10.3390/ijms10093793openalex-snapshot
Trehalose Metabolism: From Osmoprotection to Signaling
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Functional analysis of the CRP and TreR-treBC regulon in trehalose utilization of Vibrio parahaemolyticus
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Biofilm formation of Pseudomonas aeruginosa in spaceflight is minimized on lubricant impregnated surfaces
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HandKAchip - Hands-free killing assay on a chip
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Trehalase plays a role in macrophage colonization and virulence ofBurkholderia pseudomalleiin insect and mammalian hosts
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Community-led comparative genomic and phenotypic analysis of the aquaculture pathogen Pseudomonas baetica a390T sequenced by Ion semiconductor and Nanopore technologies
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The dual nature of trehalose in citrus canker disease: a virulence factor for Xanthomonas citri subsp. citri and a trigger for plant defence responses
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Trehalose Synthesis Contributes to Osmotic Stress Tolerance and Virulence of the Bacterial Wilt Pathogen Ralstonia solanacearum
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Trehalose 6‐phosphate phosphatases of Pseudomonas aeruginosa
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inferred← citeshttps://doi.org/10.3390/microorganisms9051029openalex-snapshot
What the Wild Things Do: Mechanisms of Plant Host Manipulation by Bacterial Type III-Secreted Effector Proteins
inferred← citeshttps://doi.org/10.3390/molecules29092088openalex-snapshot
Intracellular Protective Functions and Therapeutical Potential of Trehalose
inferred← citeshttps://doi.org/10.3390/plants11030296openalex-snapshot
D-Tagatose-Based Product Triggers Sweet Immunity and Resistance of Grapevine to Downy Mildew, but Not to Gray Mold Disease
inferred← citeshttps://doi.org/10.3390/plants12193394openalex-snapshot
Heterologous Expression of OtsB Increases Tuber Yield and Phenotypic Stability in Potato under Both Abiotic and Biotic Stresses
inferred← citeshttps://doi.org/10.4014/jmb.1408.08064openalex-snapshot
Investigation of Quorum Sensing-Dependent Gene Expression in Burkholderia gladioli BSR3 through RNA-seq Analyses
inferred← citeshttps://doi.org/10.5010/jpb.2026.53.011.086openalex-snapshot
Trehalose in plant stress responses: Mechanisms and agricultural applications
inferred← citeshttps://doi.org/10.5423/ppj.oa.06.2021.0087openalex-snapshot
Role of Trehalose Synthesis in Ralstonia syzygii subsp. indonesiensis PW1001 in Inducing Hypersensitive Response on Eggplant (Solanum melongena cv. Senryo-nigou)
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779352openalex-snapshot
Additional file 10 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779355openalex-snapshot
Additional file 11 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779358openalex-snapshot
Additional file 12 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779361openalex-snapshot
Additional file 13 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779364openalex-snapshot
Additional file 14 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779379openalex-snapshot
Additional file 1 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779382openalex-snapshot
Additional file 2 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779385openalex-snapshot
Additional file 3 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779388openalex-snapshot
Additional file 4 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779391openalex-snapshot
Additional file 5 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779394openalex-snapshot
Additional file 6 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779397openalex-snapshot
Additional file 7 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779400openalex-snapshot
Additional file 8 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.6084/m9.figshare.16779403openalex-snapshot
Additional file 9 of Comparative transcriptomic analysis of races 1, 2, 5 and 6 of Fusarium oxysporum f.sp. pisi in a susceptible pea host identifies differential pathogenicity profiles
inferred← citeshttps://doi.org/10.70675/5bbe4361z620cz4b92zbab6z2ac57b06363eopenalex-snapshot
Les sucres rares comme nouveaux produits pour la protection des plantes : Cas d'un produit à base de D-Tagatose dans la vigne
inferred← citeshttps://doi.org/10.70675/b5726a9bz526bz444ez96bazca9325ebd1c0openalex-snapshot
Frontières adaptatives des burkholderias en interaction avec le riz : approches génétiques et fonctionnelles
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