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Two-component systems regulate swarming in Pseudomonas aeruginosa PA14

https://doi.org/10.1101/445015
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Improving the reproducibility of Pseudomonas aeruginosa swarming motility assays
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Molecular Mechanisms of Two-Component Signal Transduction
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Cell signalling by oligosaccharides. Two-component systems in Pseudomonas aeruginosa: why so many?
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A field guide to bacterial swarming motility
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Inhibition of P. aeruginosa c-di-GMP phosphodiesterase RocR and swarming motility by a benzoisothiazolinone derivative
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Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development
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Swarming motility in undomesticated Bacillus subtilis
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.060030097openalex-snapshot
Inorganic polyphosphate is needed for swimming, swarming, and twitching motilities of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1073/pnas.0604050103openalex-snapshot
Heat-shock transcription factor (HSF)-1 pathway required for Caenorhabditis elegans immunity
inferredcites →https://doi.org/10.1073/pnas.0910934107openalex-snapshot
Cell density and mobility protect swarming bacteria against antibiotics
inferredcites →https://doi.org/10.1073/pnas.91.18.8631openalex-snapshot
Dimorphic transition in Escherichia coli and Salmonella typhimurium: surface-induced differentiation into hyperflagellate swarmer cells.
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/10.1074/jbc.m708836200openalex-snapshot
Characterization of the Histidine-containing Phosphotransfer Protein B-mediated Multistep Phosphorelay System in Pseudomonas aeruginosa PAO1
inferredcites →https://doi.org/10.1074/jbc.r115.711507openalex-snapshot
Biofilms and Cyclic di-GMP (c-di-GMP) Signaling: Lessons from Pseudomonas aeruginosa and Other Bacteria
inferredcites →https://doi.org/10.1093/femsle/fnx027openalex-snapshot
Polyphasic characterization of the thermotolerant cyanobacterium Desertifilum sp. strain IPPAS B-1220
inferredcites →https://doi.org/10.1093/femsle/fnx104openalex-snapshot
Two-component systems required for virulence in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1101/341529openalex-snapshot
Spatial Awareness of a Bacterial Swarm
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05421.xopenalex-snapshot
The impact of quorum sensing and swarming motility on Pseudomonas aeruginosa biofilm formation is nutritionally conditional
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07436.xopenalex-snapshot
A molecular mechanism that stabilizes cooperative secretions in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1126/science.1203411openalex-snapshot
Neuronal GPCR Controls Innate Immunity by Regulating Noncanonical Unfolded Protein Response Genes
inferredcites →https://doi.org/10.1128/aem.01015-12openalex-snapshot
Phosphate Starvation Promotes Swarming Motility and Cytotoxicity of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/aem.02832-14openalex-snapshot
Sensor Kinase PA4398 Modulates Swarming Motility and Biofilm Formation in Pseudomonas aeruginosa PA14
inferredcites →https://doi.org/10.1128/aem.06644-11openalex-snapshot
Imaging and Analysis of Pseudomonas aeruginosa Swarming and Rhamnolipid Production
inferredcites →https://doi.org/10.1128/br.36.4.478-503.1972openalex-snapshot
Bacterial surface translocation: a survey and a classification
inferredcites →https://doi.org/10.1128/iai.01181-08openalex-snapshot
Pseudomonas aeruginosa Infection of Zebrafish Involves both Host and Pathogen Determinants
inferredcites →https://doi.org/10.1128/iai.63.12.4868-4876.1995openalex-snapshot
Cloning and phenotypic characterization of fleS and fleR, new response regulators of Pseudomonas aeruginosa which regulate motility and adhesion to mucin
inferredcites →https://doi.org/10.1128/jb.00157-09openalex-snapshot
Swarming of Pseudomonas aeruginosa Is Controlled by a Broad Spectrum of Transcriptional Regulators, Including MetR
inferredcites →https://doi.org/10.1128/jb.00168-11openalex-snapshot
Myxococcus xanthus Swarms Are Driven by Growth and Regulated by a Pacemaker
inferredcites →https://doi.org/10.1128/jb.00196-16openalex-snapshot
PilZ Domain Protein FlgZ Mediates Cyclic Di-GMP-Dependent Swarming Motility Control in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.00586-07openalex-snapshot
BifA, a Cyclic-Di-GMP Phosphodiesterase, Inversely Regulates Biofilm Formation and Swarming Motility byPseudomonas aeruginosaPA14
inferredcites →https://doi.org/10.1128/jb.00905-09openalex-snapshot
Laboratory Strains of Bacillus subtilis Do Not Exhibit Swarming Motility
inferredcites →https://doi.org/10.1128/jb.01623-06openalex-snapshot
Identification of Genes Involved in Swarming Motility Using aPseudomonas aeruginosaPAO1 Mini-Tn5-luxMutant Library
inferredcites →https://doi.org/10.1128/jb.01659-07openalex-snapshot
Swarming ofPseudomonas aeruginosaIs a Complex Adaptation Leading to Increased Production of Virulence Factors and Antibiotic Resistance
inferredcites →https://doi.org/10.1128/jb.01824-08openalex-snapshot
Human- and Plant-Pathogenic Pseudomonas Species Produce Bacteriocins Exhibiting Colicin M-Like Hydrolase Activity towards Peptidoglycan Precursors
inferredcites →https://doi.org/10.1128/jb.182.21.5990-5996.2000openalex-snapshot
Swarming of Pseudomonas aeruginosa Is Dependent on Cell-to-Cell Signaling and Requires Flagella and Pili
inferredcites →https://doi.org/10.1128/jb.183.4.1466-1471.2001openalex-snapshot
Drosophila as a Model Host for Pseudomonas aeruginosa Infection
inferredcites →https://doi.org/10.1128/jb.187.21.7351-7361.2005openalex-snapshot
Rhamnolipids Modulate Swarming Motility Patterns ofPseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/mmbr.00043-12openalex-snapshot
Cyclic di-GMP: the First 25 Years of a Universal Bacterial Second Messenger
inferredcites →https://doi.org/10.1146/annurev.biochem.69.1.183openalex-snapshot
Two-Component Signal Transduction
inferredcites →https://doi.org/10.1146/annurev.genet.41.042007.170548openalex-snapshot
Specificity in Two-Component Signal Transduction Pathways
inferredcites →https://doi.org/10.1186/1471-2164-11-587openalex-snapshot
Gene expression in Pseudomonas aeruginosa swarming motility
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/10.1371/journal.pcbi.1004128openalex-snapshot
Neural Modularity Helps Organisms Evolve to Learn New Skills without Forgetting Old Skills
inferredcites →https://doi.org/10.1371/journal.pcbi.1004279openalex-snapshot
Integration of Metabolic and Quorum Sensing Signals Governing the Decision to Cooperate in a Bacterial Social Trait
inferredcites →https://doi.org/10.1371/journal.pone.0006018openalex-snapshot
Expression of Pseudomonas aeruginosa CupD Fimbrial Genes Is Antagonistically Controlled by RcsB and the EAL-Containing PvrR Response Regulators
inferredcites →https://doi.org/10.1371/journal.ppat.1000483openalex-snapshot
Connecting Quorum Sensing, c-di-GMP, Pel Polysaccharide, and Biofilm Formation in Pseudomonas aeruginosa through Tyrosine Phosphatase TpbA (PA3885)
inferredcites →https://doi.org/10.1371/journal.ppat.1004480openalex-snapshot
Candida albicans Ethanol Stimulates Pseudomonas aeruginosa WspR-Controlled Biofilm Formation as Part of a Cyclic Relationship Involving Phenazines
inferredcites →https://doi.org/10.3791/2437openalex-snapshot
Microtiter Dish Biofilm Formation Assay
inferredcites →https://doi.org/10.3791/52338openalex-snapshot
Preparation, Imaging, and Quantification of Bacterial Surface Motility Assays
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