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A chemosensory system that regulates biofilm formation through modulation of cyclic diguanylate levels

https://doi.org/10.1073/pnas.0507170102
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What this work says

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

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GGDEF domain is homologous to adenylyl cyclase
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[17]Gene splicing by overlap extension
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Site-directed mutagenesis by overlap extension using the polymerase chain reaction
inferredcites →https://doi.org/10.1016/s0008-6215(00)90372-0openalex-snapshot
Control of cellulose synthesis Acetobacter xylinum. A unique guanyl oligonucleotide is the immediate activator of the cellulose synthase
inferredcites →https://doi.org/10.1016/s0014-5793(97)01202-7openalex-snapshot
c‐di‐GMP‐binding protein, a new factor regulating cellulose synthesis in Acetobacter xylinum
inferredcites →https://doi.org/10.1016/s0021-9258(18)31731-9openalex-snapshot
Acetyl phosphate and the activation of two-component response regulators.
inferredcites →https://doi.org/10.1016/s0021-9258(18)34138-3openalex-snapshot
Complete analysis of cellular nucleotides by two-dimensional thin layer chromatography.
inferredcites →https://doi.org/10.1016/s0140-6736(01)05321-1openalex-snapshot
Antibiotic resistance of bacteria in biofilms
inferredcites →https://doi.org/10.1016/s0378-1097(01)00394-9openalex-snapshot
Genetic data indicate that proteins containing the GGDEF domain possess diguanylate cyclase activity
inferredcites →https://doi.org/10.1016/s0378-1119(98)00130-9openalex-snapshot
A broad-host-range Flp-FRT recombination system for site-specific excision of chromosomally-located DNA sequences: application for isolation of unmarked Pseudomonas aeruginosa mutants
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Mechanisms of biofilm resistance to antimicrobial agents
inferredcites →https://doi.org/10.1016/s1286-4579(00)01259-4openalex-snapshot
Establishment of infection: lessons from a versatile opportunist
inferredcites →https://doi.org/10.1038/416740aopenalex-snapshot
Pseudomonas biofilm formation and antibiotic resistance are linked to phenotypic variation
inferredcites →https://doi.org/10.1038/417552aopenalex-snapshot
A component of innate immunity prevents bacterial biofilm development
inferredcites →https://doi.org/10.1038/nature02122openalex-snapshot
A genetic basis for Pseudomonas aeruginosa biofilm antibiotic resistance
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Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways: a genetic analysis
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Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03401.xopenalex-snapshot
Role of the GGDEF regulator PleD in polar development of Caulobacter crescentus
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03670.xopenalex-snapshot
Biofilm formation at the air–liquid interface by the Pseudomonas fluorescens SBW25 wrinkly spreader requires an acetylated form of cellulose
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03877.xopenalex-snapshot
Genes involved in matrix formation in Pseudomonas aeruginosa PA14 biofilms
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03886.xopenalex-snapshot
The Pseudomonas aeruginosa RpoS regulon and its relationship to quorum sensing
inferredcites →https://doi.org/10.1073/pnas.0406134101openalex-snapshot
Structural basis of activity and allosteric control of diguanylate cyclase
inferredcites →https://doi.org/10.1074/jbc.m504429200openalex-snapshot
Identification and Characterization of a Cyclic di-GMP-specific Phosphodiesterase and Its Allosteric Control by GTP
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Adaptive Divergence in Experimental Populations of Pseudomonas fluorescens . I. Genetic and Phenotypic Bases of Wrinkly Spreader Fitness
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Development of improved versatile broad-host-range vectors for use in methylotrophs and other Gram-negative bacteria The GenBank accession numbers for the sequences reported in this paper are AF327711, AF327712, AF327713, AF327714, AF327715, AF327716, AF327717, AF327718, AF327719 and AF327720.
inferredcites →https://doi.org/10.1099/jmm.0.05069-0openalex-snapshot
Highly adherent small-colony variants of Pseudomonas aeruginosa in cystic fibrosis lung infection
inferredcites →https://doi.org/10.1099/mic.0.27099-0openalex-snapshot
Cyclic di-GMP as a bacterial second messenger
inferredcites →https://doi.org/10.1099/mic.0.27410-0openalex-snapshot
The pel genes of the Pseudomonas aeruginosa PAK strain are involved at early and late stages of biofilm formation
inferredcites →https://doi.org/10.1101/gad.289504openalex-snapshot
Cell cycle-dependent dynamic localization of a bacterial response regulator with a novel di-guanylate cyclase output domain
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04155.xopenalex-snapshot
Cyclic diguanylate (c‐di‐GMP) regulates Vibrio cholerae biofilm formation
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04206.xopenalex-snapshot
GGDEF and EAL domains inversely regulate cyclic di‐GMP levels and transition from sessility to motility
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04269.xopenalex-snapshot
Role of the GGDEF protein family in Salmonella cellulose biosynthesis and biofilm formation
inferredcites →https://doi.org/10.1111/j.1462-2920.2004.00618.xopenalex-snapshot
Biofilm formation by the small colony variant phenotype of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1126/science.280.5361.295openalex-snapshot
The Involvement of Cell-to-Cell Signals in the Development of a Bacterial Biofilm
inferredcites →https://doi.org/10.1128/aac.38.5.1052openalex-snapshot
Biofilm accumulation model that predicts antibiotic resistance of Pseudomonas aeruginosa biofilms
inferredcites →https://doi.org/10.1128/aem.71.8.4809-4821.2005openalex-snapshot
Characterization of Colony Morphology Variants Isolated from Pseudomonas aeruginosa Biofilms
inferredcites →https://doi.org/10.1128/jb.171.12.6649-6655.1989openalex-snapshot
Cyclic diguanylic acid and cellulose synthesis in Agrobacterium tumefaciens
inferredcites →https://doi.org/10.1128/jb.184.16.4374-4383.2002openalex-snapshot
Cluster IIcheGenes fromPseudomonas aeruginosaAre Required for an Optimal Chemotactic Response
inferredcites →https://doi.org/10.1128/jb.184.21.5946-5954.2002openalex-snapshot
Vibrio parahaemolyticus scrABC , a Novel Operon Affecting Swarming and Capsular Polysaccharide Regulation
inferredcites →https://doi.org/10.1128/jb.184.23.6481-6489.2002openalex-snapshot
Autolysis and Autoaggregation in Pseudomonas aeruginosa Colony Morphology Mutants
inferredcites →https://doi.org/10.1128/jb.184.4.1140-1154.2002openalex-snapshot
Pseudomonas aeruginosa Displays Multiple Phenotypes during Development as a Biofilm
inferredcites →https://doi.org/10.1128/jb.185.18.5431-5441.2003openalex-snapshot
Multiple Regulators Control Capsular Polysaccharide Production in Vibrio parahaemolyticus
inferredcites →https://doi.org/10.1128/jb.185.4.1384-1390.2003openalex-snapshot
Identification and Characterization of aVibrio choleraeGene,mbaA, Involved in Maintenance of Biofilm Architecture
inferredcites →https://doi.org/10.1128/jb.185.7.2066-2079.2003openalex-snapshot
Identification, Timing, and Signal Specificity of Pseudomonas aeruginosa Quorum-Controlled Genes: a Transcriptome Analysis
inferredcites →https://doi.org/10.1128/jb.186.14.4449-4456.2004openalex-snapshot
Putative Exopolysaccharide Synthesis Genes Influence Pseudomonas aeruginosa Biofilm Development
inferredcites →https://doi.org/10.1128/jb.186.14.4457-4465.2004openalex-snapshot
Two Genetic Loci Produce Distinct Carbohydrate-Rich Structural Components of thePseudomonas aeruginosaBiofilm Matrix
inferredcites →https://doi.org/10.1128/jb.186.14.4466-4475.2004openalex-snapshot
Identification ofpsl, a Locus Encoding a Potential Exopolysaccharide That Is Essential forPseudomonas aeruginosaPAO1 Biofilm Formation
inferredcites →https://doi.org/10.1128/jb.187.5.1792-1798.2005openalex-snapshot
Cyclic Diguanylate Is a Ubiquitous Signaling Molecule in Bacteria: Insights into Biochemistry of the GGDEF Protein Domain
inferredcites →https://doi.org/10.1128/mr.55.1.35-58.1991openalex-snapshot
Cellulose biosynthesis and function in bacteria

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.margen.2018.11.005openalex-snapshot
Complete genome of Pseudoalteromonas atlantica ECSMB14104, a Gammaproteobacterium inducing mussel settlement
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.118884openalex-snapshot
Seasonal and antifoulant effects on microbial–metazoan interactions in biofouling communities revealed by comprehensive eDNA metabarcoding
inferred← citeshttps://doi.org/10.1016/j.matpr.2021.05.245openalex-snapshot
Recent development in therapeutic strategies targeting Pseudomonas aeruginosa biofilms – A review
inferred← citeshttps://doi.org/10.1016/j.meegid.2021.105008openalex-snapshot
Functional analysis of pde gene and its role in the pathogenesis of Xanthomonas oryzae pv. oryzicola
inferred← citeshttps://doi.org/10.1016/j.mib.2006.02.010openalex-snapshot
Cyclic di-GMP as a second messenger
inferred← citeshttps://doi.org/10.1016/j.mib.2006.12.006openalex-snapshot
c-di-GMP-mediated regulation of virulence and biofilm formation
inferred← citeshttps://doi.org/10.1016/j.mib.2007.09.010openalex-snapshot
Role of polysaccharides in Pseudomonas aeruginosa biofilm development
inferred← citeshttps://doi.org/10.1016/j.mib.2008.09.015openalex-snapshot
Pattern formation in Pseudomonas aeruginosa biofilms
inferred← citeshttps://doi.org/10.1016/j.mib.2011.12.008openalex-snapshot
You’ve come a long way: c-di-GMP signaling
inferred← citeshttps://doi.org/10.1016/j.mib.2015.12.004openalex-snapshot
Exploiting the commons: cyclic diguanylate regulation of bacterial exopolysaccharide production
inferred← citeshttps://doi.org/10.1016/j.mib.2016.02.004openalex-snapshot
Sensational biofilms: surface sensing in bacteria
inferred← citeshttps://doi.org/10.1016/j.micinf.2009.11.009openalex-snapshot
The two-component sensor response regulator RoxS/RoxR plays a role in Pseudomonas aeruginosa interactions with airway epithelial cells
inferred← citeshttps://doi.org/10.1016/j.micpath.2008.08.007openalex-snapshot
Mutation in the S-ribosylhomocysteinase (luxS) gene involved in quorum sensing affects biofilm formation and virulence in a clinical isolate of Aeromonas hydrophila
inferred← citeshttps://doi.org/10.1016/j.micpath.2026.108833openalex-snapshot
Divergent regulation of virulence factors by FimK in classical and hypervirulent Klebsiella pneumoniae pathotypes
inferred← citeshttps://doi.org/10.1016/j.micres.2021.126869openalex-snapshot
Identification of chemoreceptor proteins for amino acids involved in host plant infection in Pseudomonas syringae pv. tabaci 6605
inferred← citeshttps://doi.org/10.1016/j.micres.2023.127302openalex-snapshot
Bacterial second messenger c-di-GMP: Emerging functions in stress resistance
inferred← citeshttps://doi.org/10.1016/j.micres.2023.127445openalex-snapshot
c-di-GMP signaling in Pseudomonas syringae complex
inferred← citeshttps://doi.org/10.1016/j.micres.2024.127935openalex-snapshot
Microbial chemotaxis in degradation of xenobiotics: Current trends and opportunities
inferred← citeshttps://doi.org/10.1016/j.microb.2025.100538openalex-snapshot
Small colony variants and their role in biofilm associated infections
inferred← citeshttps://doi.org/10.1016/j.mimet.2009.07.013openalex-snapshot
Characterization of pNC1, a small and mobilizable plasmid for use in genetic manipulation of Desulfovibrio africanus
inferred← citeshttps://doi.org/10.1016/j.mimet.2011.11.015openalex-snapshot
A chemical proteomics approach to identify c-di-GMP binding proteins in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2019.100804openalex-snapshot
Contact lens-related corneal infection: Intrinsic resistance and its compromise
inferred← citeshttps://doi.org/10.1016/j.resmic.2009.04.004openalex-snapshot
Phenotypic variation in the Pseudomonas fluorescens clinical strain MFN1032
inferred← citeshttps://doi.org/10.1016/j.resmic.2016.01.002openalex-snapshot
Functional characterization and transcriptome analysis reveal multiple roles for prc in the pathogenicity of the black rot pathogen Xanthomonas campestris pv. campestris
inferred← citeshttps://doi.org/10.1016/j.sajb.2021.11.039openalex-snapshot
Natural compounds underpinning the genetic regulation of biofilm formation: An overview
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.172967openalex-snapshot
Advancements in bacterial chemotaxis: Utilizing the navigational intelligence of bacteria and its practical applications
inferred← citeshttps://doi.org/10.1016/j.str.2009.06.010openalex-snapshot
Structural Analysis of the GGDEF-EAL Domain-Containing c-di-GMP Receptor FimX
inferred← citeshttps://doi.org/10.1016/j.str.2012.01.003openalex-snapshot
The Bacterial Stressosome: A Modular System that Has Been Adapted to Control Secondary Messenger Signaling
inferred← citeshttps://doi.org/10.1016/j.tim.2008.02.006openalex-snapshot
Rhodobacter sphaeroides: complexity in chemotactic signalling
inferred← citeshttps://doi.org/10.1016/j.tim.2008.07.004openalex-snapshot
Living on a surface: swarming and biofilm formation
inferred← citeshttps://doi.org/10.1016/j.tim.2012.02.008openalex-snapshot
When the PilZ don’t work: effectors for cyclic di-GMP action in bacteria
inferred← citeshttps://doi.org/10.1016/j.tim.2014.04.004openalex-snapshot
Chemosensory signaling systems that control bacterial survival
inferred← citeshttps://doi.org/10.1016/j.tim.2014.05.002openalex-snapshot
Biofilms, flagella, and mechanosensing of surfaces by bacteria
inferred← citeshttps://doi.org/10.1016/j.tim.2015.03.004openalex-snapshot
Positioning of bacterial chemoreceptors
inferred← citeshttps://doi.org/10.1016/j.vaccine.2006.10.033openalex-snapshot
The bacterial second messenger cyclic diGMP exhibits potent adjuvant properties
inferred← citeshttps://doi.org/10.1016/j.vaccine.2009.12.045openalex-snapshot
The member of the cyclic di-nucleotide family bis-(3′, 5′)-cyclic dimeric inosine monophosphate exerts potent activity as mucosal adjuvant
inferred← citeshttps://doi.org/10.1016/j.xpro.2023.102269openalex-snapshot
Protocol to assess metabolic activity of Pseudomonas aeruginosa by measuring heat flow using isothermal calorimetry
inferred← citeshttps://doi.org/10.1016/j.ygeno.2014.09.007openalex-snapshot
Parallel evolution of small colony variants in Burkholderia cenocepacia biofilms
inferred← citeshttps://doi.org/10.1016/s0021-9258(19)84115-7openalex-snapshot
Allosteric Control of Cyclic di-GMP Signaling
inferred← citeshttps://doi.org/10.1016/s0076-6879(06)22001-9openalex-snapshot
Comparative Genomic and Protein Sequence Analyses of a Complex System Controlling Bacterial Chemotaxis
inferred← citeshttps://doi.org/10.1016/s0076-6879(10)71010-7openalex-snapshot
Biophysical Assays for Protein Interactions in the Wsp Sensory System and Biofilm Formation
inferred← citeshttps://doi.org/10.1017/s1462399410001420openalex-snapshot
Interference ofPseudomonas aeruginosasignalling and biofilm formation for infection control
inferred← citeshttps://doi.org/10.1021/acs.biochem.6b00338openalex-snapshot
Biochemical and Cellular Characterization and Inhibitor Discovery of Pseudomonas aeruginosa 15-Lipoxygenase
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b01184openalex-snapshot
Synthesis of Triazole-Linked Analogues of c-di-GMP and Their Interactions with Diguanylate Cyclase
inferred← citeshttps://doi.org/10.1021/acs.langmuir.0c00643openalex-snapshot
Synergy between Sophorolipid Biosurfactant and SDS Increases the Efficiency of P. aeruginosa Biofilm Disruption
inferred← citeshttps://doi.org/10.1021/acsami.3c18656openalex-snapshot
Carboxylated Nanoparticle Surfaces Enhance Association with Mucoid Pseudomonas aeruginosa Biofilms
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.3c00481openalex-snapshot
pH-Responsive, Charge-Reversing Layer-by-Layer Nanoparticle Surfaces Enhance Biofilm Penetration and Eradication
inferred← citeshttps://doi.org/10.1021/acsestengg.2c00216openalex-snapshot
Quorum Quenching-Mediated Biofilm Mitigation on Functionalized Ultrafiltration Membranes via Atom Transfer Radical Polymerization
inferred← citeshttps://doi.org/10.1021/acsestwater.5c00865openalex-snapshot
Review: Extracellular Electron Transfer Mechanisms and Enhancement Strategies of Electroactive Microorganisms in Bioelectrochemical Systems
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c01907openalex-snapshot
Activated Carbon Facilitates Anaerobic Digestion of Furfural Wastewater: Effect of Direct Interspecies Electron Transfer
inferred← citeshttps://doi.org/10.1021/acssynbio.3c00009openalex-snapshot
In VivoSampling of Intracellular Heterogeneity ofPseudomonas putidaEnables Multiobjective Optimization of Genetic Devices
inferred← citeshttps://doi.org/10.1021/acssynbio.7b00273openalex-snapshot
Optogenetics Manipulation Enables Prevention of Biofilm Formation of Engineered Pseudomonas aeruginosa on Surfaces
inferred← citeshttps://doi.org/10.1021/bi901409gopenalex-snapshot
An Oxygen-Sensing Diguanylate Cyclase and Phosphodiesterase Couple for c-di-GMP Control
inferred← citeshttps://doi.org/10.1021/bk-2019-1323.ch002openalex-snapshot
Role of Exopolysaccharides in Biofilm Formation
inferred← citeshttps://doi.org/10.1021/cb400485kopenalex-snapshot
High-Throughput Screening Using the Differential Radial Capillary Action of Ligand Assay Identifies Ebselen As an Inhibitor of Diguanylate Cyclases
inferred← citeshttps://doi.org/10.1021/cr100354fopenalex-snapshot
Listening to a New Language: DSF-Based Quorum Sensing in Gram-Negative Bacteria
inferred← citeshttps://doi.org/10.1021/cr300011sopenalex-snapshot
(3′-5′)-Cyclic Dinucleotides: Synthetic Strategies and Biological Potential
inferred← citeshttps://doi.org/10.1021/ja1091062openalex-snapshot
Thiazole Orange-Induced c-di-GMP Quadruplex Formation Facilitates a Simple Fluorescent Detection of This Ubiquitous Biofilm Regulating Molecule
inferred← citeshttps://doi.org/10.1021/ja1112029openalex-snapshot
Conservative Change to the Phosphate Moiety of Cyclic Diguanylic Monophosphate Remarkably Affects Its Polymorphism and Ability To Bind DGC, PDE, and PilZ Proteins
inferred← citeshttps://doi.org/10.1021/ja9057103openalex-snapshot
Locked Chromophore Analogs Reveal That Photoactive Yellow Protein Regulates Biofilm Formation in the Deep Sea Bacterium Idiomarina loihiensis
inferred← citeshttps://doi.org/10.1038/441300aopenalex-snapshot
The superficial life of microbes
inferred← citeshttps://doi.org/10.1038/ismej.2017.83openalex-snapshot
Co-evolution with Staphylococcus aureus leads to lipopolysaccharide alterations in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1038/nchembio.2337openalex-snapshot
Versatile modes of cellular regulation via cyclic dinucleotides
inferred← citeshttps://doi.org/10.1038/ncomms10508openalex-snapshot
Rapid radiation in bacteria leads to a division of labour
inferred← citeshttps://doi.org/10.1038/ng.3148openalex-snapshot
Convergent evolution and adaptation of Pseudomonas aeruginosa within patients with cystic fibrosis
inferred← citeshttps://doi.org/10.1038/nmeth946openalex-snapshot
SCALEs: multiscale analysis of library enrichment
inferred← citeshttps://doi.org/10.1038/nprot.2015.115openalex-snapshot
Precision-engineering the Pseudomonas aeruginosa genome with two-step allelic exchange
inferred← citeshttps://doi.org/10.1038/nrd4000openalex-snapshot
Applying insights from biofilm biology to drug development — can a new approach be developed?
inferred← citeshttps://doi.org/10.1038/nrmicro1770openalex-snapshot
Chemosensory pathways, motility and development in Myxococcus xanthus
inferred← citeshttps://doi.org/10.1038/nrmicro2109openalex-snapshot
Principles of c-di-GMP signalling in bacteria
inferred← citeshttps://doi.org/10.1038/nrmicro2203openalex-snapshot
Structural and mechanistic determinants of c-di-GMP signalling
inferred← citeshttps://doi.org/10.1038/nrmicro2505openalex-snapshot
Signal processing in complex chemotaxis pathways
inferred← citeshttps://doi.org/10.1038/s41396-018-0332-5openalex-snapshot
Niche-directed evolution modulates genome architecture in freshwater Planctomycetes
inferred← citeshttps://doi.org/10.1038/s41396-020-00779-9openalex-snapshot
Biofilm matrix disrupts nematode motility and predatory behavior
inferred← citeshttps://doi.org/10.1038/s41396-022-01190-2openalex-snapshot
Biofilm matrix cloaks bacterial quorum sensing chemoattractants from predator detection
inferred← citeshttps://doi.org/10.1038/s41467-021-22176-2openalex-snapshot
Bacterial cyclic diguanylate signaling networks sense temperature
inferred← citeshttps://doi.org/10.1038/s41467-025-60567-xopenalex-snapshot
Combinatorial discovery of microtopographical landscapes that resist biofilm formation through quorum sensing mediated autolubrication
inferred← citeshttps://doi.org/10.1038/s41467-025-64557-xopenalex-snapshot
Stress-hardening behaviour of biofilm streamers
inferred← citeshttps://doi.org/10.1038/s41522-020-00165-5openalex-snapshot
The phosphorylated regulator of chemotaxis is crucial throughout biofilm biogenesis in Shewanella oneidensis
inferred← citeshttps://doi.org/10.1038/s41522-021-00225-4openalex-snapshot
Identification of small molecules that interfere with c-di-GMP signaling and induce dispersal of Pseudomonas aeruginosa biofilms
inferred← citeshttps://doi.org/10.1038/s41522-021-00257-wopenalex-snapshot
Carbohydrates from Pseudomonas aeruginosa biofilms interact with immune C-type lectins and interfere with their receptor function
inferred← citeshttps://doi.org/10.1038/s41522-022-00365-1openalex-snapshot
The Wsp chemosensory system modulates c-di-GMP-dependent biofilm formation by integrating DSF quorum sensing through the WspR-RpfG complex in Lysobacter
inferred← citeshttps://doi.org/10.1038/s41522-024-00523-7openalex-snapshot
Bacterial c-di-GMP triggers metamorphosis of mussel larvae through a STING receptor
inferred← citeshttps://doi.org/10.1038/s41522-024-00644-zopenalex-snapshot
Hypermutability bypasses genetic constraints in SCV phenotypic switching in Pseudomonas aeruginosa biofilms
inferred← citeshttps://doi.org/10.1038/s41522-025-00673-2openalex-snapshot
Echinacoside reduces intracellular c-di-GMP levels and potentiates tobramycin activity against Pseudomonas aeruginosa biofilm aggregates
inferred← citeshttps://doi.org/10.1038/s41522-025-00710-0openalex-snapshot
SadB, a mediator of AmrZ proteolysis and biofilm development in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1038/s41522-025-00841-4openalex-snapshot
Two unrelated Pseudomonas aeruginosa phages require the exopolysaccharide Psl for infection
inferred← citeshttps://doi.org/10.1038/s41522-025-00863-yopenalex-snapshot
Competition between Pseudomonas species constrains ecological diversification in polymicrobial biofilms
inferred← citeshttps://doi.org/10.1038/s41564-023-01403-0openalex-snapshot
A genetic switch controls Pseudomonas aeruginosa surface colonization
inferred← citeshttps://doi.org/10.1038/s41564-023-01468-xopenalex-snapshot
Bacterial c-di-GMP has a key role in establishing host–microbe symbiosis
inferred← citeshttps://doi.org/10.1038/s41564-024-01842-3openalex-snapshot
Pseudomonas aeruginosa faces a fitness trade-off between mucosal colonization and antibiotic tolerance during airway infection
inferred← citeshttps://doi.org/10.1038/s41564-025-02087-4openalex-snapshot
Pseudomonas aeruginosa senses exopolysaccharide trails using type IV pili and adhesins during biofilm formation
inferred← citeshttps://doi.org/10.1038/s41598-017-09926-3openalex-snapshot
The EAL-domain protein FcsR regulates flagella, chemotaxis and type III secretion system in Pseudomonas aeruginosa by a phosphodiesterase independent mechanism
inferred← citeshttps://doi.org/10.1038/s41598-018-20283-7openalex-snapshot
The activity of the C4-dicarboxylic acid chemoreceptor of Pseudomonas aeruginosa is controlled by chemoattractants and antagonists
inferred← citeshttps://doi.org/10.1038/s41598-019-42952-xopenalex-snapshot
Anaerobiosis influences virulence properties of Pseudomonas aeruginosa cystic fibrosis isolates and the interaction with Staphylococcus aureus
inferred← citeshttps://doi.org/10.1038/s41598-019-49697-7openalex-snapshot
The involvement of McpB chemoreceptor from Pseudomonas aeruginosa PAO1 in virulence
inferred← citeshttps://doi.org/10.1038/s42003-022-03453-2openalex-snapshot
The Pel polysaccharide is predominantly composed of a dimeric repeat of α-1,4 linked galactosamine and N-acetylgalactosamine
inferred← citeshttps://doi.org/10.1038/s42003-025-08693-6openalex-snapshot
Coordination of virulence factors and lifestyle transition in Pseudomonas aeruginosa through single-cell analysis
inferred← citeshttps://doi.org/10.1038/s44328-025-00052-zopenalex-snapshot
Zwitterionic nanoplasmonic bio-meshes for in situ spatiotemporal SERS monitoring of Pseudomonas aeruginosa biofilms
inferred← citeshttps://doi.org/10.1038/srep25318openalex-snapshot
Raffinose, a plant galactoside, inhibits Pseudomonas aeruginosa biofilm formation via binding to LecA and decreasing cellular cyclic diguanylate levels
inferred← citeshttps://doi.org/10.1038/srep29499openalex-snapshot
Dcsbis (PA2771) from Pseudomonas aeruginosa is a highly active diguanylate cyclase with unique activity regulation
inferred← citeshttps://doi.org/10.1039/b908047copenalex-snapshot
Interplay of heritage and habitat in the distribution of bacterial signal transduction systems
inferred← citeshttps://doi.org/10.1039/c2mb05430bopenalex-snapshot
A C-di-GMP–proflavine–hemin supramolecular complex has peroxidase activity—implication for a simple colorimetric detection
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