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Involvement of Two-Component Signaling on Bacterial Motility and Biofilm Development

https://doi.org/10.1128/jb.00259-17
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What this work says

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

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Two regulatory fim genes, fimB and fimE, control the phase variation of type 1 fimbriae in Escherichia coli.
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Crystal structure of nonphosphorylated receiver domain of the stress response regulator RcsB from Escherichia coli
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Interacting Components of the Flagellar Motor ofEscherichia coliRevealed by the Two-hybrid System in Yeast
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The N terminus of the flagellar switch protein, FliM, is the binding domain for the chemotactic response regulator, CheY
inferredcites →https://doi.org/10.1007/82_2016_53openalex-snapshot
Flagellar Regulation and Virulence in the Entomopathogenic Bacteria—Xenorhabdus nematophila and Photorhabdus luminescens
inferredcites →https://doi.org/10.1007/978-3-319-20215-0_12openalex-snapshot
The Epinephrine/Norepinephrine /Autoinducer-3 Interkingdom Signaling System in Escherichia coli O157:H7
inferredcites →https://doi.org/10.1007/s002030050626openalex-snapshot
Acetyl phosphate and the phosphorylation of OmpR are involved in the regulation of the cell division rate in Escherichia coli
inferredcites →https://doi.org/10.1007/s00294-015-0552-4openalex-snapshot
Bacterial protein acetylation: new discoveries unanswered questions
inferredcites →https://doi.org/10.1007/s00726-011-1140-7openalex-snapshot
Involvement of AtoSC two-component system in Escherichia coli flagellar regulon
inferredcites →https://doi.org/10.1007/s12275-013-2212-zopenalex-snapshot
Mutations upregulating the flhDC operon of Escherichia coli K-12
inferredcites →https://doi.org/10.1016/0014-5793(89)80617-9openalex-snapshot
Location of phosphorylation site and DNA‐binding site of a positive regulator, OmpR, involved in activation of the osmoregulatory genes of Escherichia coli
inferredcites →https://doi.org/10.1016/0014-5793(90)80626-topenalex-snapshot
Phosphorylation of a bacterial activator protein, OmpR, by a protein kinase, EnvZ, stimulates the transcription of the ompF and ompC genes in Escherichia coli
inferredcites →https://doi.org/10.1016/0022-2836(81)90218-7openalex-snapshot
Genetic analysis of the ompB locus in Escherichia coli K-12
inferredcites →https://doi.org/10.1016/0092-8674(92)90247-aopenalex-snapshot
Assembly of an MCP receptor, CheW, and kinase CheA complex in the bacterial chemotaxis signal transduction pathway
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Signal transduction by the EnvZ-OmpR phosphotransfer system in bacteria
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The Central Metabolic Pathways of Escherichia coli: Relationship between Flux and Control at a Branch Point, Efficiency of Conversion to Biomass, and Excretion of Acetate
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Enhanced biofilm formation and/or cell viability by polyamines through stimulation of response regulators UvrY and CpxR in the two-component signal transducing systems, and ribosome recycling factor
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Responding to chemical gradients: bacterial chemotaxis
inferredcites →https://doi.org/10.1016/j.jmb.2007.12.070openalex-snapshot
In Vivo Acetylation of CheY, a Response Regulator in Chemotaxis of Escherichia coli
inferredcites →https://doi.org/10.1016/j.jmb.2016.08.003openalex-snapshot
Molecular Mechanisms of Two-Component Signal Transduction
inferredcites →https://doi.org/10.1016/j.mib.2016.02.004openalex-snapshot
Sensational biofilms: surface sensing in bacteria
inferredcites →https://doi.org/10.1016/j.resmic.2005.02.005openalex-snapshot
Role of bacterial cell surface structures in Escherichia coli biofilm formation
inferredcites →https://doi.org/10.1016/j.resmic.2005.11.005openalex-snapshot
The role of the Rcs phosphorelay in Enterobacteriaceae
inferredcites →https://doi.org/10.1016/j.resmic.2010.04.002openalex-snapshot
RcsB plays a central role in H-NS-dependent regulation of motility and acid stress resistance in Escherichia coli
inferredcites →https://doi.org/10.1016/j.tibs.2007.03.002openalex-snapshot
Bacterial response regulators: versatile regulatory strategies from common domains
inferredcites →https://doi.org/10.1016/j.tim.2008.11.001openalex-snapshot
The developmental model of microbial biofilms: ten years of a paradigm up for review
inferredcites →https://doi.org/10.1016/j.tim.2012.07.003openalex-snapshot
Non-genetic diversity shapes infectious capacity and host resistance
inferredcites →https://doi.org/10.1016/j.tim.2015.03.003openalex-snapshot
Signaling and sensory adaptation in Escherichia coli chemoreceptors: 2015 update
inferredcites →https://doi.org/10.1016/j.ymeth.2016.09.012openalex-snapshot
Mechanistic study of base-pairing small regulatory RNAs in bacteria
inferredcites →https://doi.org/10.1016/s0021-9258(18)83200-8openalex-snapshot
Protein phosphorylation in chemotaxis and two-component regulatory systems of bacteria
inferredcites →https://doi.org/10.1016/s0021-9258(18)98646-1openalex-snapshot
Crystal structure of Escherichia coli CheY refined at 1.7-A resolution
inferredcites →https://doi.org/10.1016/s1369-5274(00)00070-9openalex-snapshot
Two-component and phosphorelay signal transduction
inferredcites →https://doi.org/10.1021/bi00121a034openalex-snapshot
Correlation between phosphorylation of the chemotaxis protein CheY and its activity at the flagellar motor
inferredcites →https://doi.org/10.1021/bi300147mopenalex-snapshot
Solution Structure of a Complex of the Histidine Autokinase CheA with Its Substrate CheY
inferredcites →https://doi.org/10.1021/bi9925524openalex-snapshot
The 1.9 Å Resolution Crystal Structure of Phosphono-CheY, an Analogue of the Active Form of the Response Regulator, CheY,
inferredcites →https://doi.org/10.1038/83053openalex-snapshot
Crystal structure of an activated response regulator bound to its target.
inferredcites →https://doi.org/10.1038/ismej.2011.27openalex-snapshot
IS 5 inserts upstream of the master motility operon flhDC in a quasi-Lamarckian way
inferredcites →https://doi.org/10.1038/nrmicro2109openalex-snapshot
Principles of c-di-GMP signalling in bacteria
inferredcites →https://doi.org/10.1038/nsb0198-25openalex-snapshot
Structure of the CheY-binding domain of histidine kinase CheA in complex with CheY
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02380.xopenalex-snapshot
Positive regulation of motility and flhDC expression by the RNA‐binding protein CsrA of Escherichia coli
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02393.xopenalex-snapshot
A novel feature of the multistep phosphorelay in Escherichia coli: a revised model of the RcsC → YojN → RcsB signalling pathway implicated in capsular synthesis and swarming behaviour
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.02803.xopenalex-snapshot
Quorum sensing Escherichia coli regulators B and C (QseBC): a novel two‐component regulatory system involved in the regulation of flagella and motility by quorum sensing in E. coli
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03032.xopenalex-snapshot
LrhA as a new transcriptional key regulator of flagella, motility and chemotaxis genes in Escherichia coli
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03457.xopenalex-snapshot
Evidence that acetyl phosphate functions as a global signal during biofilm development
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03601.xopenalex-snapshot
RcsCDB His‐Asp phosphorelay system negatively regulates the flhDC operon in Escherichia coli
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03815.xopenalex-snapshot
The RcsC sensor kinase is required for normal biofilm formation in Escherichia coli K‐12 and controls the expression of a regulon in response to growth on a solid surface
inferredcites →https://doi.org/10.1073/pnas.0604343103openalex-snapshot
The QseC sensor kinase: A bacterial adrenergic receptor
inferredcites →https://doi.org/10.1073/pnas.1612836114openalex-snapshot
QseC inhibition as an antivirulence approach for colitis-associated bacteria
inferredcites →https://doi.org/10.1073/pnas.86.16.6052openalex-snapshot
Phosphorylation of OmpR by the osmosensor EnvZ modulates expression of the ompF and ompC genes in Escherichia coli.
inferredcites →https://doi.org/10.1073/pnas.88.14.6269openalex-snapshot
Bacterial chemotaxis signaling complexes: formation of a CheA/CheW complex enhances autophosphorylation and affinity for CheY.
inferredcites →https://doi.org/10.1073/pnas.90.19.8787openalex-snapshot
Phosphorylation-dependent binding of a signal molecule to the flagellar switch of bacteria.
inferredcites →https://doi.org/10.1074/jbc.273.37.24030openalex-snapshot
Enhanced Binding of Altered H-NS Protein to Flagellar Rotor Protein FliG Causes Increased Flagellar Rotational Speed and Hypermotility in Escherichia coli
inferredcites →https://doi.org/10.1074/jbc.274.6.3300openalex-snapshot
Identification of an RcsA/RcsB Recognition Motif in the Promoters of Exopolysaccharide Biosynthetic Operons from Erwinia amylovora and Pantoea stewartii Subspeciesstewartii
inferredcites →https://doi.org/10.1074/jbc.275.10.7013openalex-snapshot
The RcsAB Box
inferredcites →https://doi.org/10.1074/jbc.m114.565762openalex-snapshot
The CpxR/CpxA Two-component Regulatory System Up-regulates the Multidrug Resistance Cascade to Facilitate Escherichia coli Resistance to a Model Antimicrobial Peptide
inferredcites →https://doi.org/10.1074/jbc.m115.696815openalex-snapshot
Interaction of the RcsB Response Regulator with Auxiliary Transcription Regulators in Escherichia coli
inferredcites →https://doi.org/10.1074/jbc.m303201200openalex-snapshot
Binding of the Chemotaxis Response Regulator CheY to the Isolated, Intact Switch Complex of the Bacterial Flagellar Motor
inferredcites →https://doi.org/10.1093/femsle/fnw011openalex-snapshot
In vitroevidence that RNA Polymerase acetylation and acetyl phosphate-dependent CpxR phosphorylation affectcpxPtranscription regulation
inferredcites →https://doi.org/10.1093/nar/gks869openalex-snapshot
Structural insight of a concentration-dependent mechanism by which YdiV inhibits Escherichia coli flagellum biogenesis and motility
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a122817openalex-snapshot
Phosphorylation of a Bacterial Activator Protein, OmpR, by a Protein Kinase, EnvZ, Results in Stimulation of Its DNA-Binding Ability1
inferredcites →https://doi.org/10.1097/ta.0000000000001007openalex-snapshot
The role of the sensor kinase, QseC, an adrenergic receptor of Escherichia coli, in bacterial translocation during hemorrhagic shock
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The Enzymic Interconversion of Acetate and Acetyl-coenzyme A in Escherichia coli
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Analysis of the fim cluster of an avian O2 strain of Escherichia coli: serogroup-specific sites within fimA and nucleotide sequence of fimI
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Deletion analysis of RcsC reveals a novel signalling pathway controlling poly-N-acetylglucosamine synthesis and biofilm formation in Escherichia coli
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Virulence adaptations of Pseudomonas aeruginosa isolated from patients with non-cystic fibrosis bronchiectasis
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Functional and expressional analyses of the anti-FlhD4C2 factor gene ydiV in Escherichia coli
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The fimbriae activator MatA switches off motility in Escherichia coli by repression of the flagellar master operon flhDC
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OmpR regulation of the uropathogenic Escherichia coli fimB gene in an acidic/high osmolality environment
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Integration host factor (IHF) mediates repression of flagella in enteropathogenic and enterohaemorrhagic Escherichia coli
inferredcites →https://doi.org/10.1101/gad.1700308openalex-snapshot
Signal integration in bacterial two-component regulatory systems
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Cell cycle-dependent dynamic localization of a bacterial response regulator with a novel di-guanylate cyclase output domain
inferredcites →https://doi.org/10.1101/gad.475808openalex-snapshot
Inverse regulatory coordination of motility and curli-mediated adhesion in Escherichia coli
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Regulation of acetyl phosphate synthesis and degradation, and the control of flagellar expression in Escherichia coli
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Cyclic diguanylate (c‐di‐GMP) regulates Vibrio cholerae biofilm formation
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GGDEF and EAL domains inversely regulate cyclic di‐GMP levels and transition from sessility to motility
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C‐di‐GMP: the dawning of a novel bacterial signalling system
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Transcriptional regulation of flhDC by QseBC and σ 28 (FliA) in enterohaemorrhagic Escherichia coli
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NsrR targets in the Escherichia coli genome: new insights into DNA sequence requirements for binding and a role for NsrR in the regulation of motility
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QseC‐mediated dephosphorylation of QseB is required for expression of genes associated with virulence in uropathogenic Escherichia coli
inferredcites →https://doi.org/10.1111/j.1365-2958.2012.08209.xopenalex-snapshot
A complex network of small non‐coding RNAs regulate motility in E scherichia coli
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The fimA gene encoding the type‐1 fimbrial subunit of Escherichia coli
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Post‐transcriptional regulation on a global scale: form and function of Csr/Rsm systems
inferredcites →https://doi.org/10.1111/mmi.12828openalex-snapshot
Mutually repressing repressor functions and multi‐layered cellular heterogeneity regulate the bistable S almonella fliC census
inferredcites →https://doi.org/10.1111/mmi.12858openalex-snapshot
CheY's acetylation sites responsible for generating clockwise flagellar rotation in E scherichia coli
inferredcites →https://doi.org/10.1111/mmi.13161openalex-snapshot
Protein acetylation dynamics in response to carbon overflow in E scherichia coli
inferredcites →https://doi.org/10.1111/mmi.13427openalex-snapshot
RflM mediates target specificity of the RcsCDB phosphorelay system for transcriptional repression of flagellar synthesis in Salmonella enterica
inferredcites →https://doi.org/10.1126/science.1160354openalex-snapshot
Targeting QseC Signaling and Virulence for Antibiotic Development
inferredcites →https://doi.org/10.1128/aem.02998-12openalex-snapshot
Hha Controls Escherichia coli O157:H7 Biofilm Formation by Differential Regulation of Global Transcriptional Regulators FlhDC and CsgD
inferredcites →https://doi.org/10.1128/iai.00369-16openalex-snapshot
Fur Represses Adhesion to, Invasion of, and Intracellular Bacterial Community Formation within Bladder Epithelial Cells and Motility in Uropathogenic Escherichia coli
inferredcites →https://doi.org/10.1128/iai.00630-07openalex-snapshot
Differential Effects of Epinephrine, Norepinephrine, and Indole on Escherichia coli O157:H7 Chemotaxis, Colonization, and Gene Expression
inferredcites →https://doi.org/10.1128/iai.70.3.1391-1402.2002openalex-snapshot
Osmolarity and pH Growth Conditions Regulate fim Gene Transcription and Type 1 Pilus Expression in Uropathogenic Escherichia coli
inferredcites →https://doi.org/10.1128/jb.00309-15openalex-snapshot
Function of the Histone-Like Protein H-NS in Motility of Escherichia coli: Multiple Regulatory Roles Rather than Direct Action at the Flagellar Motor
inferredcites →https://doi.org/10.1128/jb.00383-13openalex-snapshot
Acetylation of the Response Regulator RcsB Controls Transcription from a Small RNA Promoter
inferredcites →https://doi.org/10.1128/jb.00384-15openalex-snapshot
Lessons in Fundamental Mechanisms and Diverse Adaptations from the 2015 Bacterial Locomotion and Signal Transduction Meeting
inferredcites →https://doi.org/10.1128/jb.00455-15openalex-snapshot
Mutations That StimulateflhDCExpression in Escherichia coli K-12
inferredcites →https://doi.org/10.1128/jb.00564-07openalex-snapshot
The Intracellular Concentration of Acetyl Phosphate in Escherichia coli Is Sufficient for Direct Phosphorylation of Two-Component Response Regulators
inferredcites →https://doi.org/10.1128/jb.00799-06openalex-snapshot
FliT Acts as an Anti-FlhD 2 C 2 Factor in the Transcriptional Control of the Flagellar Regulon in Salmonella enterica Serovar Typhimurium
inferredcites →https://doi.org/10.1128/jb.00861-16openalex-snapshot
Genetic and Mechanistic Analyses of the Periplasmic Domain of the Enterohemorrhagic Escherichia coli QseC Histidine Sensor Kinase
inferredcites →https://doi.org/10.1128/jb.01685-09openalex-snapshot
The Physiological Stimulus for the BarA Sensor Kinase
inferredcites →https://doi.org/10.1128/jb.01780-05openalex-snapshot
A Complex Transcription Network Controls the Early Stages of Biofilm Development byEscherichia coli
inferredcites →https://doi.org/10.1128/jb.01996-07openalex-snapshot
FliZ Is a Posttranslational Activator of FlhD 4 C 2 -Dependent Flagellar Gene Expression
inferredcites →https://doi.org/10.1128/jb.02065-14openalex-snapshot
Chemotaxis of Escherichia coli to Norepinephrine (NE) Requires Conversion of NE to 3,4-Dihydroxymandelic Acid
inferredcites →https://doi.org/10.1128/jb.160.1.184-191.1984openalex-snapshot
lon transcriptional regulation of genes necessary for capsular polysaccharide synthesis in Escherichia coli K-12
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Regulation of capsular polysaccharide synthesis in Escherichia coli K-12: characterization of three regulatory genes
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Flagellar transcriptional activators FlbB and FlaI: gene sequences and 5' consensus sequences of operons under FlbB and FlaI control
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Fine-structure mapping and identification of two regulators of capsule synthesis in Escherichia coli K-12
inferredcites →https://doi.org/10.1128/jb.171.9.5190-5193.1989openalex-snapshot
Both CheA and CheW are required for reconstitution of chemotactic signaling in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.172.2.659-669.1990openalex-snapshot
RcsB and RcsC: a two-component regulator of capsule synthesis in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.173.17.5308-5314.1991openalex-snapshot
Roles of fimB and fimE in site-specific DNA inversion associated with phase variation of type 1 fimbriae in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.174.19.6256-6263.1992openalex-snapshot
DnaK, DnaJ, and GrpE are required for flagellum synthesis in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.175.10.2793-2798.1993openalex-snapshot
Is acetyl phosphate a global signal in Escherichia coli?
inferredcites →https://doi.org/10.1128/jb.175.7.2097-2101.1993openalex-snapshot
The carboxy-terminal portion of the CheA kinase mediates regulation of autophosphorylation by transducer and CheW
inferredcites →https://doi.org/10.1128/jb.176.17.5537-5540.1994openalex-snapshot
The H-NS protein is involved in the biogenesis of flagella in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.177.16.4696-4702.1995openalex-snapshot
Modulation of flagellar expression in Escherichia coli by acetyl phosphate and the osmoregulator OmpR
inferredcites →https://doi.org/10.1128/jb.178.3.668-674.1996openalex-snapshot
A regulator of the flagellar regulon of Escherichia coli, flhD, also affects cell division
inferredcites →https://doi.org/10.1128/jb.180.3.722-731.1998openalex-snapshot
Curli Fibers Are Highly Conserved between Salmonella typhimurium and Escherichia coli with Respect to Operon Structure and Regulation
inferredcites →https://doi.org/10.1128/jb.181.21.6772-6778.1999openalex-snapshot
The CpxRA Signal Transduction System of Escherichia coli : Growth-Related Autoactivation and Control of Unanticipated Target Operons
inferredcites →https://doi.org/10.1128/jb.181.24.7500-7508.1999openalex-snapshot
Multiple Control of Flagellum Biosynthesis in Escherichia coli : Role of H-NS Protein and the Cyclic AMP-Catabolite Activator Protein Complex in Transcription of the flhDC Master Operon
inferredcites →https://doi.org/10.1128/jb.183.24.7213-7223.2001openalex-snapshot
Complex Regulatory Network Controls Initial Adhesion and Biofilm Formation in Escherichia coli via Regulation of the csgD Gene
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.186.22.7529-7537.2004openalex-snapshot
Increased Motility of Escherichia coli by Insertion Sequence Element Integration into the Regulatory Region of the flhD Operon
inferredcites →https://doi.org/10.1128/jb.187.6.2038-2049.2005openalex-snapshot
CpxR/OmpR Interplay Regulates Curli Gene Expression in Response to Osmolarity inEscherichia coli
inferredcites →https://doi.org/10.1128/jb.188.1.305-316.2006openalex-snapshot
Autoinducer 2 Controls Biofilm Formation in Escherichia coli through a Novel Motility Quorum-Sensing Regulator (MqsR, B3022)
inferredcites →https://doi.org/10.1128/mbio.01611-14openalex-snapshot
A Nutrient-Tunable Bistable Switch Controls Motility in Salmonella enterica Serovar Typhimurium
inferredcites →https://doi.org/10.1128/mmbr.00020-06openalex-snapshot
Stimulus Perception in Bacterial Signal-Transducing Histidine Kinases
inferredcites →https://doi.org/10.1128/msphere.00009-17openalex-snapshot
Transcriptome-Level Signatures in Gene Expression and Gene Expression Variability during Bacterial Adaptive Evolution
inferredcites →https://doi.org/10.1146/annurev-cellbio-101011-155705openalex-snapshot
Second Messenger Regulation of Biofilm Formation: Breakthroughs in Understanding c-di-GMP Effector Systems
inferredcites →https://doi.org/10.1146/annurev.biochem.69.1.183openalex-snapshot
Two-Component Signal Transduction
inferredcites →https://doi.org/10.1146/annurev.micro.56.012302.160705openalex-snapshot
Biofilms as Complex Differentiated Communities
inferredcites →https://doi.org/10.1159/000333108openalex-snapshot
Transposon-Mediated Adaptive and Directed Mutations and Their Potential Evolutionary Benefits
inferredcites →https://doi.org/10.1186/1471-2180-13-182openalex-snapshot
OmpR and RcsB abolish temporal and spatial changes in expression of flhD in Escherichia coli Biofilm
inferredcites →https://doi.org/10.1186/s12866-016-0878-1openalex-snapshot
Spontaneous mutations in the flhD operon generate motility heterogeneity in Escherichia coli biofilm
inferredcites →https://doi.org/10.1186/s12866-017-0966-xopenalex-snapshot
Disruption of rcsB by a duplicated sequence in a curli-producing Escherichia coli O157:H7 results in differential gene expression in relation to biofilm formation, stress responses and metabolism
inferredcites →https://doi.org/10.1248/bpb.20.327openalex-snapshot
Decrease in Expression of the Master Operon of Flagellin Synthesis in a dnaA46 Mutant of Escherichia coli.
inferredcites →https://doi.org/10.1371/journal.pone.0094816openalex-snapshot
Structural, Kinetic and Proteomic Characterization of Acetyl Phosphate-Dependent Bacterial Protein Acetylation
inferredcites →https://doi.org/10.1371/journal.pone.0145035openalex-snapshot
Genomic Targets and Features of BarA-UvrY (-SirA) Signal Transduction Systems
inferredcites →https://doi.org/10.1371/journal.ppat.1000553openalex-snapshot
The QseC Adrenergic Signaling Cascade in Enterohemorrhagic E. coli (EHEC)
inferredcites →https://doi.org/10.15252/msb.20145227openalex-snapshot
Protein acetylation affects acetate metabolism, motility and acid stress response in Escherichia coli
inferredcites →https://doi.org/10.2210/pdb3chy/pdbopenalex-snapshot
CRYSTAL STRUCTURE OF ESCHERICHIA COLI CHEY REFINED AT 1.7-ANGSTROM RESOLUTION
inferredcites →https://doi.org/10.2217/fmb.10.83openalex-snapshot
The Rcs Phosphorelay: More Than Just A Two-Component Pathway
inferredcites →https://doi.org/10.3389/fcimb.2016.00011openalex-snapshot
The Two-Component System CpxRA Negatively Regulates the Locus of Enterocyte Effacement of Enterohemorrhagic Escherichia coli Involving σ32 and Lon protease
inferredcites →https://doi.org/10.3389/fmicb.2017.00029openalex-snapshot
Phenotypic Microdiversity and Phylogenetic Signal Analysis of Traits Related to Social Interaction in Bacillus spp. from Sediment Communities

What points at this work

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

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Reciprocal Regulation of OmpR and Hfq and Their Regulatory Actions on the Vi Polysaccharide Capsular Antigen in Salmonella enterica Serovar Typhi
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Backbone resonance assignment of the catalytic and ATP-binding domain of CpxA from Escherichia coli
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Bacterial Interactions With PEEK
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Biofilm formation and persister cells
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Epigenetic Mechanisms in Bacteria Bridge Physiology, Growth and Host–Pathogen Interactions
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Key signaling pathways hijacked by biofilms
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Orphan response regulator Rv3143 increases antibiotic sensitivity by regulating cell wall permeability in Mycobacterium smegmatis
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Pseudomonas aeruginosa zinc homeostasis: Key issues for an opportunistic pathogen
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Recent advances in the development of bacterial response regulators inhibitors as antibacterial and/or antibiotic adjuvant agent: A new approach to combat bacterial resistance
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Tannic acid inhibits Escherichia coli biofilm formation and underlying molecular mechanisms: Biofilm regulator CsgD
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Sugar-coated cannonballs for effective antibacterial treatments but with negligible cytotoxicity based on silver (copper) -containing carbon dots and their mechanism analysis
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Rhein against Staphylococcus xylosus by interfering with respiratory metabolism and inducing oxidative stress
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Waterlogging-induced restructuring of phyllosphere microbiota associated with mycotoxin accumulation
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Antimicrobial activity of Duea ching (Ficus botryocarpa Miq.) fruit extract toward Listeria monocytogenes and Staphylococcus aureus and the synergism with UV-C and modified atmosphere packaging in refrigerated Asian seabass slices
inferred← citeshttps://doi.org/10.1016/j.foodres.2024.115039openalex-snapshot
Complete genome sequence provides information on quorum sensing related spoilage and virulence of Aeromonas salmonicida GMT3 isolated from spoiled sturgeon
inferred← citeshttps://doi.org/10.1016/j.foodres.2026.118369openalex-snapshot
Resveratrol blocks the spoilage and virulence phenotypes of Aeromonas salmonicida isolated from sturgeon by inhibiting quorum sensing
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2022.109784openalex-snapshot
Biofilm formation and genomic features of Listeria monocytogenes strains isolated from meat and dairy industries located in Piedmont (Italy)
inferred← citeshttps://doi.org/10.1016/j.isci.2019.05.022openalex-snapshot
Inefficient Secretion of Anti-Sigma Factor FlgM Inhibits Bacterial Motility at High Temperature
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Multi-omics elucidates how humic acid-biochar composite empowers sulfate-reducing bacteria for efficient biomineralization of cadmium and lead
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inferred← citeshttps://doi.org/10.1016/j.resmic.2023.104047openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.rhisph.2026.101264openalex-snapshot
Benzoxazinoids and plant growth-promoting bacteria: A pathway to sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.150911openalex-snapshot
Transcriptome expression analysis of the gene regulation mechanism of bacterial mineralization tolerance to high concentrations of Cd2+
inferred← citeshttps://doi.org/10.1016/j.softx.2023.101377openalex-snapshot
SBTAnalyzer: A data processing software package for single-bacterium tracking microscopy at material surfaces
inferred← citeshttps://doi.org/10.1016/j.tips.2026.01.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.vetmic.2017.10.017openalex-snapshot
Different activated methyl cycle pathways affect the pathogenicity of avian pathogenic Escherichia coli
inferred← citeshttps://doi.org/10.1021/acsami.7b14197openalex-snapshot
Prediction of Broad-Spectrum Pathogen Attachment to Coating Materials for Biomedical Devices
inferred← citeshttps://doi.org/10.1021/acsinfecdis.8b00255openalex-snapshot
Exploring the Links between Nucleotide Signaling and Quorum Sensing Pathways in Regulating Bacterial Virulence
inferred← citeshttps://doi.org/10.1021/acssensors.0c00008openalex-snapshot
Design of a Histidine Kinase FRET Sensor to Detect Complex Signal Integration within Living Bacteria
inferred← citeshttps://doi.org/10.1038/s41429-021-00475-6openalex-snapshot
Antibacterial and anti-biofilm activities of histidine kinase YycG inhibitors against Streptococcus agalactiae
inferred← citeshttps://doi.org/10.1038/s41467-022-31819-xopenalex-snapshot
Auxotrophic and prototrophic conditional genetic networks reveal the rewiring of transcription factors in Escherichia coli
inferred← citeshttps://doi.org/10.1038/s41467-024-48986-8openalex-snapshot
Interplay of two small RNAs fine-tunes hierarchical flagella gene expression in Campylobacter jejuni
inferred← citeshttps://doi.org/10.1038/s41467-025-66735-3openalex-snapshot
A small periplasmic protein governs broad physiological adaptations in Vibrio cholerae via regulation of the DbfRS two-component system
inferred← citeshttps://doi.org/10.1038/s41598-020-79762-5openalex-snapshot
Colony spreading of the gliding bacterium Flavobacterium johnsoniae in the absence of the motility adhesin SprB
inferred← citeshttps://doi.org/10.1038/s41598-021-97135-4openalex-snapshot
Refrigeration of eggs influences the virulence of Salmonella Typhimurium
inferred← citeshttps://doi.org/10.1080/03639045.2025.2464793openalex-snapshot
Formulation of topical gel contains a novel benzoic acid derivative for skin infection treatment: in vitro and in vivo evaluations
inferred← citeshttps://doi.org/10.1080/21505594.2021.1950268openalex-snapshot
Importance of twitching and surface-associated motility in the virulence of Acinetobacter baumannii
inferred← citeshttps://doi.org/10.1093/femsle/fnz210openalex-snapshot
Differential regulation of physiological activities by RcsB and OmpR in Yersinia enterocolitica
inferred← citeshttps://doi.org/10.1093/femsre/fuaa008openalex-snapshot
Molecular determinants of surface colonisation in diarrhoeagenicEscherichia coli(DEC): from bacterial adhesion to biofilm formation
inferred← citeshttps://doi.org/10.1093/femsre/fuab038openalex-snapshot
Multiple functions of flagellar motility and chemotaxis in bacterial physiology
inferred← citeshttps://doi.org/10.1093/femsre/fuy001openalex-snapshot
Emergent heterogeneous microenvironments in biofilms: substratum surface heterogeneity and bacterial adhesion force-sensing
inferred← citeshttps://doi.org/10.1093/femsre/fuz029openalex-snapshot
How bacteria recognise and respond to surface contact
inferred← citeshttps://doi.org/10.1099/mic.0.000947openalex-snapshot
Novel regulators of the csgD gene encoding the master regulator of biofilm formation in Escherichia coli K-12
inferred← citeshttps://doi.org/10.1101/2023.04.21.537696openalex-snapshot
Interplay of two small RNAs fine-tunes hierarchical flagellar gene expression in the foodborne pathogen Campylobacter jejuni
inferred← citeshttps://doi.org/10.1101/2023.07.05.547789openalex-snapshot
Variations in bacterial community at Chlorophyll Maximum (C-Max) depths along the west coast of India due to seasonal changes in the primary productivity
inferred← citeshttps://doi.org/10.1101/2024.10.01.616199openalex-snapshot
The genome of Gallaecimonas pentaromativorans strain 10A, isolated from a Pacific oyster, reveals the potential for hydrocarbon degradation and CRISPR-Cas defense
inferred← citeshttps://doi.org/10.1101/747618openalex-snapshot
Photo sensing and quorum sensing are integrated to control bacterial group behaviors
inferred← citeshttps://doi.org/10.1111/1462-2920.14083openalex-snapshot
2‐Tridecanone impacts surface‐associated bacterial behaviours and hinders plant–bacteria interactions
inferred← citeshttps://doi.org/10.1111/1462-2920.70087openalex-snapshot
Metagenome‐Assembled Genomes and Metatranscriptome Analysis of Perfluorooctane Sulfonate‐Reducing Bacteria Enriched From Activated Sludge
inferred← citeshttps://doi.org/10.1111/mmi.14823openalex-snapshot
Motility control through an anti‐activation mechanism in Agrobacterium tumefaciens
inferred← citeshttps://doi.org/10.1111/mpp.13219openalex-snapshot
The phytopathogen Dickeya dadantii 3937 cpxR locus gene participates in the regulation of virulence and the global c‐di‐GMP network
inferred← citeshttps://doi.org/10.1111/nph.18886openalex-snapshot
Deciphering the mechanism of fungal pathogen‐induced disease‐suppressive soil
inferred← citeshttps://doi.org/10.1111/omi.12311openalex-snapshot
Role of the RprY response regulator in P. gingivalis community development and virulence
inferred← citeshttps://doi.org/10.1111/pce.70356openalex-snapshot
Erwinia sp. PSI‐03 Promotes Plant Growth and Detoxifies Selenite Through Selenium Nanoparticles Biosynthesis
inferred← citeshttps://doi.org/10.1128/aem.00229-25openalex-snapshot
Role of a single MCP in evolutionary adaptation of Shewanella putrefaciens for swimming in planktonic and structured environments
inferred← citeshttps://doi.org/10.1128/aem.02052-20openalex-snapshot
Regulator RcsB Controls Prodigiosin Synthesis and Various Cellular Processes in Serratia marcescens JNB5-1
inferred← citeshttps://doi.org/10.1128/jb.00281-25openalex-snapshot
Effects of multiple cell regulators on curli gene expression in Escherichia coli
inferred← citeshttps://doi.org/10.1128/jb.00420-21openalex-snapshot
The hdeD Gene Represses the Expression of Flagellum Biosynthesis via LrhA in Escherichia coli K-12
inferred← citeshttps://doi.org/10.1128/msystems.00372-24openalex-snapshot
Combinatorial control of Pseudomonas aeruginosa biofilm development by quorum-sensing and nutrient-sensing regulators
inferred← citeshttps://doi.org/10.1128/msystems.00981-20openalex-snapshot
Pangenome Analytics Reveal Two-Component Systems as Conserved Targets in ESKAPEE Pathogens
inferred← citeshttps://doi.org/10.1128/spectrum.02236-23openalex-snapshot
Mapping niche-specific two-component system requirements in uropathogenic Escherichia coli
inferred← citeshttps://doi.org/10.1128/spectrum.02892-24openalex-snapshot
Comprehensive genomic analysis of a novel Bacillus cereus decomposing toluene potentially applicable in bioremediation
inferred← citeshttps://doi.org/10.1146/annurev-micro-090817-062640openalex-snapshot
The Complex Rcs Regulatory Cascade
inferred← citeshttps://doi.org/10.11606/t.11.2024.tde-06062024-083116openalex-snapshot
Benzoxazinoids influence rhizosphere establishment and root colonization by PGPB
inferred← citeshttps://doi.org/10.1186/s12866-020-01988-0openalex-snapshot
Exogenous polyunsaturated fatty acids (PUFAs) promote changes in growth, phospholipid composition, membrane permeability and virulence phenotypes in Escherichia coli
inferred← citeshttps://doi.org/10.1186/s12918-017-0494-1openalex-snapshot
Genome-wide analysis of E. coli cell-gene interactions
inferred← citeshttps://doi.org/10.1186/s43141-021-00242-yopenalex-snapshot
Bacterial exo-polysaccharides in biofilms: role in antimicrobial resistance and treatments
inferred← citeshttps://doi.org/10.1371/journal.pone.0270198openalex-snapshot
Characterization of a Treponema denticola ATCC 35405 mutant strain with mutation accumulation, including a lack of phage-derived genes
inferred← citeshttps://doi.org/10.1371/journal.pone.0334406openalex-snapshot
The genome of Gallaecimonas pentaromativorans strain 10A, isolated from a Pacific oyster, sheds light on an environmentally widespread genus with remarkable metabolic potential
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3836308/v1openalex-snapshot
Anti-biofilm activity of antimicrobial peptide CRAMP-34 by regulating 2-dehydro-3-deoxy-D-gluconate 5-dehydrogenase (KduD) of Escherichia coli
inferred← citeshttps://doi.org/10.2217/fmb-2019-0002openalex-snapshot
Roles of Two-Component Regulatory Systems in Antibiotic Resistance
inferred← citeshttps://doi.org/10.32920/19911538openalex-snapshot
EHEC utilizes two-component systems to modulate expression of the major flagellar subunit protein, FliC, in response to host intestinal cues
inferred← citeshttps://doi.org/10.33612/diss.129244743openalex-snapshot
Bacterial Adhesion-force Sensing in Oral Biofilms
inferred← citeshttps://doi.org/10.3389/fcimb.2019.00198openalex-snapshot
Two-Component Systems in Francisella Species
inferred← citeshttps://doi.org/10.3389/fmicb.2018.02405openalex-snapshot
Phosphorylated OmpR Is Required for Type 3 Fimbriae Expression in Klebsiella pneumoniae Under Hypertonic Conditions
inferred← citeshttps://doi.org/10.3389/fmicb.2018.02459openalex-snapshot
The EnvZ-OmpR Two-Component Signaling System Is Inactivated in a Mutant Devoid of Osmoregulated Periplasmic Glucans in Dickeya dadantii
inferred← citeshttps://doi.org/10.3389/fmicb.2019.01308openalex-snapshot
Gene Targets in Ocular Pathogenic Escherichia coli for Mitigation of Biofilm Formation to Overcome Antibiotic Resistance
inferred← citeshttps://doi.org/10.3389/fmicb.2020.00122openalex-snapshot
Osmoregulated Periplasmic Glucans Transmit External Signals Through Rcs Phosphorelay Pathway in Yersinia enterocolitica
inferred← citeshttps://doi.org/10.3389/fmicb.2020.586214openalex-snapshot
Peptidoglycan Endopeptidase Spr of Uropathogenic Escherichia coli Contributes to Kidney Infections and Competitive Fitness During Bladder Colonization
inferred← citeshttps://doi.org/10.3389/fmicb.2021.640923openalex-snapshot
Biocide-Induced Emergence of Antibiotic Resistance in Escherichia coli
inferred← citeshttps://doi.org/10.3389/fmicb.2021.657404openalex-snapshot
The CRISPR-Cas System Is Involved in OmpR Genetic Regulation for Outer Membrane Protein Synthesis in Salmonella Typhi
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1041146openalex-snapshot
Transcriptional factor OmpR positively regulates prodigiosin biosynthesis in Serratia marcescens FZSF02 by binding with the promoter of the prodigiosin cluster
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1051425openalex-snapshot
Toxic effect and inability of L-homoserine to be a nitrogen source for growth of Escherichia coli resolved by a combination of in vivo evolution engineering and omics analyses
inferred← citeshttps://doi.org/10.3389/fmicb.2022.928480openalex-snapshot
In silico metatranscriptomic approach for tracking biofilm-related effectors in dairies and its importance for improving food safety
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1447485openalex-snapshot
Caspofungin enhances the potency of rifampin against Gram-negative bacteria
inferred← citeshttps://doi.org/10.3389/fpls.2022.1033192openalex-snapshot
Two-component system ArcBA modulates cell motility and biofilm formation in Dickeya oryzae
inferred← citeshttps://doi.org/10.3390/agronomy15051235openalex-snapshot
The Overexpression of an EnvZ-like Protein Improves the Symbiotic Performance of Mesorhizobia
inferred← citeshttps://doi.org/10.3390/ani14030437openalex-snapshot
The cAMP Receptor Protein (CRP) of Vibrio mimicus Regulates Its Bacterial Growth, Type II Secretion System, Flagellum Formation, Adhesion Genes, and Virulence
inferred← citeshttps://doi.org/10.3390/applmicrobiol4020053openalex-snapshot
Genes of Salmonella enterica Serovar Enteritidis Involved in Biofilm Formation
inferred← citeshttps://doi.org/10.3390/microorganisms10081491openalex-snapshot
An Age Effect of Rumen Microbiome in Dairy Buffaloes Revealed by Metagenomics
inferred← citeshttps://doi.org/10.3390/microorganisms13081829openalex-snapshot
RcsB and H-NS Both Contribute to the Repression the Expression of the csgDEFG Operon
inferred← citeshttps://doi.org/10.5495/wjcid.v10.i1.14openalex-snapshot
GadE regulates fliC gene transcription and motility in Escherichia coli
inferred← citeshttps://doi.org/10.5772/intechopen.80341openalex-snapshot
Alternative Approaches to Combat Medicinally Important Biofilm-Forming Pathogens
inferred← citeshttps://doi.org/10.64898/2026.01.28.702333openalex-snapshot
RB-TnSeq analysis reveals alcohol and salt tolerance systems in a plant root colonizer Paraburkholderia graminis OAS925
inferred← citeshttps://doi.org/10.64898/2026.06.15.732377openalex-snapshot
Development of binding and activity inhibition assays for the antibiotic resistance-associated protein PhoQ
inferred← citeshttps://doi.org/10.70675/7e01e369zc5bez4125za868zb6fea14dddc5openalex-snapshot
Caractérisation du rôle de l'Antigène 43 dans le processus de colonisation d'Escherichia coli O157∶H7
inferred← citeshttps://doi.org/10.70675/c9050b99z21fbz4c57z8bb1z66909bf9e3deopenalex-snapshot
Rôle du phosphorelais EnvZ/OmpR chez la bactérie phytopathogène Dickeya dadantii
inferred← citeshttps://doi.org/10.7554/elife.87151openalex-snapshot
σ28-dependent small RNA regulation of flagella biosynthesis
inferred← citeshttps://doi.org/10.7554/elife.87151.1openalex-snapshot
σ28-dependent small RNA regulation of flagella biosynthesis
inferred← citeshttps://doi.org/10.7554/elife.87151.1.sa0openalex-snapshot
Reviewer #3 (Public Review): σ28-dependent small RNA regulation of flagella biosynthesis
inferred← citeshttps://doi.org/10.7554/elife.87151.1.sa2openalex-snapshot
Reviewer #1 (Public Review): σ28-dependent small RNA regulation of flagella biosynthesis
inferred← citeshttps://doi.org/10.7554/elife.87151.1.sa3openalex-snapshot
eLife Assessment: σ28-dependent small RNA regulation of flagella biosynthesis
inferred← citeshttps://doi.org/10.7554/elife.87151.1.sa4openalex-snapshot
Author Response: σ28-dependent small RNA regulation of flagella biosynthesis
inferred← citeshttps://doi.org/10.7554/elife.87151.2openalex-snapshot
σ28-dependent small RNA regulation of flagella biosynthesis
inferred← citeshttps://doi.org/10.7554/elife.87151.3openalex-snapshot
σ28-dependent small RNA regulation of flagella biosynthesis
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