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Under Elevated c-di-GMP in Escherichia coli, YcgR Alters Flagellar Motor Bias and Speed Sequentially, with Additional Negative Control of the Flagellar Regulon via the Adaptor Protein RssB

https://doi.org/10.1128/jb.00578-19
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Outgoing claims: the papers this work cites, builds on, or argues with.

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The response regulator RssB controls stability of the sigma(S) subunit of RNA polymerase in Escherichia coli.
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Two novel flagellar components and H-NS are involved in the motor function of Escherichia coli
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Coordinated Reversal of Flagellar Motors on a Single Escherichia coli Cell
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Bacterial flagellar motor
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Functional Suppression of HAMP Domain Signaling Defects in the E. coli Serine Chemoreceptor
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The c-di-GMP Binding Protein YcgR Controls Flagellar Motor Direction and Speed to Affect Chemotaxis by a “Backstop Brake” Mechanism
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The Bacterial Flagellar Motor: Structure and Function of a Complex Molecular Machine
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In Vivo Measurement by FRET of Pathway Activity in Bacterial Chemotaxis
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Conformational Change in the Stator of the Bacterial Flagellar Motor
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Flagellar rotation and the mechanism of bacterial motility
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Torque-generating units of the flagellar motor of Escherichia coli have a high duty ratio
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The multicellular morphotypes of Salmonella typhimurium and Escherichia coli produce cellulose as the second component of the extracellular matrix
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The maximum number of torque-generating units in the flagellar motor of Escherichia coli is at least 11
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Resurrection of the flagellar rotary motor near zero load
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One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products
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Stress sigma factor RpoS degradation and translation are sensitive to the state of central metabolism
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MotI (DgrA) acts as a molecular clutch on the flagellar stator protein MotA in Bacillus subtilis
inferredcites →https://doi.org/10.1073/pnas.192463199openalex-snapshot
Binding of the Escherichia coli response regulator CheY to its target measured in vivo by fluorescence resonance energy transfer
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The response regulator SprE controls the stability of RpoS.
inferredcites →https://doi.org/10.1073/pnas.95.1.201openalex-snapshot
Control of direction of flagellar rotation in bacterial chemotaxis
inferredcites →https://doi.org/10.1073/pnas.96.11.6439openalex-snapshot
Regulation of RpoS proteolysis in Escherichia coli : The response regulator RssB is a recognition factor that interacts with the turnover element in RpoS
inferredcites →https://doi.org/10.1074/jbc.c600179200openalex-snapshot
The PilZ Domain Is a Receptor for the Second Messenger c-di-GMP
inferredcites →https://doi.org/10.1074/jbc.m114.593749openalex-snapshot
FliT Selectively Enhances Proteolysis of FlhC Subunit in FlhD4C2 Complex by an ATP-dependent Protease, ClpXP
inferredcites →https://doi.org/10.1074/jbc.ra119.009009openalex-snapshot
Regulation of flagellar motor switching by c-di-GMP phosphodiesterases in Pseudomonas aeruginosa
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A Miniature Flow Cell Designed for Rapid Exchange of Media Under High-power Microscope Objectives
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The yjbEFGH locus in Escherichia coli K-12 is an operon encoding proteins involved in exopolysaccharide production
inferredcites →https://doi.org/10.1101/gad.353705openalex-snapshot
A two-component phosphotransfer network involving ArcB, ArcA, and RssB coordinates synthesis and proteolysis of σS (RpoS) in E. coli
inferredcites →https://doi.org/10.1101/gad.475808openalex-snapshot
Inverse regulatory coordination of motility and curli-mediated adhesion in Escherichia coli
inferredcites →https://doi.org/10.1101/gad.864401openalex-snapshot
The RssB response regulator directly targets ςS for degradation by ClpXP
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Multiple pathways for regulation of σ S (RpoS) stability in Escherichia coli via the action of multiple anti‐adaptors
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A post‐translational, c‐di‐GMP‐dependent mechanism regulating flagellar motility
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The fimA gene encoding the type‐1 fimbrial subunit of Escherichia coli
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Cyclic di‐ GMP inhibits V ibrio cholerae motility by repressing induction of transcription and inducing extracellular polysaccharide production
inferredcites →https://doi.org/10.1126/science.1157877openalex-snapshot
A Molecular Clutch Disables Flagella in the Bacillus subtilis Biofilm
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.00424-15openalex-snapshot
Systematic Nomenclature for GGDEF and EAL Domain-Containing Cyclic Di-GMP Turnover Proteins of Escherichia coli
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Uncovering a Large Set of Genes That Affect Surface Motility inSalmonella entericaSerovar Typhimurium
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The Tail Sheath of Bacteriophage N4 Interacts with the Escherichia coli Receptor
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Analysis of Factors That Affect FlgM-Dependent Type III Secretion for Protein Purification with Salmonella enterica Serovar Typhimurium
inferredcites →https://doi.org/10.1128/jb.01789-12openalex-snapshot
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inferredcites →https://doi.org/10.1128/jb.01996-07openalex-snapshot
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Construction of a minimum-size functional flagellin of Escherichia coli
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Two overlapping genes encoding membrane proteins required for bacteriophage N4 adsorption
inferredcites →https://doi.org/10.1128/jb.180.5.1154-1158.1998openalex-snapshot
Regulation of Proteolysis of the Stationary-Phase Sigma Factor RpoS
inferredcites →https://doi.org/10.1128/jb.183.17.5187-5197.2001openalex-snapshot
Quorum Sensing Is a Global Regulatory Mechanism in Enterohemorrhagic Escherichia coli O157:H7
inferredcites →https://doi.org/10.1128/jb.183.20.5974-5981.2001openalex-snapshot
RpoS-Dependent Transcriptional Control of sprE : Regulatory Feedback Loop
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The ClpXP ATP-Dependent Protease Regulates Flagellum Synthesis inSalmonella entericaSerovar Typhimurium
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RpoS Proteolysis Is Regulated by a Mechanism That Does Not Require the SprE (RssB) Response Regulator Phosphorylation Site
inferredcites →https://doi.org/10.1128/jb.186.9.2724-2734.2004openalex-snapshot
The pgaABCD Locus of Escherichia coli Promotes the Synthesis of a Polysaccharide Adhesin Required for Biofilm Formation
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Identification of New Flagellar Genes ofSalmonella entericaSerovar Typhimurium
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Nonchemotactic Mutants of Escherichia coli
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Integration of the Second Messenger c-di-GMP into the Chemotactic Signaling Pathway
inferredcites →https://doi.org/10.1128/mbio.00822-16openalex-snapshot
A Diguanylate Cyclase Acts as a Cell Division Inhibitor in a Two-Step Response to Reductive and Envelope Stresses
inferredcites →https://doi.org/10.1128/mbio.02367-14openalex-snapshot
A New Player at the Flagellar Motor: FliL Controls both Motor Output and Bias
inferredcites →https://doi.org/10.1128/mmbr.00043-12openalex-snapshot
Cyclic di-GMP: the First 25 Years of a Universal Bacterial Second Messenger
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Cellulose biosynthesis and function in bacteria
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What points at this work

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

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Regulatory Interplay of RpoS and RssB Controls Motility and Colonization in Vibrio cholerae
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Updates on therapeutic targeting of diguanylate cyclase for addressing bacterial infections: A comprehensive review
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Regulatory interplay of RpoS and RssB controls motility and colonization in Vibrio cholerae
inferred← citeshttps://doi.org/10.1016/j.mib.2025.102632openalex-snapshot
Swimming or sessile: the interplay between c-di-GMP signalling and flagellar motility
inferred← citeshttps://doi.org/10.1016/j.micres.2024.127811openalex-snapshot
Cyclic diguanylate differentially regulates the expression of virulence factors and pathogenesis-related phenotypes in Clostridioides difficile
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Cyclic di-GMP in E. coli: Roles in pathogenesis, host-pathogen interactions, and therapeutic potentials
inferred← citeshttps://doi.org/10.1038/s42003-024-07392-yopenalex-snapshot
ArgR regulates motility and virulence through positive control of flagellar genes and inhibition of diguanylate cyclase expression in Aeromonas veronii
inferred← citeshttps://doi.org/10.1038/s42003-025-09475-wopenalex-snapshot
Altering chemotaxis as a strategy to enhance the foraging range of motility-restricted bacteria
inferred← citeshttps://doi.org/10.1080/08927014.2020.1826939openalex-snapshot
Molecules involved in motility regulation inEscherichia colicells: a review
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Bacterial motility in rhizosphere colonization: mechanisms, constraints, and implications for microbial inoculants
inferred← citeshttps://doi.org/10.1099/mgen.0.000673openalex-snapshot
Massively parallel transposon mutagenesis identifies temporally essential genes for biofilm formation in Escherichia coli
inferred← citeshttps://doi.org/10.1101/2023.02.14.528454openalex-snapshot
Escherichia coli aggregates mediated by native or synthetic adhesins exhibit both core and adhesin-specific transcriptional responses
inferred← citeshttps://doi.org/10.1101/2025.01.04.631324openalex-snapshot
C-di-GMP is Required for Swarming in E. coli : a Role for DgcO and Colanic Acid
inferred← citeshttps://doi.org/10.1101/2025.11.30.691477openalex-snapshot
Aer is a bidirectional redox sensor mediating negative chemotaxis to antibiotic-induced ROS in E. coli
inferred← citeshttps://doi.org/10.1111/gtc.12921openalex-snapshot
Roles of the second messenger c‐di‐GMP in bacteria: Focusing on the topics of flagellar regulation and Vibrio spp.
inferred← citeshttps://doi.org/10.1111/mpp.13200openalex-snapshot
Cyclic di‐GMP modulates sessile‐motile phenotypes and virulence in Dickeya oryzae via two PilZ domain receptors
inferred← citeshttps://doi.org/10.1128/jb.00063-26openalex-snapshot
Understanding c-di-GMP-mediated regulation of flagellar motility, one step at a time
inferred← citeshttps://doi.org/10.1128/jb.00353-25openalex-snapshot
Texas 2-step: a new model for YcgR::c-di-GMP action at the flagellar motor
inferred← citeshttps://doi.org/10.1128/jb.00406-23openalex-snapshot
Helicobacter pylori cheV1 mutants recover semisolid agar migration due to loss of a previously uncharacterized Type IV filament membrane alignment complex homolog
inferred← citeshttps://doi.org/10.1128/mbio.00381-26openalex-snapshot
Aer is a bidirectional redox sensor mediating negative chemotaxis to antibiotic-induced ROS in Escherichia coli
inferred← citeshttps://doi.org/10.1128/mbio.00619-23openalex-snapshot
A Second Role for the Second Messenger Cyclic-di-GMP in E. coli: Arresting Cell Growth by Altering Metabolic Flow
inferred← citeshttps://doi.org/10.1128/mbio.00916-25openalex-snapshot
c-di-GMP is required for swarming in E. coli , producing colanic acid that acts as surfactant
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PlzD modifies Vibrio vulnificus foraging behavior and virulence in response to elevated c-di-GMP
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inferred← citeshttps://doi.org/10.1146/annurev-micro-090816-093411openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmicb.2021.689619openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmicb.2023.1159974openalex-snapshot
Flagellar brake protein YcgR interacts with motor proteins MotA and FliG to regulate the flagellar rotation speed and direction
inferred← citeshttps://doi.org/10.3389/fnut.2022.1076932openalex-snapshot
The enhanced expression of genes encoding diguanylate cyclases under cold stress contributes to the adhesion and biofilm formation of Shewanella putrefaciens WS13
inferred← citeshttps://doi.org/10.3390/antibiotics15050494openalex-snapshot
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ccdC Regulates Biofilm Dispersal in Bacillus velezensis FZB42
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