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Escherichia coli O157:H7 responds to phosphate starvation by modifying LPS involved in biofilm formation

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

inferredcites →https://doi.org/10.1002/mbo3.40openalex-snapshot
Survival of enterohemorrhagic E scherichia coli in the presence of A canthamoeba castellanii and its dependence on P ho regulon
inferredcites →https://doi.org/10.1007/978-1-4939-6958-6_16openalex-snapshot
Micromethods for Isolation and Structural Characterization of Lipid A, and Polysaccharide Regions of Bacterial Lipopolysaccharides
inferredcites →https://doi.org/10.1007/s00253-008-1359-8openalex-snapshot
Temporal regulation of enterohemorrhagic Escherichia coli virulence mediated by autoinducer-2
inferredcites →https://doi.org/10.1007/s00284-009-9549-xopenalex-snapshot
Membrane Homeostasis Requires Intact pst in Extraintestinal Pathogenic Escherichia coli
inferredcites →https://doi.org/10.1007/s12275-011-0360-6openalex-snapshot
Identification of PhoB binding sites of the yibD and ytfK promoter regions in Escherichia coli
inferredcites →https://doi.org/10.1016/0378-1119(88)90440-4openalex-snapshot
Tightly regulated tac promoter vectors useful for the expression of unfused and fused proteins in Escherichia coli
inferredcites →https://doi.org/10.1016/j.biochi.2018.12.011openalex-snapshot
A comparative study of the complete lipopolysaccharide structures and biosynthesis loci of Bordetella avium, B. hinzii, and B. trematum
inferredcites →https://doi.org/10.1016/j.carres.2006.10.025openalex-snapshot
The structure of the core–O-chain linkage region of the lipopolysaccharide from Bordetella hinzii
inferredcites →https://doi.org/10.1016/j.ijmm.2015.06.001openalex-snapshot
Phosphate starvation enhances the pathogenesis of Bacillus anthracis
inferredcites →https://doi.org/10.1016/j.resmic.2012.10.013openalex-snapshot
Phosphorus limitation increases attachment in Agrobacterium tumefaciens and reveals a conditional functional redundancy in adhesin biosynthesis
inferredcites →https://doi.org/10.1016/j.vetmic.2011.05.043openalex-snapshot
The Pho regulon and the pathogenesis of Escherichia coli
inferredcites →https://doi.org/10.1038/ki.1996.136openalex-snapshot
Signal transduction in the control of phosphate-regulated genes of Escherichia coli
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02641.xopenalex-snapshot
Expression of the Pho regulon negatively regulates biofilm formation by Pseudomonas aureofaciens PA147‐2
inferredcites →https://doi.org/10.1073/pnas.120163297openalex-snapshot
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products
inferredcites →https://doi.org/10.1074/jbc.m111.291799openalex-snapshot
Molecular Basis of Lipopolysaccharide Heterogeneity in Escherichia coli
inferredcites →https://doi.org/10.1074/jbc.m112.445981openalex-snapshot
Molecular and Structural Basis of Inner Core Lipopolysaccharide Alterations in Escherichia coli
inferredcites →https://doi.org/10.1074/jbc.m401879200openalex-snapshot
Chromosomal and Plasmid-encoded Enzymes Are Required for Assembly of the R3-type Core Oligosaccharide in the Lipopolysaccharide of Escherichia coli O157:H7
inferredcites →https://doi.org/10.1074/jbc.m708163200openalex-snapshot
PagP Activation in the Outer Membrane Triggers R3 Core Oligosaccharide Truncation in the Cytoplasm of Escherichia coli O157:H7
inferredcites →https://doi.org/10.1089/fpd.2010.0673openalex-snapshot
Escherichia coli O157:H7: Animal Reservoir and Sources of Human Infection
inferredcites →https://doi.org/10.1089/fpd.2015.2099openalex-snapshot
Biofilm Formation, Virulence Gene Profiles, and Antimicrobial Resistance of Nine Serogroups of Non-O157 Shiga Toxin–Producing Escherichia coli
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btr703openalex-snapshot
Artemis: an integrated platform for visualization and analysis of high-throughput sequence-based experimental data
inferredcites →https://doi.org/10.1093/bioinformatics/btt656openalex-snapshot
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
inferredcites →https://doi.org/10.1093/nar/gkl365openalex-snapshot
Genome prediction of PhoB regulated promoters in Sinorhizobium meliloti and twelve proteobacteria
inferredcites →https://doi.org/10.1099/00221287-148-5-1593openalex-snapshot
Regulatory interactions between the Pho and σB-dependent general stress regulons of Bacillus subtilis
inferredcites →https://doi.org/10.1099/mic.0.2008/016634-0openalex-snapshot
The pst operon of enteropathogenic Escherichia coli enhances bacterial adherence to epithelial cells
inferredcites →https://doi.org/10.1111/j.1365-2672.2010.04756.xopenalex-snapshot
Biofilm formation and the food industry, a focus on the bacterial outer surface
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05539.xopenalex-snapshot
Phosphate‐dependent modulation of c‐di‐GMP levels regulates Pseudomonas fluorescens Pf0‐1 biofilm formation by controlling secretion of the adhesin LapA
inferredcites →https://doi.org/10.1111/j.1472-765x.2004.01591.xopenalex-snapshot
Attachment and biofilm formation on stainless steel by Escherichia coli O157:H7 as affected by curli production
inferredcites →https://doi.org/10.1111/j.1574-6968.2006.00440.xopenalex-snapshot
Novel gene members in the Pho regulon of Escherichia coli
inferredcites →https://doi.org/10.1111/j.1574-6968.2009.01837.xopenalex-snapshot
The PhoB regulatory system modulates biofilm formation and stress response in El Tor biotypeVibrio cholerae
inferredcites →https://doi.org/10.1111/j.1758-2229.2009.00049.xopenalex-snapshot
The Pho regulon influences biofilm formation and type three secretion in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1111/jam.13524openalex-snapshot
Characterization of the phosphate-specific transport system inCronobacter sakazakiiBAA-894
inferredcites →https://doi.org/10.1128/aem.00360-07openalex-snapshot
EnterohemorrhagicEscherichia coliBiofilms Are Inhibited by 7-Hydroxyindole and Stimulated by Isatin
inferredcites →https://doi.org/10.1128/aem.00743-08openalex-snapshot
Characterization of an Escherichia coli O157:H7 O-Antigen Deletion Mutant and Effect of the Deletion on Bacterial Persistence in the Mouse Intestine and Colonization at the Bovine Terminal Rectal Mucosa
inferredcites →https://doi.org/10.1128/aem.02983-15openalex-snapshot
Biofilm-Forming Abilities of Shiga Toxin-Producing Escherichia coli Isolates Associated with Human Infections
inferredcites →https://doi.org/10.1128/iai.00156-10openalex-snapshot
Genome-Wide Transposon Mutagenesis Reveals a Role for pO157 Genes in Biofilm Development in Escherichia coli O157:H7 EDL933
inferredcites →https://doi.org/10.1128/iai.53.1.135-140.1986openalex-snapshot
Two toxin-converting phages from Escherichia coli O157:H7 strain 933 encode antigenically distinct toxins with similar biologic activities
inferredcites →https://doi.org/10.1128/iai.64.11.4795-4801.1996openalex-snapshot
Role of the Escherichia coli O157:H7 O side chain in adherence and analysis of an rfb locus
inferredcites →https://doi.org/10.1128/iai.70.4.1739-1749.2002openalex-snapshot
Immune Responses to Recombinant Pneumococcal PspA Antigen Delivered by Live Attenuated Salmonella enterica Serovar Typhimurium Vaccine
inferredcites →https://doi.org/10.1128/jb.00708-09openalex-snapshot
PhoB Regulates Motility, Biofilms, and Cyclic di-GMP inVibrio cholerae
inferredcites →https://doi.org/10.1128/jb.01012-12openalex-snapshot
Transposon Mutagenesis Identifies Uropathogenic Escherichia coli Biofilm Factors
inferredcites →https://doi.org/10.1128/jb.01536-07openalex-snapshot
Modulation of Hexa-Acyl Pyrophosphate Lipid A Population underEscherichia coliPhosphate (Pho) Regulon Activation
inferredcites →https://doi.org/10.1128/jb.05483-11openalex-snapshot
Systematic Analysis of Diguanylate Cyclases That Promote Biofilm Formation by Pseudomonas fluorescens Pf0-1
inferredcites →https://doi.org/10.1128/jb.154.1.269-277.1983openalex-snapshot
Morphological heterogeneity among Salmonella lipopolysaccharide chemotypes in silver-stained polyacrylamide gels
inferredcites →https://doi.org/10.1128/jb.178.15.4344-4366.1996openalex-snapshot
Global analysis of proteins synthesized during phosphorus restriction in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.186.14.4492-4501.2004openalex-snapshot
Phosphorus Limitation Enhances Biofilm Formation of the Plant Pathogen Agrobacterium tumefaciens through the PhoR-PhoB Regulatory System
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
inferredcites →https://doi.org/10.1128/mbio.01116-14openalex-snapshot
Biofilms Formed by Gram-Negative Bacteria Undergo Increased Lipid A Palmitoylation, Enhancing In Vivo Survival
inferredcites →https://doi.org/10.1139/o86-004openalex-snapshot
Structure of the O-chain polysaccharide of the phenol-phase soluble lipopolysaccharide of Escherichia coli 0:157:H7
inferredcites →https://doi.org/10.1146/annurev.biochem.71.110601.135414openalex-snapshot
Lipopolysaccharide Endotoxins
inferredcites →https://doi.org/10.1155/2013/607258openalex-snapshot
Relevance of Biofilms in the Pathogenesis of Shiga‐Toxin‐Producing Escherichia coli Infection
inferredcites →https://doi.org/10.1186/s13099-018-0252-yopenalex-snapshot
N-Acetyl-glucosamine influences the biofilm formation of Escherichia coli
inferredcites →https://doi.org/10.1371/journal.pone.0051241openalex-snapshot
Enhanced Biofilm Formation by Escherichia coli LPS Mutants Defective in Hep Biosynthesis
inferredcites →https://doi.org/10.1371/journal.pone.0094285openalex-snapshot
PhoB Activates Escherichia coli O157:H7 Virulence Factors in Response to Inorganic Phosphate Limitation
inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot
Cutadapt removes adapter sequences from high-throughput sequencing reads
inferredcites →https://doi.org/10.2527/jas.2006-508openalex-snapshot
Shiga toxin-producing Escherichia coli: An overview1
inferredcites →https://doi.org/10.3354/ame010015openalex-snapshot
Content of carbon, nitrogen, oxygen, sulfur and phosphorus in native aquatic and cultured bacteria
inferredcites →https://doi.org/10.3389/fcimb.2016.00082openalex-snapshot
Mutation of the Enterohemorrhagic Escherichia coli Core LPS Biosynthesis Enzyme RfaD Confers Hypersusceptibility to Host Intestinal Innate Immunity In vivo
inferredcites →https://doi.org/10.3389/fcimb.2017.00134openalex-snapshot
The NAG Sensor NagC Regulates LEE Gene Expression and Contributes to Gut Colonization by Escherichia coli O157:H7
inferredcites →https://doi.org/10.3389/fmicb.2014.00317openalex-snapshot
Life on the outside: role of biofilms in environmental persistence of Shiga-toxin producing Escherichia coli
inferredcites →https://doi.org/10.3791/3916openalex-snapshot
Purification and Visualization of Lipopolysaccharide from Gram-negative Bacteria by Hot Aqueous-phenol Extraction

What points at this work

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

inferred← citeshttps://doi.org/10.1080/21505594.2025.2545559openalex-snapshot
Roles of Pho regulon in bacterial pathogenicity
inferred← citeshttps://doi.org/10.1101/749887openalex-snapshot
Experimental evolution reveals the genetic basis and systems biology of superoxide stress tolerance
inferred← citeshttps://doi.org/10.1128/msystems.00980-20openalex-snapshot
Elucidation of Regulatory Modes for Five Two-Component Systems in Escherichia coli Reveals Novel Relationships
inferred← citeshttps://doi.org/10.3390/ijms25052760openalex-snapshot
Deciphering the Interrelationship of arnT Involved in Lipid-A Alteration with the Virulence of Salmonella Typhimurium
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