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Deletion of σ 54 ( rpoN ) Alters the Rate of Autolysis and Biofilm Formation in Enterococcus faecalis

https://doi.org/10.1128/jb.06046-11
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What this work says

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

inferredcites →https://doi.org/10.1007/bf00259462openalex-snapshot
High efficiency introduction of plasmid DNA into glycine treated Enterococcus faecalis by electroporation
inferredcites →https://doi.org/10.1007/bf00315808openalex-snapshot
Construction of an Azospirillum brasilense Sp7 recA mutant
inferredcites →https://doi.org/10.1007/s002840010164openalex-snapshot
The rpoN Gene of Enterococcus faecalis Directs Sensitivity to Subclass IIa Bacteriocins
inferredcites →https://doi.org/10.1016/j.femsle.2004.06.005openalex-snapshot
What drives bacteria to produce a biofilm?
inferredcites →https://doi.org/10.1016/j.ijantimicag.2009.12.011openalex-snapshot
Antibiotic resistance of bacterial biofilms
inferredcites →https://doi.org/10.1016/j.jhin.2006.06.028openalex-snapshot
Bacterial biofilms within the clinical setting: what healthcare professionals should know
inferredcites →https://doi.org/10.1016/j.micpath.2007.05.005openalex-snapshot
Adherence of Streptococcus pneumoniae to polystyrene plates, effect of serum on adhesion, and virulence in the gerbil otitis media model
inferredcites →https://doi.org/10.1016/s0065-2911(06)51004-5openalex-snapshot
Surface Adhesins of Staphylococcus aureus
inferredcites →https://doi.org/10.1016/s0147-619x(03)00020-9openalex-snapshot
Construction of the mobilizable plasmid pMV158GFP, a derivative of pMV158 that carries the gene encoding the green fluorescent protein
inferredcites →https://doi.org/10.1016/s0378-1097(03)00097-1openalex-snapshot
The alternative sigma factor RpoN regulates the quorum sensing generhlIinPseudomonas aeruginosa
inferredcites →https://doi.org/10.1038/nrmicro2415openalex-snapshot
The biofilm matrix
inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01846.xopenalex-snapshot
Dual regulation of mucoidy in Pseudomonas aeruginosa and sigma factor antagonism
inferredcites →https://doi.org/10.1073/pnas.0610226104openalex-snapshot
The cidA murein hydrolase regulator contributes to DNA release and biofilm development in Staphylococcus aureus
inferredcites →https://doi.org/10.1086/591861openalex-snapshot
Antimicrobial-Resistant Pathogens Associated With Healthcare-Associated Infections: Annual Summary of Data Reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2006–2007
inferredcites →https://doi.org/10.1093/nar/gkp1123openalex-snapshot
Promoter and regulon analysis of nitrogen assimilation factor, σ54, reveal alternative strategy for E. coli MG1655 flagellar biosynthesis
inferredcites →https://doi.org/10.1099/00221287-143-12-3849openalex-snapshot
RpoN of the fish pathogen Vibrio (Listonella) anguillarum is essential for flagellum production and virulence by the water-borne but not intraperitoneal route of inoculation
inferredcites →https://doi.org/10.1099/00221287-145-10-2977openalex-snapshot
Physiological characterization of Streptococcus bovis mutants that can resist 2-deoxyglucose-induced lysis
inferredcites →https://doi.org/10.1099/00221287-146-6-1267openalex-snapshot
Quantitative detection of Streptococcus pneumoniae cells harbouring single or multiple copies of the gene encoding the green fluorescent protein
inferredcites →https://doi.org/10.1099/00221287-147-12-3263openalex-snapshot
A σ54-dependent PTS permease of the mannose family is responsible for sensitivity of Listeria monocytogenes to mesentericin Y105
inferredcites →https://doi.org/10.1099/00221287-147-6-1575openalex-snapshot
Analysis of σ54-dependent genes in Enterococcus faecalis: a mannose PTS permease (EIIMan) is involved in sensitivity to a bacteriocin, mesentericin Y105
inferredcites →https://doi.org/10.1099/mic.0.032631-0openalex-snapshot
Inactivation of alternative sigma factor 54 (RpoN) leads to increased acid resistance, and alters locus of enterocyte effacement (LEE) expression in Escherichia coli O157 : H7
inferredcites →https://doi.org/10.1099/mic.0.033381-0openalex-snapshot
Influence of RpoN on isocitrate lyase activity in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1099/mic.0.034165-0openalex-snapshot
σ 54-mediated control of the mannose phosphotransferase sytem in Lactobacillus plantarum impacts on carbohydrate metabolism
inferredcites →https://doi.org/10.1099/mic.0.2006/004812-0openalex-snapshot
Identification of new genes associated with intermediate resistance of Enterococcus faecalis to divercin V41, a pediocin-like bacteriocin
inferredcites →https://doi.org/10.1099/mic.0.2007/006031-0openalex-snapshot
Role of autolysin-mediated DNA release in biofilm formation of Staphylococcus epidermidis
inferredcites →https://doi.org/10.1111/j.1365-2958.1993.tb00961.xopenalex-snapshot
In a class of its own — the RNA polymerase sigma factor σ;54 (σN)
inferredcites →https://doi.org/10.1111/j.1365-2958.2005.05020.xopenalex-snapshot
A major protein component of the Bacillus subtilis biofilm matrix
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05527.xopenalex-snapshot
Role of NtrC in biofilm formation via controlling expression of the gene encoding an ADP‐glycero‐manno‐heptose‐6‐epimerase in the pathogenic bacterium, Vibrio vulnificus
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06703.xopenalex-snapshot
A fratricidal mechanism is responsible for eDNA release and contributes to biofilm development of Enterococcus faecalis
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07054.xopenalex-snapshot
A dual role of extracellular DNA during biofilm formation of Neisseria meningitidis
inferredcites →https://doi.org/10.1111/j.1574-6968.2006.00405.xopenalex-snapshot
The sigma factor RpoN (σ54) is involved in osmotolerance inListeria monocytogenes
inferredcites →https://doi.org/10.1111/j.1574-6976.2007.00092.xopenalex-snapshot
Sigma factors inPseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/aac.33.9.1588openalex-snapshot
In vitro susceptibility studies of vancomycin-resistant Enterococcus faecalis
inferredcites →https://doi.org/10.1128/aac.45.4.999-1007.2001openalex-snapshot
Riddle of Biofilm Resistance
inferredcites →https://doi.org/10.1128/aem.02361-09openalex-snapshot
Role of Extracellular DNA during Biofilm Formation by Listeria monocytogenes
inferredcites →https://doi.org/10.1128/aem.70.4.2520-2524.2004openalex-snapshot
Vibrio fischeri σ 54 Controls Motility, Biofilm Formation, Luminescence, and Colonization
inferredcites →https://doi.org/10.1128/cmr.15.2.155-166.2002openalex-snapshot
Bacterial Adhesion: Seen Any Good Biofilms Lately?
inferredcites →https://doi.org/10.1128/iai.00111-06openalex-snapshot
Alanine Esters of Enterococcal Lipoteichoic Acid Play a Role in Biofilm Formation and Resistance to Antimicrobial Peptides
inferredcites →https://doi.org/10.1128/iai.00711-10openalex-snapshot
Enterococcal Biofilm Formation and Virulence in an Optimized Murine Model of Foreign Body-Associated Urinary Tract Infections
inferredcites →https://doi.org/10.1128/iai.01167-07openalex-snapshot
Burkholderia cenocepacia Requires the RpoN Sigma Factor for Biofilm Formation and Intracellular Trafficking within Macrophages
inferredcites →https://doi.org/10.1128/iai.68.5.2579-2586.2000openalex-snapshot
Effects of Enterococcus faecalis fsr Genes on Production of Gelatinase and a Serine Protease and Virulence
inferredcites →https://doi.org/10.1128/jb.00314-08openalex-snapshot
Regulation of Autolysis-Dependent Extracellular DNA Release by Enterococcus faecalis Extracellular Proteases Influences Biofilm Development
inferredcites →https://doi.org/10.1128/jb.00592-09openalex-snapshot
Capsular Polysaccharide Production in Enterococcus faecalis and Contribution of CpsF to Capsule Serospecificity
inferredcites →https://doi.org/10.1128/jb.01152-08openalex-snapshot
Flagellar Biogenesis of Xanthomonas campestris Requires the Alternative Sigma Factors RpoN2 and FliA and Is Temporally Regulated by FlhA, FlhB, and FlgM
inferredcites →https://doi.org/10.1128/jb.01202-06openalex-snapshot
Analysis ofPseudomonas aeruginosaConditional Psl Variants Reveals Roles for the Psl Polysaccharide in Adhesion and Maintaining Biofilm Structure Postattachment
inferredcites →https://doi.org/10.1128/jb.01311-07openalex-snapshot
Full Activation of Enterococcus faecalis Gelatinase by a C-Terminal Proteolytic Cleavage
inferredcites →https://doi.org/10.1128/jb.01441-07openalex-snapshot
The Genome and Structural Proteome of YuA, a New Pseudomonas aeruginosa Phage Resembling M6
inferredcites →https://doi.org/10.1128/jb.183.11.3372-3382.2001openalex-snapshot
Characterization of fsr , a Regulator Controlling Expression of Gelatinase and Serine Protease in Enterococcus faecalis OG1RF
inferredcites →https://doi.org/10.1128/jb.185.12.3613-3623.2003openalex-snapshot
Role of the Enterococcus faecalis GelE Protease in Determination of Cellular Chain Length, Supernatant Pheromone Levels, and Degradation of Fibrin and Misfolded Surface Proteins
inferredcites →https://doi.org/10.1128/jb.186.17.5629-5639.2004openalex-snapshot
TheEnterococcus faecalis fsrTwo-Component System Controls Biofilm Development through Production of Gelatinase
inferredcites →https://doi.org/10.1128/jb.188.3.902-908.2006openalex-snapshot
Peptidoglycan O Acetylation and Autolysin Profile ofEnterococcus faecalisin the Viable but Nonculturable State
inferredcites →https://doi.org/10.1128/mbio.00140-10openalex-snapshot
The Pseudomonas aeruginosa Exopolysaccharide Psl Facilitates Surface Adherence and NF-κB Activation in A549 Cells
inferredcites →https://doi.org/10.1128/mmbr.00014-09openalex-snapshot
Streptococcus Adherence and Colonization
inferredcites →https://doi.org/10.1128/mmbr.69.4.527-543.2005openalex-snapshot
Alternative Sigma Factors and Their Roles in Bacterial Virulence
inferredcites →https://doi.org/10.1371/journal.pone.0000582openalex-snapshot
Genetic Diversity among Enterococcus faecalis
inferredcites →https://doi.org/10.1371/journal.pone.0005822openalex-snapshot
Modulation of eDNA Release and Degradation Affects Staphylococcus aureus Biofilm Maturation
inferredcites →https://doi.org/10.1371/journal.pone.0006734openalex-snapshot
Quorum Sensing Regulation of the Two hcp Alleles in Vibrio cholerae O1 Strains
inferredcites →https://doi.org/10.1371/journal.pone.0010146openalex-snapshot
Identification of Genes Involved in Polysaccharide-Independent Staphylococcus aureus Biofilm Formation
inferredcites →https://doi.org/10.3103/s0891416808040010openalex-snapshot
Regulation of biofilm formation in Escherichia coli K12: Effect of mutations in the genes HNS, STRA, LON, and RPON
inferredcites →https://doi.org/10.4049/jimmunol.0901640openalex-snapshot
Extracellular DNA: A Major Proinflammatory Component of Pseudomonas aeruginosa Biofilms

What points at this work

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

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Intestinal Bile Acids Induce a Morphotype Switch in Vancomycin-Resistant Enterococcus that Facilitates Intestinal Colonization
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Diverse Enterococcus faecalis strains show heterogeneity in biofilm properties
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Diffusible signal factor enhances the saline-alkaline resistance and rhizosphere colonization of Stenotrophomonas rhizophila by coordinating optimal metabolism
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Exploiting biofilm phenotypes for functional characterization of hypothetical genes in Enterococcus faecalis
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Pheromone killing of multidrug-resistant Enterococcus faecalis V583 by native commensal strains
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Genome-wide screen for genes involved in eDNA release during biofilm formation by Staphylococcus aureus
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Influence of tick and mammalian physiological temperatures on Borrelia burgdorferi biofilms
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Virulence-linked adhesin drives mutualist colonization of the bee gut via biofilm formation
inferred← citeshttps://doi.org/10.1111/1348-0421.13109openalex-snapshot
RpoN (sigma factor 54) contributes to bacterial fitness during tracheal colonization of Bordetella bronchiseptica
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Life after death: the critical role of extracellular DNA in microbial biofilms
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