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RecA levels modulate biofilm development in Acinetobacter baumannii

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What this work says

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

inferredcites →https://doi.org/10.1002/emopenalex-snapshot
Long-Lasting Genomic Instability Following Arsenite Exposure inMammalian Cells: The Role of Reactive Oxygen Species
inferredcites →https://doi.org/10.1006/prep.1993.1056openalex-snapshot
Overproduction and Purification of σ32, the Escherichia coli Heat Shock Transcription Factor
inferredcites →https://doi.org/10.1007/s00284-002-3793-7openalex-snapshot
Complementation of Bacteriophage Induction and Recombination Defects in Escherichia coli RecA − Mutants by Expression of the Cloned T4 Bacteriophage uvsX Gene
inferredcites →https://doi.org/10.1016/j.chembiol.2016.02.010openalex-snapshot
RecA Inhibitors Potentiate Antibiotic Activity and Block Evolution of Antibiotic Resistance
inferredcites →https://doi.org/10.1016/j.jmb.2018.02.002openalex-snapshot
The Structure of the Biofilm-controlling Response Regulator BfmR from Acinetobacter baumannii Reveals Details of Its DNA-binding Mechanism
inferredcites →https://doi.org/10.1016/j.pep.2005.01.016openalex-snapshot
Protein production by auto-induction in high-density shaking cultures
inferredcites →https://doi.org/10.1021/acssynbio.3c00167openalex-snapshot
AspFlex: Molecular Tools to Study Gene Expression and Regulation in Acinetobacter baumannii
inferredcites →https://doi.org/10.1021/acssynbio.6b00031openalex-snapshot
EcoFlex: A Multifunctional MoClo Kit for E. coli Synthetic Biology
inferredcites →https://doi.org/10.1038/nmeth819openalex-snapshot
A guide to choosing fluorescent proteins
inferredcites →https://doi.org/10.1038/nmicrobiol.2016.77openalex-snapshot
MicrobeJ, a tool for high throughput bacterial cell detection and quantitative analysis
inferredcites →https://doi.org/10.1038/nrmicro2960openalex-snapshot
Sticking together: building a biofilm the Bacillus subtilis way
inferredcites →https://doi.org/10.1038/nrmicro3380openalex-snapshot
Molecular mechanisms of antibiotic resistance
inferredcites →https://doi.org/10.1038/s41522-017-0016-3openalex-snapshot
Bacillus subtilis utilizes the DNA damage response to manage multicellular development
inferredcites →https://doi.org/10.1038/s41598-018-25661-9openalex-snapshot
Biofilm formation is not associated with worse outcome in Acinetobacter baumannii bacteraemic pneumonia
inferredcites →https://doi.org/10.1073/pnas.0608949103openalex-snapshot
Antibiotics as intermicrobial signaling agents instead of weapons
inferredcites →https://doi.org/10.1073/pnas.1212429109openalex-snapshot
Localized cell death focuses mechanical forces during 3D patterning in a biofilm
inferredcites →https://doi.org/10.1073/pnas.1800961115openalex-snapshot
Structural basis for Acinetobacter baumannii biofilm formation
inferredcites →https://doi.org/10.1074/jbc.m803934200openalex-snapshot
Defective Dissociation of a “Slow” RecA Mutant Protein Imparts an Escherichia coli Growth Defect
inferredcites →https://doi.org/10.1086/533452openalex-snapshot
Federal Funding for the Study of Antimicrobial Resistance in Nosocomial Pathogens: No ESKAPE
inferredcites →https://doi.org/10.1093/femspd/ftw056openalex-snapshot
Penetration barrier contributes to bacterial biofilm-associated resistance against only select antibiotics, and exhibits genus-, strain- and antibiotic-specific differences
inferredcites →https://doi.org/10.1093/jac/36.4.743openalex-snapshot
Ofloxacin, norfloxacin and ceftazidime increase the production of alginate and promote the formation of biofilm of Pscudomonas aeruginosa in vitro
inferredcites →https://doi.org/10.1093/jac/48.suppl_1.5openalex-snapshot
Determination of minimum inhibitory concentrations
inferredcites →https://doi.org/10.1099/mic.0.075317-0openalex-snapshot
Adherence to abiotic surface induces SOS response in Escherichia coli K-12 strains under aerobic and anaerobic conditions
inferredcites →https://doi.org/10.1099/mic.0.2008/019471-0openalex-snapshot
Characterization of a two-component regulatory system from Acinetobacter baumannii that controls biofilm formation and cellular morphology
inferredcites →https://doi.org/10.1099/mic.0.26541-0openalex-snapshot
Attachment to and biofilm formation on abiotic surfaces by Acinetobacter baumannii: involvement of a novel chaperone-usher pili assembly system
inferredcites →https://doi.org/10.1100/2012/973436openalex-snapshot
Characterization of eDNA from the Clinical Strain Acinetobacter baumannii AIIMS 7 and Its Role in Biofilm Formation
inferredcites →https://doi.org/10.1101/cshperspect.a012674openalex-snapshot
DNA Damage Responses in Prokaryotes: Regulating Gene Expression, Modulating Growth Patterns, and Manipulating Replication Forks
inferredcites →https://doi.org/10.1101/cshperspect.a012682openalex-snapshot
Translesion DNA Synthesis and Mutagenesis in Prokaryotes
inferredcites →https://doi.org/10.1101/gad.1510307openalex-snapshot
New insights into Acinetobacter baumannii pathogenesis revealed by high-density pyrosequencing and transposon mutagenesis
inferredcites →https://doi.org/10.1111/j.1399-302x.2008.00480.xopenalex-snapshot
Effects of recombinase A deficiency on biofilm formation by Streptococcus mutans
inferredcites →https://doi.org/10.1111/j.1574-6968.2012.02618.xopenalex-snapshot
The Acinetobacter regulatory UmuDAb protein cleaves in response to DNA damage with chimeric LexA/UmuD characteristics
inferredcites →https://doi.org/10.1111/mmi.12541openalex-snapshot
Activation of phenotypic subpopulations in response to ciprofloxacin treatment in A cinetobacter baumannii
inferredcites →https://doi.org/10.1128/aac.00101-17openalex-snapshot
Impact of Mucositis on Absorption and Systemic Drug Exposure of Isavuconazole
inferredcites →https://doi.org/10.1128/aac.00778-17openalex-snapshot
Subinhibitory Concentrations of Trimethoprim and Sulfamethoxazole Prevent Biofilm Formation by Acinetobacter baumannii through Inhibition of Csu Pilus Expression
inferredcites →https://doi.org/10.1128/aac.00877-15openalex-snapshot
Biofilm Formation Caused by Clinical Acinetobacter baumannii Isolates Is Associated with Overexpression of the AdeFGH Efflux Pump
inferredcites →https://doi.org/10.1128/aac.44.7.1818-1824.2000openalex-snapshot
Role of Antibiotic Penetration Limitation in Klebsiella pneumoniae Biofilm Resistance to Ampicillin and Ciprofloxacin
inferredcites →https://doi.org/10.1128/aem.02289-09openalex-snapshot
Characterization of Extracellular Polymeric Substances from Acidophilic Microbial Biofilms
inferredcites →https://doi.org/10.1128/aem.18.5.834-837.1969openalex-snapshot
Congo Red-Agar Plating Medium for Detecting Pigmentation in Pasteurella pestis
inferredcites →https://doi.org/10.1128/aem.49.1.1-7.1985openalex-snapshot
A new medium for the enumeration and subculture of bacteria from potable water
inferredcites →https://doi.org/10.1128/aem.70.10.6188-6196.2004openalex-snapshot
Stratified Growth in Pseudomonas aeruginosa Biofilms
inferredcites →https://doi.org/10.1128/cmr.00058-07openalex-snapshot
Acinetobacter baumannii : Emergence of a Successful Pathogen
inferredcites →https://doi.org/10.1128/iai.00016-10openalex-snapshot
Identification and Characterization of a Glycosyltransferase Involved in Acinetobacter baumannii Lipopolysaccharide Core Biosynthesis
inferredcites →https://doi.org/10.1128/iai.05913-11openalex-snapshot
The Acinetobacter baumannii Biofilm-Associated Protein Plays a Role in Adherence to Human Epithelial Cells
inferredcites →https://doi.org/10.1128/jb.00131-15openalex-snapshot
Resources for Genetic and Genomic Analysis of Emerging Pathogen Acinetobacter baumannii
inferredcites →https://doi.org/10.1128/jb.00389-11openalex-snapshot
Acinetobacter baumannii RecA Protein in Repair of DNA Damage, Antimicrobial Resistance, General Stress Response, and Virulence
inferredcites →https://doi.org/10.1128/jb.00536-18openalex-snapshot
Lon Protease Has Multifaceted Biological Functions in Acinetobacter baumannii
inferredcites →https://doi.org/10.1128/jb.00647-09openalex-snapshot
The pgaABCD Locus of Acinetobacter baumannii Encodes the Production of Poly-β-1-6- N -Acetylglucosamine, Which Is Critical for Biofilm Formation
inferredcites →https://doi.org/10.1128/jb.00799-16openalex-snapshot
RNA-Mediated cis Regulation in Acinetobacter baumannii Modulates Stress-Induced Phenotypic Variation
inferredcites →https://doi.org/10.1128/jb.01349-12openalex-snapshot
A Single Residue Unique to DinB-Like Proteins Limits Formation of the Polymerase IV Multiprotein Complex in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.01416-07openalex-snapshot
Identification and Characterization of an Acinetobacter baumannii Biofilm-Associated Protein
inferredcites →https://doi.org/10.1128/jb.01464-06openalex-snapshot
Complete and SOS-Mediated Response of Staphylococcus aureus to the Antibiotic Ciprofloxacin
inferredcites →https://doi.org/10.1128/jb.01740-05openalex-snapshot
Ectopic Overexpression of Wild-Type and Mutant hipA Genes in Escherichia coli : Effects on Macromolecular Synthesis and Persister Formation
inferredcites →https://doi.org/10.1128/jb.02176-12openalex-snapshot
Antibiotic Resistance Acquired through a DNA Damage-Inducible Response in Acinetobacter baumannii
inferredcites →https://doi.org/10.1128/mbio.00392-15openalex-snapshot
Acetic Acid Acts as a Volatile Signal To Stimulate Bacterial Biofilm Formation
inferredcites →https://doi.org/10.1128/mbio.01163-14openalex-snapshot
Genome-Wide Identification of Acinetobacter baumannii Genes Necessary for Persistence in the Lung
inferredcites →https://doi.org/10.1128/msphere.00055-15openalex-snapshot
Uropathogenic Escherichia coli Metabolite-Dependent Quiescence and Persistence May Explain Antibiotic Tolerance during Urinary Tract Infection
inferredcites →https://doi.org/10.1146/annurev.mi.49.100195.003431openalex-snapshot
MICROBIAL BIOFILMS
inferredcites →https://doi.org/10.1369/jhc.4a6428.2004openalex-snapshot
High-resolution Visualization of the Microbial Glycocalyx with Low-voltage Scanning Electron Microscopy: Dependence on Cationic Dyes
inferredcites →https://doi.org/10.1371/journal.pone.0067950openalex-snapshot
Purification and Characterization of Biofilm-Associated EPS Exopolysaccharides from ESKAPE Organisms and Other Pathogens
inferredcites →https://doi.org/10.1371/journal.pone.0072626openalex-snapshot
Neural and Behavioral Evidence for an Intrinsic Cost of Self-Control
inferredcites →https://doi.org/10.1371/journal.pone.0072968openalex-snapshot
Whole Transcriptome Analysis of Acinetobacter baumannii Assessed by RNA-Sequencing Reveals Different mRNA Expression Profiles in Biofilm Compared to Planktonic Cells
inferredcites →https://doi.org/10.1371/journal.pone.0093861openalex-snapshot
Prophage Induction and Differential RecA and UmuDAb Transcriptome Regulation in the DNA Damage Responses of Acinetobacter baumannii and Acinetobacter baylyi
inferredcites →https://doi.org/10.1371/journal.pone.0111660openalex-snapshot
Characterisation of Pellicles Formed by Acinetobacter baumannii at the Air-Liquid Interface
inferredcites →https://doi.org/10.1371/journal.pone.0144763openalex-snapshot
The SOS Response Master Regulator LexA Is Associated with Sporulation, Motility and Biofilm Formation in Clostridium difficile
inferredcites →https://doi.org/10.1371/journal.pone.0152013openalex-snapshot
UmuDAb: An Error-Prone Polymerase Accessory Homolog Whose N-Terminal Domain Is Required for Repression of DNA Damage Inducible Gene Expression in Acinetobacter baylyi
inferredcites →https://doi.org/10.1371/journal.pone.0191962openalex-snapshot
Semaphorin3A induces nerve regeneration in the adult cornea-a switch from its repulsive role in development
inferredcites →https://doi.org/10.1371/journal.pone.0205638openalex-snapshot
Desiccation tolerance in Acinetobacter baumannii is mediated by the two-component response regulator BfmR
inferredcites →https://doi.org/10.1371/journal.ppat.1004691openalex-snapshot
Antibiotic Modulation of Capsular Exopolysaccharide and Virulence in Acinetobacter baumannii
inferredcites →https://doi.org/10.2147/idr.s169894openalex-snapshot
Acinetobacter baumannii biofilms: effects of physicochemical factors, virulence, antibiotic resistance determinants, gene regulation, and future antimicrobial treatments
inferredcites →https://doi.org/10.2217/fmb.09.5openalex-snapshot
Regulation of Acinetobacter Baumannii Biofilm Formation
inferredcites →https://doi.org/10.3389/fmicb.2017.00288openalex-snapshot
RNA Primer Extension Hinders DNA Synthesis by Escherichia coli Mutagenic DNA Polymerase IV
inferredcites →https://doi.org/10.3389/fmicb.2017.01020openalex-snapshot
Predicting Species-Resolved Macronutrient Acquisition during Succession in a Model Phototrophic Biofilm Using an Integrated ‘Omics Approach
inferredcites →https://doi.org/10.3391/mbi.2014.5.1.01openalex-snapshot
Tackling Invasive Alien Species in Europe: the top 20 issues
inferredcites →https://doi.org/10.3391/mbi.2015.6.1.01openalex-snapshot
Concepts for biocontrol in marine environments: is there a way forward?
inferredcites →https://doi.org/10.7554/elife.39324openalex-snapshot
Consolidation alters motor sequence-specific distributed representations
inferredcites →https://doi.org/10.7554/elife.42761openalex-snapshot
Spatial and temporal organization of RecA in the Escherichia coli DNA-damage response
inferredcites →https://doi.org/10.7554/elife.47612openalex-snapshot
Evolutionary pathways to antibiotic resistance are dependent upon environmental structure and bacterial lifestyle

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

inferred← citeshttps://doi.org/10.1016/j.crmicr.2022.100131openalex-snapshot
Factors mediating Acinetobacter baumannii biofilm formation: Opportunities for developing therapeutics
inferred← citeshttps://doi.org/10.1128/spectrum.03774-22openalex-snapshot
Distinct Screening Approaches Uncover PA14_36820 and RecA as Negative Regulators of Biofilm Phenotypes in Pseudomonas aeruginosa PA14
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