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Quorum-sensing agr system of Staphylococcus aureus primes gene expression for protection from lethal oxidative stress
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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/j.1460-2075.1993.tb06074.xopenalex-snapshot
Synthesis of staphylococcal virulence factors is controlled by a regulatory RNA molecule.
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Activation of alpha‐toxin translation in Staphylococcus aureus by the trans‐encoded antisense RNA, RNAIII.
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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/bf02191645openalex-snapshot
Theagr P2 operon: An autocatalytic sensory transduction system inStaphylococcus aureus
inferredcites →https://doi.org/10.1016/0076-6879(91)04029-nopenalex-snapshot
[27] Genetic systems in Staphylococci
inferredcites →https://doi.org/10.1016/j.cell.2007.06.049openalex-snapshot
A Common Mechanism of Cellular Death Induced by Bactericidal Antibiotics
inferredcites →https://doi.org/10.1016/j.celrep.2013.01.026openalex-snapshot
YihE Kinase Is a Central Regulator of Programmed Cell Death in Bacteria
inferredcites →https://doi.org/10.1016/j.chom.2011.07.004openalex-snapshot
Nutrient Metal Sequestration by Calprotectin Inhibits Bacterial Superoxide Defense, Enhancing Neutrophil Killing of Staphylococcus aureus
inferredcites →https://doi.org/10.1016/j.chom.2022.12.003openalex-snapshot
MRSA lineage USA300 isolated from bloodstream infections exhibit altered virulence regulation
inferredcites →https://doi.org/10.1016/j.molcel.2008.08.005openalex-snapshot
RNAIII-Independent Target Gene Control by the agr Quorum-Sensing System: Insight into the Evolution of Virulence Regulation in Staphylococcus aureus
inferredcites →https://doi.org/10.1016/j.plasmid.2009.01.003openalex-snapshot
Improved lux reporters for use in Staphylococcus aureus
inferredcites →https://doi.org/10.1016/j.plasmid.2014.08.001openalex-snapshot
Single-copy vectors for integration at the SaPI1 attachment site for Staphylococcus aureus
inferredcites →https://doi.org/10.1016/s0140-6736(02)08713-5openalex-snapshot
Genome and virulence determinants of high virulence community-acquired MRSA
inferredcites →https://doi.org/10.1021/np5000704openalex-snapshot
Polyhydroxyanthraquinones as Quorum Sensing Inhibitors from the Guttates of Penicillium restrictum and Their Analysis by Desorption Electrospray Ionization Mass Spectrometry
inferredcites →https://doi.org/10.1038/nature13469openalex-snapshot
Optimization of lag time underlies antibiotic tolerance in evolved bacterial populations
inferredcites →https://doi.org/10.1038/ng0295-202openalex-snapshot
Mouse model of X–linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production
inferredcites →https://doi.org/10.1038/nm1656openalex-snapshot
Identification of novel cytolytic peptides as key virulence determinants for community-associated MRSA
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1038/nmicrobiol.2016.51openalex-snapshot
Persister formation in Staphylococcus aureus is associated with ATP depletion
inferredcites →https://doi.org/10.1038/s41564-019-0627-yopenalex-snapshot
Reactive oxygen species induce antibiotic tolerance during systemic Staphylococcus aureus infection
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03526.xopenalex-snapshot
Autoinduction and signal transduction in the regulation of staphylococcal virulence
inferredcites →https://doi.org/10.1073/pnas.0407661102openalex-snapshot
Transient interference with staphylococcal quorum sensing blocks abscess formation
inferredcites →https://doi.org/10.1073/pnas.1200603109openalex-snapshot
Quorum-sensing agr mediates bacterial oxidation response via an intramolecular disulfide redox switch in the response regulator AgrA
inferredcites →https://doi.org/10.1073/pnas.1509743112openalex-snapshot
Antibiotic efficacy is linked to bacterial cellular respiration
inferredcites →https://doi.org/10.1073/pnas.1707466114openalex-snapshot
Lethality of MalE-LacZ hybrid protein shares mechanistic attributes with oxidative component of antibiotic lethality
inferredcites →https://doi.org/10.1073/pnas.1902752116openalex-snapshot
Oxidative stress drives the selection of quorum sensing mutants in the Staphylococcus aureus population
inferredcites →https://doi.org/10.1073/pnas.2118566119openalex-snapshot
A broadly applicable, stress-mediated bacterial death pathway regulated by the phosphotransferase system (PTS) and the cAMP-Crp cascade
inferredcites →https://doi.org/10.1074/jbc.m710227200openalex-snapshot
Identification of Ligand Specificity Determinants in AgrC, the Staphylococcus aureus Quorum-sensing Receptor
inferredcites →https://doi.org/10.1080/14787210.2021.1840353openalex-snapshot
Bacterial death from treatment with fluoroquinolones and other lethal stressors
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/bioinformatics/btu170openalex-snapshot
Trimmomatic: a flexible trimmer for Illumina sequence data
inferredcites →https://doi.org/10.1099/00221287-6-1-2-95openalex-snapshot
Staphylococcal Coagulase: Mode of Action and Antigenicity
inferredcites →https://doi.org/10.1099/00222615-34-3-143openalex-snapshot
A chemically defined medium for slime production by coagulase-negative staphylococci
inferredcites →https://doi.org/10.1111/1462-2920.13223openalex-snapshot
Microbial stress priming: a meta‐analysis
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05292.xopenalex-snapshot
Inhibition of rot translation by RNAIII, a key feature of agr function
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06518.xopenalex-snapshot
A new oxidative sensing and regulation pathway mediated by the MgrA homologue SarZ in Staphylococcus aureus
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07105.xopenalex-snapshot
Redox sensing by a Rex‐family repressor is involved in the regulation of anaerobic gene expression in Staphylococcus aureus
inferredcites →https://doi.org/10.1111/j.1365-2958.2011.07720.xopenalex-snapshot
Staphylococcus aureus regulates the expression and production of the staphylococcal superantigen‐like secreted proteins in a Rot‐dependent manner
inferredcites →https://doi.org/10.1126/science.1155207openalex-snapshot
A Nitric Oxide–Inducible Lactate Dehydrogenase Enables Staphylococcus aureus to Resist Innate Immunity
inferredcites →https://doi.org/10.1126/science.1175439openalex-snapshot
Endogenous Nitric Oxide Protects Bacteria Against a Wide Spectrum of Antibiotics
inferredcites →https://doi.org/10.1126/science.1209855openalex-snapshot
H 2 S: A Universal Defense Against Antibiotics in Bacteria
inferredcites →https://doi.org/10.1126/science.276.5321.2027openalex-snapshot
Bacterial Interference Caused by Autoinducing Peptide Variants
inferredcites →https://doi.org/10.1126/science.abd8377openalex-snapshot
Inhibitors of bacterial H 2 S biogenesis targeting antibiotic resistance and tolerance
inferredcites →https://doi.org/10.1126/sciimmunol.aam8929openalex-snapshot
The lung is a host defense niche for immediate neutrophil-mediated vascular protection
inferredcites →https://doi.org/10.1128/aac.00592-22openalex-snapshot
Moxifloxacin-Mediated Killing of Mycobacterium tuberculosis Involves Respiratory Downshift, Reductive Stress, and Accumulation of Reactive Oxygen Species
inferredcites →https://doi.org/10.1128/aac.01703-20openalex-snapshot
The Promises and Limitations of N -Acetylcysteine as a Potentiator of First-Line and Second-Line Tuberculosis Drugs
inferredcites →https://doi.org/10.1128/iai.00146-21openalex-snapshot
Staphylococcus aureus Peptide Methionine Sulfoxide Reductases Protect from Human Whole-Blood Killing
inferredcites →https://doi.org/10.1128/iai.01036-08openalex-snapshot
Interconnections between Sigma B, agr , and Proteolytic Activity in Staphylococcus aureus Biofilm Maturation
inferredcites →https://doi.org/10.1128/iai.01074-13openalex-snapshot
Importance of Bacillithiol in the Oxidative Stress Response of Staphylococcus aureus
inferredcites →https://doi.org/10.1128/iai.70.11.6373-6382.2002openalex-snapshot
Staphylococcus aureus Aconitase Inactivation Unexpectedly Inhibits Post-Exponential-Phase Growth and Enhances Stationary-Phase Survival
inferredcites →https://doi.org/10.1128/jb.00042-13openalex-snapshot
Inactivation of the Pta-AckA Pathway Causes Cell Death in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.00081-07openalex-snapshot
Anaerobic Gene Expression in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.00229-16openalex-snapshot
Regulatory Requirements for Staphylococcus aureus Nitric Oxide Resistance
inferredcites →https://doi.org/10.1128/jb.00706-12openalex-snapshot
Rot and SaeRS Cooperate To Activate Expression of the Staphylococcal Superantigen-Like Exoproteins
inferredcites →https://doi.org/10.1128/jb.01524-06openalex-snapshot
Catalase (KatA) and Alkyl Hydroperoxide Reductase (AhpC) Have Compensatory Roles in Peroxide Stress Resistance and Are Required for Survival, Persistence, and Nasal Colonization in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.06685-11openalex-snapshot
Allele-Dependent Differences in Quorum-Sensing Dynamics Result in Variant Expression of Virulence Genes in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.181.13.3898-3903.1999openalex-snapshot
Characterization of the Major Superoxide Dismutase of Staphylococcus aureus and Its Role in Starvation Survival, Stress Resistance, and Pathogenicity
inferredcites →https://doi.org/10.1128/jb.183.24.7173-7181.2001openalex-snapshot
Alkyl Hydroperoxide Reductase Is the Primary Scavenger of Endogenous Hydrogen Peroxide in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.184.5.1430-1437.2002openalex-snapshot
In Vitro Serial Passage of Staphylococcus aureus : Changes in Physiology, Virulence Factor Production, and agr Nucleotide Sequence
inferredcites →https://doi.org/10.1128/jb.188.5.1899-1910.2006openalex-snapshot
Transcription Profiling of the mgrA Regulon in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/mbio.00045-15openalex-snapshot
Glycolytic Dependency of High-Level Nitric Oxide Resistance and Virulence in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/mbio.00358-17openalex-snapshot
Alternative Evolutionary Pathways for Drug-Resistant Small Colony Variant Mutants in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/mbio.00537-12openalex-snapshot
A Genetic Resource for Rapid and Comprehensive Phenotype Screening of Nonessential Staphylococcus aureus Genes
inferredcites →https://doi.org/10.1128/mbio.00696-13openalex-snapshot
The Staphylococcus aureus SrrAB Two-Component System Promotes Resistance to Nitrosative Stress and Hypoxia
inferredcites →https://doi.org/10.1128/mbio.00818-16openalex-snapshot
Staphylococcus aureus Coordinates Leukocidin Expression and Pathogenesis by Sensing Metabolic Fluxes via RpiRc
inferredcites →https://doi.org/10.1128/mbio.01476-17openalex-snapshot
Tuning of the Lethal Response to Multiple Stressors with a Single-Site Mutation during Clinical Infection by Staphylococcus aureus
inferredcites →https://doi.org/10.1128/mbio.02188-21openalex-snapshot
The Intersection of the Staphylococcus aureus Rex and SrrAB Regulons: an Example of Metabolic Evolution That Maximizes Resistance to Immune Radicals
inferredcites →https://doi.org/10.1146/annurev-micro-092412-155746openalex-snapshot
Neutrophils Versus Staphylococcus aureus : A Biological Tug of War
inferredcites →https://doi.org/10.1146/annurev-micro-102215-095708openalex-snapshot
Staphylococcus aureus RNAIII and Its Regulon Link Quorum Sensing, Stress Responses, Metabolic Adaptation, and Regulation of Virulence Gene Expression
inferredcites →https://doi.org/10.1146/annurev.biochem.77.061606.161055openalex-snapshot
Cellular Defenses against Superoxide and Hydrogen Peroxide
inferredcites →https://doi.org/10.1146/annurev.genet.42.110807.091640openalex-snapshot
Quorum Sensing in Staphylococci
inferredcites →https://doi.org/10.1186/1471-2180-5-8openalex-snapshot
Genome-scale reconstruction of the metabolic network in Staphylococcus aureus N315: an initial draft to the two-dimensional annotation
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
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/10.1371/journal.pone.0023909openalex-snapshot
A Toxin-Antitoxin Module in Bacillus subtilis Can Both Mitigate and Amplify Effects of Lethal Stress
inferredcites →https://doi.org/10.1371/journal.pone.0157101openalex-snapshot
E-Flux2 and SPOT: Validated Methods for Inferring Intracellular Metabolic Flux Distributions from Transcriptomic Data
inferredcites →https://doi.org/10.1371/journal.pone.0170283openalex-snapshot
The Staphylococcus aureus SrrAB Regulatory System Modulates Hydrogen Peroxide Resistance Factors, Which Imparts Protection to Aconitase during Aerobic Growth
inferredcites →https://doi.org/10.1371/journal.pone.0238689openalex-snapshot
Assessment of transcriptomic constraint-based methods for central carbon flux inference
inferredcites →https://doi.org/10.1371/journal.ppat.1005341openalex-snapshot
Bacterial Hypoxic Responses Revealed as Critical Determinants of the Host-Pathogen Outcome by TnSeq Analysis of Staphylococcus aureus Invasive Infection
inferredcites →https://doi.org/10.1517/13543784.2015.1019062openalex-snapshot
Investigational therapies targeting quorum-sensing for the treatment of Staphylococcus aureus infections
inferredcites →https://doi.org/10.3389/fcimb.2012.00033openalex-snapshot
Staphylococcal response to oxidative stress
inferredcites →https://doi.org/10.3389/fmicb.2019.00863openalex-snapshot
Absence of Protein A Expression Is Associated With Higher Capsule Production in Staphylococcal Isolates
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/2023.10.15.562438openalex-snapshot
Bacillus subtilis maintains antibiofilm activity against Staphylococcus aureus following adaptive laboratory evolution
inferred← citeshttps://doi.org/10.26599/fshw.2024.9250337openalex-snapshot
Quorum sensing: its roles in mediating biofilm and viable but non-culturable state formation, and strategies for the prevention and control of foodborne bacteria via quorum quenching
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