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MRSA emerges through natural transformation
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/82_2015_5019openalex-snapshot
The Role of Two-Component Signal Transduction Systems in Staphylococcus aureus Virulence Regulation
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Mobile genetic elements of Staphylococcus aureus
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A Staphylococcus aureus Regulatory System that Responds to Host Heme and Modulates Virulence
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Phage release from biofilm and planktonicStaphylococcus aureuscells
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Genomic variation and evolution of Staphylococcus aureus
inferredcites →https://doi.org/10.1016/j.ijmm.2014.05.010openalex-snapshot
The Staphylococcal Cassette Chromosome mec type V from Staphylococcus aureus ST398 is packaged into bacteriophage capsids
inferredcites →https://doi.org/10.1016/j.tim.2017.05.011openalex-snapshot
Transfer of Antibiotic Resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1016/s0140-6736(09)61999-1openalex-snapshot
Community-associated meticillin-resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1016/s0378-1097(99)00282-7openalex-snapshot
The sae locus of Staphylococcus aureus encodes a two-component regulatory system
inferredcites →https://doi.org/10.1016/s0966-842x(02)02400-9openalex-snapshot
Is quorum sensing a side effect of diffusion sensing?
inferredcites →https://doi.org/10.1016/s1368-7646(03)00003-7openalex-snapshot
Insights on antibiotic resistance of Staphylococcus aureus from its whole genome: genomic island SCC
inferredcites →https://doi.org/10.1021/ja2071835openalex-snapshot
AirSR, a [2Fe-2S] Cluster-Containing Two-Component System, Mediates Global Oxygen Sensing and Redox Signaling in Staphylococcus aureus
inferredcites →https://doi.org/10.1038/305709a0openalex-snapshot
The toxic shock syndrome exotoxin structural gene is not detectably transmitted by a prophage
inferredcites →https://doi.org/10.1038/nrdp.2018.33openalex-snapshot
Methicillin-resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1038/nrmicro2200openalex-snapshot
Waves of resistance: Staphylococcus aureus in the antibiotic era
inferredcites →https://doi.org/10.1038/s41467-017-00903-yopenalex-snapshot
Quorum sensing integrates environmental cues, cell density and cell history to control bacterial competence
inferredcites →https://doi.org/10.1038/s41467-018-02949-yopenalex-snapshot
Sensory deprivation in Staphylococcus aureus
inferredcites →https://doi.org/10.1046/j.1365-2443.2003.00668.xopenalex-snapshot
A new staphylococcal sigma factor in the conserved gene cassette: functional significance and implication for the evolutionary processes
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Transmembrane topology and histidine protein kinase activity of AgrC, the agr signal receptor in Staphylococcus aureus
inferredcites →https://doi.org/10.1046/j.1365-2958.1998.01122.xopenalex-snapshot
Pho signal transduction network reveals direct transcriptional regulation of one two‐component system by another two‐component regulator: Bacillus subtilis PhoP directly regulates production of ResD
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03599.xopenalex-snapshot
Two‐component system VraSR positively modulates the regulation of cell‐wall biosynthesis pathway in Staphylococcus aureus
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03618.xopenalex-snapshot
Biphasic intracellular expression of Staphylococcus aureus virulence factors and evidence for Agr‐mediated diffusion sensing
inferredcites →https://doi.org/10.1073/pnas.0402521101openalex-snapshot
Complete genomes of two clinical Staphylococcus aureus strains: Evidence for the rapid evolution of virulence and drug resistance
inferredcites →https://doi.org/10.1073/pnas.0502950102openalex-snapshot
Whole genome sequence of Staphylococcus saprophyticus reveals the pathogenesis of uncomplicated urinary tract infection
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/10.1089/mdr.1996.2.435openalex-snapshot
Tracking the Evolutionary Origin of the Methicillin Resistance Gene: Cloning and Sequencing of a Homologue of mecA from a Methicillin Susceptible Strain of Staphylococcus sciuri
inferredcites →https://doi.org/10.1093/jac/dks494openalex-snapshot
Expression of SCCmec cassette chromosome recombinases in methicillin-resistant Staphylococcus aureus and Staphylococcus epidermidis
inferredcites →https://doi.org/10.1099/jmm.0.021956-0openalex-snapshot
A simplified multiplex PCR assay for fast and easy discrimination of globally distributed staphylococcal cassette chromosome mec types in meticillin-resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1099/mic.0.049692-0openalex-snapshot
NsaRS is a cell-envelope-stress-sensing two-component system of Staphylococcus aureus
inferredcites →https://doi.org/10.1099/mic.0.26575-0openalex-snapshot
The staphylococcal saeRS system coordinates environmental signals with agr quorum sensing
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05034.xopenalex-snapshot
The role of proton motive force in expression of the Staphylococcus aureus cid and lrg operons
inferredcites →https://doi.org/10.1111/j.1365-2958.2011.07735.xopenalex-snapshot
Bacitracin and nisin resistance in Staphylococcus aureus : a novel pathway involving the BraS/BraR two‐component system (SA2417/SA2418) and both the BraD/BraE and VraD/VraE ABC transporters
inferredcites →https://doi.org/10.1111/j.1365-3164.2012.01072.xopenalex-snapshot
Are all meticillin‐resistantStaphylococcus aureus(MRSA) equal in all hosts? Epidemiological and genetic comparison between animal and human MRSA
inferredcites →https://doi.org/10.1111/j.1462-5822.2012.01832.xopenalex-snapshot
MRSA virulence and spread
inferredcites →https://doi.org/10.1111/j.1574-6976.2009.00164.xopenalex-snapshot
The genetic transformation machinery: composition, localization, and mechanism
inferredcites →https://doi.org/10.1111/j.1758-2229.2012.00378.xopenalex-snapshot
Bacteriophages of S taphylococcus aureus efficiently package various bacterial genes and mobile genetic elements including SCC mec with different frequencies
inferredcites →https://doi.org/10.1111/mmi.12767openalex-snapshot
S taphylococcus aureus competence genes: mapping of the SigH , ComK 1 and ComK 2 regulons by transcriptome sequencing
inferredcites →https://doi.org/10.1111/mmi.13340openalex-snapshot
Transfer of the methicillin resistance genomic island among staphylococci by conjugation
inferredcites →https://doi.org/10.1111/mmi.13634openalex-snapshot
Staphylococcus aureus biofilm: a complex developmental organism
inferredcites →https://doi.org/10.1126/science.284.5418.1318openalex-snapshot
Bacterial Biofilms: A Common Cause of Persistent Infections
inferredcites →https://doi.org/10.1128/aac.00356-06openalex-snapshot
Role of VraSR in Antibiotic Resistance and Antibiotic-Induced Stress Response in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.00356-10openalex-snapshot
Origin and Molecular Evolution of the Determinant of Methicillin Resistance in Staphylococci
inferredcites →https://doi.org/10.1128/aac.00412-13openalex-snapshot
Role of the LytSR Two-Component Regulatory System in Adaptation to Cationic Antimicrobial Peptides in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.00575-09openalex-snapshot
Staphylococcal Cassette Chromosome mec -Like Element in Macrococcus caseolyticus
inferredcites →https://doi.org/10.1128/aac.01058-13openalex-snapshot
Transduction of Staphylococcal Cassette Chromosome mec Elements between Strains of Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.02008-12openalex-snapshot
Staphylococcus aureus Biofilms Promote Horizontal Transfer of Antibiotic Resistance
inferredcites →https://doi.org/10.1128/aac.38.11.2590openalex-snapshot
Reassessment of the number of auxiliary genes essential for expression of high-level methicillin resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.40.12.2680openalex-snapshot
Suppression of methicillin resistance in a mecA-containing pre-methicillin-resistant Staphylococcus aureus strain is caused by the mecI-mediated repression of PBP 2' production
inferredcites →https://doi.org/10.1128/aac.43.6.1449openalex-snapshot
Cloning and Nucleotide Sequence Determination of the Entire mec DNA of Pre-Methicillin-Resistant Staphylococcus aureus N315
inferredcites →https://doi.org/10.1128/aac.44.6.1549-1555.2000openalex-snapshot
A New Class of Genetic Element, Staphylococcus Cassette Chromosome mec , Encodes Methicillin Resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.45.5.1323-1336.2001openalex-snapshot
Structural Comparison of Three Types of Staphylococcal Cassette Chromosome mec Integrated in the Chromosome in Methicillin-Resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.46.4.1147-1152.2002openalex-snapshot
Novel Type of Staphylococcal Cassette Chromosome mec Identified in Community-Acquired Methicillin-Resistant Staphylococcus aureus Strains
inferredcites →https://doi.org/10.1128/aac.47.12.3926-3934.2003openalex-snapshot
Evolutionary Models of the Emergence ofMethicillin-Resistant Staphylococcusaureus
inferredcites →https://doi.org/10.1128/aac.48.6.2295-2297.2004openalex-snapshot
Fitness Cost of SCC mec and Methicillin Resistance Levels in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.48.7.2637-2651.2004openalex-snapshot
Novel Type V Staphylococcal Cassette Chromosome mec Driven by a Novel Cassette Chromosome Recombinase, ccrC
inferredcites →https://doi.org/10.1128/aac.49.8.3404-3413.2005openalex-snapshot
DNA Microarray-Based Identification of Genes Associated with Glycopeptide Resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aem.70.11.6887-6891.2004openalex-snapshot
New Vector for Efficient Allelic Replacement in Naturally Nontransformable, Low-GC-Content, Gram-Positive Bacteria
inferredcites →https://doi.org/10.1128/cmr.00020-18openalex-snapshot
Methicillin-Resistant Staphylococcus aureus: Molecular Characterization, Evolution, and Epidemiology
inferredcites →https://doi.org/10.1128/iai.00371-18openalex-snapshot
PhoPR Contributes to Staphylococcus aureus Growth during Phosphate Starvation and Pathogenesis in an Environment-Specific Manner
inferredcites →https://doi.org/10.1128/iai.03109-14openalex-snapshot
Characterization of a Novel Two-Component Regulatory System, HptRS, the Regulator for the Hexose Phosphate Transport System in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.00905-08openalex-snapshot
Characterization of the Oxygen-Responsive NreABC Regulon of Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.01520-09openalex-snapshot
Roles of CcrA and CcrB in Excision and Integration of Staphylococcal Cassette Chromosome mec , a Staphylococcus aureus Genomic Island
inferredcites →https://doi.org/10.1128/jb.104.3.1158-1167.1970openalex-snapshot
Transduction of Methicillin Resistance in Staphylococcus aureus Dependent on an Unusual Specificity of the Recipient Strain
inferredcites →https://doi.org/10.1128/jb.123.3.905-915.1975openalex-snapshot
Transformation reveals a chromosomal locus of the gene(s) for methicillin resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.178.19.5810-5812.1996openalex-snapshot
Identification of LytSR-regulated genes from Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.181.12.3666-3673.1999openalex-snapshot
Role in Cell Permeability of an Essential Two-Component System inStaphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.182.14.3955-3964.2000openalex-snapshot
A New Two-Component Regulatory System Involved in Adhesion, Autolysis, and Extracellular Proteolytic Activity of Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.183.4.1113-1123.2001openalex-snapshot
Identification of a Novel Two-Component Regulatory System That Acts in Global Regulation of Virulence Factors of Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.184.13.3623-3629.2002openalex-snapshot
Type 1 Capsule Genes of Staphylococcus aureus Are Carried in a Staphylococcal Cassette Chromosome Genetic Element
inferredcites →https://doi.org/10.1128/jb.185.18.5465-5472.2003openalex-snapshot
Jumping the Barrier to β-Lactam Resistance in Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.186.4.1175-1181.2004openalex-snapshot
Identification of Genes Controlled by the Essential YycG/YycF Two-Component System ofStaphylococcus aureus
inferredcites →https://doi.org/10.1128/jb.187.15.5486-5492.2005openalex-snapshot
Global Regulation of Gene Expression by ArlRS, a Two-Component Signal Transduction Regulatory System of Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jcm.22.6.996-1006.1985openalex-snapshot
Adherence of coagulase-negative staphylococci to plastic tissue culture plates: a quantitative model for the adherence of staphylococci to medical devices
inferredcites →https://doi.org/10.1128/mbio.01137-19openalex-snapshot
Identification of Extracellular DNA-Binding Proteins in the Biofilm Matrix
inferredcites →https://doi.org/10.1128/mbio.01341-14openalex-snapshot
Temporal and Stochastic Control of Staphylococcus aureus Biofilm Development
inferredcites →https://doi.org/10.1128/microbiolspec.vmbf-0022-2015openalex-snapshot
The Staphylococcal Biofilm: Adhesins, Regulation, and Host Response
inferredcites →https://doi.org/10.1146/annurev.genet.42.110807.091640openalex-snapshot
Quorum Sensing in Staphylococci
inferredcites →https://doi.org/10.1172/jci18535openalex-snapshot
Antimicrobial resistance: the example of Staphylococcus aureus
inferredcites →https://doi.org/10.1172/jci200318535openalex-snapshot
Antimicrobial resistance: the example of Staphylococcus aureus
inferredcites →https://doi.org/10.1186/1471-2164-10-429openalex-snapshot
Transcriptome analysis of the responses of Staphylococcus aureus to antimicrobial peptides and characterization of the roles of vraDE and vraSR in antimicrobial resistance
inferredcites →https://doi.org/10.1186/1471-2180-11-13openalex-snapshot
Staphylococcus aureus requires cardiolipin for survival under conditions of high salinity
inferredcites →https://doi.org/10.1371/journal.pone.0021323openalex-snapshot
Investigation of the Staphylococcus aureus GraSR Regulon Reveals Novel Links to Virulence, Stress Response and Cell Wall Signal Transduction Pathways
inferredcites →https://doi.org/10.1371/journal.ppat.1000888openalex-snapshot
Alternative Sigma Factor σH Modulates Prophage Integration and Excision in Staphylococcus aureus
inferredcites →https://doi.org/10.1371/journal.ppat.1003003openalex-snapshot
Expression of a Cryptic Secondary Sigma Factor Gene Unveils Natural Competence for DNA Transformation in Staphylococcus aureus
inferredcites →https://doi.org/10.1371/journal.ppat.1003201openalex-snapshot
The KdpD/KdpE Two-Component System: Integrating K+ Homeostasis and Virulence
inferredcites →https://doi.org/10.1371/journal.ppat.1003819openalex-snapshot
The Staphylococcus aureus ArlRS Two-Component System Is a Novel Regulator of Agglutination and Pathogenesis
inferredcites →https://doi.org/10.1529/biophysj.104.047134openalex-snapshot
Forces during Bacteriophage DNA Packaging and Ejection
inferredcites →https://doi.org/10.2323/jgam.52.259openalex-snapshot
Genetic characterization of the natural SigB variants found in clinical isolates of Staphylococcus aureus
inferredcites →https://doi.org/10.3389/fmicb.2018.02723openalex-snapshot
Factors Contributing to the Evolution of mecA-Mediated β-lactam Resistance in Staphylococci: Update and New Insights From Whole Genome Sequencing (WGS)
inferredcites →https://doi.org/10.3390/v4123316openalex-snapshot
The Staphylococci Phages Family: An Overview
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/2022.04.06.487305openalex-snapshot
Microaerobic conditions and the complex regulation of natural competence in Staphylococcus aureus
inferred← citeshttps://doi.org/10.70675/e10d34a0ze450z4abczbf8bz5182f982ce81openalex-snapshot
Natural competence for genetic transformation in Staphylococcus aureus
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