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Enterococcus faecium Biofilm Formation: Identification of Major Autolysin AtlA Efm , Associated Acm Surface Localization, and AtlA Efm -Independent Extracellular DNA Release

https://doi.org/10.1128/mbio.00154-13
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What this work says

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

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Lytic transglycosylases in macromolecular transport systems of Gram-negative bacteria
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A general system for generating unlabelled gene replacements in bacterial chromosomes
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[1] The collagens: An overview and update
inferredcites →https://doi.org/10.1016/j.copbio.2010.10.016openalex-snapshot
Biofilm formation and dispersal in Gram-positive bacteria
inferredcites →https://doi.org/10.1016/j.febslet.2009.08.010openalex-snapshot
Impact of peptidoglycan O‐acetylation on autolytic activities of the Enterococcus faecalis N‐acetylglucosaminidase AtlA and N‐acetylmuramidase AtlB
inferredcites →https://doi.org/10.1016/j.jmb.2011.11.039openalex-snapshot
Inhibition of Pseudomonas aeruginosa Virulence: Characterization of the AprA–AprI Interface and Species Selectivity
inferredcites →https://doi.org/10.1016/j.tim.2011.11.001openalex-snapshot
Optimizing future treatment of enterococcal infections: attacking the biofilm?
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.4101774.xopenalex-snapshot
Evidence for autolysin‐mediated primary attachment of Staphylococcus epidermidis to a polystyrene surface
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03417.xopenalex-snapshot
Clinical isolates of Enterococcus faecium exhibit strain‐specific collagen binding mediated by Acm, a new member of the MSCRAMM family
inferredcites →https://doi.org/10.1074/jbc.m802323200openalex-snapshot
Role of N-Acetylglucosaminidase and N-Acetylmuramidase Activities in Enterococcus faecalis Peptidoglycan Metabolism
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/gks1243openalex-snapshot
CDD: conserved domains and protein three-dimensional structure
inferredcites →https://doi.org/10.1099/00221287-146-10-2395openalex-snapshot
Quantification of biofilm structures by the novel computer program comstat
inferredcites →https://doi.org/10.1099/jmm.0.05201-0openalex-snapshot
Correlation between enterococcal biofilm formation in vitro and medical-device-related infection potential in vivo
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.1365-2958.2005.05008.xopenalex-snapshot
A characterization of DNA release in Pseudomonas aeruginosa cultures and biofilms
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06211.xopenalex-snapshot
LysM, a widely distributed protein motif for binding to (peptido)glycans
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.1365-2958.2009.07007.xopenalex-snapshot
Role of staphylococcal wall teichoic acid in targeting the major autolysin Atl
inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02355.xopenalex-snapshot
A genetic element present on megaplasmids allows Enterococcus faecium to use raffinose as carbon source
inferredcites →https://doi.org/10.1111/j.1574-6968.2007.00688.xopenalex-snapshot
icaand beyond: biofilm mechanisms and regulation inStaphylococcus epidermidisandStaphylococcus aureus
inferredcites →https://doi.org/10.1128/aac.42.11.2883openalex-snapshot
Effect of Disruption of a Gene Encoding an Autolysin of Enterococcus faecalis OG1RF
inferredcites →https://doi.org/10.1128/aem.01317-08openalex-snapshot
DNA as an Adhesin: Bacillus cereus Requires Extracellular DNA To Form Biofilms
inferredcites →https://doi.org/10.1128/aem.02073-07openalex-snapshot
Differential Roles of Poly- N -Acetylglucosamine Surface Polysaccharide and Extracellular DNA in Staphylococcus aureus and Staphylococcus epidermidis Biofilms
inferredcites →https://doi.org/10.1128/aem.68.3.1196-1203.2002openalex-snapshot
Functional Genomics Approach to Identifying Genes Required for Biofilm Development by Streptococcus mutans
inferredcites →https://doi.org/10.1128/cmr.15.2.167-193.2002openalex-snapshot
Biofilms: Survival Mechanisms of Clinically Relevant Microorganisms
inferredcites →https://doi.org/10.1128/iai.00275-09openalex-snapshot
SgrA, a Nidogen-Binding LPXTG Surface Adhesin Implicated in Biofilm Formation, and EcbA, a Collagen Binding MSCRAMM, Are Two Novel Adhesins of Hospital-Acquired Enterococcus faecium
inferredcites →https://doi.org/10.1128/iai.69.2.712-718.2001openalex-snapshot
Staphylococcus caprae Strains Carry Determinants Known To Be Involved in Pathogenicity: a Gene Encoding an Autolysin-Binding Fibronectin and the ica Operon Involved in Biofilm Formation
inferredcites →https://doi.org/10.1128/iai.69.5.3423-3426.2001openalex-snapshot
Key Role of Teichoic Acid Net Charge in Staphylococcus aureus Colonization of Artificial Surfaces
inferredcites →https://doi.org/10.1128/iai.72.6.3658-3663.2004openalex-snapshot
Influence of Origin of Isolates, Especially Endocarditis Isolates, and Various Genes on Biofilm Formation by Enterococcus faecalis
inferredcites →https://doi.org/10.1128/iai.73.6.3512-3520.2005openalex-snapshot
Identification and Characterization of an Autolysin-Encoding Gene of Streptococcus mutans
inferredcites →https://doi.org/10.1128/iai.73.8.4793-4802.2005openalex-snapshot
The Multifunctional Staphylococcus aureus Autolysin Aaa Mediates Adherence to Immobilized Fibrinogen and Fibronectin
inferredcites →https://doi.org/10.1128/jb.00056-11openalex-snapshot
The Major Autolysin of Streptococcus gordonii Is Subject to Complex Regulation and Modulates Stress Tolerance, Biofilm Formation, and Extracellular-DNA Release
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.00536-06openalex-snapshot
The atlA Operon of Streptococcus mutans : Role in Autolysin Maturation and Cell Surface Biogenesis
inferredcites →https://doi.org/10.1128/jb.00664-07openalex-snapshot
Five Genes Encoding Surface-Exposed LPXTG Proteins Are Enriched in Hospital-Adapted Enterococcus faecium Clonal Complex 17 Isolates
inferredcites →https://doi.org/10.1128/jb.01145-06openalex-snapshot
Functional Analysis of AtlA, the MajorN-Acetylglucosaminidase ofEnterococcus faecalis
inferredcites →https://doi.org/10.1128/jb.01205-07openalex-snapshot
Enterococcal Surface Protein Esp Is Important for Biofilm Formation of Enterococcus faecium E1162
inferredcites →https://doi.org/10.1128/jb.06231-11openalex-snapshot
Characterization and Functional Analysis of atl , a Novel Gene Encoding Autolysin in Streptococcus suis
inferredcites →https://doi.org/10.1128/jb.184.10.2699-2708.2002openalex-snapshot
A Quorum-Sensing Signaling System Essential for Genetic Competence in Streptococcus mutans Is Involved in Biofilm Formation
inferredcites →https://doi.org/10.1128/jb.184.22.6333-6342.2002openalex-snapshot
Novel Two-Component Regulatory System Involved in Biofilm Formation and Acid Resistance inStreptococcus mutans
inferredcites →https://doi.org/10.1128/jb.187.13.4392-4400.2005openalex-snapshot
DNA Binding-Uptake System: a Link between Cell-to-Cell Communication and Biofilm Formation
inferredcites →https://doi.org/10.1128/jb.188.10.3622-3630.2006openalex-snapshot
Cation-Induced Transcriptional Regulation of the dlt Operon of Staphylococcus aureus
inferredcites →https://doi.org/10.1128/mbio.00193-12openalex-snapshot
Enterococcus faecalis Produces Abundant Extracellular Structures Containing DNA in the Absence of Cell Lysis during Early Biofilm Formation
inferredcites →https://doi.org/10.1146/annurev.micro.54.1.49openalex-snapshot
Biofilm Formation as Microbial Development
inferredcites →https://doi.org/10.1186/1471-2164-10-291openalex-snapshot
Comprehensive identification of essential Staphylococcus aureus genes using Transposon-Mediated Differential Hybridisation (TMDH)
inferredcites →https://doi.org/10.1186/1471-2164-11-239openalex-snapshot
Pyrosequencing-based comparative genome analysis of the nosocomial pathogen Enterococcus faecium and identification of a large transferable pathogenicity island
inferredcites →https://doi.org/10.1371/journal.pgen.1002804openalex-snapshot
Genome-Wide Identification of Ampicillin Resistance Determinants in Enterococcus faecium
inferredcites →https://doi.org/10.1371/journal.pone.0042244openalex-snapshot
Contribution of the Staphylococcus aureus Atl AM and GL Murein Hydrolase Activities in Cell Division, Autolysis, and Biofilm Formation
inferredcites →https://doi.org/10.3390/molecules16108848openalex-snapshot
Transcriptional and Functional Analysis Shows Sodium Houttuyfonate-Mediated Inhibition of Autolysis in Staphylococcus aureus

What points at this work

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

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4-Hydroxyboesenbergin B of Alpinia japonica protected gastrointestinal tract by inhibiting vancomycin-resistant enterococcus and balancing intestinal microbiota
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Clinical outcomes and molecular epidemiology of vancomycin-resistant Enterococcus faecium bloodstream infection: The importance of appropriate therapy and ST17 predominance
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YajC, a predicted membrane protein, promotes Enterococcus faecium biofilm formation in vitro and in a rat endocarditis model
inferred← citeshttps://doi.org/10.1093/femsmc/xtae018openalex-snapshot
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inferred← citeshttps://doi.org/10.1128/aem.02083-20openalex-snapshot
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