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The rise of the Enterococcus: beyond vancomycin resistance
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.1952.02930230016005openalex-snapshot
STREPTOCOCCUS VIRIDANS SUBACUTE BACTERIAL ENDOCARDITIS
inferredcites →https://doi.org/10.1001/jama.308.17.1813-bopenalex-snapshot
Harrison’s Principles of Internal Medicine
inferredcites →https://doi.org/10.1007/s00018-002-8500-0openalex-snapshot
The 2.4-Å crystal structure of the penicillin-resistant penicillin-binding protein PBP5fm from Enterococcus faecium in complex with benzylpenicillin
inferredcites →https://doi.org/10.1016/0147-619x(85)90052-6openalex-snapshot
Nucleotide sequence analysis of a gene encoding a streptomycin/spectinomycin adenyltransferase
inferredcites →https://doi.org/10.1016/j.ijmm.2010.08.015openalex-snapshot
A multiresistance megaplasmid pLG1 bearing a hylEfm genomic island in hospital Enterococcus faecium isolates
inferredcites →https://doi.org/10.1016/j.mib.2010.08.004openalex-snapshot
Horizontal gene transfer and the genomics of enterococcal antibiotic resistance
inferredcites →https://doi.org/10.1016/j.micinf.2011.08.006openalex-snapshot
Contribution of the enterococcal surface protein Esp to pathogenesis of Enterococcus faecium endocarditis
inferredcites →https://doi.org/10.1016/j.molcel.2007.04.005openalex-snapshot
The Site of Action of Oxazolidinone Antibiotics in Living Bacteria and in Human Mitochondria
inferredcites →https://doi.org/10.1016/j.tim.2009.06.004openalex-snapshot
LPxTG surface proteins of enterococci
inferredcites →https://doi.org/10.1016/s0140-6736(88)91037-9openalex-snapshot
VANCOMYCIN-RESISTANT ENTEROCOCCI
inferredcites →https://doi.org/10.1016/s0195-6701(96)90065-1openalex-snapshot
Heat and chemical resistance of enterococci
inferredcites →https://doi.org/10.1016/s0891-5520(20)30509-2openalex-snapshot
AMINOGLYCOSIDE RESISTANT ENTEROCOCCAL ENDOCARDITIS
inferredcites →https://doi.org/10.1021/bi992025kopenalex-snapshot
Protein-Sulfenic Acids: Diverse Roles for an Unlikely Player in Enzyme Catalysis and Redox Regulation
inferredcites →https://doi.org/10.1034/j.1399-302x.2003.00059.xopenalex-snapshot
Influence of Enterococcus faecalis proteases and the collagen‐binding protein, Ace, on adhesion to dentin
inferredcites →https://doi.org/10.1038/nature07250openalex-snapshot
Vancomycin-resistant enterococci exploit antibiotic-induced innate immune deficits
inferredcites →https://doi.org/10.1046/j.1365-2958.1996.831449.xopenalex-snapshot
Structural analysis and proteolytic activation of Enterococcus faecalis cytolysin, a novel lantibiotic
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/10.1056/nejm198807213190307openalex-snapshot
Plasmid-Mediated Resistance to Vancomycin and Teicoplanin in Enterococcus Faecium
inferredcites →https://doi.org/10.1056/nejm200012283432604openalex-snapshot
Effect of Antibiotic Therapy on the Density of Vancomycin-Resistant Enterococci in the Stool of Colonized Patients
inferredcites →https://doi.org/10.1056/nejmoa1011138openalex-snapshot
Genetic Basis for In Vivo Daptomycin Resistance in Enterococci
inferredcites →https://doi.org/10.1073/pnas.032448299openalex-snapshot
The capsular polysaccharide of Enterococcus faecalis and its relationship to other polysaccharides in the cell wall
inferredcites →https://doi.org/10.1073/pnas.0701809104openalex-snapshot
Structural basis for streptogramin B resistance in Staphylococcus aureus by virginiamycin B lyase
inferredcites →https://doi.org/10.1073/pnas.0804276105openalex-snapshot
The oxazolidinone antibiotics perturb the ribosomal peptidyl-transferase center and effect tRNA positioning
inferredcites →https://doi.org/10.1073/pnas.0806350105openalex-snapshot
The molecular switch that activates the cell wall anchoring step of pilus assembly in gram-positive bacteria
inferredcites →https://doi.org/10.1073/pnas.1000139107openalex-snapshot
Mechanism of chromosomal transfer of Enterococcus faecalis pathogenicity island, capsule, antimicrobial resistance, and other traits
inferredcites →https://doi.org/10.1073/pnas.1006855107openalex-snapshot
Inducible expression eliminates the fitness cost of vancomycin resistance in enterococci
inferredcites →https://doi.org/10.1073/pnas.96.12.6908openalex-snapshot
Vancomycin-resistant enterococci in intensive-care hospital settings: Transmission dynamics, persistence, and the impact of infection control programs
inferredcites →https://doi.org/10.1074/jbc.m303766200openalex-snapshot
Structural Basis of Synercid® (Quinupristin-Dalfopristin) Resistance in Gram-positive Bacterial Pathogens
inferredcites →https://doi.org/10.1074/jbc.m611137200openalex-snapshot
The Enterococcus faecalis MSCRAMM ACE Binds Its Ligand by the Collagen Hug Model
inferredcites →https://doi.org/10.1084/jem.4.5-6.521openalex-snapshot
A CASE OF ACUTE ENDOCARDITIS CAUSED BY MICROCOCCUS ZYMOGENES (NOV. SPEC.), WITH A DESCRIPTION OF THE MICROORGANISM
inferredcites →https://doi.org/10.1086/313949openalex-snapshot
Aminoglycoside Resistance in Enterococci
inferredcites →https://doi.org/10.1086/314453openalex-snapshot
Generation and Testing of Mutants ofEnterococcus faecalisin a Mouse Peritonitis Model
inferredcites →https://doi.org/10.1086/381150openalex-snapshot
A Putative Sugar‐Binding Transcriptional Regulator in a Novel Gene Locus inEnterococcus faecalisContributes to Production of Biofilm and Prolonged Bacteremia in Mice
inferredcites →https://doi.org/10.1086/502924openalex-snapshot
SHEA Guideline for Preventing Nosocomial Transmission of Multidrug-Resistant Strains ofStaphylococcus aureusandEnterococcus
inferredcites →https://doi.org/10.1086/515605openalex-snapshot
Penicillin-Binding Protein 5 Sequence Alterations in Clinical Isolates of Enterococcus faecium with Different Levels of -Lactam Resistance
inferredcites →https://doi.org/10.1086/517524openalex-snapshot
Importance of theebp(Endocarditis‐ and Biofilm‐Associated Pilus) Locus in the Pathogenesis ofEnterococcus faecalisAscending Urinary Tract Infection
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/10.1086/593956openalex-snapshot
Secular Trends of Hospitalization With Vancomycin-Resistant Enterococcus Infection in the United States, 2000–2006
inferredcites →https://doi.org/10.1086/595986openalex-snapshot
Transferable Capacity for Gastrointestinal Colonization inEnterococcus faeciumin a Mouse Model
inferredcites →https://doi.org/10.1086/600124openalex-snapshot
Importance of theepaLocus ofEnterococcus faecalisOG1RF in a Mouse Model of Ascending Urinary Tract Infection
inferredcites →https://doi.org/10.1086/605609openalex-snapshot
Enterococcal Surface Protein Transiently AggravatesEnterococcus faecium–Induced Urinary Tract Infection in Mice
inferredcites →https://doi.org/10.1086/644790openalex-snapshot
Analysis of Clonality and Antibiotic Resistance among Early Clinical Isolates of Enterococcus faecium in the United States
inferredcites →https://doi.org/10.1086/650203openalex-snapshot
Bacterial Flagellin Stimulates Toll‐Like Receptor 5–Dependent Defense against Vancomycin‐Resistant Enterococcus Infection
inferredcites →https://doi.org/10.1089/mdr.1996.2.209openalex-snapshot
Intrinsic Penicillin Resistance in Enterococci
inferredcites →https://doi.org/10.1089/mdr.2011.0025openalex-snapshot
Molecular Characterization of Vancomycin-Resistant Enterococci in a Chinese Hospital Between 2003 and 2009
inferredcites →https://doi.org/10.1093/infdis/163.4.780openalex-snapshot
Evidence for Clonal Spread of a Single Strain of -Lactamase-Producing Enterococcus (Streptococcus) faecalis to Six Hospitals in Five States
inferredcites →https://doi.org/10.1093/infdis/170.6.1549openalex-snapshot
A Plasmid-Encoded Surface Protein On Enterococcus Faecalis Augments Its Internalization By Cultured Intestinal Epithelial Cells
inferredcites →https://doi.org/10.1093/infdis/jiq160openalex-snapshot
Importance of Two Enterococcus faecium Loci Encoding Gls-like Proteins for In Vitro Bile Salts Stress Response and Virulence
inferredcites →https://doi.org/10.1093/nar/gkr012openalex-snapshot
A simple and efficient method to search for selected primary transcripts: non-coding and antisense RNAs in the human pathogen Enterococcus faecalis
inferredcites →https://doi.org/10.1099/mic.0.2008/017319-0openalex-snapshot
Identification and phenotypic characterization of a second collagen adhesin, Scm, and genome-based identification and analysis of 13 other predicted MSCRAMMs, including four distinct pilus loci, in Enterococcus faecium
inferredcites →https://doi.org/10.1099/mic.0.2008/020891-0openalex-snapshot
Expression of two distinct types of pili by a hospital-acquired Enterococcus faecium isolate
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04045.xopenalex-snapshot
An amino‐terminal domain of Enterococcus faecalis aggregation substance is required for aggregation, bacterial internalization by epithelial cells and binding to lipoteichoic acid
inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05744.xopenalex-snapshot
Acquisition of a natural resistance gene renders a clinical strain of methicillin‐resistantStaphylococcus aureusresistant to the synthetic antibiotic linezolid
inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05987.xopenalex-snapshot
Comparative study of the physiological roles of three peroxidases (NADH peroxidase, Alkyl hydroperoxide reductase and Thiol peroxidase) in oxidative stress response, survival inside macrophages and virulence of Enterococcus faecalis
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06587.xopenalex-snapshot
Glycolipids are involved in biofilm accumulation and prolonged bacteraemia in Enterococcus faecalis
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.1469-0691.2010.03201.xopenalex-snapshot
Genome-based insights into the evolution of enterococci
inferredcites →https://doi.org/10.1111/j.1469-0691.2010.03226.xopenalex-snapshot
Mobile genetic elements and their contribution to the emergence of antimicrobial resistant Enterococcus faecalis and Enterococcus faecium
inferredcites →https://doi.org/10.1111/j.1574-6976.2011.00284.xopenalex-snapshot
Population biology of Gram-positive pathogens: high-risk clones for dissemination of antibiotic resistance
inferredcites →https://doi.org/10.1126/science.1080613openalex-snapshot
Role of Mobile DNA in the Evolution of Vancomycin-Resistant Enterococcus faecalis
inferredcites →https://doi.org/10.1126/science.1110591openalex-snapshot
Diversity of the Human Intestinal Microbial Flora
inferredcites →https://doi.org/10.1126/science.1183605openalex-snapshot
A Catalog of Reference Genomes from the Human Microbiome
inferredcites →https://doi.org/10.1128/aac.00099-11openalex-snapshot
Analysis of PBP5 of Early U.S. Isolates of Enterococcus faecium: Sequence Variation Alone Does Not Explain Increasing Ampicillin Resistance over Time
inferredcites →https://doi.org/10.1128/aac.00134-10openalex-snapshot
Global Spread of the hyl Efm Colonization-Virulence Gene in Megaplasmids of the Enterococcus faecium CC17 Polyclonal Subcluster
inferredcites →https://doi.org/10.1128/aac.00207-11openalex-snapshot
Genetic Basis for Daptomycin Resistance in Enterococci
inferredcites →https://doi.org/10.1128/aac.00242-09openalex-snapshot
Cotransfer of Antibiotic Resistance Genes and a hyl Efm -Containing Virulence Plasmid in Enterococcus faecium
inferredcites →https://doi.org/10.1128/aac.01633-08openalex-snapshot
Influence of Recombination on Development of Mutational Resistance to Linezolid in Enterococcus faecalis JH2-2
inferredcites →https://doi.org/10.1128/aac.31.2.139openalex-snapshot
Continuous-infusion ampicillin therapy of enterococcal endocarditis in rats
inferredcites →https://doi.org/10.1128/aac.34.4.543openalex-snapshot
Antimicrobial susceptibility of vancomycin-resistant Leuconostoc, Pediococcus, and Lactobacillus species
inferredcites →https://doi.org/10.1128/aac.36.11.2355openalex-snapshot
Beta-lactamase-producing enterococci
inferredcites →https://doi.org/10.1128/aac.37.8.1563openalex-snapshot
Genetics and mechanisms of glycopeptide resistance in enterococci
inferredcites →https://doi.org/10.1128/aac.41.5.931openalex-snapshot
Influence of inducible cross-resistance to macrolides, lincosamides, and streptogramin B-type antibiotics in Enterococcus faecium on activity of quinupristin-dalfopristin in vitro and in rabbits with experimental endocarditis
inferredcites →https://doi.org/10.1128/aac.43.4.727openalex-snapshot
Aminoglycosides: Activity and Resistance
inferredcites →https://doi.org/10.1128/aac.46.6.1845-1850.2002openalex-snapshot
An Enterococcus faecalis ABC Homologue (Lsa) Is Required for the Resistance of This Species to Clindamycin and Quinupristin-Dalfopristin
inferredcites →https://doi.org/10.1128/aac.47.10.3318-3320.2003openalex-snapshot
Recombination Proficiency Influences Frequency and Locus of Mutational Resistance to Linezolid in Enterococcus faecalis
inferredcites →https://doi.org/10.1128/aac.49.10.4227-4233.2005openalex-snapshot
Glycopeptide ResistancevanAOperons inPaenibacillusStrains Isolated from Soil
inferredcites →https://doi.org/10.1128/cmr.00027-10openalex-snapshot
Hospital Epidemiology and Infection Control in Acute-Care Settings
inferredcites →https://doi.org/10.1128/cmr.3.1.46openalex-snapshot
The life and times of the Enterococcus
inferredcites →https://doi.org/10.1128/iai.00038-11openalex-snapshot
Relative Contributions of Ebp Pili and the Collagen Adhesin Ace to Host Extracellular Matrix Protein Adherence and Experimental Urinary Tract Infection by Enterococcus faecalis OG1RF
inferredcites →https://doi.org/10.1128/iai.00039-11openalex-snapshot
Conservation of Ebp-Type Pilus Genes among Enterococci and Demonstration of Their Role in Adherence of Enterococcus faecalis to Human Platelets
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.00149-09openalex-snapshot
Further Characterization of the epa Gene Cluster and Epa Polysaccharides of Enterococcus faecalis
inferredcites →https://doi.org/10.1128/iai.00165-10openalex-snapshot
Role of Methionine Sulfoxide Reductases A and B of Enterococcus faecalis in Oxidative Stress and Virulence
inferredcites →https://doi.org/10.1128/iai.00279-07openalex-snapshot
Enterococcal Leucine-Rich Repeat-Containing Protein Involved in Virulence and Host Inflammatory Response
inferredcites →https://doi.org/10.1128/iai.00375-08openalex-snapshot
A Functional Collagen Adhesin Gene, acm , in Clinical Isolates of Enterococcus faecium Correlates with the Recent Success of This Emerging Nosocomial Pathogen
inferredcites →https://doi.org/10.1128/iai.00476-06openalex-snapshot
Ligand-Signaled Upregulation of Enterococcus faecalis ace Transcription, a Mechanism for Modulating Host- E. faecalis Interaction
inferredcites →https://doi.org/10.1128/iai.00570-06openalex-snapshot
Opsonic Antibodies to Enterococcus faecalis Strain 12030 Are Directed against Lipoteichoic Acid
inferredcites →https://doi.org/10.1128/iai.00576-09openalex-snapshot
Enterococcus faecalis Capsular Polysaccharide Serotypes C and D and Their Contributions to Host Innate Immune Evasion
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.00930-08openalex-snapshot
An AraC-Type Transcriptional Regulator Encoded on the Enterococcus faecalis Pathogenicity Island Contributes to Pathogenesis and Intracellular Macrophage Survival
inferredcites →https://doi.org/10.1128/iai.01118-09openalex-snapshot
Gelatinase Contributes to the Pathogenesis of Endocarditis Caused byEnterococcus faecalis
inferredcites →https://doi.org/10.1128/iai.01218-08openalex-snapshot
ace , Which Encodes an Adhesin in Enterococcus faecalis , Is Regulated by Ers and Is Involved in Virulence
inferredcites →https://doi.org/10.1128/iai.45.2.528-530.1984openalex-snapshot
Hemolysin of Streptococcus faecalis subspecies zymogenes contributes to virulence in mice
inferredcites →https://doi.org/10.1128/iai.59.4.1239-1246.1991openalex-snapshot
Molecular characterization of the Enterococcus faecalis cytolysin activator
inferredcites →https://doi.org/10.1128/iai.60.6.2445-2452.1992openalex-snapshot
Contribution of the pAD1-encoded cytolysin to the severity of experimental Enterococcus faecalis endophthalmitis
inferredcites →https://doi.org/10.1128/iai.65.10.4207-4215.1997openalex-snapshot
Enterococcus faecalis antigens in human infections
inferredcites →https://doi.org/10.1128/iai.66.1.218-223.1998openalex-snapshot
Aggregation and Binding Substances Enhance Pathogenicity in Rabbit Models ofEnterococcus faecalisEndocarditis
inferredcites →https://doi.org/10.1128/iai.68.2.815-823.2000openalex-snapshot
Analysis of a Gene Cluster ofEnterococcus faecalisInvolved in Polysaccharide Biosynthesis
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/iai.69.7.4366-4372.2001openalex-snapshot
Role of Enterococcus faecalis Surface Protein Esp in the Pathogenesis of Ascending Urinary Tract Infection
inferredcites →https://doi.org/10.1128/iai.70.10.5647-5650.2002openalex-snapshot
Virulence Effect of Enterococcus faecalis Protease Genes and the Quorum-Sensing Locus fsr in Caenorhabditis elegans and Mice
inferredcites →https://doi.org/10.1128/iai.70.4.2010-2015.2002openalex-snapshot
Evidence that the Enterococcal Polysaccharide Antigen Gene ( epa ) Cluster Is Widespread in Enterococcus faecalis and Influences Resistance to Phagocytic Killing of E. faecalis
inferredcites →https://doi.org/10.1128/iai.70.8.4678-4681.2002openalex-snapshot
The Enterococcus faecalis fsrB Gene, a Key Component of the fsr Quorum-Sensing System, Is Associated with Virulence in the Rabbit Endophthalmitis Model
inferredcites →https://doi.org/10.1128/iai.72.6.3628-3633.2004openalex-snapshot
Contribution of Gelatinase, Serine Protease, and fsr to the Pathogenesis of Enterococcus faecalis Endophthalmitis
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.73.11.7772-7774.2005openalex-snapshot
Decreased Virulence of a gls24 Mutant of Enterococcus faecalis OG1RF in an Experimental Endocarditis Model
inferredcites →https://doi.org/10.1128/iai.73.3.1606-1612.2005openalex-snapshot
Gelatinase Is Important for Translocation of Enterococcus faecalis across Polarized Human Enterocyte-Like T84 Cells
inferredcites →https://doi.org/10.1128/iai.73.8.4888-4894.2005openalex-snapshot
Fsr-Independent Production of Protease(s) May Explain the Lack of Attenuation of an Enterococcus faecalis fsr Mutant Versus a gelE - sprE Mutant in Induction of Endocarditis
inferredcites →https://doi.org/10.1128/jb.00153-10openalex-snapshot
High-Quality Draft Genome Sequences of 28 Enterococcus sp. Isolates
inferredcites →https://doi.org/10.1128/jb.00725-10openalex-snapshot
Enterococcus faecalis rnjB Is Required for Pilin Gene Expression and Biofilm Formation
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.05026-11openalex-snapshot
The Fsr Quorum-Sensing System of Enterococcus faecalisModulates Surface Display of the Collagen-Binding MSCRAMM Ace through Regulation of gelE
inferredcites →https://doi.org/10.1128/jb.177.4.871-876.1995openalex-snapshot
Pheromone-inducible conjugation in Enterococcus faecalis: interbacterial and host-parasite chemical communication
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.187.19.6668-6677.2005openalex-snapshot
Tn5386, a Novel Tn916-Like Mobile Element inEnterococcus faeciumD344R That Interacts with Tn916To Yield a Large Genomic Deletion
inferredcites →https://doi.org/10.1128/jb.188.6.2063-2072.2006openalex-snapshot
Putative Surface Proteins Encoded within a Novel Transferable Locus Confer a High-Biofilm Phenotype to Enterococcus faecalis
inferredcites →https://doi.org/10.1128/jcm.01351-07openalex-snapshot
Emergence of Clonal Complex 17 Enterococcus faecium in The Netherlands
inferredcites →https://doi.org/10.1128/jcm.02526-09openalex-snapshot
Molecular Epidemiology of Vancomycin-Resistant Enterococcus faecium : a Prospective, Multicenter Study in South American Hospitals
inferredcites →https://doi.org/10.1128/jcm.02596-05openalex-snapshot
Multilocus Sequence Typing Scheme for Enterococcus faecalis Reveals Hospital-Adapted Genetic Complexes in a Background of High Rates of Recombination
inferredcites →https://doi.org/10.1128/jcm.29.12.2752-2757.1991openalex-snapshot
DNA fingerprinting of Enterococcus faecium by pulsed-field gel electrophoresis may be a useful epidemiologic tool
inferredcites →https://doi.org/10.1128/mbio.00227-10openalex-snapshot
Multidrug-Resistant Enterococci Lack CRISPR- cas
inferredcites →https://doi.org/10.1128/mmbr.59.4.591-603.1995openalex-snapshot
Streptococcus pneumoniae: virulence factors, pathogenesis, and vaccines
inferredcites →https://doi.org/10.1146/annurev.mi.40.100186.003223openalex-snapshot
Conjugative Transposons and the Dissemination of Antibiotic Resistance in Streptococci
inferredcites →https://doi.org/10.1172/jci106758openalex-snapshot
Studies on antibiotic synergism against enterococci
inferredcites →https://doi.org/10.1172/jci109149openalex-snapshot
Aminoglycoside-Inactivating Enzymes in Clinical Isolates of Streptococcus Faecalis
inferredcites →https://doi.org/10.1172/jci29021openalex-snapshot
Endocarditis and biofilm-associated pili of Enterococcus faecalis
inferredcites →https://doi.org/10.1172/jci43918openalex-snapshot
Vancomycin-resistant Enterococcus domination of intestinal microbiota is enabled by antibiotic treatment in mice and precedes bloodstream invasion in humans
inferredcites →https://doi.org/10.1186/1471-2164-10-194openalex-snapshot
Comparative genomics of Enterococcus faecalis from healthy Norwegian infants
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/10.1186/1471-2180-10-17openalex-snapshot
Bicarbonate enhances expression of the endocarditis and biofilm associated pilus locus, ebpR-ebpABC, in Enterococcus faecalis
inferredcites →https://doi.org/10.1186/1471-2180-11-20openalex-snapshot
The hyl Efm gene in pHylEfm of Enterococcus faecium is not required in pathogenesis of murine peritonitis
inferredcites →https://doi.org/10.1186/1471-2334-11-80openalex-snapshot
IS element IS16 as a molecular screening tool to identify hospital-associated strains of Enterococcus faecium
inferredcites →https://doi.org/10.1186/1741-7007-2-4openalex-snapshot
Alterations at the peptidyl transferase centre of the ribosome induced by the synergistic action of the streptogramins dalfopristin and quinupristin
inferredcites →https://doi.org/10.1186/gb-2008-9-7-r110openalex-snapshot
Large scale variation in Enterococcus faecalis illustrated by the genome analysis of strain OG1RF
inferredcites →https://doi.org/10.1261/rna.2233511openalex-snapshot
Intrinsic resistance to aminoglycosides in Enterococcus faecium is conferred by the 16S rRNA m5C1404-specific methyltransferase EfmM
inferredcites →https://doi.org/10.1371/journal.pone.0009658openalex-snapshot
The Extracytoplasmic Function Sigma Factor SigV Plays a Key Role in the Original Model of Lysozyme Resistance and Virulence of Enterococcus faecalis
inferredcites →https://doi.org/10.1371/journal.pone.0011879openalex-snapshot
Screening of In Vivo Activated Genes in Enterococcus faecalis during Insect and Mouse Infections and Growth in Urine
inferredcites →https://doi.org/10.1371/journal.pone.0023948openalex-snapshot
Genome-Wide Identification of Small RNAs in the Opportunistic Pathogen Enterococcus faecalis V583
inferredcites →https://doi.org/10.1371/journal.pone.0030187openalex-snapshot
Genomic and SNP Analyses Demonstrate a Distant Separation of the Hospital and Community-Associated Clades of Enterococcus faecium
inferredcites →https://doi.org/10.1371/journal.ppat.0030007openalex-snapshot
Insertion Sequence–Driven Diversification Creates a Globally Dispersed Emerging Multiresistant Subspecies of E. faecium
inferredcites →https://doi.org/10.1371/journal.ppat.1000716openalex-snapshot
Importance of the Collagen Adhesin Ace in Pathogenesis and Protection against Enterococcus faecalis Experimental Endocarditis
inferredcites →https://doi.org/10.1586/14787210.6.5.637openalex-snapshot
Emergence and management of drug-resistant enterococcal infections
inferredcites →https://doi.org/10.2217/17460913.3.5.547openalex-snapshot
Acquired Vancomycin Resistance in Clinically Relevant Pathogens
inferredcites →https://doi.org/10.2217/fmb.09.82openalex-snapshot
Transition of Enterococcus Faecium from Commensal Organism to Nosocomial Pathogen
inferredcites →https://doi.org/10.2807/ese.13.47.19046-enopenalex-snapshot
Emergence and spread of vancomycin resistance among enterococci in Europe
inferredcites →https://doi.org/10.2807/ese.15.29.19620-enopenalex-snapshot
Alarming spread of vancomycin resistant enterococci in Sweden since 2007
inferredcites →https://doi.org/10.3201/1106.041204openalex-snapshot
Global Spread of Vancomycin-resistant Enterococcus faecium from Distinct Nosocomial Genetic Complex
inferredcites →https://doi.org/10.4049/jimmunol.181.9.6328openalex-snapshot
Immune Evasion of Enterococcus faecalis by an Extracellular Gelatinase That Cleaves C3 and iC3b
inferredcites →https://doi.org/10.4161/viru.1.4.11966openalex-snapshot
Characterization of theebpfmpilus-encoding operon ofEnterococcus faeciumand its role in biofilm formation and virulence in a murine model of urinary tract infection
inferredcites →https://doi.org/10.7326/0003-4819-108-3-499_2openalex-snapshot
Harrison's Principles of Internal Medicine.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A potentially probiotic strain of Enterococcus faecalis from human milk that is avirulent, antibiotic sensitive, and nonbreaching of the gut barrier
inferred← citeshttps://doi.org/10.1007/s00203-023-03775-7openalex-snapshot
Activity of a foam in preventing rebound of vancomycin-resistant Enterococcus faecium-containing droplets generated from the toilet bowl
inferred← citeshttps://doi.org/10.1007/s00203-024-04227-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00203-026-05054-7openalex-snapshot
A sucralose-based sweetener promotes biofilm formation and plasmid-mediated antibiotic resistance transfer in opportunistic gut bacteria
inferred← citeshttps://doi.org/10.1007/s00203-026-05077-0openalex-snapshot
Clade-specific evolution and genome plasticity underlying antimicrobial resistance in Enterococcus faecium
inferred← citeshttps://doi.org/10.1007/s00203-026-05132-wopenalex-snapshot
Enterococcus in herbal fermentation: a genus-specific perspective on enzymatic capability, biotransformation outcomes and safety
inferred← citeshttps://doi.org/10.1007/s00203-026-05223-8openalex-snapshot
Harnessing phage-ciprofloxacin synergy to overcome multidrug-resistant infections and biofilm persistence
inferred← citeshttps://doi.org/10.1007/s00210-026-05701-2openalex-snapshot
Outcomes of linezolid, glycopeptides, and other regimens in ampicillin-resistant, vancomycin-susceptible and vancomycin-resistant enterococcal bacteremia in a resource-limited setting: stewardship implications
inferred← citeshttps://doi.org/10.1007/s00216-015-8912-yopenalex-snapshot
Identification of vancomycin interaction with Enterococcus faecalis within 30 min of interaction time using Raman spectroscopy
inferred← citeshttps://doi.org/10.1007/s00216-019-02190-6openalex-snapshot
A ratiometric fluorescent probe for sensitive determination of the important glycopeptide antibiotic vancomycin
inferred← citeshttps://doi.org/10.1007/s00248-019-01464-xopenalex-snapshot
Eutrophication and Related Antibiotic Resistance of Enterococci in the Minjiang River, China
inferred← citeshttps://doi.org/10.1007/s00253-019-10277-4openalex-snapshot
Diversity of volatile organic compound production from leucine and citrate in Enterococcus faecium
inferred← citeshttps://doi.org/10.1007/s00253-023-12858-wopenalex-snapshot
IS6 family insertion sequences promote optrA dissemination between plasmids varying in transfer abilities
inferred← citeshttps://doi.org/10.1007/s00284-025-04610-6openalex-snapshot
Molecular Framework of Multidrug Resistance in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1007/s00345-024-04981-8openalex-snapshot
Epidemiology and risk factors for staphylococcal urinary tract infections in the Moroccan Casablanca area
inferred← citeshttps://doi.org/10.1007/s00438-026-02504-1openalex-snapshot
Pan-genome analysis reveals the triangle mechanisms of antibiotic resistance, pathogenicity, and biofilm formation in Enterococcus faecalis
inferred← citeshttps://doi.org/10.1007/s00438-026-02505-0openalex-snapshot
Genomic characterisation of vancomycin-resistant Enterococcus faecium with Tn1546-plasmid rep17 in obstetrics and gynaecology settings in Algeria
inferred← citeshttps://doi.org/10.1007/s00705-017-3503-1openalex-snapshot
Complete genome sequence of a novel, virulent Ahjdlikevirus bacteriophage that infects Enterococcus faecium
inferred← citeshttps://doi.org/10.1007/s00705-019-04341-7openalex-snapshot
Complete genome analysis of the novel Enterococcus faecalis phage vB_EfaS_AL3
inferred← citeshttps://doi.org/10.1007/s10096-016-2747-0openalex-snapshot
Tedizolid susceptibility in linezolid- and vancomycin-resistant Enterococcus faecium isolates
inferred← citeshttps://doi.org/10.1007/s10096-016-2867-6openalex-snapshot
Evaluation of the novel artus C. difficile QS-RGQ, VanR QS-RGQ and MRSA/SA QS-RGQ assays for the laboratory diagnosis of Clostridium difficile infection (CDI), and for vancomycin-resistant enterococci (VRE) and methicillin-resistant Staphylococcus aureus (MRSA) screening
inferred← citeshttps://doi.org/10.1007/s10096-017-3042-4openalex-snapshot
High-touch surfaces: microbial neighbours at hand
inferred← citeshttps://doi.org/10.1007/s10096-018-3193-yopenalex-snapshot
Association between duration of intravenous antibiotic administration and early-life microbiota development in late-preterm infants
inferred← citeshttps://doi.org/10.1007/s10096-018-3214-xopenalex-snapshot
The use of high-throughput sequencing to investigate an outbreak of glycopeptide-resistant Enterococcus faecium with a novel quinupristin-dalfopristin resistance mechanism
inferred← citeshttps://doi.org/10.1007/s10096-019-03801-xopenalex-snapshot
Role of linezolid combination therapy for serious infections: review of the current evidence
inferred← citeshttps://doi.org/10.1007/s10096-022-04527-zopenalex-snapshot
Web-based prediction of antimicrobial resistance in enterococcal clinical isolates by whole-genome sequencing
inferred← citeshttps://doi.org/10.1007/s10096-024-04768-0openalex-snapshot
Genetic analysis of vancomycin-variable Enterococcus faecium clinical isolates in Italy
inferred← citeshttps://doi.org/10.1007/s10096-024-04843-6openalex-snapshot
The role of time to positive blood cultures in enhancing the predictive capability of DENOVA score for diagnosing infective endocarditis in patients with Enterococcus faecalis bacteremia
inferred← citeshttps://doi.org/10.1007/s10096-024-04917-5openalex-snapshot
Clinical characteristics, predisposing factors and outcomes for Enterococcus faecalis versus Enterococcus faecium bloodstream infections: a prospective multicentre cohort study
inferred← citeshttps://doi.org/10.1007/s10096-026-05512-6openalex-snapshot
Detection of vanA-positive, glycopeptide-resistant but ampicillin-susceptible Enterococcus faecalis: two genetically distinct, unrelated clinical isolates from the United Kingdom
inferred← citeshttps://doi.org/10.1007/s10096-026-05544-yopenalex-snapshot
Factors associated with methicillin resistance in Staphylococcus aureus: a case–case–control analysis of AMR surveillance data
inferred← citeshttps://doi.org/10.1007/s10096-026-05557-7openalex-snapshot
Performance of disk diffusion and MIC gradient tests in tigecycline susceptibility testing of enterococci: a Nordic multicentre study
inferred← citeshttps://doi.org/10.1007/s10096-026-05657-4openalex-snapshot
Genomic insights into an optrA-carrying plasmid associated with linezolid resistance in clinical Enterococcus faecalis isolates, Argentina
inferred← citeshttps://doi.org/10.1007/s10123-024-00534-6openalex-snapshot
The Enterococcus secretome inhibits the growth of vancomycin-resistant Enterococcus faecalis V853 with their antiproliferative properties and nanoencapsulation effects
inferred← citeshttps://doi.org/10.1007/s10238-025-01950-2openalex-snapshot
Disinfectant-induced bacterial resistance and antibiotic cross-resistance—mechanisms and clinical relevance
inferred← citeshttps://doi.org/10.1007/s10441-014-9226-8openalex-snapshot
In Silico Analysis of Acinetobacter baumannii Phospholipase D as a Subunit Vaccine Candidate
inferred← citeshttps://doi.org/10.1007/s10482-013-0073-4openalex-snapshot
Multilocus sequence typing and antimicrobial resistance in Enterococcus faecium isolates from fresh produce
inferred← citeshttps://doi.org/10.1007/s10499-024-01435-1openalex-snapshot
Utilizing the potential of Saussurea lappa in aquaculture industry: a review on immune enhancement and pollution remediation
inferred← citeshttps://doi.org/10.1007/s10661-014-4168-9openalex-snapshot
Hierarchal clustering yields insight into multidrug-resistant bacteria isolated from a cattle feedlot wastewater treatment system
inferred← citeshttps://doi.org/10.1007/s10695-025-01560-5openalex-snapshot
Thyme-synthesized silver nanoparticles mitigate immunosuppression, oxidative damage, and histopathological alterations induced by multidrug-resistant Enterococcus faecalis in Oreochromis niloticus: in vitro and in vivo assays
inferred← citeshttps://doi.org/10.1007/s11033-024-09870-2openalex-snapshot
Antimicrobial resistance: use of phage therapy in the management of resistant infections
inferred← citeshttps://doi.org/10.1007/s11047-019-09730-0openalex-snapshot
Generation and robustness of Boolean networks to model Clostridium difficile infection
inferred← citeshttps://doi.org/10.1007/s11090-018-9930-2openalex-snapshot
Regulation of Enterococcus faecalis Biofilm Formation and Quorum Sensing Related Virulence Factors with Ultra-low Dose Reactive Species Produced by Plasma Activated Water
inferred← citeshttps://doi.org/10.1007/s11096-013-9825-5openalex-snapshot
Treatment considerations in vancomycin-resistant enterococcal bacteremia: daptomycin or linezolid? A review
inferred← citeshttps://doi.org/10.1007/s11101-026-10228-8openalex-snapshot
An in-depth review of the phytochemical profile and pharmacological potential of Oenocarpus bataua
inferred← citeshttps://doi.org/10.1007/s11259-022-09906-7openalex-snapshot
High prevalence of vancomycin non-susceptible and multi-drug resistant enterococci in farmed animals and fresh retail meats in Bangladesh
inferred← citeshttps://doi.org/10.1007/s11259-025-10978-4openalex-snapshot
Therapeutic effect of Bouea macrophylla Griffith in protecting Koi fish from Enterococcus faecalis infection and acute ammonia toxicity
inferred← citeshttps://doi.org/10.1007/s11259-026-11208-1openalex-snapshot
Enterococcus faecalis–associated infective aortic endocarditis as a cause of arterial thromboembolism in a cat
inferred← citeshttps://doi.org/10.1007/s11262-023-02016-9openalex-snapshot
Isolation and characterization of a novel lytic bacteriophage vB_Efm_LG62 infecting Enterococcus faecium
inferred← citeshttps://doi.org/10.1007/s11274-025-04389-5openalex-snapshot
Unveiling the probiotic potential of Enterococcus spp.: Mechanisms and roles in animal and human health, A comprehensive review
inferred← citeshttps://doi.org/10.1007/s11274-026-05284-3openalex-snapshot
Comparative genomic and phenotypic profiling of commercial probiotic Enterococcus faecium strains: insights into safety and functional attributes
inferred← citeshttps://doi.org/10.1007/s11356-012-1283-4openalex-snapshot
Impact of chronic exposure to low doses of chlorpyrifos on the intestinal microbiota in the Simulator of the Human Intestinal Microbial Ecosystem (SHIME®) and in the rat
inferred← citeshttps://doi.org/10.1007/s11756-026-02279-1openalex-snapshot
Isolation and functional characterization of a lytic phage SSBHU against Enterococcus faecium and its potential application in phage therapy
inferred← citeshttps://doi.org/10.1007/s11756-026-02352-9openalex-snapshot
Partial purification and characterisation of an Enterocin P-like bacteriocin from Enterococcus faecium E18
inferred← citeshttps://doi.org/10.1007/s11908-012-0270-8openalex-snapshot
Enterococcal Endocarditis: Can We Win the War?
inferred← citeshttps://doi.org/10.1007/s12010-022-03950-4openalex-snapshot
Potential of Desert Medicinal Plants for Combating Resistant Biofilms in Urinary Tract Infections
inferred← citeshttps://doi.org/10.1007/s12033-026-01578-xopenalex-snapshot
Triphala Modulates the Membrane Vesicle Transcriptome of Enterococcus durans VIT3 to Influence Antibiotic Response and Probiotic Functions
inferred← citeshttps://doi.org/10.1007/s12088-024-01216-7openalex-snapshot
Antimicrobial Susceptibility Patterns of Enterococcus Species and Molecular Detection of Enterococcus faecalis Isolated from Patients with Urinary Tract Infection in a Tertiary Care Hospital in Bangladesh
inferred← citeshttps://doi.org/10.1007/s12088-024-01384-6openalex-snapshot
A Comprehensive Review of Molecular Mechanisms Leading to the Emergence of Multidrug Resistance in Bacteria
inferred← citeshttps://doi.org/10.1007/s12104-022-10087-2openalex-snapshot
1H, 13C, and 15N resonance assignments of a conserved putative cell wall binding domain from Enterococcus faecalis
inferred← citeshttps://doi.org/10.1007/s12223-017-0521-zopenalex-snapshot
Safety assessment of commensal enterococci from dogs
inferred← citeshttps://doi.org/10.1007/s12223-017-0547-2openalex-snapshot
Severity of drug resistance and co-existence of Enterococcus faecalis in diabetic foot ulcer infections
inferred← citeshttps://doi.org/10.1007/s12223-018-0596-1openalex-snapshot
Unusual oral mucosal microbiota after hematopoietic cell transplantation with glycopeptide antibiotics: potential association with pathophysiology of oral mucositis
inferred← citeshttps://doi.org/10.1007/s12223-025-01418-6openalex-snapshot
Vancomycin-resistant enterococci in healthcare settings: clonal analysis, resistance profiles, and biofilm formation of strains isolated from hospitalized patients
inferred← citeshttps://doi.org/10.1007/s12275-014-4011-6openalex-snapshot
Enterococcus infection biology: Lessons from invertebrate host models
inferred← citeshttps://doi.org/10.1007/s12275-019-9434-7openalex-snapshot
Propionate, together with triple antibiotics, inhibits the growth of Enterococci
inferred← citeshttps://doi.org/10.1007/s12275-024-00139-8openalex-snapshot
Repeated Exposure of Vancomycin to Vancomycin-Susceptible Staphylococcus aureus (VSSA) Parent Emerged VISA and VRSA Strains with Enhanced Virulence Potentials
inferred← citeshttps://doi.org/10.1007/s12602-017-9357-8openalex-snapshot
In Silico and Experimental Data Claiming Safety Aspects and Beneficial Attributes of the Bacteriocinogenic Strain Enterococcus faecalis B3A-B3B
inferred← citeshttps://doi.org/10.1007/s12602-019-09618-6openalex-snapshot
The Increasing Issue of Vancomycin-Resistant Enterococci and the Bacteriocin Solution
inferred← citeshttps://doi.org/10.1007/s12602-020-09633-yopenalex-snapshot
What Is Wrong with Enterococcal Probiotics?
inferred← citeshttps://doi.org/10.1007/s12602-020-09711-1openalex-snapshot
Anti-Proliferative and Anti-Biofilm Potentials of Bacteriocins Produced by Non-Pathogenic Enterococcus sp.
inferred← citeshttps://doi.org/10.1007/s12602-025-10594-3openalex-snapshot
Lactic Acid Bacteria Strains Isolated from Jerusalem Artichoke (Helianthus tuberosus L.) Tubers as Potential Probiotic Candidates
inferred← citeshttps://doi.org/10.1007/s12602-026-11009-7openalex-snapshot
New Proteins from Cold: Antibiofilm Activity of Cold-Azurin and PsyOmp38 Against Enterococcus faecalis and Klebsiella pneumoniae
inferred← citeshttps://doi.org/10.1007/s12602-026-11125-4openalex-snapshot
Probiotic and Technological Potential of Enterococcus faecium EM03, Isolated From Brazilian Semi-hard Cheese
inferred← citeshttps://doi.org/10.1007/s12602-026-11153-0openalex-snapshot
Phenotypic and Whole-Genome Characterization of Enterococcus Isolates from Korean Doenjang and Meju: E. durans Edu-1 as a Food-Grade Probiotic Candidate with Epithelial Wound-Healing Activity
inferred← citeshttps://doi.org/10.1007/s12602-026-11218-0openalex-snapshot
A Novel Enterococcus Phage Exhibits Potent Anti-biofilm Activity Against Multidrug Resistant Strains and Protects Mice from Peritonitis Sepsis
inferred← citeshttps://doi.org/10.1007/s15010-014-0628-yopenalex-snapshot
Detection of opsonic antibodies against Enterococcus faecalis cell wall carbohydrates in immune globulin preparations
inferred← citeshttps://doi.org/10.1007/s15010-024-02249-2openalex-snapshot
Epidemiological trends and susceptibility patterns of bloodstream infections caused by Enterococcus spp. in six German university hospitals: a prospectively evaluated multicentre cohort study from 2016 to 2020 of the R-Net study group
inferred← citeshttps://doi.org/10.1007/s15010-024-02372-0openalex-snapshot
Enterococci independently increase the risk for initial antibiotic treatment failure and prolonged hospitalization in adult patients with complicated urinary tract infection: a retrospective cohort study
inferred← citeshttps://doi.org/10.1007/s15010-026-02979-5openalex-snapshot
Epidemiology, antimicrobial resistance trends, and predictors of mortality among vancomycin-resistant enterococci: a six-year retrospective cohort study from Oman
inferred← citeshttps://doi.org/10.1007/s40121-015-0072-zopenalex-snapshot
Real-World Treatment of Enterococcal Infections with Daptomycin: Insights from a Large European Registry (EU-CORE)
inferred← citeshttps://doi.org/10.1007/s40123-025-01113-2openalex-snapshot
In Vitro Activity of Bacteriophages Against Ocular Methicillin-resistant S. aureus Isolates Collected in the US
inferred← citeshttps://doi.org/10.1007/s40506-013-0006-9openalex-snapshot
Molecular Diagnosis Contributing for Multi-Drug Resistant Infection Control
inferred← citeshttps://doi.org/10.1007/s40506-018-0166-8openalex-snapshot
Enterococci as Increasing Bacteria in Hospitals: Why Are Infection Control Measures Challenging for This Bacteria?
inferred← citeshttps://doi.org/10.1007/s40506-020-00227-4openalex-snapshot
Vancomycin-Resistant Enterococcus in Hematology-Oncology Patients: a Review on Colonization, Screening, Infections, Resistance, and Antimicrobial Stewardship
inferred← citeshttps://doi.org/10.1007/s42770-019-00200-4openalex-snapshot
Time-kill curves of daptomycin and Monte Carlo simulation for the treatment of bacteraemia caused by Enterococcus faecium
inferred← citeshttps://doi.org/10.1007/s42770-020-00360-8openalex-snapshot
Trend of clinical vancomycin-resistant enterococci isolated in a regional Italian hospital from 2001 to 2018
inferred← citeshttps://doi.org/10.1007/s42995-022-00144-zopenalex-snapshot
An expectation–maximization algorithm for estimating proportions of deletions among bacterial populations with application to study antibiotic resistance gene transfer in Enterococcus faecalis
inferred← citeshttps://doi.org/10.1016/b978-0-08-100596-5.00848-9openalex-snapshot
Lactic Acid Bacteria: Enterococcus in Milk and Dairy Products
inferred← citeshttps://doi.org/10.1016/b978-0-12-374407-4.00528-8openalex-snapshot
Lactic Acid Bacteria | Enterococcus in Milk and Dairy Products
inferred← citeshttps://doi.org/10.1016/b978-0-12-800874-4.00015-5openalex-snapshot
Evaluation of Natural Products against Biofilm-Mediated Bacterial Resistance
inferred← citeshttps://doi.org/10.1016/b978-0-12-801214-7.00009-0openalex-snapshot
Antibiotic Resistance in Enterococci
inferred← citeshttps://doi.org/10.1016/b978-0-323-37677-8.50052-8openalex-snapshot
Streptococcus and Enterococcus Species Infections
inferred← citeshttps://doi.org/10.1016/b978-0-443-18638-7.00023-2openalex-snapshot
A systematic chemoinformatic analysis of chemical space, scaffolds and antimicrobial activity of LpxC inhibitors
inferred← citeshttps://doi.org/10.1016/b978-0-443-26726-0.00009-8openalex-snapshot
Novel approaches to tackle carbapenem-resistant ESKAPE pathogens
inferred← citeshttps://doi.org/10.1016/b978-0-443-26726-0.00013-xopenalex-snapshot
Harnessing deep learning to combat antibiotic resistance: A focus on ESKAPE pathogens
inferred← citeshttps://doi.org/10.1016/b978-0-443-27781-8.00011-7openalex-snapshot
Interactions between plants and human pathogens: Mechanisms of transmission, antimicrobial resistance, and global health challenges
inferred← citeshttps://doi.org/10.1016/b978-0-443-36518-8.00022-9openalex-snapshot
Combating antibiotic resistance: The role and impact of antibiotic resistance breakers
inferred← citeshttps://doi.org/10.1016/b978-0-7020-6285-8.00177-5openalex-snapshot
Streptococci and Enterococci
inferred← citeshttps://doi.org/10.1016/b978-1-4557-0306-7.00093-3openalex-snapshot
Gram-Positive Infections
inferred← citeshttps://doi.org/10.1016/b978-1-78548-271-7.50002-xopenalex-snapshot
Spoilage of Egg Products
inferred← citeshttps://doi.org/10.1016/b978-84-9113-248-6.00017-2openalex-snapshot
10.1016/b978-84-9113-248-6.00017-2
inferred← citeshttps://doi.org/10.1016/bs.aambs.2020.03.001openalex-snapshot
Antimicrobial resistance genes in bacteria from animal-based foods
inferred← citeshttps://doi.org/10.1016/bs.aambs.2026.07.001openalex-snapshot
A One Health approach to Antimicrobial Resistance: Concepts, challenges, and advances in omics
inferred← citeshttps://doi.org/10.1016/bs.ampbs.2022.06.004openalex-snapshot
Antimicrobial tolerance and its role in the development of resistance: Lessons from enterococci
inferred← citeshttps://doi.org/10.1016/bs.enz.2024.07.001openalex-snapshot
Bacterial α-CAs: a biochemical and structural overview
inferred← citeshttps://doi.org/10.1016/j.ab.2013.07.045openalex-snapshot
A liquid chromatography–tandem mass spectrometry assay for d-Ala-d-Lac: A key intermediate for vancomycin resistance in vancomycin-resistant enterococci
inferred← citeshttps://doi.org/10.1016/j.actbio.2017.01.011openalex-snapshot
Probiotic E. coli Nissle 1917 biofilms on silicone substrates for bacterial interference against pathogen colonization
inferred← citeshttps://doi.org/10.1016/j.adaj.2017.10.002openalex-snapshot
Outbreak of bacterial endocarditis associated with an oral surgery practice
inferred← citeshttps://doi.org/10.1016/j.ajem.2017.03.010openalex-snapshot
Emerging trends in antibiotic resistance: Implications for emergency medicine
inferred← citeshttps://doi.org/10.1016/j.ajic.2012.11.019openalex-snapshot
Low risk of apparent transmission of vancomycin-resistant Enterococci from bacteraemic patients to hospitalized contacts
inferred← citeshttps://doi.org/10.1016/j.ajic.2013.01.013openalex-snapshot
Modeling the regional spread and control of vancomycin-resistant enterococci
inferred← citeshttps://doi.org/10.1016/j.ajic.2014.01.008openalex-snapshot
Vancomycin-resistant Enterococcus spp isolated from community acquired infections and colonizations in Querétaro City, Mexico
inferred← citeshttps://doi.org/10.1016/j.ajo.2023.06.016openalex-snapshot
Microbiology of Eye Infections at the Massachusetts Eye and Ear: An 8-Year Retrospective Review Combined With Genomic Epidemiology
inferred← citeshttps://doi.org/10.1016/j.amsu.2022.104258openalex-snapshot
Epidemiology, microbiological and clinical characteristics of Enterococcus species bloodstream infections: A 10-year retrospective cohort study from Qatar
inferred← citeshttps://doi.org/10.1016/j.aninu.2020.11.019openalex-snapshot
Age-associated changes in caecal microbiome and their apparent correlations with growth performances of layer pullets
inferred← citeshttps://doi.org/10.1016/j.aninu.2022.01.005openalex-snapshot
Tracing enterococci persistence along a pork production chain from feed to food in China
inferred← citeshttps://doi.org/10.1016/j.antinf.2016.09.002openalex-snapshot
Daptomycine et infections sévères à entérocoques
inferred← citeshttps://doi.org/10.1016/j.aqrep.2021.100868openalex-snapshot
Enterococcus faecalis involved in streptococcosis like infection in silver barb (Barbonymus gonionotus)
inferred← citeshttps://doi.org/10.1016/j.aqrep.2024.102514openalex-snapshot
Effects of Vitamin E and/or selenium nanoparticles on organ histology, hemato-biochemical parameters, immunity, gene expression, and growth performance in Nile tilapia challenged with Enterococcus faecalis
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2019.734319openalex-snapshot
Experimental pathogenesis and host immune responses of Enterococcus faecalis infection in Nile tilapia (Oreochromis niloticus)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2021.737806openalex-snapshot
Dietary Bougainvillea glabra leaf meal on growth, haemato-biochemical responses and disease resistance in Nile tilapia, Oreochromis niloticus against Enterococcus faecalis
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2026.106511openalex-snapshot
Antibacterial and anti-virulence activity of juglone against Enterococcus faecalis compared with chlorhexidine
inferred← citeshttps://doi.org/10.1016/j.bbagen.2017.09.011openalex-snapshot
Novel insights into the vancomycin-resistant Enterococcus faecalis (V583) alkylhydroperoxide reductase subunit F
inferred← citeshttps://doi.org/10.1016/j.bbagen.2024.130562openalex-snapshot
Piperidinium surfactants functionalized with carbamate fragment: Aggregation, antimicrobial activity and cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.bbamem.2017.08.003openalex-snapshot
Characterization of the tertiary structure of the peptidoglycan of Enterococcus faecalis
inferred← citeshttps://doi.org/10.1016/j.bbmt.2014.01.030openalex-snapshot
Metagenomic Analysis of the Stool Microbiome in Patients Receiving Allogeneic Stem Cell Transplantation: Loss of Diversity Is Associated with Use of Systemic Antibiotics and More Pronounced in Gastrointestinal Graft-versus-Host Disease
inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.11.023openalex-snapshot
Structural study of acyl carrier protein of Enterococcus faecalis and its interaction with enzymes in de novo fatty acid synthesis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.152884openalex-snapshot
Microbiota diversity and its influence on diabetic osteoporosis development
inferred← citeshttps://doi.org/10.1016/j.bcp.2016.10.001openalex-snapshot
History of antimicrobial drug discovery: Major classes and health impact
inferred← citeshttps://doi.org/10.1016/j.biochi.2019.01.012openalex-snapshot
Kinetic mechanism of Enterococcus faecium d-aspartate ligase
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2025.123141openalex-snapshot
A nano-enabled adjunctive therapy to prevent vancomycin resistance evolution: Toward nano-anti-antibiotics
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