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Enterococci facilitate polymicrobial infections
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Plant Natural Flavonoids Against Multidrug Resistant Pathogens
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Interactions of microorganisms within a urinary catheter polymicrobial biofilm model
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Pathogen colonization of the gastrointestinal microbiome at intensive care unit admission and risk for subsequent death or infection
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In vitro virulence activity of Pseudomonas aeruginosa, enhanced by either Acinetobacter baumannii or Enterococcus faecium through the polymicrobial interactions
inferredcites →https://doi.org/10.1007/s12223-015-0401-3openalex-snapshot
Polymicrobial biofilms by diabetic foot clinical isolates
inferredcites →https://doi.org/10.1016/j.ajic.2010.10.024openalex-snapshot
Implications for vancomycin-resistant Enterococcus colonization associated with Clostridium difficile infections
inferredcites →https://doi.org/10.1016/j.ajic.2018.07.011openalex-snapshot
Bacterial burden is associated with increased transmission to health care workers from patients colonized with vancomycin-resistant Enterococcus
inferredcites →https://doi.org/10.1016/j.ajog.2021.09.018openalex-snapshot
Recurrent bacterial vaginosis following metronidazole treatment is associated with microbiota richness at diagnosis
inferredcites →https://doi.org/10.1016/j.bjm.2016.12.012openalex-snapshot
Detection of vancomycin-resistant enterococci (VRE) in stool specimens submitted for Clostridium difficile toxin testing
inferredcites →https://doi.org/10.1016/j.cell.2022.02.002openalex-snapshot
Emerging enterococcus pore-forming toxins with MHC/HLA-I as receptors
inferredcites →https://doi.org/10.1016/j.chom.2016.09.004openalex-snapshot
Enterococcal Metabolite Cues Facilitate Interspecies Niche Modulation and Polymicrobial Infection
inferredcites →https://doi.org/10.1016/j.chom.2017.04.002openalex-snapshot
Cooperating Commensals Restore Colonization Resistance to Vancomycin-Resistant Enterococcus faecium
inferredcites →https://doi.org/10.1016/j.ijantimicag.2004.02.001openalex-snapshot
Bacterial resistance to antimicrobials in urinary isolates
inferredcites →https://doi.org/10.1016/j.immuni.2016.09.009openalex-snapshot
Enterococcus hirae and Barnesiella intestinihominis Facilitate Cyclophosphamide-Induced Therapeutic Immunomodulatory Effects
inferredcites →https://doi.org/10.1016/j.jiac.2018.01.001openalex-snapshot
Clinical management of non-faecium non-faecalis vancomycin-resistant enterococci infection. Focus on Enterococcus gallinarum and Enterococcus casseliflavus/flavescens
inferredcites →https://doi.org/10.1016/j.jmb.2019.05.030openalex-snapshot
Dr. Jekyll and Mr. Hide: How Enterococcus faecalis Subverts the Host Immune Response to Cause Infection
inferredcites →https://doi.org/10.1016/j.joen.2010.09.007openalex-snapshot
Resazurin Metabolism Assay for Root Canal Disinfectant Evaluation on Dual-species Biofilms
inferredcites →https://doi.org/10.1016/j.mib.2017.11.030openalex-snapshot
Evolution of virulence in Enterococcus faecium, a hospital-adapted opportunistic pathogen
inferredcites →https://doi.org/10.1016/j.otohns.2004.08.007openalex-snapshot
Intracranial complications of otitis media: 15 years of experience in 33 patients
inferredcites →https://doi.org/10.1016/j.pedneo.2020.01.004openalex-snapshot
Enterococci and food safety – Are all probiotics beneficial?
inferredcites →https://doi.org/10.1016/j.tim.2022.07.003openalex-snapshot
Dual species biofilms are enhanced by metabolite cross-feeding
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Probiotic for pathogen-specific Staphylococcus aureus decolonisation in Thailand: a phase 2, double-blind, randomised, placebo-controlled trial
inferredcites →https://doi.org/10.1038/nature07250openalex-snapshot
Vancomycin-resistant enterococci exploit antibiotic-induced innate immune deficits
inferredcites →https://doi.org/10.1038/nature12729openalex-snapshot
Antibacterial membrane attack by a pore-forming intestinal C-type lectin
inferredcites →https://doi.org/10.1038/nature15524openalex-snapshot
Bacteriocin production augments niche competition by enterococci in the mammalian gastrointestinal tract
inferredcites →https://doi.org/10.1038/nrmicro2761openalex-snapshot
The rise of the Enterococcus: beyond vancomycin resistance
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Unveiling the role of Gardnerella vaginalis in polymicrobial Bacterial Vaginosis biofilms: the impact of other vaginal pathogens living as neighbors
inferredcites →https://doi.org/10.1038/s41396-022-01248-1openalex-snapshot
Heme cross-feeding can augment Staphylococcus aureus and Enterococcus faecalis dual species biofilms
inferredcites →https://doi.org/10.1038/s41467-017-00796-xopenalex-snapshot
Gastric acid suppression promotes alcoholic liver disease by inducing overgrowth of intestinal Enterococcus
inferredcites →https://doi.org/10.1038/s41467-022-29493-0openalex-snapshot
Collateral sensitivity to pleuromutilins in vancomycin-resistant Enterococcus faecium
inferredcites →https://doi.org/10.1038/s41467-022-35380-5openalex-snapshot
Microbiome-mediated fructose depletion restricts murine gut colonization by vancomycin-resistant Enterococcus
inferredcites →https://doi.org/10.1038/s41564-020-0723-zopenalex-snapshot
A broad-spectrum antibiotic adjuvant reverses multidrug-resistant Gram-negative pathogens
inferredcites →https://doi.org/10.1038/s41579-018-0107-zopenalex-snapshot
Biofilm-associated infection by enterococci
inferredcites →https://doi.org/10.1038/s41579-022-00682-4openalex-snapshot
Tolerance and resistance of microbial biofilms
inferredcites →https://doi.org/10.1038/s41579-022-00838-2openalex-snapshot
Helping C. difficile to thrive
inferredcites →https://doi.org/10.1038/s41586-019-1501-zopenalex-snapshot
Microbiota-derived lantibiotic restores resistance against vancomycin-resistant Enterococcus
inferredcites →https://doi.org/10.1038/s41586-022-05438-xopenalex-snapshot
Enterococci enhance Clostridioides difficile pathogenesis
inferredcites →https://doi.org/10.1038/s41591-019-0626-9openalex-snapshot
Genomic and epidemiological evidence of bacterial transmission from probiotic capsule to blood in ICU patients
inferredcites →https://doi.org/10.1038/s41598-019-45441-3openalex-snapshot
Intestinal translocation of enterococci requires a threshold level of enterococcal overgrowth in the lumen
inferredcites →https://doi.org/10.1038/s41598-022-12552-3openalex-snapshot
Adaptation of the gut pathobiont Enterococcus faecalis to deoxycholate and taurocholate bile acids
inferredcites →https://doi.org/10.1073/pnas.1917130117openalex-snapshot
Evolution of vancomycin-resistant Enterococcus faecium during colonization and infection in immunocompromised pediatric patients
inferredcites →https://doi.org/10.1080/08927014.2021.1993836openalex-snapshot
Coexistence of Candida albicans and Enterococcus faecalis increases biofilm virulence and periapical lesions in rats
inferredcites →https://doi.org/10.1080/23744235.2022.2125066openalex-snapshot
Enterococcus hirae infections in the clinical practice
inferredcites →https://doi.org/10.1086/317549openalex-snapshot
Vancomycin-Resistant Enterococci among Chronic Hemodialysis Patients: A Prospective Study of Acquisition
inferredcites →https://doi.org/10.1086/502207openalex-snapshot
Colonization and Infection With Multiple Nosocomial Pathogens Among Patients Colonized With Vancomycin-ResistantEnterococcus
inferredcites →https://doi.org/10.1086/502357openalex-snapshot
Occurrence of Co-colonization or Co-Infection with Vancomycin-Resistant Enterococci and Methicillin-ResistantStaphylococcus aureusin a Medical Intensive Care Unit
inferredcites →https://doi.org/10.1086/527394openalex-snapshot
Prior Environmental Contamination Increases the Risk of Acquisition of Vancomycin-Resistant Enterococci
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/10.1086/650203openalex-snapshot
Bacterial Flagellin Stimulates Toll‐Like Receptor 5–Dependent Defense against Vancomycin‐Resistant Enterococcus Infection
inferredcites →https://doi.org/10.1089/mdr.2006.12.63openalex-snapshot
Vancomycin-Resistant Enterococci May Obtain Nutritional Support by Scavenging Carbohydrate Fragments Generated During Mucin Degradation by the Anaerobic Microbiota of the Colon
inferredcites →https://doi.org/10.1093/cid/cis580openalex-snapshot
Intestinal Domination and the Risk of Bacteremia in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation
inferredcites →https://doi.org/10.1093/jac/dkab211openalex-snapshot
Capability ofEnterococcus faecalisto shield Gram-negative pathogens from aminoglycoside exposure
inferredcites →https://doi.org/10.1093/jac/dki336openalex-snapshot
Evidence of vancomycin resistance gene transfer between enterococci of human origin in the gut of mice harbouring human microbiota
inferredcites →https://doi.org/10.1093/jac/dkm057openalex-snapshot
Co-transfer of vanA and aggregation substance genes from Enterococcus faecalis isolates in intra- and interspecies matings
inferredcites →https://doi.org/10.1093/ofid/ofac475openalex-snapshot
Polymicrobial Foot Infection Patterns Are Common and Associated With Treatment Failure
inferredcites →https://doi.org/10.1099/ijsem.0.002786openalex-snapshot
LPSN – List of Prokaryotic names with Standing in Nomenclature (bacterio.net), 20 years on
inferredcites →https://doi.org/10.1099/jmm.0.055830-0openalex-snapshot
Quantitative detection of Staphylococcus aureus, Enterococcus faecalis and Pseudomonas aeruginosa in human oral epithelial cells from subjects with periodontitis and periodontal health
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.1469-0691.2010.03214.xopenalex-snapshot
Management of multidrug-resistant enterococcal infections
inferredcites →https://doi.org/10.1111/j.1574-695x.2012.00948.xopenalex-snapshot
Kinetics and morphology of polymicrobial biofilm formation on polypropylene mesh
inferredcites →https://doi.org/10.1111/j.1574-6968.2004.tb09614.xopenalex-snapshot
Conjugal transfer of aminoglycoside and macrolide resistance betweenEnterococcus faeciumisolates in the intestine of streptomycin-treated mice
inferredcites →https://doi.org/10.1111/j.1742-481x.2006.00159.xopenalex-snapshot
Multiple bacterial species reside in chronic wounds: a longitudinal study
inferredcites →https://doi.org/10.1111/jam.15567openalex-snapshot
Nigella sativa oil extract: A natural novel specific conjugal transfer inhibitor of vancomycin resistance from vanA/B-resistant Enterococcus faecium to Staphylococcus aureus
inferredcites →https://doi.org/10.1126/sciadv.add9280openalex-snapshot
Mitoxantrone targets both host and bacteria to overcome vancomycin resistance in Enterococcus faecalis
inferredcites →https://doi.org/10.1126/science.1090956openalex-snapshot
Genetic Analysis of a High-Level Vancomycin-Resistant Isolate of Staphylococcus aureus
inferredcites →https://doi.org/10.1126/science.1240537openalex-snapshot
The Intestinal Microbiota Modulates the Anticancer Immune Effects of Cyclophosphamide
inferredcites →https://doi.org/10.1126/science.aax3760openalex-snapshot
Lactose drives Enterococcus expansion to promote graft-versus-host disease
inferredcites →https://doi.org/10.1126/science.aaz7595openalex-snapshot
Immunostimulatory gut bacteria
inferredcites →https://doi.org/10.1126/scitranslmed.aad6663openalex-snapshot
TLR-7 activation enhances IL-22–mediated colonization resistance against vancomycin-resistant enterococcus
inferredcites →https://doi.org/10.1128/aac.00576-06openalex-snapshot
High-Level Vancomycin-Resistant Staphylococcus aureus Isolates Associated with a Polymicrobial Biofilm
inferredcites →https://doi.org/10.1128/aac.01587-12openalex-snapshot
pSK41-Like Plasmid Is Necessary for Inc18-Like vanA Plasmid Transfer from Enterococcus faecalis to Staphylococcus aureus In Vitro
inferredcites →https://doi.org/10.1128/aac.47.5.1571-1576.2003openalex-snapshot
Presence of a vanA -Carrying Pheromone Response Plasmid (pBRG1) in a Clinical Isolate of Enterococcus faecium
inferredcites →https://doi.org/10.1128/aem.01182-17openalex-snapshot
Molecular Determinants of the Thickened Matrix in a Dual-Species Pseudomonas aeruginosa and Enterococcus faecalis Biofilm
inferredcites →https://doi.org/10.1128/aem.02638-17openalex-snapshot
Autoinducer 2-Dependent Escherichia coli Biofilm Formation Is Enhanced in a Dual-Species Coculture
inferredcites →https://doi.org/10.1128/cmr.00058-18openalex-snapshot
The Enterococcus: a Model of Adaptability to Its Environment
inferredcites →https://doi.org/10.1128/iai.00378-17openalex-snapshot
Enterococcus faecalis Promotes Innate Immune Suppression and Polymicrobial Catheter-Associated Urinary Tract Infection
inferredcites →https://doi.org/10.1128/iai.00808-16openalex-snapshot
The Pathogenic Potential of Proteus mirabilis Is Enhanced by Other Uropathogens during Polymicrobial Urinary Tract Infection
inferredcites →https://doi.org/10.1128/iai.00863-08openalex-snapshot
Neutrophils Are Essential for Rapid Clearance ofEnterococcus faeciumin Mice
inferredcites →https://doi.org/10.1128/iai.62.10.4534-4541.1994openalex-snapshot
Enterococcus faecalis aggravates pyelonephritis caused by Pseudomonas aeruginosa in experimental ascending mixed urinary tract infection in mice
inferredcites →https://doi.org/10.1128/iai.65.1.144-149.1997openalex-snapshot
Evidence of the proinflammatory role of Enterococcus faecalis in polymicrobial peritonitis in rats
inferredcites →https://doi.org/10.1128/jb.00177-21openalex-snapshot
Let Me Upgrade You: Impact of Mobile Genetic Elements on Enterococcal Adaptation and Evolution
inferredcites →https://doi.org/10.1128/jb.00530-19openalex-snapshot
“It Takes a Village”: Mechanisms Underlying Antimicrobial Recalcitrance of Polymicrobial Biofilms
inferredcites →https://doi.org/10.1128/mbio.01321-22openalex-snapshot
Interactions between Enterohemorrhagic Escherichia coli (EHEC) and Gut Commensals at the Interface of Human Colonoids
inferredcites →https://doi.org/10.1128/mbio.01346-15openalex-snapshot
Antibiotic-Driven Dysbiosis Mediates Intraluminal Agglutination and Alternative Segregation of Enterococcus faecium from the Intestinal Epithelium
inferredcites →https://doi.org/10.1128/mbio.02547-19openalex-snapshot
Enterococcus faecalis Enhances Expression and Activity of the Enterohemorrhagic Escherichia coli Type III Secretion System
inferredcites →https://doi.org/10.1128/microbiolspec.gpp3-0053-2018openalex-snapshot
Pathogenicity of Enterococci
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/s12879-022-07382-7openalex-snapshot
Distribution and drug sensitivity of pathogenic bacteria in diabetic foot ulcer patients with necrotizing fasciitis at a diabetic foot center in China
inferredcites →https://doi.org/10.1186/s12941-019-0327-8openalex-snapshot
Determining the clinical significance of co-colonization of vancomycin-resistant enterococci and methicillin-resistant Staphylococcus aureus in the intestinal tracts of patients in intensive care units: a case–control study
inferredcites →https://doi.org/10.1371/journal.pone.0082665openalex-snapshot
Infective Endocarditis Epidemiology Over Five Decades: A Systematic Review
inferredcites →https://doi.org/10.1371/journal.ppat.1004653openalex-snapshot
Phage-mediated Dispersal of Biofilm and Distribution of Bacterial Virulence Genes Is Induced by Quorum Sensing
inferredcites →https://doi.org/10.1371/journal.ppat.1011108openalex-snapshot
A fiber-enriched diet alleviates Staphylococcus aureus-induced mastitis by activating the HDAC3-mediated antimicrobial program in macrophages via butyrate production in mice
inferredcites →https://doi.org/10.2903/j.efsa.2007.587openalex-snapshot
Introduction of a Qualified Presumption of Safety (QPS) approach for assessment of selected microorganisms referred to EFSA - Opinion of the Scientific Committee
inferredcites →https://doi.org/10.3201/eid1110.050508openalex-snapshot
Methicillin-resistant Staphylococcus aureus and Vancomycin-resistant Enterococci Co-colonization1
inferredcites →https://doi.org/10.3389/fmicb.2018.01791openalex-snapshot
The Genus Enterococcus: Between Probiotic Potential and Safety Concerns—An Update
inferredcites →https://doi.org/10.3390/foods10112846openalex-snapshot
Emerging Risks in Food: Probiotic Enterococci Pose a Threat to Public Health through the Food Chain
inferredcites →https://doi.org/10.3390/microorganisms11010143openalex-snapshot
Pepsin and Trypsin Treatment Combined with Carvacrol: An Efficient Strategy to Fight Pseudomonas aeruginosa and Enterococcus faecalis Biofilms
inferredcites →https://doi.org/10.3390/microorganisms9071501openalex-snapshot
In Vitro Reduction of Interleukin-8 Response to Enterococcus faecalis by Escherichia coli Strains Isolated from the Same Polymicrobial Urines
inferredcites →https://doi.org/10.3390/pathogens11101177openalex-snapshot
Culture Supernatant of Enterococcus faecalis Promotes the Hyphal Morphogenesis and Biofilm Formation of Candida albicans
inferredcites →https://doi.org/10.3390/pathogens9100835openalex-snapshot
Enterococcus faecalis Polymicrobial Interactions Facilitate Biofilm Formation, Antibiotic Recalcitrance, and Persistent Colonization of the Catheterized Urinary Tract
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/10.5005/jp-journals-10071-23916openalex-snapshot
Increasing Trend of Vancomycin-resistant Enterococci Bacteremia in a Tertiary Care Hospital of South India: A Three-year Prospective Study
inferredcites →https://doi.org/10.7150/thno.56205openalex-snapshot
Drug repurposing for next-generation combination therapies against multidrug-resistant bacteria
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Mechanistic study of the immune defense function of the CRISPR1-Cas system in Enterococcus faecalis
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Community context influences the conjugation efficiency of Escherichia coli
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Community context influences the conjugation efficiency of E. coli
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Pyocyanin produced by Pseudomonas aeruginosa creates legacy effects that promote antibiotic resistance evolution in enterococci
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Case report of Enterococcus thailandicus bacteremia, with genomic characterization of its clinical isolate
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MiFoDB, a workflow for microbial food metagenomic characterization, enables high-resolution analysis of fermented food microbial dynamics
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Gut microbiota was highly related to the immune status in chronic obstructive pulmonary disease patients
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Plasma cell-free DNA Droplet Digital PCR provides rapid and efficient infectious microbiology diagnosis for febrile haematological patients
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Species-level taxonomic characterization of gut microbiota in HIV-infected individuals
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inferred← citeshttps://doi.org/10.34172/ijep.5633openalex-snapshot
C A Review of Genes Related to Biofilm Formation in Enterococcus
inferred← citeshttps://doi.org/10.52276/25792822-2023.4-359openalex-snapshot
Heat Stress and Cultivable Intestinal Bacteria of Lehmann Brown Hens
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