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Increased rates of genomic mutation in a biofilm co-culture model of Pseudomonas aeruginosa and Staphylococcus aureus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s10534-015-9848-6openalex-snapshot
Spoils of war: iron at the crux of clinical and ecological fitness of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1016/j.abb.2011.12.008openalex-snapshot
Non-heme manganese catalase – The ‘other’ catalase
inferredcites →https://doi.org/10.1016/j.mbs.2005.03.011openalex-snapshot
New algorithms for Luria–Delbrück fluctuation analysis
inferredcites →https://doi.org/10.1016/j.mrfmmm.2015.04.002openalex-snapshot
Methods for comparing mutation rates using fluctuation assay data
inferredcites →https://doi.org/10.1016/s0076-6879(05)09012-9openalex-snapshot
Methods for Determining Spontaneous Mutation Rates
inferredcites →https://doi.org/10.1021/acs.biochem.6b01135openalex-snapshot
Mechanism of Action of a Membrane-Active Quinoline-Based Antimicrobial on Natural and Model Bacterial Membranes
inferredcites →https://doi.org/10.1038/ismej.2017.83openalex-snapshot
Co-evolution with Staphylococcus aureus leads to lipopolysaccharide alterations in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1038/nrmicro.2017.99openalex-snapshot
Targeting microbial biofilms: current and prospective therapeutic strategies
inferredcites →https://doi.org/10.1038/s41522-017-0035-0openalex-snapshot
Staphylococcus aureus interaction with Pseudomonas aeruginosa biofilm enhances tobramycin resistance
inferredcites →https://doi.org/10.1073/pnas.0711949105openalex-snapshot
Bacterial addiction module toxin Doc inhibits translation elongation through its association with the 30S ribosomal subunit
inferredcites →https://doi.org/10.1093/bioinformatics/btp253openalex-snapshot
Fluctuation AnaLysis CalculatOR: a web tool for the determination of mutation rate using Luria–Delbrück fluctuation analysis
inferredcites →https://doi.org/10.1093/bioinformatics/btu153openalex-snapshot
Prokka: rapid prokaryotic genome annotation
inferredcites →https://doi.org/10.1093/femspd/fty003openalex-snapshot
Interaction between Staphylococcus aureus and Pseudomonas aeruginosa is beneficial for colonisation and pathogenicity in a mixed biofilm
inferredcites →https://doi.org/10.1093/jac/dkn044openalex-snapshot
Increased mutability of Pseudomonas aeruginosa in biofilms
inferredcites →https://doi.org/10.1093/nar/gkt1226openalex-snapshot
The SEED and the Rapid Annotation of microbial genomes using Subsystems Technology (RAST)
inferredcites →https://doi.org/10.1099/mic.0.000220openalex-snapshot
Iron acquisition in the cystic fibrosis lung and potential for novel therapeutic strategies
inferredcites →https://doi.org/10.1099/mic.0.000352openalex-snapshot
An ex vivo lung model to study bronchioles infected with Pseudomonas aeruginosa biofilms
inferredcites →https://doi.org/10.1126/science.aaj2191openalex-snapshot
Antibiotic tolerance facilitates the evolution of resistance
inferredcites →https://doi.org/10.1128/aac.03676-14openalex-snapshot
Antibiotic-Loaded Synthetic Calcium Sulfate Beads for Prevention of Bacterial Colonization and Biofilm Formation in Periprosthetic Infections
inferredcites →https://doi.org/10.1128/iai.02198-14openalex-snapshot
Synergistic Interactions of Pseudomonas aeruginosa and Staphylococcus aureus in an In Vitro Wound Model
inferredcites →https://doi.org/10.1128/jb.00059-15openalex-snapshot
Coculture of Staphylococcus aureus with Pseudomonas aeruginosa Drives S. aureus towards Fermentative Metabolism and Reduced Viability in a Cystic Fibrosis Model
inferredcites →https://doi.org/10.1128/jb.187.15.5267-5277.2005openalex-snapshot
Cystic Fibrosis Sputum Supports Growth and Cues Key Aspects of Pseudomonas aeruginosa Physiology
inferredcites →https://doi.org/10.1128/jb.187.2.554-566.2005openalex-snapshot
Staphylococcus aureus Serves as an Iron Source for Pseudomonas aeruginosa during In Vivo Coculture
inferredcites →https://doi.org/10.1128/mbio.00557-13openalex-snapshot
Ferrous Iron Is a Significant Component of Bioavailable Iron in Cystic Fibrosis Airways
inferredcites →https://doi.org/10.1146/annurev.micro.112408.134247openalex-snapshot
TonB-Dependent Transporters: Regulation, Structure, and Function
inferredcites →https://doi.org/10.1183/13993003.00612-2017openalex-snapshot
Primary ciliary dyskinesia ciliated airway cells show increased susceptibility toHaemophilus influenzaebiofilm formation
inferredcites →https://doi.org/10.1186/1471-2164-9-75openalex-snapshot
The RAST Server: Rapid Annotations using Subsystems Technology
inferredcites →https://doi.org/10.1186/s12890-015-0062-7openalex-snapshot
Clinical outcomes associated with Staphylococcus aureus and Pseudomonas aeruginosa airway infections in adult cystic fibrosis patients
inferredcites →https://doi.org/10.1186/s12918-016-0334-8openalex-snapshot
Metabolic modeling of a chronic wound biofilm consortium predicts spatial partitioning of bacterial species
inferredcites →https://doi.org/10.1371/journal.pbio.2003981openalex-snapshot
Pseudomonas aeruginosa exoproducts determine antibiotic efficacy against Staphylococcus aureus
inferredcites →https://doi.org/10.1371/journal.pcbi.1005595openalex-snapshot
Unicycler: Resolving bacterial genome assemblies from short and long sequencing reads
inferredcites →https://doi.org/10.1371/journal.pone.0011818openalex-snapshot
A New Approach for the Discovery of Antibiotics by Targeting Non-Multiplying Bacteria: A Novel Topical Antibiotic for Staphylococcal Infections
inferredcites →https://doi.org/10.1371/journal.pone.0042897openalex-snapshot
Comparative Analysis of Single-Species and Polybacterial Wound Biofilms Using a Quantitative, In Vivo, Rabbit Ear Model
inferredcites →https://doi.org/10.1371/journal.pone.0047695openalex-snapshot
Increased Mutability of Staphylococci in Biofilms as a Consequence of Oxidative Stress
inferredcites →https://doi.org/10.1371/journal.pone.0056794openalex-snapshot
Contrasting Diversity Values: Statistical Inferences Based on Overlapping Confidence Intervals
inferredcites →https://doi.org/10.1371/journal.pone.0089614openalex-snapshot
Adaptation of Pseudomonas aeruginosa in Cystic Fibrosis Airways Influences Virulence of Staphylococcus aureus In Vitro and Murine Models of Co-Infection
inferredcites →https://doi.org/10.1586/14787210.2015.1023291openalex-snapshot
Chronic wound infections: the role of Pseudomonas aeruginosa and Staphylococcus aureus
inferredcites →https://doi.org/10.3390/pathogens2020288openalex-snapshot
From in vitro to in vivo Models of Bacterial Biofilm-Related Infections
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s11274-025-04338-2openalex-snapshot
Antimicrobial applications of inorganic radiosensitizers and their potential in biofilm control
inferred← citeshttps://doi.org/10.1016/j.cels.2024.09.007openalex-snapshot
Evolution in microbial microcosms is highly parallel, regardless of the presence of interacting species
inferred← citeshttps://doi.org/10.1099/mic.0.001506openalex-snapshot
Selective colonization of microplastics, wood and glass by antimicrobial-resistant and pathogenic bacteria
inferred← citeshttps://doi.org/10.1099/mic.0.001749openalex-snapshot
Microbial interactions as key players shaping the emergence and spread of de novo resistance mutations
inferred← citeshttps://doi.org/10.1101/2024.10.15.618514openalex-snapshot
Magnesium depletion unleashes two unusual modes of colistin resistance with different fitness costs
inferred← citeshttps://doi.org/10.1128/aem.01155-23openalex-snapshot
Competitive interactions facilitate resistance development against antimicrobials
inferred← citeshttps://doi.org/10.1146/annurev-micro-041320-031627openalex-snapshot
Microbial Interspecies Interactions and Their Impact on the Emergence and Spread of Antimicrobial Resistance
inferred← citeshttps://doi.org/10.1186/s13568-021-01210-yopenalex-snapshot
The inhibitory effects of Staphylococcus aureus on the antibiotic susceptibility and virulence factors of Pseudomonas aeruginosa: A549 cell line model
inferred← citeshttps://doi.org/10.12688/f1000research.55140.1openalex-snapshot
An in vitro model for the cultivation of polymicrobial biofilms under continuous-flow conditions
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003673openalex-snapshot
Magnesium depletion by Candida albicans unleashes two unusual modes of colistin resistance in Pseudomonas aeruginosa with different fitness costs
inferred← citeshttps://doi.org/10.2217/fmb-2019-0200openalex-snapshot
Recapitulation of Polymicrobial Communities Associated with Cystic Fibrosis Airway Infections: A Perspective
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