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Metabolite transfer with the fermentation product 2,3-butanediol enhances virulence by Pseudomonas aeruginosa

https://doi.org/10.1038/ismej.2013.232

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1 of the 54 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.1165/rcmb.2012-0088oc (notice 2018-12-29).

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What this work says

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

inferredcites →https://doi.org/10.1016/j.biotechadv.2011.01.007openalex-snapshot

Microbial 2,3-butanediol production: A state-of-the-art review

inferredcites →https://doi.org/10.1016/j.elecom.2010.01.019openalex-snapshot

Quorum sensing regulates electric current generation of Pseudomonas aeruginosa PA14 in bioelectrochemical systems

inferredcites →https://doi.org/10.1016/j.jcf.2010.09.004openalex-snapshot

Lactate in cystic fibrosis sputum

inferredcites →https://doi.org/10.1016/j.resmic.2010.01.003openalex-snapshot

Phenazines affect biofilm formation by Pseudomonas aeruginosa in similar ways at various scales

inferredcites →https://doi.org/10.1016/s0022-2836(67)80070-6openalex-snapshot

DNA replication and the division cycle in Escherichia coli

inferredcites →https://doi.org/10.1016/s0140-6736(03)12567-6openalex-snapshot

Cystic fibrosis

inferredcites →https://doi.org/10.1016/s0169-409x(02)00144-8openalex-snapshot

An overview of the pathogenesis of cystic fibrosis lung disease

inferredcites →https://doi.org/10.1021/bi6024403openalex-snapshot

Structural and Functional Analysis of the Pyocyanin Biosynthetic Protein PhzM from Pseudomonas aeruginosa,

inferredcites →https://doi.org/10.1021/es048563oopenalex-snapshot

Microbial Phenazine Production Enhances Electron Transfer in Biofuel Cells

inferredcites →https://doi.org/10.1021/es702290aopenalex-snapshot

Redox Reactions of Phenazine Antibiotics with Ferric (Hydr)oxides and Molecular Oxygen

inferredcites →https://doi.org/10.1038/35037627openalex-snapshot

Quorum-sensing signals indicate that cystic fibrosis lungs are infected with bacterial biofilms

inferredcites →https://doi.org/10.1038/417552aopenalex-snapshot

A component of innate immunity prevents bacterial biofilm development

inferredcites →https://doi.org/10.1038/ismej.2010.88openalex-snapshot

Phylogenetic and metabolic diversity of bacteria associated with cystic fibrosis

inferredcites →https://doi.org/10.1038/ismej.2011.167openalex-snapshot

Bacterial cis-2-unsaturated fatty acids found in the cystic fibrosis airway modulate virulence and persistence of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1038/ismej.2012.5openalex-snapshot

The gut anaerobe Faecalibacterium prausnitzii uses an extracellular electron shuttle to grow at oxic–anoxic interphases

inferredcites →https://doi.org/10.1038/ismej.2013.229openalex-snapshot

Breath gas metabolites and bacterial metagenomes from cystic fibrosis airways indicate active pH neutral 2,3-butanedione fermentation

inferredcites →https://doi.org/10.1039/c1ee01377gopenalex-snapshot

Metabolite-based mutualism between Pseudomonas aeruginosa PA14 and Enterobacter aerogenes enhances current generation in bioelectrochemical systems

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03803.xopenalex-snapshot

Modulation of Pseudomonas aeruginosa gene expression by host microflora through interspecies communication

inferredcites →https://doi.org/10.1073/pnas.0511100103openalex-snapshot

An ordered, nonredundant library of Pseudomonas aeruginosa strain PA14 transposon insertion mutants

inferredcites →https://doi.org/10.1073/pnas.060030097openalex-snapshot

Inorganic polyphosphate is needed for swimming, swarming, and twitching motilities of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1073/pnas.0710525105openalex-snapshot

Shewanella secretes flavins that mediate extracellular electron transfer

inferredcites →https://doi.org/10.1073/pnas.0804326105openalex-snapshot

A polymicrobial perspective of pulmonary infections exposes an enigmatic pathogen in cystic fibrosis patients

inferredcites →https://doi.org/10.1073/pnas.1107857108openalex-snapshot

Intestinal inflammation allows Salmonella to use ethanolamine to compete with the microbiota

inferredcites →https://doi.org/10.1073/pnas.1120577109openalex-snapshot

Decade-long bacterial community dynamics in cystic fibrosis airways

inferredcites →https://doi.org/10.1073/pnas.91.1.197openalex-snapshot

Structure of the autoinducer required for expression of Pseudomonas aeruginosa virulence genes.

inferredcites →https://doi.org/10.1073/pnas.96.24.13904openalex-snapshot

Identification of genes controlled by quorum sensing in Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1086/514631openalex-snapshot

Microbiology of Sputum from Patients at Cystic Fibrosis Centers in the United States

inferredcites →https://doi.org/10.1099/mic.0.022764-0openalex-snapshot

Revisiting the quorum-sensing hierarchy in Pseudomonas aeruginosa: the transcriptional regulator RhlR regulates LasR-specific factors

inferredcites →https://doi.org/10.1099/mic.0.27566-0openalex-snapshot

Expression of the quorum-sensing regulatory protein LasR is strongly affected by iron and oxygen concentrations in cultures of Pseudomonas aeruginosa irrespective of cell density

inferredcites →https://doi.org/10.1101/sqb.1957.022.01.039openalex-snapshot

Concluding Remarks

inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05772.xopenalex-snapshot

Responses of Pseudomonas aeruginosa to low oxygen indicate that growth in the cystic fibrosis lung is by aerobic respiration

inferredcites →https://doi.org/10.1111/j.1462-2920.2009.01996.xopenalex-snapshot

Absolute quantification of Dehalococcoides proteins: enzyme bioindicators of chlorinated ethene dehalorespiration

inferredcites →https://doi.org/10.1128/cmr.00068-09openalex-snapshot

The Changing Microbial Epidemiology in Cystic Fibrosis

inferredcites →https://doi.org/10.1128/cmr.15.2.194-222.2002openalex-snapshot

Lung Infections Associated with Cystic Fibrosis

inferredcites →https://doi.org/10.1128/iai.56.9.2515-2517.1988openalex-snapshot

Measurement of Pseudomonas aeruginosa phenazine pigments in sputum and assessment of their contribution to sputum sol toxicity for respiratory epithelium

inferredcites →https://doi.org/10.1128/iai.60.2.328-336.1992openalex-snapshot

Response of Pseudomonas aeruginosa to pyocyanin: mechanisms of resistance, antioxidant defenses, and demonstration of a manganese-cofactored superoxide dismutase

inferredcites →https://doi.org/10.1128/jb.00396-11openalex-snapshot

Phenazine-1-Carboxylic Acid Promotes Bacterial Biofilm Development via Ferrous Iron Acquisition

inferredcites →https://doi.org/10.1128/jb.01138-07openalex-snapshot

Nutritional Cues Control Pseudomonas aeruginosa Multicellular Behavior in Cystic Fibrosis Sputum

inferredcites →https://doi.org/10.1128/jb.02273-12openalex-snapshot

Bacterial Community Morphogenesis Is Intimately Linked to the Intracellular Redox State

inferredcites →https://doi.org/10.1128/jb.160.3.928-934.1984openalex-snapshot

Pseudomonas aeruginosa mutants affected in anaerobic growth on arginine: evidence for a four-gene cluster encoding the arginine deiminase pathway

inferredcites →https://doi.org/10.1128/jb.181.13.3890-3897.1999openalex-snapshot

Effect of rpoS Mutation on the Stress Response and Expression of Virulence Factors in Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/jb.182.10.2702-2708.2000openalex-snapshot

The Pseudomonas Quinolone Signal Regulates rhl Quorum Sensing in Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/jb.183.3.1047-1057.2001openalex-snapshot

Role of Alginate and Its O Acetylation in Formation of Pseudomonas aeruginosa Microcolonies and Biofilms

inferredcites →https://doi.org/10.1128/jb.184.10.2576-2586.2002openalex-snapshot

Advancing the Quorum in Pseudomonas aeruginosa : MvaT and the Regulation of N -Acylhomoserine Lactone Production and Virulence Gene Expression

inferredcites →https://doi.org/10.1128/jb.185.7.2080-2095.2003openalex-snapshot

Microarray Analysis of Pseudomonas aeruginosa Quorum-Sensing Regulons: Effects of Growth Phase and Environment

inferredcites →https://doi.org/10.1136/thoraxjnl-2011-200932openalex-snapshot

Long-term cultivation-independent microbial diversity analysis demonstrates that bacterial communities infecting the adult cystic fibrosis lung show stability and resilience

inferredcites →https://doi.org/10.1152/ajplung.1998.274.6.l893openalex-snapshot

Pseudomonaspyocyanine alters calcium signaling in human airway epithelial cells

inferredcites →https://doi.org/10.1165/rcmb.2012-0088ocopenalex-snapshot

Phenazine Content in the Cystic Fibrosis Respiratory Tract Negatively Correlates with Lung Function and Microbial Complexity

inferredcites →https://doi.org/10.1371/journal.pone.0022702openalex-snapshot

Culture Enriched Molecular Profiling of the Cystic Fibrosis Airway Microbiome

inferredcites →https://doi.org/10.1371/journal.pone.0027091openalex-snapshot

Pseudomonas aeruginosa Elastase Provides an Escape from Phagocytosis by Degrading the Pulmonary Surfactant Protein-A

inferredcites →https://doi.org/10.1371/journal.pone.0058299openalex-snapshot

Pyocyanin Facilitates Extracellular DNA Binding to Pseudomonas aeruginosa Influencing Cell Surface Properties and Aggregation

inferredcites →https://doi.org/10.1371/journal.ppat.1000184openalex-snapshot

Discerning the Complexity of Community Interactions Using a Drosophila Model of Polymicrobial Infections

inferredcites →https://doi.org/10.1371/journal.ppat.1000712openalex-snapshot

Nutrient Availability as a Mechanism for Selection of Antibiotic Tolerant Pseudomonas aeruginosa within the CF Airway

inferredcites →https://doi.org/10.2217/fmb.12.55openalex-snapshot

Microbial Diversity in the Cystic Fibrosis Airways: Where is thy Sting?

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GC-MS Analysis of Volatiles Present in Pappea Capensis Extracts

inferred← citeshttps://doi.org/10.70675/6f838ff3z76faz4f1ezb358zf37e099d6a38openalex-snapshot

Improve the principles for selecting new bacterial biocontrol agents for FHB

inferred← citeshttps://doi.org/10.70675/8a056a1ez60bcz434az9009z1ec9be6277c7openalex-snapshot

Impact des génotypes de blé sur le métabolisme secondaire des Pseudomonas et conséquences sur leurs interactions avec la plante hôte

inferred← citeshttps://doi.org/10.70675/fd86f51dzd853z4f5az9f76zc38b311986f3openalex-snapshot

Identification et caractérisation de composés produits par des bactéries environnementales pour la lutte biologique contre Legionella pneumophila

inferred← citeshttps://doi.org/10.7759/cureus.58660openalex-snapshot

Phytochemical Composition and Antimicrobial Efficacy of Salvadora persica Root Extracts Against Carbapenem-Resistant Acinetobacter baumannii

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