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Mucin-enriched environment shapes bacteriophage protection against Pseudomonas aeruginosa in airway epithelial cells

https://doi.org/10.1101/2025.10.17.683030
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Control of the Proinflammatory State in Cystic Fibrosis Lung Epithelial Cells by Genes from the TNF-αR/NFκB Pathway
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Distinct effects of mucin on phage-host interactions in model systems of beneficial and pathogenic bacteria
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Cellular and Molecular Biology of Airway Mucins
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Relationships between bacteria and the mucus layer
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Chemical Genetics Reveals Environment-Specific Roles for Quorum Sensing Circuits in Pseudomonas aeruginosa
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High levels of interleukin-6 in the exhaled breath condensate of patients with COPD
inferredcites →https://doi.org/10.1016/s0140-6736(24)01867-1openalex-snapshot
Global burden of bacterial antimicrobial resistance 1990–2021: a systematic analysis with forecasts to 2050
inferredcites →https://doi.org/10.1021/acs.biomac.1c00073openalex-snapshot
Structural Alterations of Mucins Are Associated with Losses in Functionality
inferredcites →https://doi.org/10.1038/bjc.2013.748openalex-snapshot
Interleukin-6 released by colon cancer-associated fibroblasts is critical for tumour angiogenesis: anti-interleukin-6 receptor antibody suppressed angiogenesis and inhibited tumour–stroma interaction
inferredcites →https://doi.org/10.1038/mi.2015.131openalex-snapshot
Signal transducer and activator of transcription-3 licenses Toll-like receptor 4-dependent interleukin (IL)-6 and IL-8 production via IL-6 receptor-positive feedback in endometrial cells
inferredcites →https://doi.org/10.1038/nrmicro2315openalex-snapshot
Bacteriophage resistance mechanisms
inferredcites →https://doi.org/10.1038/s41467-022-31330-3openalex-snapshot
Mucin induces CRISPR-Cas defense in an opportunistic pathogen
inferredcites →https://doi.org/10.1038/s41467-024-48560-2openalex-snapshot
Bacteriophage defends murine gut from Escherichia coli invasion via mucosal adherence
inferredcites →https://doi.org/10.1038/s41522-018-0067-0openalex-snapshot
Mucins trigger dispersal of Pseudomonas aeruginosa biofilms
inferredcites →https://doi.org/10.1038/s41564-019-0581-8openalex-snapshot
Mucin glycans attenuate the virulence of Pseudomonas aeruginosa in infection
inferredcites →https://doi.org/10.1038/s41564-024-01705-xopenalex-snapshot
Personalized bacteriophage therapy outcomes for 100 consecutive cases: a multicentre, multinational, retrospective observational study
inferredcites →https://doi.org/10.1038/s41591-025-03678-8openalex-snapshot
Personalized inhaled bacteriophage therapy for treatment of multidrug-resistant Pseudomonas aeruginosa in cystic fibrosis
inferredcites →https://doi.org/10.1038/s41598-019-52794-2openalex-snapshot
Impact of bacteria motility in the encounter rates with bacteriophage in mucus
inferredcites →https://doi.org/10.1038/s42003-024-07269-0openalex-snapshot
Mucosal-adapted bacteriophages as a preventive strategy for a lethal Pseudomonas aeruginosa challenge in mice
inferredcites →https://doi.org/10.1042/bst20170455openalex-snapshot
Role of mucins in lung homeostasis: regulated expression and biosynthesis in health and disease
inferredcites →https://doi.org/10.1073/pnas.0609213104openalex-snapshot
Population structure of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1073/pnas.1305923110openalex-snapshot
Bacteriophage adhering to mucus provide a non–host-derived immunity
inferredcites →https://doi.org/10.1073/pnas.2116197119openalex-snapshot
Bacteriophages evolve enhanced persistence to a mucosal surface
inferredcites →https://doi.org/10.1080/01902148.2019.1665147openalex-snapshot
Pseudomonas aeruginosa-derived flagellin stimulates IL-6 and IL-8 production in human bronchial epithelial cells: A potential mechanism for progression and exacerbation of COPD
inferredcites →https://doi.org/10.1089/107999099313866openalex-snapshot
Regulation of Interleukin-8 Gene Expression
inferredcites →https://doi.org/10.1101/cshperspect.a016295openalex-snapshot
IL-6 in Inflammation, Immunity, and Disease
inferredcites →https://doi.org/10.1126/scitranslmed.abo7728openalex-snapshot
Chronic airway epithelial hypoxia exacerbates injury in muco-obstructive lung disease through mucus hyperconcentration
inferredcites →https://doi.org/10.1128/aem.00026-12openalex-snapshot
Catabolite Repression Control of Pyocyanin Biosynthesis at an Intersection of Primary and Secondary Metabolism in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/cmr.00062-22openalex-snapshot
Reassessment of Historical Clinical Trials Supports the Effectiveness of Phage Therapy
inferredcites →https://doi.org/10.1128/jb.00505-07openalex-snapshot
Pyocyanin Alters Redox Homeostasis and Carbon Flux through Central Metabolic Pathways in Pseudomonas aeruginosa PA14
inferredcites →https://doi.org/10.1128/jb.01184-12openalex-snapshot
The CRISPR/Cas Adaptive Immune System of Pseudomonas aeruginosa Mediates Resistance to Naturally Occurring and Engineered Phages
inferredcites →https://doi.org/10.1128/jvi.01789-24openalex-snapshot
Escherichia coli phage ΦPNJ-9 adheres to mucus via a variant Hoc protein
inferredcites →https://doi.org/10.1128/mbio.00275-18openalex-snapshot
Mixed Communities of Mucoid and Nonmucoid Pseudomonas aeruginosa Exhibit Enhanced Resistance to Host Antimicrobials
inferredcites →https://doi.org/10.1128/mbio.00831-25openalex-snapshot
Flagellar motility and the mucus environment influence aggregation-mediated antibiotic tolerance of Pseudomonas aeruginosa in chronic lung infection
inferredcites →https://doi.org/10.1128/mbio.01984-19openalex-snapshot
Bacteriophage Adherence to Mucus Mediates Preventive Protection against Pathogenic Bacteria
inferredcites →https://doi.org/10.1128/mbio.03451-23openalex-snapshot
Mucus polymer concentration and in vivo adaptation converge to define the antibiotic response of Pseudomonas aeruginosa during chronic lung infection
inferredcites →https://doi.org/10.1128/mbio.03474-20openalex-snapshot
Targeting of Mammalian Glycans Enhances Phage Predation in the Gastrointestinal Tract
inferredcites →https://doi.org/10.1128/msystems.00171-24openalex-snapshot
Metapopulation model of phage therapy of an acute Pseudomonas aeruginosa lung infection
inferredcites →https://doi.org/10.1128/spectrum.01601-24openalex-snapshot
Synergistic action of mucoactive drugs and phages against Pseudomonas aeruginosa and Klebsiella pneumoniae
inferredcites →https://doi.org/10.1128/spectrum.02072-22openalex-snapshot
Characterization of Phage Resistance and Their Impacts on Bacterial Fitness in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/spectrum.03520-23openalex-snapshot
Relevance of the bacteriophage adherence to mucus model for Pseudomonas aeruginosa phages
inferredcites →https://doi.org/10.1139/cjm-2013-0570openalex-snapshot
Mucin inhibits Pseudomonas aeruginosa biofilm formation by significantly enhancing twitching motility
inferredcites →https://doi.org/10.1152/ajplung.00383.2001openalex-snapshot
Identification ofPseudomonas aeruginosaflagellin as an adhesin for Muc1 mucin
inferredcites →https://doi.org/10.1152/ajplung.2001.280.1.l181openalex-snapshot
Muc1 mucins on the cell surface are adhesion sites forPseudomonas aeruginosa
inferredcites →https://doi.org/10.1165/rcmb.2018-0007ocopenalex-snapshot
Lung Defense through IL-8 Carries a Cost of Chronic Lung Remodeling and Impaired Function
inferredcites →https://doi.org/10.1172/jci117676openalex-snapshot
A distinct array of proinflammatory cytokines is expressed in human colon epithelial cells in response to bacterial invasion.
inferredcites →https://doi.org/10.1172/jci200213870openalex-snapshot
Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients
inferredcites →https://doi.org/10.1172/jci6277openalex-snapshot
The innate immune system in cystic fibrosis lung disease
inferredcites →https://doi.org/10.1183/09031936.00141514openalex-snapshot
The innate immune function of airway epithelial cells in inflammatory lung disease
inferredcites →https://doi.org/10.1183/09031936.03.00040703openalex-snapshot
Chronic obstructive pulmonary disease: molecular and cellularmechanisms
inferredcites →https://doi.org/10.1183/13993003.00903-2016openalex-snapshot
Hypoxia and sterile inflammation in cystic fibrosis airways: mechanisms and potential therapies
inferredcites →https://doi.org/10.1186/1755-7682-1-24openalex-snapshot
Pulmonary bacterial pathogens in cystic fibrosis patients and antibiotic therapy: a tool for the health workers
inferredcites →https://doi.org/10.1371/journal.ppat.1005846openalex-snapshot
Evidence and Role for Bacterial Mucin Degradation in Cystic Fibrosis Airway Disease
inferredcites →https://doi.org/10.23937/2378-3516/1410098openalex-snapshot
A Comparison between Two Pathophysiologically Different yet Microbiologically Similar Lung Diseases: Cystic Fibrosis and Chronic Obstructive Pulmonary Disease
inferredcites →https://doi.org/10.3389/fimmu.2023.1255533openalex-snapshot
Interleukin 6: at the interface of human health and disease
inferredcites →https://doi.org/10.3389/fmicb.2015.00343openalex-snapshot
Virulence reduction in bacteriophage resistant bacteria
inferredcites →https://doi.org/10.3389/fmicb.2015.01036openalex-snapshot
Clinical utilization of genomics data produced by the international Pseudomonas aeruginosa consortium
inferredcites →https://doi.org/10.3389/fmicb.2023.1286046openalex-snapshot
Molecular studies of phages-Klebsiella pneumoniae in mucoid environment: innovative use of mucolytic agents prior to the administration of lytic phages
inferredcites →https://doi.org/10.3390/antibiotics9060339openalex-snapshot
The Basis for Natural Multiresistance to Phage in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.3390/ijms252413653openalex-snapshot
Expression Levels of MUC5AC and MUC5B in Airway Goblet Cells Are Associated with Traits of COPD and Progression of Chronic Airflow Limitation
inferredcites →https://doi.org/10.3390/jcm6120112openalex-snapshot
Airway Mucus and Asthma: The Role of MUC5AC and MUC5B
inferredcites →https://doi.org/10.3390/microorganisms9030509openalex-snapshot
Exploring Mucin as Adjunct to Phage Therapy
inferredcites →https://doi.org/10.3390/molecules25132981openalex-snapshot
Biological Activity of Porcine Gastric Mucin on Stress Resistance and Immunomodulation
inferredcites →https://doi.org/10.3390/v13071332openalex-snapshot
Emerging Phage Resistance in Pseudomonas aeruginosa PAO1 Is Accompanied by an Enhanced Heterogeneity and Reduced Virulence
inferredcites →https://doi.org/10.7554/elife.73679openalex-snapshot
Parallel evolution of Pseudomonas aeruginosa phage resistance and virulence loss in response to phage treatment in vivo and in vitro
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