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Pseudomonas aeruginosa- mediated cardiac dysfunction is driven by extracellular vesicles released during infection
Pseudomonas aeruginosa- mediated cardiac dysfunction is driven by extracellular vesicles released during infection
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Pseudomonas aeruginosa- mediated cardiac dysfunction is driven by extracellular vesicles released during infection
Pseudomonas aeruginosa- mediated cardiac dysfunction is driven by extracellular vesicles released during infection
Journal Article

Pseudomonas aeruginosa- mediated cardiac dysfunction is driven by extracellular vesicles released during infection

2026
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Overview
Bacterial pneumonia can lead to severe cardiovascular complications and is a major contributor to increased mortality among hospitalized patients, either directly or indirectly. Pseudomonas aeruginosa , an opportunistic pathogen frequently encountered in hospital settings, accounts for nearly 20% of all infections in intensive care units (ICUs). Our previous studies demonstrated that P. aeruginosa lung infection induces profound cardiac electrical abnormalities and left ventricular (LV) dysfunction, despite minimal bacterial dissemination to the heart. In the present study, we identify exosomes released from infected host cells and outer membrane vesicles (OMVs) secreted by P. aeruginosa as critical mediators of this cardiac dysfunction. We show that host-derived exosomes are enriched with bacterial OMVs containing toxins and other immunogenic molecules, which promote systemic inflammation and tissue injury, ultimately contributing to cardiac impairment.
Publisher
American Society for Microbiology,American Society for Microbiology (ASM)
Subject

Animal Infection Models

/ Animals

/ Bacteria

/ Bacterial infections

/ Bacterial Pathogenesis

/ Bacterial Pneumonia

/ Bacteriology

/ Bronchopulmonary infection

/ cardiac dysfunction

/ Cardiomyocytes

/ Cardiovascular diseases

/ Clinical Microbiology and Infectious Diseases

/ Communication

/ Comorbidity

/ Congestive heart failure

/ Disease Models, Animal

/ Exosomes

/ Extracellular vesicles

/ Extracellular Vesicles - metabolism

/ Health care

/ Healthcare-Associated Infections

/ Heart diseases

/ Heart failure

/ Hospital-Acquired Pneumonia

/ Host-Microbial Interactions

/ human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs)

/ Humans

/ Immunogenicity

/ Induced Pluripotent Stem Cells

/ Intensive care units

/ Liquid chromatography

/ Lungs

/ Macrophages

/ Mass spectroscopy

/ Medical Microbiology

/ Membrane vesicles

/ Mice

/ Microbial Pathogenesis and Immunology

/ Microbial Physiology and Genetics

/ microelectrode array (MEA)

/ Model Organisms

/ Mortality

/ Murine Pneumonia Models

/ Muscle contraction

/ Myocytes, Cardiac - microbiology

/ Nosocomial Infections

/ Opportunist infection

/ outer membrane vesicles (OMVs)

/ Pathogenesis

/ Pathogens

/ Physiology

/ Pluripotency

/ Pneumonia

/ Propagation

/ Pseudomonas aeruginosa

/ Pseudomonas aeruginosa - pathogenicity

/ Pseudomonas aeruginosa - physiology

/ Pseudomonas Infections - complications

/ Pseudomonas Infections - microbiology

/ Pseudomonas Species

/ Public Health Microbiology

/ Research Article

/ Respiratory Infections

/ Sepsis and Systemic Infections

/ Ventilator-Associated Pneumonia

/ Ventricle