Clinical and Lung Microbiome Impact of Chronic Versus Intermittent Pseudomonas aeruginosa Infection in Bronchiectasis

Laia Fernández-Barat1, Ruben López-Aladid1, Victoria Alcaraz-Serrano1

  • 1CELLEX Research Laboratories, CibeRes (Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, 06/06/0028), Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain; School of Medicine, Department of Medicine & Department of Biophysics and Bioengineering, University of Barcelona, Spain; Pulmonology Department, Hospital Clínic, Barcelona, Spain.

PubMed
Abstract

Insights

Chronic Pseudomonas aeruginosa (PA) infection in bronchiectasis (BE) patients is linked to lower quality of life but fewer hospitalizations. This distinction impacts patient care and lung microbiome diversity.

Area of Science:

  • Pulmonary Medicine
  • Microbiology
  • Immunology

Background:

  • Non-cystic fibrosis bronchiectasis (BE) patients with Pseudomonas aeruginosa (PA) show varied exacerbation rates.
  • Previous studies did not differentiate between chronic and intermittent PA infection stages.

Purpose of the Study:

  • To investigate if chronic or intermittent PA infection in BE patients correlates with exacerbation rates, quality of life, and respiratory microbiome biodiversity over one year.
  • To compare clinical and microbiological outcomes between chronic and intermittent PA infection phenotypes.

Main Methods:

  • A 1-year longitudinal study involving 80 BE patients (61 chronic, 19 intermittent PA infection).
  • Sequential 3-monthly measurements of microbiological (PA load, phenotype, biofilms), immunological (serum IgGs), and clinical data (Quality-of-Life, exacerbations).
  • 16S rRNA gene sequencing for respiratory microbiome analysis, comparing mucoid PA in chronic vs. non-mucoid PA in intermittent infections.

Main Results:

  • Chronically infected patients reported reduced quality of life but fewer hospitalized exacerbations compared to intermittently infected patients.
  • Chronic PA infection was associated with decreased sputum microbiome biodiversity.
  • Higher systemic IgGs against P. aeruginosa correlated with fewer hospitalized exacerbations in chronically infected patients.

Conclusions:

  • Distinguishing between chronic and intermittent P. aeruginosa infection in BE patients is clinically significant.
  • These infection phenotypes influence quality of life, exacerbation frequency, and lung microbiome diversity.
  • This differentiation is readily achievable in clinical practice.

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