Evidence map›Paper›PMID 39987197›Full record

ArticleScientific reports2025

Virulence factors of Pseudomonas aeruginosa and immune response during exacerbations and stable phase in bronchiectasis.

Roberto Cabrera, Nona Rovira-Ribalta, Anna Motos, Leticia Bueno-Freire, Nil Vázquez, Alba Soler-Comas, Victoria Alcaraz-Serrano, Rubén López-Aladid, Laura Muñoz, Jordi Vila and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Co-infection withFrontiers in medicine · 2026
    Review
  3. Observational
  4. Microbiome and its role in bronchiectasis.Therapeutic advances in respiratory disease
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Roberto CabreraHospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain.
Nona Rovira-RibaltaHospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain.
Anna MotosHospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain.
Leticia Bueno-FreireHospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain.
Nil VázquezHospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain.
Alba Soler-ComasHospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain.
Victoria Alcaraz-SerranoHospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain.
Rubén López-AladidHospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain.
Laura MuñozDepartment of Clinical Microbiology, Hospital Clínic, CIBERINFEC, Barcelona Global Health Institute, University of Barcelona, Barcelona, Spain.
Jordi VilaDepartment of Clinical Microbiology, Hospital Clínic, CIBERINFEC, Barcelona Global Health Institute, University of Barcelona, Barcelona, Spain.
Antoni Torres *Hospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain. atorres@recerca.clinic.cat.
Laia Fernández-Barat *Hospital Clínic, Cellex Laboratory, CIBERES (Center for Net Biomedical Research Respiratory Diseases, 06/06/0028), FCRB-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), School of Medicine, University of Barcelona, Barcelona, Spain. lfernan1@recerca.clinic.cat.

Funding

CIBER ES18PI01X1-2021ISCIII-FEDER PI18/00145ISCIII-FOS FI19/00090SEPAR 208, 628, 1428
6 · The paper itself

Abstract

The study of key Pseudomonas aeruginosa (PA) virulence factors, the molecular basis of pathogenicity, as well as their correlation with the immune response during exacerbations in patients with non-cystic fibrosis bronchiectasis can help to identify novel targets and biomarkers for clinical management. The objective was to compare P. aeruginosa virulence and the patient's immune response during stable phases and exacerbations of bronchiectasis. We used polymerase chain reaction (PCR) and real-time quantitative PCR (qRT-PCR) to perform molecular characterization of the genomic islands and virulence genes present in 42 P. aeruginosa strains obtained from the sputum of patients with bronchiectasis during stability and exacerbations. Immunoglobulin (Ig) and interleukin (IL) levels in 32 serum samples were analyze by ELISA and Luminex assay. A greater presence of the conjugative element pKLC102, specific virulence genes (exoS, exoY) and pyoverdine production characterize the P. aeruginosa strains obtained during exacerbations. The expression levels of type III secretion system (exoS, exoY) showed an important role in the humoral immune response during exacerbations. Exacerbations were associated with high levels of IL-6. The presence of specific genomic islands, virulence genes, and increased IL-6 levels provide an accurate characterization on bronchiectasis exacerbations. These targets could be useful in the prevention, management and treatment of these exacerbations.

Indexed as

BronchiectasisPseudomonas aeruginosaPseudomonas InfectionsVirulence FactorsAgedBacterial ProteinsFemaleGenomic IslandsHumansInterleukin-6MaleMiddle AgedSputumVirulenceBacterial ProteinsInterleukin-6Virulence FactorsBiomarkersBronchiectasisPathogenicityPseudomonas aeruginosaRespiratory diseases

Identifiers

PMID39987197
PMCPMC11846832

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.