Evidence map›Paper›PMID 42168836›Full record

Observational studyBMC microbiology2026

Antibiotic pressure does not uncover intra-host heterogeneity of Pseudomonas aeruginosa in patients with chronic lung disease.

Lisa Göpel, Espen E Groth, Sina Minke, Hinrich Schulenburg, Barbara Kalsdorf, Laura Kirchhoff, Leif Tueffers, Klaus F Rabe, Sébastien Boutin, Dennis Nurjadi and 1 more

Abstract readObservational Study
In one paragraph

Observational study in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Lisa Göpel *Institute of Medical Microbiology, University of Luebeck and University Hospital Schleswig-Holstein Campus Lübeck, Lübeck, Germany. lisamarie.goepel@uksh.de.
Espen E Groth *Department of Pneumology, LungenClinic Grosshansdorf, Großhansdorf, Germany.
Sina MinkeInstitute of Medical Microbiology, University of Luebeck and University Hospital Schleswig-Holstein Campus Lübeck, Lübeck, Germany.
Hinrich SchulenburgDepartment of Evolutionary Ecology and Genetics, Zoological Institute, Kiel University, Kiel, Germany.
Barbara KalsdorfDivision of Clinical Infectious Diseases, Research Center Borstel, Leibniz Lung Center, Borstel, Germany.
Laura KirchhoffInstitute of Medical Microbiology, University of Luebeck and University Hospital Schleswig-Holstein Campus Lübeck, Lübeck, Germany.
Leif TueffersInstitute of Medical Microbiology, University of Luebeck and University Hospital Schleswig-Holstein Campus Lübeck, Lübeck, Germany.
Klaus F RabeDepartment of Pneumology, LungenClinic Grosshansdorf, Großhansdorf, Germany.
Sébastien BoutinInstitute of Medical Microbiology, University of Luebeck and University Hospital Schleswig-Holstein Campus Lübeck, Lübeck, Germany.
Dennis NurjadiInstitute of Medical Microbiology, University of Luebeck and University Hospital Schleswig-Holstein Campus Lübeck, Lübeck, Germany.
Jan RuppInstitute of Medical Microbiology, University of Luebeck and University Hospital Schleswig-Holstein Campus Lübeck, Lübeck, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudomonas aeruginosa colonization and infection in patients with chronic obstructive pulmonary disease (COPD) or non-cystic fibrosis bronchiectasis (NCFBE) are associated with increased airway inflammation and mortality. Pseudomonas-active antibiotic therapy is a frequent therapeutic intervention in acute bacteria-driven exacerbation or when eradication of P. aeruginosa colonization is intended. However, the impact of intra-patient heterogeneity of P. aeruginosa on eradication outcomes remains unclear.We enrolled 30 patients receiving inpatient care for COPD and/or NCFBE exacerbation with known or newly detected P. aeruginosa colonization into an observational study. The analysis cohort consisted of 22 participants receiving in-hospital antibiotic eradication therapy, from whom a total of 91 lower respiratory tract samples were collected prior to, during, and after antibiotic therapy. To explore intra-host clonal heterogeneity, a maximum of 10 randomly selected P. aeruginosa isolates were collected from all patient samples containing Pseudomonas.P. aeruginosa-positive cultures were detected in 11 of 22 patients at baseline or during antibiotic therapy. Among these patients, short-term microbiological eradication, defined as a Pseudomonas-negative culture during or at the conclusion of antibiotic treatment, was achieved in 10 of 11 cases (90.9%). Extended antimicrobial susceptibility testing was performed on all isolates and indicated low levels of resistance in isolates obtained from patients before the initiation of eradication therapy and overall limited intra-host phenotypic resistance variability. Whole-genome sequencing of isolates from four patients with at least three longitudinal P. aeruginosa-positive samples confirmed colonization by a single clonal lineage in each case.While concordance between phenotypic resistance and detected genetic resistance determinants was limited, overall resistance levels were low. Our data suggest that P. aeruginosa colonization in our cohort of COPD/NCFBE patients was predominantly associated with a single clonal lineage and with limited intra-host resistance heterogeneity. These findings, based on a small sample size, suggest that susceptibility testing of a single isolate could inform eradication therapy in selected patients. The high rate of short-term eradication success is consistent with the effectiveness of current antibiotic regimens. Yet, more comprehensive longitudinal studies with larger patient numbers and more diverse patient backgrounds are warranted to clarify persistence and re-infection dynamics.Trial registrationGerman Clinical Trials Register (DRKS), DRKS00023975. Registered 28 December 2020. Retrospectively registered.

Indexed as

Anti-Bacterial AgentsPseudomonas aeruginosaPseudomonas InfectionsPulmonary Disease, Chronic ObstructiveAgedBronchiectasisFemaleHumansMaleMicrobial Sensitivity TestsMiddle AgedAnti-Bacterial AgentsAntimicrobial resistanceChronic obstructive pulmonary diseaseEradication therapyIntra-host heterogeneityNon-cystic fibrosis bronchiectasisPseudomonas aeruginosa

Identifiers

PMID42168836
PMCPMC13192145

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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.