Evidence map›Paper›PMID 26714629›Full record

ArticleBMC genomics2015

Comparative genomics and biological characterization of sequential Pseudomonas aeruginosa isolates from persistent airways infection.

Irene Bianconi, Julie Jeukens, Luca Freschi, Beatriz Alcalá-Franco, Marcella Facchini, Brian Boyle, Antonio Molinaro, Irena Kukavica-Ibrulj, Burkhard Tümmler, Roger C Levesque and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. BioMed research international · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Frontiers in immunology · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Comparative Genomics ofAntibiotics (Basel, Switzerland) · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Effect of iron chelation on anti-pseudomonal activity of doxycycline.International journal of antimicrobial agents · 2021
    Article
  14. International journal of molecular sciences · 2021
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. UnderstandingCells · 2020
    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

11 authors at 4 institutions in 3 countries.

Irene BianconiInfections and Cystic Fibrosis Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy. bianconi.irene@hsr.it.
Julie JeukensInstitut de biologie intégrative et des systèmes (IBIS), Université Laval, Quebec, Canada. julie.jeukens.1@ulaval.ca.
Luca FreschiInstitut de biologie intégrative et des systèmes (IBIS), Université Laval, Quebec, Canada. luca.freschi@bio.ulaval.ca.
Beatriz Alcalá-FrancoInfections and Cystic Fibrosis Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy. alcalafranco.beatriz@hsr.it.
Marcella FacchiniInfections and Cystic Fibrosis Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy. facchini.marcella@hsr.it.
Brian BoyleInstitut de biologie intégrative et des systèmes (IBIS), Université Laval, Quebec, Canada. Brian.Boyle@ibis.ulaval.ca.
Antonio MolinaroUniversità di Napoli Federico II, Napoli, Italy. molinaro@unina.it.
Irena Kukavica-IbruljInstitut de biologie intégrative et des systèmes (IBIS), Université Laval, Quebec, Canada. kukavica@fmed.ulaval.ca.
Burkhard TümmlerMedizinische Hochschule Hannover, Hannover, Germany. Tuemmler.Burkhard@mh-hannover.de.
Roger C LevesqueInstitut de biologie intégrative et des systèmes (IBIS), Université Laval, Quebec, Canada. rclevesq@ibis.ulaval.ca.
Alessandra BragonziInfections and Cystic Fibrosis Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy. bragonzi.alessandra@hsr.it.
Université Laval · CAVita-Salute San Raffaele University · ITMedizinische Hochschule Hannover · DEUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPseudomonas aeruginosa establishes life-long chronic airway infections in cystic fibrosis (CF) patients. As the disease progresses, P. aeruginosa pathoadaptive variants are distinguished from the initially acquired strain. However, the genetic basis and the biology of host-bacteria interactions leading to a persistent lifestyle of P. aeruginosa are not understood. As a model system to study long term and persistent CF infections, the P. aeruginosa RP73, isolated 16.9 years after the onset of airways colonization from a CF patient, was investigated. Comparisons with strains RP1, isolated at the onset of the colonization, and clonal RP45, isolated 7 years before RP73 were carried out to better characterize genomic evolution of P. aeruginosa in the context of CF pathogenicity.

resultsVirulence assessments in disease animal model, genome sequencing and comparative genomics analysis were performed for clinical RP73, RP45, RP1 and prototype strains. In murine model, RP73 showed lower lethality and a remarkable capability of long-term persistence in chronic airways infection when compared to other strains. Pathological analysis of murine lungs confirmed advanced chronic pulmonary disease, inflammation and mucus secretory cells hyperplasia. Genomic analysis predicted twelve genomic islands in the RP73 genome, some of which distinguished RP73 from other prototype strains and corresponded to regions of genome plasticity. Further, comparative genomic analyses with sequential RP isolates showed signatures of pathoadaptive mutations in virulence factors potentially linked to the development of chronic infections in CF.

conclusionsThe genome plasticity of P. aeruginosa particularly in the RP73 strain strongly indicated that these alterations may form the genetic basis defining host-bacteria interactions leading to a persistent lifestyle in human lungs.

Indexed as

AnimalsCystic FibrosisDisease Models, AnimalGenome, BacterialGenomicsInflammationMaleMiceMice, Inbred C57BLPseudomonas aeruginosaRespiratory Tract InfectionsVirulence FactorsVirulence Factors

Identifiers

PMID26714629
PMCPMC4696338
OpenAlexW2219728682

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.