Evidence map›Paper›PMID 23573242›Full record

ArticlePloS one2013

Phenotypic heterogeneity of Pseudomonas aeruginosa populations in a cystic fibrosis patient.

Matthew L Workentine, Christopher D Sibley, Bryan Glezerson, Swathi Purighalla, Jens C Norgaard-Gron, Michael D Parkins, Harvey R Rabin, Michael G Surette

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

111 citing papers in PubMed, 185 citations in OpenAlex.

  1. Intrapulmonary percussive ventilation improves lung function in cystic fibrosis patients chronically colonized with Pseudomonas aeruginosa: a pilot cross-over study.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2018
    Trial
  2. Pseudomonas aeruginosa phenotypes associated with eradication failure in children with cystic fibrosis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2014
    Trial
  3. Article
  4. Beyond Resistance Genes:Life (Basel, Switzerland) · 2026
    Review
  5. Article
  6. Phage-Based Approaches to ChronicAntibiotics (Basel, Switzerland) · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Insights onMicroorganisms · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

51 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Matthew L WorkentineFarncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
Christopher D Sibley
Bryan Glezerson
Swathi Purighalla
Jens C Norgaard-Gron
Michael D Parkins
Harvey R Rabin
Michael G Surette
University of Calgary · CAPopulation Health Research Institute · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

The opportunistic pathogen Pseudomonas aeruginosa chronically infects the lower airways of patients with cystic fibrosis. Throughout the course of infection this organism undergoes adaptations that contribute to its long-term persistence in the airways. While P. aeruginosa diversity has been documented, it is less clear to what extent within-patient diversity contributes to the overall population structure as most studies have been limited to the analysis of only a few isolates per patient per time point. To examine P. aeruginosa population structure in more detail we collected multiple isolates from individual sputum samples of a patient chronically colonized with P. aeruginosa. This strain collection, comprised of 169 clonal isolates and representing three pulmonary exacerbations as well as clinically stable periods, was assayed for a wide selection of phenotypes. These phenotypes included colony morphology, motility, quorum sensing, protease activity, auxotrophy, siderophore levels, antibiotic resistance, and growth profiles. Each phenotype displayed significant variation even within isolates of the same colony morphotype from the same sample. Isolates demonstrated a large degree of individuality across phenotypes, despite being part of a single clonal lineage, suggesting that the P. aeruginosa population in the cystic fibrosis airways is being significantly under-sampled.

Indexed as

AdultBacterial LoadCluster AnalysisCystic FibrosisDrug Resistance, BacterialElectrophoresis, Gel, Pulsed-FieldGenetic HeterogeneityGenetics, PopulationHumansMaleOpportunistic InfectionsPhenotypePseudomonas aeruginosaPseudomonas InfectionsRespiratory Tract InfectionsSputum

Identifiers

PMID23573242
PMCPMC3616088
OpenAlexW2062652176

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.