Evidence map›Paper›PMID 19047519›Full record

ArticleGenome research2009

Newly introduced genomic prophage islands are critical determinants of in vivo competitiveness in the Liverpool Epidemic Strain of Pseudomonas aeruginosa.

Craig Winstanley, Morgan G I Langille, Joanne L Fothergill, Irena Kukavica-Ibrulj, Catherine Paradis-Bleau, François Sanschagrin, Nicholas R Thomson, Geoff L Winsor, Michael A Quail, Nicola Lennard and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Genome research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 197 papers.

0numbers the graph read from it
0cells of the map it votes in
197citing 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

197 citing papers in PubMed, 339 citations in OpenAlex.

  1. Revisiting the life cycle of temperate phages.Nature reviews. Microbiology · 2026
    Review
  2. Prophage: agent provocateur?Archives of microbiology · 2026
    Review
  3. Article
  4. Co-infection withISME communications · 2026
    Article
  5. Genomic islands inNAR genomics and bioinformatics · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Genomic characterization of group BMicrobial genomics · 2025
    Article
  12. Review
  13. Genotypic and phenotypic analyses of two distinct sets ofJournal of medical microbiology · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Revisiting typing systems for group BMicrobial genomics · 2024
    Article
  19. Article
  20. Targeted deletion of Pf prophages from diverseJournal of bacteriology · 2024
    Article

137 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

19 authors at 5 institutions in 2 countries.

Craig WinstanleyDivision of Medical Microbiology and Genitourinary Medicine, University of Liverpool, Liverpool L69 3GA, United Kingdom.
Morgan G I Langille
Joanne L Fothergill
Irena Kukavica-Ibrulj
Catherine Paradis-Bleau
François Sanschagrin
Nicholas R Thomson
Geoff L Winsor
Michael A Quail
Nicola Lennard
Alexandra Bignell
Louise Clarke
Kathy Seeger
David Saunders
David Harris
Julian Parkhill
Robert E W Hancock
Fiona S L Brinkman
Roger C Levesque
Wellcome Sanger Institute · GBUniversité Laval · CASimon Fraser University · CAUniversity of Liverpool · GBUniversity of British Columbia · CA

Funding

Wellcome Trust
6 · The paper itself

Abstract

Pseudomonas aeruginosa isolates have a highly conserved core genome representing up to 90% of the total genomic sequence with additional variable accessory genes, many of which are found in genomic islands or islets. The identification of the Liverpool Epidemic Strain (LES) in a children's cystic fibrosis (CF) unit in 1996 and its subsequent observation in several centers in the United Kingdom challenged the previous widespread assumption that CF patients acquire only unique strains of P. aeruginosa from the environment. To learn about the forces that shaped the development of this important epidemic strain, the genome of the earliest archived LES isolate, LESB58, was sequenced. The sequence revealed the presence of many large genomic islands, including five prophage clusters, one defective (pyocin) prophage cluster, and five non-phage islands. To determine the role of these clusters, an unbiased signature tagged mutagenesis study was performed, followed by selection in the chronic rat lung infection model. Forty-seven mutants were identified by sequencing, including mutants in several genes known to be involved in Pseudomonas infection. Furthermore, genes from four prophage clusters and one genomic island were identified and in direct competition studies with the parent isolate; four were demonstrated to strongly impact on competitiveness in the chronic rat lung infection model. This strongly indicates that enhanced in vivo competitiveness is a major driver for maintenance and diversifying selection of these genomic prophage genes.

Indexed as

AnimalsDisease OutbreaksDrug Resistance, BacterialEnglandFimbriae ProteinsGenes, BacterialGenes, ViralGenome, BacterialHumansMultigene FamilyMutagenesisO AntigensProphagesPseudomonas aeruginosaPseudomonas InfectionsPseudomonas PhagesFimbriae ProteinsO Antigens

Identifiers

PMID19047519
PMCPMC2612960
OpenAlexW2165913026

What OpenQuestion holds

Textmetadata
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.