Evidence map›Paper›PMID 26401445›Full record

ArticlePeerJ2015

Comparative genomics of non-pseudomonal bacterial species colonising paediatric cystic fibrosis patients.

Kate L Ormerod, Narelle M George, James A Fraser, Claire Wainwright, Philip Hugenholtz

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Pathogens (Basel, Switzerland) · 2021
    Review
  3. Genes · 2021
    Review
  4. Antimicrobial agents and chemotherapy · 2020
    Review
  5. Genomic information on Stenotrophomonas maltophilia ST264 isolated from a cystic fibrosis pediatric patient in Brazil.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2020
    Article
  6. Article
  7. Article
  8. Emergence and spread of worldwideInfection and drug resistance · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Evolution ofFrontiers in microbiology · 2017
    Article
  14. Article
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

5 authors at 2 institutions in 1 country.

Kate L OrmerodAustralian Infectious Diseases Research Centre, School of Chemistry and Molecular Biosciences, University of Queensland , Brisbane, Queensland , Australia.
Narelle M GeorgeHealth Support Queensland, Department of Health, Queensland Government , Herston, Queensland , Australia.
James A FraserAustralian Infectious Diseases Research Centre, School of Chemistry and Molecular Biosciences, University of Queensland , Brisbane, Queensland , Australia.
Claire WainwrightSchool of Medicine, University of Queensland , Brisbane, Queensland , Australia ; Department of Respiratory and Sleep Medicine, Lady Cilento Children's Hospital , South Brisbane, Queensland , Australia ; Queensland Children's Medical Research Insitute , Herston, Queensland , Australia.
Philip HugenholtzAustralian Infectious Diseases Research Centre, School of Chemistry and Molecular Biosciences, University of Queensland , Brisbane, Queensland , Australia ; Australian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, University of Queensland , Brisbane, Queensland , Australia.
University of Queensland · AUQueensland Government · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genetic disorder cystic fibrosis is a life-limiting condition affecting ∼70,000 people worldwide. Targeted, early, treatment of the dominant infecting species, Pseudomonas aeruginosa, has improved patient outcomes; however, there is concern that other species are now stepping in to take its place. In addition, the necessarily long-term antibiotic therapy received by these patients may be providing a suitable environment for the emergence of antibiotic resistance. To investigate these issues, we employed whole-genome sequencing of 28 non-Pseudomonas bacterial strains isolated from three paediatric patients. We did not find any trend of increasing antibiotic resistance (either by mutation or lateral gene transfer) in these isolates in comparison with other examples of the same species. In addition, each isolate contained a virulence gene repertoire that was similar to other examples of the relevant species. These results support the impaired clearance of the CF lung not demanding extensive virulence for survival in this habitat. By analysing serial isolates of the same species we uncovered several examples of strain persistence. The same strain of Staphylococcus aureus persisted for nearly a year, despite administration of antibiotics to which it was shown to be sensitive. This is consistent with previous studies showing antibiotic therapy to be inadequate in cystic fibrosis patients, which may also explain the lack of increasing antibiotic resistance over time. Serial isolates of two naturally multi-drug resistant organisms, Achromobacter xylosoxidans and Stenotrophomonas maltophilia, revealed that while all S. maltophilia strains were unique, A. xylosoxidans persisted for nearly five years, making this a species of particular concern. The data generated by this study will assist in developing an understanding of the non-Pseudomonas species associated with cystic fibrosis.

Indexed as

Antibiotic resistanceComparative genomicsCystic fibrosisHost adaptationLateral gene transferMicroevolutionSerial isolates

Identifiers

PMID26401445
PMCPMC4579023
OpenAlexW1901808137

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.