Evidence map›Paper›PMID 28273168›Full record

ArticlePloS one2017

Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis.

Laura J Sherrard, Anna S Tai, Bryan A Wee, Kay A Ramsay, Timothy J Kidd, Nouri L Ben Zakour, David M Whiley, Scott A Beatson, Scott C Bell

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Clearance of hypermutator XDRASM case reports · 2026
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  11. β-lactam Resistance inPathogens (Basel, Switzerland) · 2021
    Review
  12. A panel of diverseJAC-antimicrobial resistance · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Laura J SherrardLung Bacteria Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Anna S TaiLung Bacteria Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Bryan A WeeSchool of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia.
Kay A RamsayLung Bacteria Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Timothy J KiddSchool of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia.
Nouri L Ben ZakourSchool of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia.
David M WhileyUQ Centre for Clinical Research, The University of Queensland, Brisbane, QLD, Australia.
Scott A BeatsonSchool of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia.
Scott C BellLung Bacteria Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A Pseudomonas aeruginosa AUST-02 strain sub-type (M3L7) has been identified in Australia, infects the lungs of some people with cystic fibrosis and is associated with antibiotic resistance. Multiple clonal lineages may emerge during treatment with mutations in chromosomally encoded antibiotic resistance genes commonly observed. Here we describe the within-host diversity and antibiotic resistance of M3L7 during and after antibiotic treatment of an acute pulmonary exacerbation using whole genome sequencing and show both variation and shared mutations in important genes. Eleven isolates from an M3L7 population (n = 134) isolated over 3 months from an individual with cystic fibrosis underwent whole genome sequencing. A phylogeny based on core genome SNPs identified three distinct phylogenetic groups comprising two groups with higher rates of mutation (hypermutators) and one non-hypermutator group. Genomes were screened for acquired antibiotic resistance genes with the result suggesting that M3L7 resistance is principally driven by chromosomal mutations as no acquired mechanisms were detected. Small genetic variations, shared by all 11 isolates, were found in 49 genes associated with antibiotic resistance including frame-shift mutations (mexA, mexT), premature stop codons (oprD, mexB) and mutations in quinolone-resistance determining regions (gyrA, parE). However, whole genome sequencing also revealed mutations in 21 genes that were acquired following divergence of groups, which may also impact the activity of antibiotics and multi-drug efflux pumps. Comparison of mutations with minimum inhibitory concentrations of anti-pseudomonal antibiotics could not easily explain all resistance profiles observed. These data further demonstrate the complexity of chronic and antibiotic resistant P. aeruginosa infection where a multitude of co-existing genotypically diverse sub-lineages might co-exist during and after intravenous antibiotic treatment.

Indexed as

Genome, BacterialAdultAnti-Bacterial AgentsChromosome MappingCystic FibrosisDrug Resistance, MicrobialFrameshift MutationHigh-Throughput Nucleotide SequencingHumansMaleMicrobial Sensitivity TestsPhylogenyPseudomonas aeruginosaPseudomonas InfectionsQuinolonesSequence Analysis, DNAAnti-Bacterial AgentsQuinolones

Identifiers

PMID28273168
PMCPMC5342179

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.