Evidence map›Paper›PMID 22195037›Full record

ArticlePloS one2011

Phenotypic and genome-wide analysis of an antibiotic-resistant small colony variant (SCV) of Pseudomonas aeruginosa.

Qing Wei, Saeed Tarighi, Andreas Dötsch, Susanne Häussler, Mathias Müsken, Victoria J Wright, Miguel Cámara, Paul Williams, Steven Haenen, Bart Boerjan and 10 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 129 citations in OpenAlex.

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  9. The Building Blocks of Antimicrobial Resistance inFrontiers in cellular and infection microbiology · 2021
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  13. Selection and dissemination of antimicrobial resistance in Agri-food production.Antimicrobial resistance and infection control · 2019
    Review
  14. Commentary: Tolerance and Resistance ofFrontiers in microbiology · 2019
    Article
  15. Article
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  19. Article
  20. Frontiers in cellular and infection microbiology · 2017
    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

20 authors at 6 institutions in 4 countries.

Qing WeiResearch Group Microbiology, VIB Department of Structural Biology, Vrije Universiteit Brussel, Brussels, Belgium.
Saeed Tarighi
Andreas Dötsch
Susanne Häussler
Mathias Müsken
Victoria J Wright
Miguel Cámara
Paul Williams
Steven Haenen
Bart Boerjan
Annelies Bogaerts
Evy Vierstraete
Peter Verleyen
Liliane Schoofs
Ronnie Willaert
Valérie N De Groote
Jan Michiels
Ken Vercammen
Aurélie Crabbé
Pierre Cornelis
KU Leuven · BEVrije Universiteit Brussel · BEUniversity of Nottingham · GBHelmholtz Centre for Infection Research · DEArizona State University · USCenter for Experimental and Clinical Infection Research · DE

Funding

Biotechnology and Biological Sciences Research Council BB/F014392/1Biotechnology and Biological Sciences Research Council BBF0143921
6 · The paper itself

Abstract

backgroundSmall colony variants (SCVs) are slow-growing bacteria, which often show increased resistance to antibiotics and cause latent or recurrent infections. It is therefore important to understand the mechanisms at the basis of this phenotypic switch. METHODOLOGY/PRINCIPAL

findingsOne SCV (termed PAO-SCV) was isolated, showing high resistance to gentamicin and to the cephalosporine cefotaxime. PAO-SCV was prone to reversion as evidenced by emergence of large colonies with a frequency of 10(-5) on media without antibiotics while it was stably maintained in presence of gentamicin. PAO-SCV showed a delayed growth, defective motility, and strongly reduced levels of the quorum sensing Pseudomonas quinolone signal (PQS). Whole genome expression analysis further suggested a multi-layered antibiotic resistance mechanism, including simultaneous over-expression of two drug efflux pumps (MexAB-OprM, MexXY-OprM), the LPS modification operon arnBCADTEF, and the PhoP-PhoQ two-component system. Conversely, the genes for the synthesis of PQS were strongly down-regulated in PAO-SCV. Finally, genomic analysis revealed the presence of mutations in phoP and phoQ genes as well as in the mexZ gene encoding a repressor of the mexXY and mexAB-oprM genes. Only one mutation occurred only in REV, at nucleotide 1020 of the tufA gene, a paralog of tufB, both encoding the elongation factor Tu, causing a change of the rarely used aspartic acid codon GAU to the more common GAC, possibly causing an increase of tufA mRNA translation. High expression of phoP and phoQ was confirmed for the SCV variant while the revertant showed expression levels reduced to wild-type levels.

conclusionsBy combining data coming from phenotypic, gene expression and proteome analysis, we could demonstrate that resistance to aminoglycosides in one SCV mutant is multifactorial including overexpression of efflux mechanisms, LPS modification and is accompanied by a drastic down-regulation of the Pseudomonas quinolone signal quorum sensing system.

Indexed as

Anti-Bacterial AgentsBacterial ProteinsColony Count, MicrobialDown-RegulationDrug Resistance, BacterialGene Expression ProfilingGene Expression Regulation, BacterialGenes, BacterialGenetic VariationGenome, BacterialGentamicinsMicrobial Sensitivity TestsOligonucleotide Array Sequence AnalysisPhenotypeProteomePseudomonas aeruginosa2-heptyl-3-hydroxy-4-quinoloneAnti-Bacterial AgentsBacterial ProteinsGentamicinsProteomeQuinolones

Identifiers

PMID22195037
PMCPMC3240657
OpenAlexW2151795920

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.