Evidence map›Paper›PMID 26696268›Full record

ArticlePloS one2015

Escherichia coli under Ionic Silver Stress: An Integrative Approach to Explore Transcriptional, Physiological and Biochemical Responses.

Claire Saulou-Bérion, Ignacio Gonzalez, Brice Enjalbert, Jean-Nicolas Audinot, Isabelle Fourquaux, Frédéric Jamme, Muriel Cocaign-Bousquet, Muriel Mercier-Bonin, Laurence Girbal

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. The good, the bad, and the ugly of metals as antimicrobials.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2024
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Silver and Antibiotic, New Facts to an Old Story.Antibiotics (Basel, Switzerland) · 2018
    Review
  9. Article
  10. Toxicity of Food-Grade TiOFrontiers in microbiology · 2018
    Article
  11. 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

9 authors.

Claire Saulou-BérionUniversité de Toulouse, INSA, UPS, INPT, LISBP, Toulouse, France.
Ignacio GonzalezUniversité de Toulouse, INSA, UPS, INPT, LISBP, Toulouse, France.
Brice EnjalbertUniversité de Toulouse, INSA, UPS, INPT, LISBP, Toulouse, France.
Jean-Nicolas AudinotLuxembourg Institute of Science and Technology (LIST), Material Research & Technology Department (MRT), Belvaux, Luxembourg.
Isabelle FourquauxFaculté de Médecine Rangueil, Centre de Microscopie Electronique Appliquée à la Biologie (CMEAB), Toulouse Cedex, France.
Frédéric JammeINRA, UAR1008, CEPIA, Nantes, France.
Muriel Cocaign-BousquetUniversité de Toulouse, INSA, UPS, INPT, LISBP, Toulouse, France.
Muriel Mercier-BoninUniversité de Toulouse, INSA, UPS, INPT, LISBP, Toulouse, France.
Laurence GirbalUniversité de Toulouse, INSA, UPS, INPT, LISBP, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For a better understanding of the systemic effect of sub-lethal micromolar concentrations of ionic silver on Escherichia coli, we performed a multi-level characterization of cells under Ag+-mediated stress using an integrative biology approach combining physiological, biochemical and transcriptomic data. Physiological parameters, namely bacterial growth and survival after Ag+ exposure, were first quantified and related to the accumulation of intracellular silver, probed for the first time by nano secondary ion mass spectroscopy at sub-micrometer lateral resolution. Modifications in E. coli biochemical composition were evaluated under Ag+-mediated stress by in situ synchrotron Fourier-transform infrared microspectroscopy and a comprehensive transcriptome response was also determined. Using multivariate statistics, correlations between the physiological parameters, the extracellular concentration of AgNO3 and the intracellular silver content, gene expression profiles and micro-spectroscopic data were investigated. We identified Ag+-dependent regulation of gene expression required for growth (e.g. transporter genes, transcriptional regulators, ribosomal proteins), for ionic silver transport and detoxification (e.g. copA, cueO, mgtA, nhaR) and for coping with various types of stress (dnaK, pspA, metA,R, oxidoreductase genes). The silver-induced shortening of the acyl chain of fatty acids, mostly encountered in cell membrane, was highlighted by microspectroscopy and correlated with the down-regulated expression of genes involved in fatty acid transport (fadL) and synthesis/modification of lipid A (lpxA and arnA). The increase in the disordered secondary structure of proteins in the presence of Ag+ was assessed through the conformational shift shown for amides I and II, and further correlated with the up-regulated expression of peptidase (hfq) and chaperone (dnaJ), and regulation of transpeptidase expression (ycfS and ycbB). Interestingly, as these transpeptidases act on the structural integrity of the cell wall, regulation of their expression may explain the morphological damage reported under Ag+-mediated stress. This result clearly demonstrates that the cell membrane is a key target of ionic silver.

Indexed as

Escherichia coli K12Escherichia coli ProteinsGene Expression Regulation, BacterialSilverSilver NitrateStress, PhysiologicalTranscription, GeneticEscherichia coli ProteinsSilverSilver Nitrate

Identifiers

PMID26696268
PMCPMC4699211

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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.