Evidence map›Paper›PMID 25166615›Full record

ArticlePloS one2014

Levels of alpha-toxin correlate with distinct phenotypic response profiles of blood mononuclear cells and with agr background of community-associated Staphylococcus aureus isolates.

Srikanth Mairpady Shambat, Axana Haggar, Francois Vandenesch, Gerard Lina, Willem J B van Wamel, Gayathri Arakere, Mattias Svensson, Anna Norrby-Teglund

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Virulence · 2026
    Article
  2. Article
  3. Mucosa-Associated Invariant T Cell Hypersensitivity toJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Oncoimmunology · 2020
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. 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

8 authors.

Srikanth Mairpady ShambatKarolinska Institutet, Centre for Infectious Medicine, Stockholm, Sweden.
Axana HaggarKarolinska Institutet, Centre for Infectious Medicine, Stockholm, Sweden.
Francois VandeneschCIRI, International Center for Infectiology Research, LabEx Ecofect, Université Lyon 1, Inserm U1111, Ecole Normale Supérieure de Lyon, CNRS UMR5308, Centre National de Référence des Staphylocoques, Hospices civils de Lyon, Lyon, France.
Gerard LinaCIRI, International Center for Infectiology Research, LabEx Ecofect, Université Lyon 1, Inserm U1111, Ecole Normale Supérieure de Lyon, CNRS UMR5308, Centre National de Référence des Staphylocoques, Hospices civils de Lyon, Lyon, France.
Willem J B van WamelDepartment of Medical Microbiology and Infectious Diseases, Erasmus Medical Centre, Rotterdam, Netherlands.
Gayathri ArakereSociety for Innovation and Development, Indian Institute of Science Campus, Bangalore, India.
Mattias SvenssonKarolinska Institutet, Centre for Infectious Medicine, Stockholm, Sweden.
Anna Norrby-TeglundKarolinska Institutet, Centre for Infectious Medicine, Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidemiological studies of Staphylococcus aureus have shown a relation between certain clones and the presence of specific virulence genes, but how this translates into virulence-associated functional responses is not fully elucidated. Here we addressed this issue by analyses of community-acquired S. aureus strains characterized with respect to antibiotic resistance, ST types, agr types, and virulence gene profiles. Supernatants containing exotoxins were prepared from overnight bacterial cultures, and tested in proliferation assays using human peripheral blood mononuclear cells (PBMC). The strains displayed stable phenotypic response profiles, defined by either a proliferative or cytotoxic response. Although, virtually all strains elicited superantigen-mediated proliferative responses, the strains with a cytotoxic profile induced proliferation only in cultures with the most diluted supernatants. This indicated that the superantigen-response was masked by a cytotoxic effect which was also confirmed by flow cytometry analysis. The cytotoxic supernatants contained significantly higher levels of α-toxin than did the proliferative supernatants. Addition of α-toxin to supernatants characterized as proliferative switched the response into cytotoxic profiles. In contrast, no effect of Panton Valentine Leukocidin, δ-toxin or phenol soluble modulin α-3 was noted in the proliferative assay. Furthermore, a significant association between agr type and phenotypic profile was found, where agrII and agrIII strains had predominantly a proliferative profile whereas agrI and IV strains had a predominantly cytotoxic profile. The differential response profiles associated with specific S. aureus strains with varying toxin production could possibly have an impact on disease manifestations, and as such may reflect specific pathotypes.

Indexed as

Bacterial ToxinsCell ProliferationCommunity-Acquired InfectionsDrug Resistance, BacterialFlow CytometryHumansLeukocytes, MononuclearPhenotypeStaphylococcal InfectionsStaphylococcus aureusSuperantigensBacterial ToxinsSuperantigens

Identifiers

PMID25166615
PMCPMC4148398

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.