Evidence map›Paper›PMID 23372719›Full record

ArticlePloS one2013

Proteomic biomarkers associated with Streptococcus agalactiae invasive genogroups.

Philippe Lanotte, Marylise Perivier, Eve Haguenoer, Laurent Mereghetti, Christophe Burucoa, Stéphane Claverol, Christo Atanassov

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Secretome analysis and virulence assessment inJournal of oral microbiology · 2024
    Article
  3. Automated classification of group BFrontiers in molecular biosciences · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Rapid Classification of Multilocus Sequence Subtype for Group BFrontiers in cellular and infection microbiology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Proteomic Analysis and Virulence Assessment ofFrontiers in cellular and infection microbiology · 2019
    Article
  13. Article
  14. Molecular epidemiology and distribution of serotypes, genotypes, and antibiotic resistance genes of Streptococcus agalactiae clinical isolates from Guelma, Algeria and Marseille, France.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2015
    Article
  15. 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

7 authors.

Philippe LanotteEquipe Bactéries et risque materno-fœtal, UMR 1282 ISP, Université François Rabelais de Tours, Tours, France.
Marylise Perivier
Eve Haguenoer
Laurent Mereghetti
Christophe Burucoa
Stéphane Claverol
Christo Atanassov

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Group B streptococcus (GBS, Streptococcus agalactiae) is a leading cause of meningitis and sepsis in newborns and an etiological agent of meningitis, endocarditis, osteoarticular and soft tissue infections in adults. GBS isolates are routinely clustered in serotypes and in genotypes. At present one GBS sequence type (i.e. ST17) is considered to be closely associated with bacterial invasiveness and novel proteomic biomarkers could make a valuable contribution to currently available GBS typing data. For that purpose we analyzed the protein profiles of 170 genotyped GBS isolates by Surface-Enhanced Laser Desorption/Ionization Time-of-Flight Mass Spectrometry (SELDI). Univariate statistical analysis of the SELDI profiles identified four protein biomarkers significantly discriminating ST17 isolates from those of the other sequence types. Two of these biomarkers (MW of 7878 Da and 12200 Da) were overexpressed and the other two (MW of 6258 Da and 10463 Da) were underexpressed in ST17. The four proteins were isolated by mass spectrometry-assisted purification and their tryptic peptides analyzed by LC-MS/MS. They were thereby identified as the small subunit of exodeoxyribonuclease VII, the 50S ribosomal protein L7/L12, a CsbD-like protein and thioredoxin, respectively. In conclusion, we identified four candidate biomarkers of ST17 by SELDI for high-throughput screening. These markers may serve as a basis for further studies on the pathophysiology of GBS infection, and for the development of novel vaccines.

Indexed as

AdultBacterial ProteinsBiomarkersCell Adhesion MoleculesChild, PreschoolExodeoxyribonucleasesHumansMeningitis, BacterialPhylogenyProteomicsRibosomal ProteinsSerotypingSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationStreptococcal InfectionsStreptococcus agalactiaeThioredoxinsBacterial ProteinsBiomarkersCell Adhesion MoleculesExodeoxyribonucleasesexodeoxyribonuclease VIIRibosomal ProteinsThioredoxins

Identifiers

PMID23372719
PMCPMC3553121

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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.