Evidence map›Paper›PMID 28765563›Full record

ArticleScientific reports2017

Quantitative Proteomics of Cerebrospinal Fluid in Paediatric Pneumococcal Meningitis.

Guadalupe Gómez-Baena, Richard J Bennett, Carmen Martínez-Rodríguez, Małgorzata Wnęk, Gavin Laing, Graeme Hickey, Lynn McLean, Robert J Beynon, Enitan D Carrol

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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  9. Role of Exosomes in Brain Diseases.Frontiers in cellular neuroscience · 2021
    Review
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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.

Guadalupe Gómez-BaenaCentre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, United Kingdom.
Richard J BennettCentre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, United Kingdom.
Carmen Martínez-RodríguezDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, United Kingdom.
Małgorzata WnękDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, United Kingdom.
Gavin LaingDepartment of Molecular Biology and Parasitology, School of Tropical Medicine, Liverpool, L3 5QA, United Kingdom.
Graeme HickeyDepartment of Biostatistics, Institute of Translational Medicine, Liverpool, L69 3BX, United Kingdom.ORCID 0000-0002-4989-0054
Lynn McLeanCentre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, United Kingdom.
Robert J BeynonCentre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, United Kingdom.
Enitan D CarrolDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, University of Liverpool, Liverpool, L69 7BE, United Kingdom. edcarrol@liverpool.ac.uk.

Funding

Medical Research Council MR/M009114/1Wellcome Trust 068026
6 · The paper itself

Abstract

Streptococcus pneumoniae is responsible for diseases causing major global public health problems, including meningitis, pneumonia and septicaemia. Despite recent advances in antimicrobial therapy, pneumococcal meningitis remains a life-threatening disease. Furthermore, long-term sequelae are a major concern for survivors. Hence, a better understanding of the processes occurring in the central nervous system is crucial to the development of more effective management strategies. We used mass spectrometry based quantitative proteomics to identify protein changes in cerebrospinal fluid from children with Streptococcus pneumoniae infection, compared with children admitted to hospital with bacterial meningitis symptoms but negative diagnosis. Samples were analysed, by label free proteomics, in two independent cohorts (cohort 1: cases (n = 8) and hospital controls (n = 4); cohort 2: cases (n = 8), hospital controls (n = 8)). Over 200 human proteins were differentially expressed in each cohort, of which 65% were common to both. Proteins involved in the immune response and exosome signalling were significantly enriched in the infected samples. For a subset of proteins derived from the proteome analysis, we corroborated the proteomics data in a third cohort (hospital controls (n = 15), healthy controls (n = 5), cases (n = 20)) by automated quantitative western blotting, with excellent agreement with our proteomics findings. Proteomics data are available via ProteomeXchange with identifier PXD004219.

Indexed as

AdolescentBlotting, WesternCerebrospinal FluidChildChild, PreschoolFemaleHumansInfantMaleMass SpectrometryMeningitis, PneumococcalProteomeProteomicsProteome

Identifiers

PMID28765563
PMCPMC5539295

What OpenQuestion holds

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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.