Evidence map›Paper›PMID 10816464›Full record

ArticleInfection and immunity2000

Identification of an immunodominant ABC transporter in methicillin-resistant Staphylococcus aureus infections.

J P Burnie, R C Matthews, T Carter, E Beaulieu, M Donohoe, C Chapman, P Williamson, S J Hodgetts

Registry-linked trialAbstract read
In one paragraph

Article in Infection and immunity, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00217841 (A Multi Centre, Double-Blind, Randomised, Placebo Controlled Prospective Study on the Safety and Efficacy of Aurograb in Patients With Severe, Deep-Seated Staphylococcal Infections Receiving Vancomycin), which is not on this map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.3field-weighted citation impact, top 20% 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.

NCT00217841 phase3completednot on this mapstarted 2004, after this paper: background citation

A Multi Centre, Double-Blind, Randomised, Placebo Controlled Prospective Study on the Safety and Efficacy of Aurograb in Patients With Severe, Deep-Seated Staphylococcal Infections Receiving Vancomycin

TypeinterventionalSponsorNeuTec PharmaRan2004 to 2006Enrolled180ConditionsStaphylococcal InfectionsArmsAurograb
3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 81 citations in OpenAlex.

  1. Methicillin-resistantCurrent pharmaceutical biotechnology · 2025
    Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Phenol-soluble modulins and staphylococcal infection.Nature reviews. Microbiology · 2013
    Review
  16. Will there ever be a universal Staphylococcus aureus vaccine?Human vaccines & immunotherapeutics · 2013
    Article
  17. Article
  18. Article
  19. Article
  20. 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 at 1 institution in 1 country.

J P BurnieNeuTec Pharma plc, University of Manchester, Central Manchester Healthcare Trust, Manchester M13 9WL, United Kingdom.
R C Matthews
T Carter
E Beaulieu
M Donohoe
C Chapman
P Williamson
S J Hodgetts
University of Manchester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunoblotting sera from 26 patients with septicemia due to an epidemic strain of methicillin-resistant Staphylococcus aureus (EMRSA-15), 6 of whom died, revealed an immunodominant EMRSA-15 antigen at 61 kDa. There was a statistically significant correlate (P < 0.001) between survival and immunoglobulin G to the 61-kDa band. The antigen was identified by sequencing positive clones obtained by screening a genomic expression library of EMRSA-15 with pooled sera from patients taken after the septicemic episode. Eluted antibody reacted with the 61-kDa antigen on immunoblots. The amino terminus was obtained by searching the S. aureus NCTC 8325 and MRSA strain COL databases, and the whole protein was expressed in Escherichia coli TOP 10F'. The derived amino acid sequence showed homology with ABC transporters, with paired Walker A and Walker B motifs and 73% homology to YkpA from Bacillus subtilis. Epitope mapping of the derived amino acid sequence with sera from patients who had recovered from EMRSA-15 septicemia delineated seven epitopes. Three of these epitopes, represented by peptides 1 (KIKVYVGNYDFWYQS), 2 (TVIVVSHDRHFLYNNV), and 3 (TETFLRGFLGRMLFS), were synthesized and used to isolate human recombinant antibodies from a phage antibody display library. Recombinant antibodies against peptides 1 and 2 gave logarithmic reductions in organ colony counts, compared with control groups, in a mouse model of the infection. This study suggests the potential role of an ABC transporter as a target for immunotherapy.

Indexed as

Antigens, BacterialImmunodominant EpitopesMethicillin ResistanceAmino Acid SequenceAnimalsAntibodies, BacterialATP-Binding Cassette TransportersBacteremiaDisease OutbreaksEpitope MappingFemaleGenes, BacterialHumansImmunoblottingKidneyLiverAntibodies, BacterialAntigens, BacterialATP-Binding Cassette TransportersImmunodominant EpitopesRecombinant Proteins

Identifiers

PMID10816464
PMCPMC97562
OpenAlexW2137334317

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.