Evidence map›Paper›PMID 19654871›Full record

ArticlePloS one2009

Immunogenic Burkholderia pseudomallei outer membrane proteins as potential candidate vaccine targets.

Yuka Hara, Rahmah Mohamed, Sheila Nathan

Abstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Antibodies toMicroorganisms · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Infection and drug resistance · 2025
    Review
  8. Review
  9. Article
  10. Vaccines · 2024
    Review
  11. Article
  12. Vaccinomics to Design a Multi-Epitopes Vaccine forInternational journal of environmental research and public health · 2022
    Article
  13. Article
  14. Recent Progress inPathogens (Basel, Switzerland) · 2021
    Review
  15. Article
  16. Use of RecombinantPathogens (Basel, Switzerland) · 2021
    Article
  17. Review
  18. Article
  19. Evaluation of the Whole Proteome ofFrontiers in medicine · 2021
    Article
  20. Current Advances inCells · 2020
    Review
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

3 authors.

Yuka HaraMalaysia Genome Institute, UKM-MTDC Smart Technology Centre, Bangi, Selangor, Malaysia.
Rahmah Mohamed
Sheila Nathan

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBurkholderia pseudomallei is the causative agent of melioidosis, a disease of significant morbidity and mortality in both human and animals in endemic areas. There is no vaccine towards the bacterium available in the market, and the efficacy of many of the bacterium's surface and secreted proteins are currently being evaluated as vaccine candidates. METHODOLOGY/PRINCIPAL

findingsWith the availability of the B. pseudomallei whole genome sequence, we undertook to identify genes encoding the known immunogenic outer membrane protein A (OmpA). Twelve OmpA domains were identified and ORFs containing these domains were fully annotated. Of the 12 ORFs, two of these OmpAs, Omp3 and Omp7, were successfully cloned, expressed as soluble protein and purified. Both proteins were recognised by antibodies in melioidosis patients' sera by Western blot analysis. Purified soluble fractions of Omp3 and Omp7 were assessed for their ability to protect BALB/c mice against B. pseudomallei infection. Mice were immunised with either Omp3 or Omp7, subsequently challenged with 1x10(6) colony forming units (cfu) of B. pseudomallei via the intraperitoneal route, and examined daily for 21 days post-challenge. This pilot study has demonstrated that whilst all control unimmunised mice died by day 9 post-challenge, two mice (out of 4) from both immunised groups survived beyond 21 days post-infection. CONCLUSIONS/SIGNIFICANCE: We have demonstrated that B. pseudomallei OmpA proteins are immunogenic in mice as well as melioidosis patients and should be further assessed as potential vaccine candidates against B. pseudomallei infection.

Indexed as

Bacterial VaccinesAmino Acid SequenceAnimalsAntibodies, BacterialBacterial Outer Membrane ProteinsBlotting, WesternBurkholderia pseudomalleiGenome, BacterialHumansMelioidosisMiceMice, Inbred BALB CMolecular Sequence DataPilot ProjectsSequence Homology, Amino AcidAntibodies, BacterialBacterial Outer Membrane ProteinsBacterial Vaccines

Identifiers

PMID19654871
PMCPMC2716516

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.