Evidence map›Paper›PMID 27144565›Full record

ArticleInternational journal of molecular sciences2016

Comprehensive Identification of Immunodominant Proteins of Brucella abortus and Brucella melitensis Using Antibodies in the Sera from Naturally Infected Hosts.

Gamal Wareth, Murat Eravci, Christoph Weise, Uwe Roesler, Falk Melzer, Lisa D Sprague, Heinrich Neubauer, Jayaseelan Murugaiyan

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 6% 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.

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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. A Dual, Systematic Approach to Malaria Diagnostic Biomarker Discovery.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Comparative proteomics ofOne health (Amsterdam, Netherlands) · 2021
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Proteomics ofMicroorganisms · 2020
    Article
  14. Proteomics of Brucella.Proteomes · 2020
    Review
  15. Isolate Specific Cold Response ofFrontiers in microbiology · 2019
    Article
  16. Proteogenomic Analysis and Discovery of Immune Antigens inMolecular & cellular proteomics : MCP · 2017
    Article
  17. 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 2 institutions in 2 countries.

Gamal WarethInstitute of Animal Hygiene and Environmental Health, Centre for Infectious Medicine, Freie Universität Berlin, Robert-von-Ostertag-Str. 7-13, Berlin 14163, Germany. Gamal.Wareth@fli.bund.de.
Murat EravciInstitute of Chemistry and Biochemistry, Freie Universität Berlin, Thielallee 63, Berlin 14195, Germany. eravci@zedat.fu-berlin.de.
Christoph WeiseInstitute of Chemistry and Biochemistry, Freie Universität Berlin, Thielallee 63, Berlin 14195, Germany. chris.weise@biochemie.fu-berlin-de.
Uwe RoeslerInstitute of Animal Hygiene and Environmental Health, Centre for Infectious Medicine, Freie Universität Berlin, Robert-von-Ostertag-Str. 7-13, Berlin 14163, Germany. Uwe.Roesler@fu-berlin.de.
Falk MelzerFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Bacterial Infections and Zoonoses, Naumburger Str. 96a, Jena 07743, Germany. Falk.Melzer@fli.bund.de.
Lisa D SpragueFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Bacterial Infections and Zoonoses, Naumburger Str. 96a, Jena 07743, Germany. Lisa.Sprague@fli.bund.de.
Heinrich NeubauerFriedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Bacterial Infections and Zoonoses, Naumburger Str. 96a, Jena 07743, Germany. Heinrich.Neubauer@fli.bund.de.
Jayaseelan MurugaiyanInstitute of Animal Hygiene and Environmental Health, Centre for Infectious Medicine, Freie Universität Berlin, Robert-von-Ostertag-Str. 7-13, Berlin 14163, Germany. jayaseelan.murugaiyan@fu-berlin.de.
Freie Universität Berlin · DEFriedrich-Loeffler-Institut · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brucellosis is a debilitating zoonotic disease that affects humans and animals. The diagnosis of brucellosis is challenging, as accurate species level identification is not possible with any of the currently available serology-based diagnostic methods. The present study aimed at identifying Brucella (B.) species-specific proteins from the closely related species B. abortus and B. melitensis using sera collected from naturally infected host species. Unlike earlier reported investigations with either laboratory-grown species or vaccine strains, in the present study, field strains were utilized for analysis. The label-free quantitative proteomic analysis of the naturally isolated strains of these two closely related species revealed 402 differentially expressed proteins, among which 63 and 103 proteins were found exclusively in the whole cell extracts of B. abortus and B. melitensis field strains, respectively. The sera from four different naturally infected host species, i.e., cattle, buffalo, sheep, and goat were applied to identify the immune-binding protein spots present in the whole protein extracts from the isolated B. abortus and B. melitensis field strains and resolved on two-dimensional gel electrophoresis. Comprehensive analysis revealed that 25 proteins of B. abortus and 20 proteins of B. melitensis were distinctly immunoreactive. Dihydrodipicolinate synthase, glyceraldehyde-3-phosphate dehydrogenase and lactate/malate dehydrogenase from B. abortus, amino acid ABC transporter substrate-binding protein from B. melitensis and fumarylacetoacetate hydrolase from both species were reactive with the sera of all the tested naturally infected host species. The identified proteins could be used for the design of serological assays capable of detecting pan-Brucella, B. abortus- and B. melitensis-specific antibodies.

Indexed as

AnimalsAntibodiesAntigens, BacterialBacterial ProteinsBlotting, WesternBrucella abortusBrucella melitensisBrucellosis, BovineCattleChromatography, High Pressure LiquidElectrophoresis, Gel, Two-DimensionalGlyceraldehyde-3-Phosphate DehydrogenasesHydro-LyasesProteomeSpectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization4-hydroxy-tetrahydrodipicolinate synthaseAntibodiesAntigens, BacterialBacterial ProteinsGlyceraldehyde-3-Phosphate DehydrogenasesHydro-LyasesProteome2D-PAGEBrucellahost specificityLiquid chromatography–mass spectrometry (LC-MS)mass spectrometryMatrix-assisted laser desorption/ionization-Tine of Flight-Mass Spectrometry MALDI-TOF MSproteomicstwo dimensional electrophoresisWestern blot

Identifiers

PMID27144565
PMCPMC4881485
OpenAlexW2344372525

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.