Evidence map›Paper›PMID 26579096›Full record

ReviewFrontiers in microbiology2015

Analyzing the molecular mechanism of lipoprotein localization in Brucella.

Shivani Goolab, Robyn L Roth, Henriette van Heerden, Michael C Crampton

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. TheAnnual review of microbiology · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Epitope-Based Vaccine of aFrontiers in immunology · 2021
    Article
  8. Article
  9. Frontiers in microbiology · 2020
    Article
  10. Journal of bacteriology · 2019
    Article
  11. Omp19 EnablesFrontiers in immunology · 2019
    Article
  12. Article
  13. 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

4 authors at 2 institutions in 1 country.

Shivani GoolabProtein Technologies, Biosciences, Council for Scientific and Industrial Research Pretoria, South Africa ; Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of Pretoria Pretoria, South Africa.
Robyn L RothProtein Technologies, Biosciences, Council for Scientific and Industrial Research Pretoria, South Africa.
Henriette van HeerdenDepartment of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of Pretoria Pretoria, South Africa.
Michael C CramptonProtein Technologies, Biosciences, Council for Scientific and Industrial Research Pretoria, South Africa.
Council for Scientific and Industrial Research · ZAUniversity of Pretoria · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial lipoproteins possess diverse structure and functionality, ranging from bacterial physiology to pathogenic processes. As such many lipoproteins, originating from Brucella are exploited as potential vaccines to countermeasure brucellosis infection in the host. These membrane proteins are translocated from the cytoplasm to the cell membrane where they are anchored peripherally by a multifaceted targeting mechanism. Although much research has focused on the identification and classification of Brucella lipoproteins and their potential use as vaccine candidates for the treatment of Brucellosis, the underlying route for the translocation of these lipoproteins to the outer surface of the Brucella (and other pathogens) outer membrane (OM) remains mostly unknown. This is partly due to the complexity of the organism and evasive tactics used to escape the host immune system, the variation in biological structure and activity of lipoproteins, combined with the complex nature of the translocation machinery. The biosynthetic pathway of Brucella lipoproteins involves a distinct secretion system aiding translocation from the cytoplasm, where they are modified by lipidation, sorted by the lipoprotein localization machinery pathway and thereafter equipped for export to the OM. Surface localized lipoproteins in Brucella may employ a lipoprotein flippase or the β-barrel assembly complex for translocation. This review provides an overview of the characterized Brucella OM proteins that form part of the OM, including a handful of other characterized bacterial lipoproteins and their mechanisms of translocation. Lipoprotein localization pathways in gram negative bacteria will be used as a model to identify gaps in Brucella lipoprotein localization and infer a potential pathway. Of particular interest are the dual topology lipoproteins identified in Escherichia coli and Haemophilus influenza. The localization and topology of these lipoproteins from other gram negative bacteria are well characterized and may be useful to infer a solution to better understand the translocation process in Brucella.

Indexed as

Brucella lipoproteinBrucella vaccine targetlipoprotein localizationlipoprotein secretionLol pathwayouter membrane proteinpathogen-associated molecular patternstoll-like receptors

Identifiers

PMID26579096
PMCPMC4623201
OpenAlexW2180873639

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.