Evidence map›Paper›PMID 22624012›Full record

ArticlePloS one2012

Expression of an epitope-tagged virulence protein in Rickettsia parkeri using transposon insertion.

Matthew D Welch, Shawna C O Reed, Rebecca L Lamason, Alisa W Serio

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–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

16 citing papers in PubMed.

  1. Article
  2. Transformation and allelic exchange inbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. PathogenicJournal of bacteriology · 2024
    Review
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  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

4 authors.

Matthew D WelchDepartment of Molecular & Cell Biology, University of California, Berkeley, California, United States of America. welch@berkeley.edu
Shawna C O Reed
Rebecca L Lamason
Alisa W Serio

Funding

Manipulation of the actin cytoskeleton by spotted fever group RickettsiaR01AI074760 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI WELCH, MATTHEW D · 2007 to 2011
$1.8M
NIAID NIH HHS AI-074760NIAID NIH HHS R01 AI074760
6 · The paper itself

Abstract

Despite recent advances in our ability to genetically manipulate Rickettsia, little has been done to employ genetic tools to study the expression and localization of Rickettsia virulence proteins. Using a mariner-based Himar1 transposition system, we expressed an epitope-tagged variant of the actin polymerizing protein RickA under the control of its native promoter in Rickettsia parkeri, allowing the detection of RickA using commercially-available antibodies. Native RickA and epitope-tagged RickA exhibited similar levels of expression and were specifically localized to bacteria. To further facilitate protein expression in Rickettsia, we also developed a plasmid for Rickettsia insertion and expression (pRIE), containing a variant Himar1 transposon with enhanced flexibility for gene insertion, and used it to generate R. parkeri strains expressing diverse fluorescent proteins. Expression of epitope-tagged proteins in Rickettsia will expand our ability to assess the regulation and function of important virulence factors.

Indexed as

AnimalsBacterial ProteinsChlorocebus aethiopsFluorescent Antibody TechniqueGene Expression Regulation, BacterialImmunoblottingMicroscopy, FluorescencePhysical Chromosome MappingPlasmidsRickettsiaVero CellsVirulence FactorsBacterial ProteinsRickA protein, RickettsiaVirulence Factors

Identifiers

PMID22624012
PMCPMC3356282

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.