Evidence map›Paper›PMID 22479512›Full record

ArticlePloS one2012

Identification of chromosomal genes in Yersinia pestis that influence type III secretion and delivery of Yops into target cells.

Andrew S Houppert, Elizabeth Kwiatkowski, Elizabeth M Glass, Kristin L DeBord, Peter M Merritt, Olaf Schneewind, Melanie M Marketon

Open access · goldAbstract 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Regulation of the Yersinia type III secretion system: traffic control.Frontiers in cellular and infection microbiology · 2013
    Review
  8. Review
  9. 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

7 authors at 3 institutions in 1 country.

Andrew S HouppertDepartment of Biology, Indiana University, Bloomington, Indiana, United States of America.
Elizabeth Kwiatkowski
Elizabeth M Glass
Kristin L DeBord
Peter M Merritt
Olaf Schneewind
Melanie M Marketon
Indiana University Bloomington · USUniversity of Chicago · USArgonne National Laboratory · US

Funding

Vaccines and Therapies Against BotulismU54AI057153 · NIAID · UNIVERSITY OF CHICAGO · PI CROSSON, SEAN · 2003 to 2013
$87.6M
Yersinia Type III Transport of Yop Proteins into Immune CellsR01AI042797 · NIAID · UNIVERSITY OF CHICAGO · PI SCHNEEWIND, OLAF · 1998 to 2013
$4.3M
The Type III Pathway of Yersinia PestisR03AI055545 · NIAID · UNIVERSITY OF CHICAGO · PI SCHNEEWIND, OLAF · 2003 to 2004
$153k
NIAID NIH HHS 1-U54-AI-057153NIAID NIH HHS AI055545NIAID NIH HHS AI42797NIAID NIH HHS R01 AI042797NIAID NIH HHS R03 AI055545NIAID NIH HHS U54 AI057153
6 · The paper itself

Abstract

Pathogenic Yersinia species possess a type III secretion system, which is required for the delivery of effector Yop proteins into target cells during infection. Genes encoding the type III secretion machinery, its substrates, and several regulatory proteins all reside on a 70-Kb virulence plasmid. Genes encoded in the chromosome of yersiniae are thought to play important roles in bacterial perception of host environments and in the coordinated activation of the type III secretion pathway. Here, we investigate the contribution of chromosomal genes to the complex regulatory process controlling type III secretion in Yersinia pestis. Using transposon mutagenesis, we identified five chromosomal genes required for expression or secretion of Yops in laboratory media. Four out of the five chromosomal mutants were defective to various extents at injecting Yops into tissue culture cells. Interestingly, we found one mutant that was not able to secrete in vitro but was fully competent for injecting Yops into host cells, suggesting independent mechanisms for activation of the secretion apparatus. When tested in a mouse model of plague disease, three mutants were avirulent, whereas two strains were severely attenuated. Together these results demonstrate the importance of Y. pestis chromosomal genes in the proper function of type III secretion and in the pathogenesis of plague.

Indexed as

Gene Expression Regulation, BacterialAnimalsBacterial Outer Membrane ProteinsChromosomes, BacterialDNA Transposable ElementsFemaleGenetic Complementation TestHeLa CellsHumansMiceMice, Inbred BALB CMutagenesisMutationPhenotypeTemperatureTrimethoprimBacterial Outer Membrane ProteinsDNA Transposable ElementsTrimethoprim

Identifiers

PMID22479512
PMCPMC3316589
OpenAlexW2042923189

What OpenQuestion holds

Textmetadata
LicenceCC0
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.