Evidence map›Paper›PMID 15342597›Full record

ArticleJournal of bacteriology2004

A novel mutation within the central Listeria monocytogenes regulator PrfA that results in constitutive expression of virulence gene products.

Kendy K Y Wong, Nancy E Freitag

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

45 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Listeria monocytogenes: from a saprophytic to a cytosolic virulent pathogen.World journal of microbiology & biotechnology · 2025
    Review
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  7. Regulation ofMicrobiology spectrum · 2019
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  8. Switching Lifestyles Is anFrontiers in cellular and infection microbiology · 2019
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  12. Article
  13. Stochastic and Differential Activation of σFrontiers in microbiology · 2017
    Article
  14. Article
  15. Article
  16. Article
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  18. Article
  19. Article
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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

2 authors at 1 institution in 1 country.

Kendy K Y WongSeattle Biomedical Research Institute, 307 Westlake Ave. N., Suite 500, Seattle, WA 98109-5219, USA.
Nancy E Freitag
University of Washington · US

Funding

Listeria Virulence Gene Expression Within Host CellsR01AI041816 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FREITAG, NANCY ELIZABETH · 2001 to 2010
$3.9M
Listeria virulence gene expression within host cellsR56AI041816 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FREITAG, NANCY ELIZABETH · 2012 to 2012
$399k
LISTERIA VIRULENCE GENE EXPRESSION WITHIN HOST CELLSR29AI041816 · NIAID · WAYNE STATE UNIVERSITY · PI FREITAG, NANCY · 1997 to 2001
$253k
NIAID NIH HHS AI41816NIAID NIH HHS R01 AI041816NIAID NIH HHS R29 AI041816NIAID NIH HHS R56 AI041816
6 · The paper itself

Abstract

The PrfA protein of Listeria monocytogenes functions as a key regulatory factor for the coordinated expression of many virulence genes during bacterial infection of host cells. PrfA activity is controlled by multiple regulatory mechanisms, including an apparent requirement for either the presence of a cofactor or some form of posttranslational modification that regulates the activation of PrfA. In this study, we describe the identification and characterization of a novel PrfA mutation that results in constitutive activation of the PrfA protein. The PrfA L140F mutation was found to confer high-level expression of PrfA-regulated genes and to be functionally dominant over the wild-type allele. The presence of the PrfA L140F mutation resulted in the aggregation of L. monocytogenes in broth culture and, unlike previously described prfA mutations, appeared to be slightly toxic to the bacteria. High-level PrfA-dependent gene expression showed no additional increase in L. monocytogenes strains containing an additional copy of prfA L140F despite a >4-fold increase in PrfA protein levels. In contrast, the introduction of multiple copies of the wild-type prfA allele to L. monocytogenes resulted in a corresponding increase in PrfA-dependent gene expression, although overall expression levels remained far below those observed for PrfA L140F strains. These results suggest a hierarchy of PrfA regulation, such that the relative levels of PrfA protein present within the cell correlate with the levels of PrfA-dependent gene expression when the protein is not in its fully activated state; however, saturating levels of the protein are then quickly reached when PrfA is converted to its active form. Regulation of the PrfA activation status must be an important facet of L. monocytogenes survival, as mutations that result in constitutive PrfA activation may have deleterious consequences for bacterial physiology.

Indexed as

Gene Expression Regulation, BacterialMutationAdaptation, PhysiologicalAmino Acid SubstitutionArtificial Gene FusionBacterial ProteinsGenes, ReporterGlucuronidaseListeria monocytogenesModels, MolecularMutation, MissensePeptide Termination FactorsPhospholipasesTrans-ActivatorsVirulenceVirulence FactorsBacterial ProteinsGlucuronidasePeptide Termination FactorsPhospholipasesTrans-ActivatorsVirulence Factors

Identifiers

PMID15342597
PMCPMC515134
OpenAlexW2138461159

What OpenQuestion holds

Textmetadata
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.