Evidence map›Paper›PMID 24948362›Full record

ReviewCellular microbiology2014

Role of host GTPases in infection by Listeria monocytogenes.

Keith Ireton, Luciano A Rigano, Georgina C Dowd

Open access · bronzeAbstract readReview
In one paragraph

Review in Cellular microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Pathogens (Basel, Switzerland) · 2022
    Review
  5. Cancers · 2021
    Article
  6. Article
  7. Inverse control of Rab proteins byScience advances · 2020
    Article
  8. Article
  9. Epitopes for Multivalent Vaccines AgainstFrontiers in cellular and infection microbiology · 2020
    Article
  10. Article
  11. Article
  12. Review
  13. ArfGAP1 restrictsEMBO reports · 2018
    Article
  14. Article
  15. SNX8 mediates IFNγ-triggered noncanonical signaling pathway and host defense againstProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  16. Article
  17. Article
  18. 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

3 authors at 1 institution in 1 country.

Keith IretonDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Luciano A Rigano
Georgina C Dowd
University of Otago · NZ

Funding

Molecular Mechanism of cell-cell spread of Listeria in polarized epithelial cellsR01AI085072 · NIAID · UNIVERSITY OF OTAGO · PI IRETON, KEITH PATRICK · 2010 to 2013
$1.0M
NIAID NIH HHS R01 AI085072NIAID NIH HHS R01AI085072
6 · The paper itself

Abstract

The bacterial pathogen Listeria monocytogenes induces internalization into mammalian cells and uses actin-based motility to spread within tissues. Listeria accomplishes this intracellular life cycle by exploiting or antagonizing several host GTPases. Internalization into human cells is mediated by the bacterial surface proteins InlA or InlB. These two modes of uptake each require a host actin polymerization pathway comprised of the GTPase Rac1, nucleation promotion factors, and the Arp2/3 complex. In addition to Rac1, InlB-mediated internalization involves inhibition of the GTPase Arf6 and participation of Dynamin and septin family GTPases. After uptake, Listeria is encased in host phagosomes. The bacterial protein GAPDH inactivates the human GTPase Rab5, thereby delaying phagosomal acquisition of antimicrobial properties. After bacterial-induced destruction of the phagosome, cytosolic Listeria uses the surface protein ActA to stimulate actin-based motility. The GTPase Dynamin 2 reduces the density of microtubules that would otherwise limit bacterial movement. Cell-to-cell spread results when motile Listeria remodel the host plasma membrane into protrusions that are engulfed by neighbouring cells. The human GTPase Cdc42, its activator Tuba, and its effector N-WASP form a complex with the potential to restrict Listeria protrusions. Bacteria overcome this restriction through two microbial factors that inhibit Cdc42-GTP or Tuba/N-WASP interaction.

Indexed as

Animalscdc42 GTP-Binding ProteinGTP PhosphohydrolasesHumansListeria monocytogenesListeriosiscdc42 GTP-Binding ProteinGTP Phosphohydrolases

Identifiers

PMID24948362
PMCPMC4656192
OpenAlexW1522122447

What OpenQuestion holds

Textmetadata
LicenceTDM
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.