Evidence map›Paper›PMID 18383626›Full record

ArticlePLoS pathogens2008

Chlamydial entry involves TARP binding of guanine nucleotide exchange factors.

B Josh Lane, Charla Mutchler, Souhaila Al Khodor, Scott S Grieshaber, Rey A Carabeo

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

101 citing papers in PubMed, 152 citations in OpenAlex.

  1. Review
  2. ThemBio · 2026
    Article
  3. Review
  4. mSphere · 2025
    Article
  5. Chlamydia trachomatis invasion: a duet of effectors.Biochemical Society transactions · 2025
    Review
  6. Article
  7. Adaptor protein Abelson interactor 1 in homeostasis and disease.Cell communication and signaling : CCS · 2024
    Review
  8. Article
  9. Article
  10. Dynamin-dependent entry ofResearch square · 2023
    Article
  11. Requirement of GrgA forbioRxiv : the preprint server for biology · 2023
    Article
  12. Review
  13. Article
  14. Molecular pathogenesis ofFrontiers in cellular and infection microbiology · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Genetic susceptibility loci forFrontiers in immunology · 2022
    Article

41 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 1 country.

B Josh LaneDepartment of Microbiology and Immunology, University of Louisville Medical School, Louisville, Kentucky, USA.
Charla Mutchler
Souhaila Al Khodor
Scott S Grieshaber
Rey A Carabeo
University of Louisville · USUniversity of Louisville Hospital · USUniversity of Florida · US

Funding

CHLAMYDIAL INVASION OF NON-PHAGOCYTIC CELLSR01AI065545 · NIAID · WASHINGTON STATE UNIVERSITY · PI CARABEO, REY A · 2005 to 2021
$3.3M
Identification of the chlamydial adhesin and receptorK22AI052252 · NIAID · UNIVERSITY OF LOUISVILLE · PI CARABEO, REYNALDO A · 2004 to 2005
$216k
NIAID NIH HHS AI052252NIAID NIH HHS AI065545NIAID NIH HHS K22 AI052252NIAID NIH HHS R01 AI065545
6 · The paper itself

Abstract

Chlamydia trachomatis attachment to cells induces the secretion of the elementary body-associated protein TARP (Translocated Actin Recruiting Protein). TARP crosses the plasma membrane where it is immediately phosphorylated at tyrosine residues by unknown host kinases. The Rac GTPase is also activated, resulting in WAVE2 and Arp2/3-dependent recruitment of actin to the sites of chlamydia attachment. We show that TARP participates directly in chlamydial invasion activating the Rac-dependent signaling cascade to recruit actin. TARP functions by binding two distinct Rac guanine nucleotide exchange factors (GEFs), Sos1 and Vav2, in a phosphotyrosine-dependent manner. The tyrosine phosphorylation profile of the sequence YEPISTENIYESI within TARP, as well as the transient activation of the phosphatidylinositol 3-kinase (PI3-K), appears to determine which GEF is utilized to activate Rac. The first and second tyrosine residues, when phosphorylated, are utilized by the Sos1/Abi1/Eps8 and Vav2, respectively, with the latter requiring the lipid phosphatidylinositol 3,4,5-triphosphate. Depletion of these critical signaling molecules by siRNA resulted in inhibition of chlamydial invasion to varying degrees, owing to a possible functional redundancy of the two pathways. Collectively, these data implicate TARP in signaling to the actin cytoskeleton remodeling machinery, demonstrating a mechanism by which C.trachomatis invades non-phagocytic cells.

Indexed as

ActinsBacterial AdhesionChlamydia trachomatisCytoskeletal ProteinsEndocytosisGuanine Nucleotide Exchange FactorsHeLa CellsHost-Pathogen InteractionsHumansIntracellular Signaling Peptides and ProteinsNuclear ProteinsPhosphatidylinositol 3-KinasesPhosphorylationProtein BindingProto-Oncogene Proteins c-aktSignal TransductionActinsCytoskeletal ProteinsGuanine Nucleotide Exchange FactorsIntracellular Signaling Peptides and ProteinsNuclear ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTARPTyrosine

Identifiers

PMID18383626
PMCPMC2279300
OpenAlexW1967089575

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.