Evidence map›Paper›PMID 32946535›Full record

ArticlePLoS pathogens2020

The Chlamydia trachomatis secreted effector TmeA hijacks the N-WASP-ARP2/3 actin remodeling axis to facilitate cellular invasion.

Robert Faris, Alix McCullough, Shelby E Andersen, Thomas O Moninger, Mary M Weber

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.5field-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

34 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. ThemBio · 2026
    Article
  3. Review
  4. Article
  5. ThebioRxiv : the preprint server for biology · 2025
    Article
  6. mSphere · 2025
    Article
  7. Article
  8. The N-terminus of theMicrobiology spectrum · 2025
    Article
  9. Chlamydia trachomatis invasion: a duet of effectors.Biochemical Society transactions · 2025
    Review
  10. Review
  11. The N-terminus of thebioRxiv : the preprint server for biology · 2024
    Article
  12. Article
  13. mBio · 2024
    Article
  14. Article
  15. Review
  16. Dynamin-dependent entry ofResearch square · 2023
    Article
  17. Article
  18. Review
  19. TheProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  20. 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

5 authors at 1 institution in 1 country.

Robert FarisDepartment of Microbiology and Immunology, University of Iowa Carver College of Medicine, Iowa City, Iowa, United States of America.
Alix McCulloughDepartment of Microbiology and Immunology, University of Iowa Carver College of Medicine, Iowa City, Iowa, United States of America.ORCID 0000-0003-1850-9246
Shelby E AndersenDepartment of Microbiology and Immunology, University of Iowa Carver College of Medicine, Iowa City, Iowa, United States of America.ORCID 0000-0002-4573-1021
Thomas O MoningerCentral Microscopy Research Facility, University of Iowa Carver College of Medicine, Iowa City, Iowa, United States of America.
Mary M WeberDepartment of Microbiology and Immunology, University of Iowa Carver College of Medicine, Iowa City, Iowa, United States of America.ORCID 0000-0001-5126-2164
University of Iowa · US

Funding

Functional characterization of Chlamydia trachomatis inclusion membrane proteins and their role in subversion of the host vesicular traffickingR01AI150812 · NIAID · UNIVERSITY OF IOWA · PI Mary Weber · 2020 to 2026
$3.5M
NIAID NIH HHS R01 AI150812
6 · The paper itself

Abstract

As an obligate intracellular pathogen, host cell invasion is paramount to Chlamydia trachomatis proliferation. While the mechanistic underpinnings of this essential process remain ill-defined, it is predicted to involve delivery of prepackaged effector proteins into the host cell that trigger plasma membrane remodeling and cytoskeletal reorganization. The secreted effector proteins TmeA and TarP, have risen to prominence as putative key regulators of cellular invasion and bacterial pathogenesis. Although several studies have begun to unravel molecular details underlying the putative function of TarP, the physiological function of TmeA during host cell invasion is unknown. Here, we show that TmeA employs molecular mimicry to bind to the GTPase binding domain of N-WASP, which results in recruitment of the actin branching ARP2/3 complex to the site of chlamydial entry. Electron microscopy revealed that TmeA mutants are deficient in filopodia capture, suggesting that TmeA/N-WASP interactions ultimately modulate host cell plasma membrane remodeling events necessary for chlamydial entry. Importantly, while both TmeA and TarP are necessary for effective host cell invasion, we show that these effectors target distinct pathways that ultimately converge on activation of the ARP2/3 complex. In line with this observation, we show that a double mutant suffers from a severe entry defect nearly identical to that observed when ARP3 is chemically inhibited or knocked down. Collectively, our study highlights both TmeA and TarP as essential regulators of chlamydial invasion that modulate the ARP2/3 complex through distinct signaling platforms, resulting in plasma membrane remodeling events that are essential for pathogen uptake.

Indexed as

Bacterial ProteinsChlamydia trachomatisActin-Related Protein 2-3 ComplexCell MembraneHeLa CellsHumansMutationProtein DomainsPseudopodiaWiskott-Aldrich Syndrome Protein, NeuronalActin-Related Protein 2-3 ComplexBacterial ProteinsWASL protein, humanWiskott-Aldrich Syndrome Protein, Neuronal

Identifiers

PMID32946535
PMCPMC7526919
OpenAlexW3087641904

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.