Evidence map›Paper›PMID 36395759›Full record

ArticleCell host & microbe2022

Chlamydia repurposes the actin-binding protein EPS8 to disassemble epithelial tight junctions and promote infection.

Lee Dolat, Victoria K Carpenter, Yi-Shan Chen, Michitaka Suzuki, Erin P Smith, Ozge Kuddar, Raphael H Valdivia

Open access · greenAbstract read
In one paragraph

Article in Cell host & microbe, 2022. 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
2.6field-weighted citation impact, top 10% 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, 19 citations in OpenAlex.

  1. ThemBio · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. ThebioRxiv : the preprint server for biology · 2025
    Article
  8. mSphere · 2025
    Article
  9. Journal of bacteriology · 2025
    Review
  10. Study Models forMicroorganisms · 2025
    Review
  11. Article
  12. Review
  13. Insights into innate immune cell evasion byFrontiers in immunology · 2024
    Review
  14. ATG9A supportsMicrobiology spectrum · 2023
    Article
  15. Review
  16. Review
  17. Review
  18. Genome organization and genomics inFrontiers in cellular and infection microbiology · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Lee DolatDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Victoria K CarpenterDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Yi-Shan ChenDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Michitaka SuzukiDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Erin P SmithDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Ozge KuddarDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Raphael H ValdiviaDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA. Electronic address: raphael.valdivia@duke.edu.
Duke Medical Center · USDuke University · US

Funding

Structure-Function Analysis of Chlamydia Secretion ChaperonesR01AI123083 · NIAID · DUKE UNIVERSITY · PI VALDIVIA, RAPHAEL H, ZHOU, PEI · 2016 to 2020
$2.6M
Functional characterization of early Chlamydia effectorsR01AI134891 · NIAID · DUKE UNIVERSITY · PI VALDIVIA, RAPHAEL H · 2018 to 2022
$2.4M
Subversion of the host cell cytoskeleton and innate immunity by Chlamydia trachomatisF32AI138372 · NIAID · DUKE UNIVERSITY · PI DOLAT, LEE · 2019 to 2021
$235k
NIAID NIH HHS F32 AI138372NIAID NIH HHS R01 AI123083NIAID NIH HHS R01 AI134891
6 · The paper itself

Abstract

Invasive microbial pathogens often disrupt epithelial barriers, yet the mechanisms used to dismantle tight junctions are poorly understood. Here, we show that the obligate pathogen Chlamydia trachomatis uses the effector protein TepP to transiently disassemble tight junctions early during infection. TepP alters the tyrosine phosphorylation status of host proteins involved in cytoskeletal regulation, including the filamentous actin-binding protein EPS8. We determined that TepP and EPS8 are necessary and sufficient to remodel tight junctions and that the ensuing disruption of epithelial barrier function promotes secondary invasion events. The genetic deletion of EPS8 renders epithelial cells and endometrial organoids resistant to TepP-mediated tight junction remodeling. Finally, TepP and EPS8 promote infection in murine models of infections, with TepP mutants displaying defects in ascension to the upper genital tract. These findings reveal a non-canonical function of EPS8 in the disassembly of epithelial junctions and an important role for Chlamydia pathogenesis.

Indexed as

Adaptor Proteins, Signal TransducingChlamydia InfectionsMicrofilament ProteinsTight JunctionsAnimalsChlamydia trachomatisEpithelial CellsHost-Pathogen InteractionsMiceAdaptor Proteins, Signal TransducingEps8 protein, mouseMicrofilament ProteinsChlamydiaepitheliainfectionsecreted effectorstight junctionsupper genital tract

Identifiers

PMID36395759
PMCPMC9793342
OpenAlexW4309367571

What OpenQuestion holds

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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.