Evidence map›Paper›PMID 36084633›Full record

ArticleCell host & microbe2022

The bacterial effector GarD shields Chlamydia trachomatis inclusions from RNF213-mediated ubiquitylation and destruction.

Stephen C Walsh, Jeffrey R Reitano, Mary S Dickinson, Miriam Kutsch, Dulcemaria Hernandez, Alyson B Barnes, Benjamin H Schott, Liuyang Wang, Dennis C Ko, So Young Kim and 3 more

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 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
8.4field-weighted citation impact, top 1% 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

52 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. RNF213-dependent lytic destruction ofProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Genome-wide association studies ofInfection and immunity · 2026
    Article
  5. Review
  6. Review
  7. Inclusion Membrane Proteins ofMicroorganisms · 2026
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Anti-International journal of molecular sciences · 2026
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. TheeLife · 2025
    Article
  19. HoweLife · 2025
    Article
  20. Complete deletion of theInfection and immunity · 2025
    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

13 authors at 2 institutions in 1 country.

Stephen C WalshDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Jeffrey R ReitanoDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA; Department of Immunology, Duke University Medical Center, Durham, NC, USA.
Mary S DickinsonDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Miriam KutschDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Dulcemaria HernandezDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Alyson B BarnesDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Benjamin H SchottDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Liuyang WangDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Dennis C KoDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
So Young KimDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Raphael H ValdiviaDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Robert J BastidasDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA.
Jörn CoersDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC, USA; Department of Immunology, Duke University Medical Center, Durham, NC, USA. Electronic address: jorn.coers@duke.edu.
Duke University Hospital · USDuke Medical Center · US

Funding

Serologic Biomarkers of Human Sexually Transmitted Infection and DiseaseU19AI084044 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI TETTELIN, HERVE S · 2009 to 2018
$22.8M
IRGM-driven host responses to Chlamydia trachomatis infectionsR01AI103197 · NIAID · DUKE UNIVERSITY · PI COERS, JOERN · 2013 to 2023
$4.2M
Basic Immunology Training ProgramT32AI052077 · NIAID · DUKE UNIVERSITY · PI KRANGEL, MICHAEL S · 2002 to 2024
$4.2M
Genetics and Genomics Training GrantT32GM136627 · NIGMS · DUKE UNIVERSITY · PI ALLISON E ASHLEY-KOCH · 2020 to 2026
$3.1M
Interferon-inducible cell-intrinsic host defense against Chlamydia trachomatisR37AI103197 · NIAID · DUKE UNIVERSITY · PI Jorn Coers · 2024 to 2026
$1.6M
Posttranslational modifications of host proteins by Chlamydia effectorsR21AI140019 · NIAID · DUKE UNIVERSITY · PI BASTIDAS, ROBERT J · 2018 to 2019
$441k
Defining human interferon-stimulated genes with novel functions in host defense to Chlamydia infectionsF31AI150106 · NIAID · DUKE UNIVERSITY · PI WALSH, STEPHEN CHARLES · 2020 to 2022
$115k
NIAID NIH HHS F31 AI150106NIAID NIH HHS R01 AI103197NIAID NIH HHS R21 AI140019NIAID NIH HHS R37 AI103197NIAID NIH HHS T32 AI052077NIAID NIH HHS U19 AI084044NIGMS NIH HHS T32 GM136627
6 · The paper itself

Abstract

Chlamydia trachomatis is the leading cause of sexually transmitted bacterial infections and a major threat to women's reproductive health in particular. This obligate intracellular pathogen resides and replicates within a cellular compartment termed an inclusion, where it is sheltered by unknown mechanisms from gamma-interferon (IFNγ)-induced cell-autonomous host immunity. Through a genetic screen, we uncovered the Chlamydia inclusion membrane protein gamma resistance determinant (GarD) as a bacterial factor protecting inclusions from cell-autonomous immunity. In IFNγ-primed human cells, inclusions formed by garD loss-of-function mutants become decorated with linear ubiquitin and are eliminated. Leveraging cellular genome-wide association data, we identified the ubiquitin E3 ligase RNF213 as a candidate anti-Chlamydia protein. We demonstrate that IFNγ-inducible RNF213 facilitates the ubiquitylation and destruction of GarD-deficient inclusions. Furthermore, we show that GarD operates as a cis-acting stealth factor barring RNF213 from targeting inclusions, thus functionally defining GarD as an RNF213 antagonist essential for chlamydial growth during IFNγ-stimulated immunity.

Indexed as

Bacterial InfectionsChlamydia InfectionsAdenosine TriphosphatasesChlamydia trachomatisFemaleGenome-Wide Association StudyHeLa CellsHumansInterferon-gammaUbiquitinationUbiquitin-Protein LigasesUbiquitinsAdenosine TriphosphatasesInterferon-gammaRNF213 protein, humanUbiquitin-Protein LigasesUbiquitinsautophagycell-autonomous immunityChlamydiainterferoninterferon-stimulated genesNDP52optineurinRNF213TAX1BP1ubiquitylation

Identifiers

PMID36084633
PMCPMC9772000
OpenAlexW4294970179

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.