Evidence map›Paper›PMID 39282383›Full record

ArticlebioRxiv : the preprint server for biology2025

The

Luz Saavedra-Sanchez, Mary S Dickinson, Shruti Apte, Yifeng Zhang, Maarten de Jong, Samantha Skavicus, Nicholas S Heaton, Neal M Alto, Jörn Coers

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

  • Updated by
    The2025
5 · Who and what money

Authors and funding

9 authors.

Luz Saavedra-SanchezDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Mary S DickinsonDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Shruti ApteDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Yifeng ZhangDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Maarten de JongDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0003-2278-286X
Samantha SkavicusDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Nicholas S HeatonDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Neal M AltoDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-7602-3853
Jörn CoersDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.ORCID 0000-0001-8707-4608

Funding

Type III effector regulation of host signal transduction systemsR01AI083359 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI ALTO, NEAL MATHEW · 2009 to 2024
$6.3M
The pathogenic effects of epithelial cells surviving direct influenza virus infectionR01AI137031 · NIAID · DUKE UNIVERSITY · PI Nicholas S Heaton · 2019 to 2026
$4.5M
Interferon-inducible cell-autonomous immunity to cytosolic bacterial pathogensR01AI139425 · NIAID · DUKE UNIVERSITY · PI Jorn Coers · 2019 to 2026
$3.4M
Control of influenza virus induced type I interferon signaling during pregnancyR01AI168107 · NIAID · DUKE UNIVERSITY · PI Nicholas S Heaton · 2023 to 2026
$2.9M
Human GBPs as regulators of immunity to intracellular bacterial pathogensR56AI139425 · NIAID · DUKE UNIVERSITY · PI COERS, JOERN · 2018 to 2018
$465k
Type III effector regulation of host GTPase signalingR56AI083359 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI ALTO, NEAL MATHEW · 2014 to 2014
$452k
NIAID NIH HHS R01 AI083359NIAID NIH HHS R01 AI137031NIAID NIH HHS R01 AI139425NIAID NIH HHS R01 AI168107NIAID NIH HHS R56 AI083359NIAID NIH HHS R56 AI139425
6 · The paper itself

Abstract

A central signal that marshals host defense against many infections is the lymphocyte-derived cytokine interferon-gamma (IFNγ). The IFNγ receptor is expressed on most human cells, and its activation leads to the expression of antimicrobial proteins that execute diverse cell-autonomous immune programs. One such immune program consists of the sequential detection, ubiquitylation, and destruction of intracellular pathogens. Recently, the IFNγ-inducible ubiquitin E3 ligase RNF213 was identified as a pivotal mediator of such a defense axis. RNF213 provides host protection against viral, bacterial, and protozoan pathogens. To establish infections, potentially susceptible intracellular pathogens must have evolved mechanisms that subdue RNF213-controlled cell-autonomous immunity. In support of this hypothesis, we demonstrate here that a causative agent of bacillary dysentery,

Identifiers

PMID39282383
PMCPMC11398459

What OpenQuestion holds

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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.