Evidence map›Paper›PMID 28669671›Full record

ArticleCell host & microbe2017

Viral Replication Complexes Are Targeted by LC3-Guided Interferon-Inducible GTPases.

Scott B Biering, Jayoung Choi, Rachel A Halstrom, Hailey M Brown, Wandy L Beatty, Sanghyun Lee, Broc T McCune, Erin Dominici, Lelia E Williams, Robert C Orchard and 5 more

Abstract read
In one paragraph

Article in Cell host & microbe, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
–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

63 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Review
  3. Article
  4. Antiviral Role of Surface Layer Protein A (SlpA) ofPathogens (Basel, Switzerland) · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The mechanisms and roles of selective autophagy in mammals.Nature reviews. Molecular cell biology · 2023
    Review
  18. Article
  19. Review
  20. Article

3 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

15 authors.

Scott B BieringCommittee on Microbiology, University of Chicago, Chicago, IL 60637, USA.
Jayoung ChoiDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA.
Rachel A HalstromDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA.
Hailey M BrownCommittee on Immunology, University of Chicago, Chicago, IL 60637, USA.
Wandy L BeattyDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Sanghyun LeeDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Broc T McCuneDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Erin DominiciDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA.
Lelia E WilliamsBiological Sciences Collegiate Division, University of Chicago, Chicago, IL 60637, USA.
Robert C OrchardDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Craig B WilenDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Masahiro YamamotoLaboratory of Immunoparasitology, World Premier International Research Center Immunology Frontier Research Center, Osaka University, Osaka 565-0871, Japan.
Jörn CoersDepartments of Medicine, Molecular Genetics and Microbiology, and Immunology, Duke University Medical Center, Durham, NC 27710, USA.
Gregory A TaylorDepartments of Medicine, Molecular Genetics and Microbiology, and Immunology, Duke University Medical Center, Durham, NC 27710, USA; GRECC, Durham VA Health Care System, Durham, NC 27705, USA.
Seungmin HwangCommittee on Microbiology, University of Chicago, Chicago, IL 60637, USA; Department of Pathology, University of Chicago, Chicago, IL 60637, USA; Committee on Immunology, University of Chicago, Chicago, IL 60637, USA. Electronic address: shwang@bsd.uchicago.edu.

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI CHIEN-MIN KAO · 1985 to 2026
$122.1M
ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI CHANG, EUGENE B · 1990 to 2025
$29.8M
Molecular And Cellular Biology Training ProgramT32GM007183 · NIGMS · UNIVERSITY OF CHICAGO · PI GLICK, BENJAMIN S, RICE, PHOEBE A · 1985 to 2021
$23.9M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
IRGM-driven host responses to Chlamydia trachomatis infectionsR01AI103197 · NIAID · DUKE UNIVERSITY · PI COERS, JOERN · 2013 to 2023
$4.2M
Interferon-inducible cell-intrinsic host defense against Chlamydia trachomatisR37AI103197 · NIAID · DUKE UNIVERSITY · PI Jorn Coers · 2024 to 2026
$1.6M
Role of virus-receptor interactions in determining norovirus tropism and pathogenesis in vivoK08AI128043 · NIAID · YALE UNIVERSITY · PI WILEN, CRAIG BRIAN · 2017 to 2021
$940k
DEFINING THE IN VIVO ROLE OF DAP1 IN AUTOPHAGY AND COLITISF31CA177194 · NCI · WASHINGTON UNIVERSITY · PI MCCUNE, BROC TAYLOR · 2013 to 2015
$87k
Regulation of Intestinal Inflammation by Irgm1I01BX002369 · VA · DURHAM VA MEDICAL CENTER · PI TAYLOR, GREGORY A · 2015 to 2018
–
BLRD VA I01 BX002369NCATS NIH HHS UL1 TR000430NCI NIH HHS F31 CA177194NCI NIH HHS P30 CA014599NIAID NIH HHS K08 AI128043NIAID NIH HHS R01 AI103197NIAID NIH HHS R37 AI103197NIAID NIH HHS T32 AI007090NIDDK NIH HHS P30 DK042086NIGMS NIH HHS T32 GM007183
6 · The paper itself

Abstract

All viruses with positive-sense RNA genomes replicate on membranous structures in the cytoplasm called replication complexes (RCs). RCs provide an advantageous microenvironment for viral replication, but it is unknown how the host immune system counteracts these structures. Here we show that interferon-gamma (IFNG) disrupts the RC of murine norovirus (MNV) via evolutionarily conserved autophagy proteins and the induction of IFN-inducible GTPases, which are known to destroy the membrane of vacuoles containing bacteria, protists, or fungi. The MNV RC was marked by the microtubule-associated-protein-1-light-chain-3 (LC3) conjugation system of autophagy and then targeted by immunity-related GTPases (IRGs) and guanylate-binding proteins (GBPs) upon their induction by IFNG. Further, the LC3 conjugation system and the IFN-inducible GTPases were necessary to inhibit MNV replication in mice and human cells. These data suggest that viral RCs can be marked and antagonized by a universal immune defense mechanism targeting diverse pathogens replicating in cytosolic membrane structures.

Indexed as

AnimalsAutophagyCaliciviridae InfectionsCarrier ProteinsCell LineCytosolFemaleFibroblastsGene Knockdown TechniquesGTP PhosphohydrolasesHeLa CellsHumansImmunity, InnateInterferon-gammaInterferonsMacrophagesCarrier ProteinsGTP PhosphohydrolasesInterferon-gammaInterferonsMap1lc3b protein, mouseMicrotubule-Associated ProteinsautophagyGBPGTPaseinterferonIRGLC3replicationRNAtargetingvirus

Identifiers

PMID28669671
PMCPMC5591033

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.