Evidence map›Paper›PMID 26048137›Full record

ArticleCell host & microbe2015

Cyclic GMP-AMP Synthase Is an Innate Immune DNA Sensor for Mycobacterium tuberculosis.

Angela C Collins, Haocheng Cai, Tuo Li, Luis H Franco, Xiao-Dong Li, Vidhya R Nair, Caitlyn R Scharn, Chelsea E Stamm, Beth Levine, Zhijian J Chen and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 248 papers.

0numbers the graph read from it
0cells of the map it votes in
248citing papers in PubMed
19.6field-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

248 citing papers in PubMed, 373 citations in OpenAlex.

  1. Trial
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  6. Article
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  8. Epigenetic Reprogramming byAntibiotics (Basel, Switzerland) · 2026
    Review
  9. CMPK2 restrictsbioRxiv : the preprint server for biology · 2026
    Article
  10. Article
  11. Review
  12. Article
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  18. Sorting nexin 5 mediates antigen presentation and immunity againstbioRxiv : the preprint server for biology · 2026
    Article
  19. Article
  20. Review

188 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Angela C CollinsDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA; Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA.
Haocheng CaiDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.
Tuo LiDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.
Luis H FrancoHoward Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA; Center for Autophagy Research, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA.
Xiao-Dong LiDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.
Vidhya R NairDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA; Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA.
Caitlyn R ScharnDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA; Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA.
Chelsea E StammDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA; Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA.
Beth LevineDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA; Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA; Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA; Center for Autophagy Research, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA.
Zhijian J ChenDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA; Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA. Electronic address: zhijian.chen@utsouthwestern.edu.
Michael U ShilohDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA; Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9113, USA. Electronic address: michael.shiloh@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · USHoward Hughes Medical Institute · USSouthwestern Medical Center · US

Funding

Genetic and Pathway Analysis CoreU19AI109725 · NIAID · WASHINGTON UNIVERSITY · PI VIRGIN, HERBERT W · 2014 to 2018
$32.7M
INTEGRATIVE IMMUNOLOGY TRAINING PROGRAMT32AI005284 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI Nan Yan · 2003 to 2026
$7.4M
MOLECULAR MICROBIOLOGY TRAINING GRANTT32AI007520 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI Julie K Pfeiffer · 1997 to 2026
$7.0M
Carbon monoxide resistance in Mycobacterium tuberculosis pathogenesisR01AI099439 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI SHILOH, MICHAEL · 2012 to 2016
$2.0M
Biochemical Dissection of the RIG-I Antiviral PathwayR01AI093967 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI CHEN, ZHIJIAN J · 2011 to 2015
$2.0M
Identification of novel M. tuberculosis secreted effector proteinsR21AI111023 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI SHILOH, MICHAEL · 2014 to 2015
$430k
Howard Hughes Medical InstituteNIAID NIH HHS AI093967NIAID NIH HHS R01 AI093967NIAID NIH HHS R01 AI099439NIAID NIH HHS R21 AI111023NIAID NIH HHS T32 AI005284NIAID NIH HHS T32AI005284NIAID NIH HHS T32 AI007520NIAID NIH HHS U19 AI109725
6 · The paper itself

Abstract

Activation of the DNA-dependent cytosolic surveillance pathway in response to Mycobacterium tuberculosis infection stimulates ubiquitin-dependent autophagy and inflammatory cytokine production, and plays an important role in host defense against M. tuberculosis. However, the identity of the host sensor for M. tuberculosis DNA is unknown. Here we show that M. tuberculosis activated cyclic guanosine monophosphate-adenosine monophosphate (cGAMP) synthase (cGAS) in macrophages to produce cGAMP, a second messenger that activates the adaptor protein stimulator of interferon genes (STING) to induce type I interferons and other cytokines. cGAS localized with M. tuberculosis in mouse and human cells and in human tuberculosis lesions. Knockdown or knockout of cGAS in human or mouse macrophages blocked cytokine production and induction of autophagy. Mice deficient in cGAS were more susceptible to lethality caused by infection with M. tuberculosis. These results demonstrate that cGAS is a vital innate immune sensor of M. tuberculosis infection.

Indexed as

AnimalsAutophagyCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDNA, BacterialDNA-Binding ProteinsHost-Pathogen InteractionsHumansImmunity, InnateInterferon-betaMacrophagesMembrane ProteinsMice, Inbred C57BLMice, Mutant StrainsMycobacterium tuberculosisNucleotidyltransferasesProto-Oncogene Proteins c-etscGAS protein, humancGAS protein, mouseCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDNA, BacterialDNA-Binding ProteinsELF3 protein, humanInterferon-betaMembrane ProteinsNucleotidyltransferasesProto-Oncogene Proteins c-etsSting1 protein, mouseSTING ProteinTranscription Factors

Identifiers

PMID26048137
PMCPMC4499468
OpenAlexW1897605380

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.