Evidence map›Paper›PMID 22522562›Full record

ArticleNature medicine2012

Lethal inflammasome activation by a multidrug-resistant pathobiont upon antibiotic disruption of the microbiota.

Janelle S Ayres, Norver J Trinidad, Russell E Vance

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed
9.4field-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

128 citing papers in PubMed, 213 citations in OpenAlex.

  1. Trial
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  10. Virulence · 2024
    Review
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  12. Evaluating the Effectiveness ofPharmaceuticals (Basel, Switzerland) · 2024
    Article
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68 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Janelle S AyresDepartment of Molecular & Cell Biology, Division of Immunology & Pathogenesis, University of California, Berkeley, USA. jayres@berkeley.edu
Norver J Trinidad
Russell E Vance
University of California, Berkeley · US

Funding

The role of Listeria cyclic-di-AMP during infection and immunityP01AI063302 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI VANCE, RUSSELL E · 2004 to 2025
$45.5M
Functional and Structural Dissection of Inflammasome ActivationR37AI075039 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI RUSSELL E VANCE · 2018 to 2026
$3.8M
Specificity and in vivo function of the Naip/Nlrc4 inflammasomesR01AI075039 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI VANCE, RUSSELL E · 2008 to 2017
$3.6M
Macrophage transcriptional responses to Legionella pneumophilaR01AI080749 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI VANCE, RUSSELL E · 2009 to 2013
$1.6M
Control of intestinal microflora and inflammation by immune sensing of flagellinF32AI091068 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI AYRES, JANELLE S · 2010 to 2012
$138k
NIAID NIH HHS AI063302NIAID NIH HHS AI075039NIAID NIH HHS AI080749NIAID NIH HHS AI091068NIAID NIH HHS F32 AI091068NIAID NIH HHS R01 AI075039NIAID NIH HHS R01 AI080749NIAID NIH HHS R37 AI075039
6 · The paper itself

Abstract

The mammalian intestine harbors a complex microbial community that provides numerous benefits to its host. However, the microbiota can also include potentially virulent species, termed pathobiont, which can cause disease when intestinal homeostasis is disrupted. The molecular mechanisms by which pathobionts cause disease remain poorly understood. Here we describe a sepsis-like disease that occurs upon gut injury in antibiotic-treated mice. Sepsis was associated with the systemic spread of a specific multidrug-resistant Escherichia coli pathobiont that expanded markedly in the microbiota of antibiotic-treated mice. Rapid sepsis-like death required a component of the innate immune system, the Naip5-Nlrc4 inflammasome. In accordance with Koch's postulates, we found the E. coli pathobiont was sufficient to activate Naip5-Nlrc4 and cause disease when injected intravenously into unmanipulated mice. These findings reveal how sepsis-like disease can result from recognition of pathobionts by the innate immune system.

Indexed as

AnimalsAnti-Bacterial AgentsApoptosis Regulatory ProteinsCalcium-Binding ProteinsDrug Resistance, Multiple, BacterialEscherichia coliImmunity, InnateInflammasomesIntestinesMetagenomeMiceMice, Inbred C57BLNeuronal Apoptosis-Inhibitory ProteinSepsisVirulence FactorsAnti-Bacterial AgentsApoptosis Regulatory ProteinsCalcium-Binding ProteinsInflammasomesIpaf protein, mouseNaip5 protein, mouseNeuronal Apoptosis-Inhibitory ProteinVirulence Factors

Identifiers

PMID22522562
PMCPMC3472005
OpenAlexW2171982502

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.