Evidence map›Paper›PMID 32846120›Full record

ArticleCell reports2020

Influenza-Induced Oxidative Stress Sensitizes Lung Cells to Bacterial-Toxin-Mediated Necroptosis.

Norberto Gonzalez-Juarbe, Ashleigh N Riegler, Alexander S Jureka, Ryan P Gilley, Jeffrey D Brand, John E Trombley, Ninecia R Scott, Maryann P Platt, Peter H Dube, Chad M Petit and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

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  13. Secondary infection withFEMS microbes · 2022
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  20. Co-infection of H9N2 Influenza A Virus andFrontiers in microbiology · 2021
    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

12 authors at 3 institutions in 1 country.

Norberto Gonzalez-JuarbeDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, AL 35294-2170, USA; Infectious Diseases and Genomic Medicine Group, J Craig Venter Institute, 9605 Medical Center Drive, Suite 150, Rockville, MD 20850, USA. Electronic address: ngonzale@jcvi.org.
Ashleigh N RieglerDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, AL 35294-2170, USA.
Alexander S JurekaDepartment of Biochemistry and Molecular Genetics, The University of Alabama at Birmingham, Birmingham, AL 35294-2170, USA.
Ryan P GilleyDepartment of Microbiology, Immunology and Molecular Genetics, The University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Jeffrey D BrandDepartment of Anesthesiology and Perioperative Medicine, The University of Alabama at Birmingham, Birmingham, AL 35294-2170, USA.
John E TrombleyDepartment of Anesthesiology and Perioperative Medicine, The University of Alabama at Birmingham, Birmingham, AL 35294-2170, USA.
Ninecia R ScottDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, AL 35294-2170, USA.
Maryann P PlattInfectious Diseases and Genomic Medicine Group, J Craig Venter Institute, 9605 Medical Center Drive, Suite 150, Rockville, MD 20850, USA.
Peter H DubeDepartment of Microbiology, Immunology and Molecular Genetics, The University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Chad M PetitDepartment of Biochemistry and Molecular Genetics, The University of Alabama at Birmingham, Birmingham, AL 35294-2170, USA.
Kevin S HarrodDepartment of Anesthesiology and Perioperative Medicine, The University of Alabama at Birmingham, Birmingham, AL 35294-2170, USA.
Carlos J OrihuelaDepartment of Microbiology, The University of Alabama at Birmingham, Birmingham, AL 35294-2170, USA.
University of Alabama at Birmingham · USThe University of Texas Health Science Center at San Antonio · USJ. Craig Venter Institute · US

Funding

The role of CARDS toxin in genesis and exacerbation of allergic inflammationU19AI070412 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI BASEMAN, JOEL BARRY · 2006 to 2015
$19.7M
IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
ZINC DIETARY ALTERATIONS OF CADMIUM INDUCED HEPATIC TOXICITY IN RATSS06GM008111 · NIGMS · FLORIDA AGRICULTURAL AND MECHANICAL UNIV · PI REAMS, ROMONIA RENEE · 1989 to 2008
$9.1M
Cardiac microlesion formation during invasive pneumococcal diseaseR01AI114800 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Carlos J Orihuela, Herve S TETTELIN · 2015 to 2026
$5.1M
Targeting MMP9 to Improve Outcomes in Serious Influenza InfectionsR01AI111475 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HARROD, KEVIN S, LEVY, BRUCE D · 2014 to 2018
$4.3M
Strain Dependent Structure and Function of the Influenza NS1 ProteinR01AI134693 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PETIT, CHAD · 2018 to 2022
$1.9M
Influenza regulation of epithelial pneumococcal host defense.R01HL149944 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HARROD, KEVIN S · 2020 to 2023
$1.5M
Pneumococcal biofilm formation is SpxB dependentR21AI146149 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ORIHUELA, CARLOS J · 2019 to 2020
$427k
Capsule protects intracellular pneumococci during vascular endothelial cell translocationR21AI148368 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ORIHUELA, CARLOS J · 2020 to 2021
$408k
SK channel antagonists as novel bronchodilators for asthmaR21AI113724 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI BRENNER, ROBERT · 2014 to 2015
$407k
Inhibition of necroptosis during inflamm-aging and pneumoniaR21AG055144 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ORIHUELA, CARLOS J · 2016 to 2017
$404k
NHLBI NIH HHS R01 HL149944NIAID NIH HHS R01 AI111475NIAID NIH HHS R01 AI114800NIAID NIH HHS R01 AI134693NIAID NIH HHS R21 AI113724NIAID NIH HHS R21 AI146149NIAID NIH HHS R21 AI148368NIAID NIH HHS T32 AI007051NIAID NIH HHS U19 AI070412NIA NIH HHS R21 AG055144NIGMS NIH HHS S06 GM008111
6 · The paper itself

Abstract

Pneumonias caused by influenza A virus (IAV) co- and secondary bacterial infections are characterized by their severity and high mortality rate. Previously, we have shown that bacterial pore-forming toxin (PFT)-mediated necroptosis is a key driver of acute lung injury during bacterial pneumonia. Here, we evaluate the impact of IAV on PFT-induced acute lung injury during co- and secondary Streptococcus pneumoniae (Spn) infection. We observe that IAV synergistically sensitizes lung epithelial cells for PFT-mediated necroptosis in vitro and in murine models of Spn co-infection and secondary infection. Pharmacoelogical induction of oxidative stress without virus sensitizes cells for PFT-mediated necroptosis. Antioxidant treatment or inhibition of necroptosis reduces disease severity during secondary bacterial infection. Our results advance our understanding on the molecular basis of co- and secondary bacterial infection to influenza and identify necroptosis inhibition and antioxidant therapy as potential intervention strategies.

Indexed as

AnimalsHumansInfluenza, HumanLungMiceNecroptosisOxidative Stresscell deathco-infectionsepithelial cellsinflammationinfluenza A virusnecroptosisoxidative stresspneumoniasecondary bacterial infectionStreptococcus pneumoniae

Identifiers

PMID32846120
PMCPMC7570217
OpenAlexW3080739719

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.