Evidence map›Paper›PMID 23166798›Full record

ArticlePloS one2012

Sidestream smoke exposure increases the susceptibility of airway epithelia to adenoviral infection.

Priyanka Sharma, Abimbola O Kolawole, Susan B Core, Adriana E Kajon, Katherine J D A Excoffon

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Priyanka SharmaDepartment of Biological Sciences, Wright State University, Dayton, Ohio, United States of America.
Abimbola O Kolawole
Susan B Core
Adriana E Kajon
Katherine J D A Excoffon
Wright State University · USLovelace Respiratory Research Institute · US

Funding

Isoform-specific Regulation of the Coxsackie and Adenovirus Receptor in Polarized EpitheliaR15AI090625 · NIAID · WRIGHT STATE UNIVERSITY · PI EXCOFFON, KATHERINE JULIE · 2010 to 2015
$881k
NIAID NIH HHS R15 AI090625NIAID NIH HHS R15AI090625
6 · The paper itself

Abstract

backgroundAlthough significant epidemiological evidence indicates that cigarette smoke exposure increases the incidence and severity of viral infection, the molecular mechanisms behind the increased susceptibility of the respiratory tract to viral pathogens are unclear. Adenoviruses are non-enveloped DNA viruses and important causative agents of acute respiratory disease. The Coxsackievirus and adenovirus receptor (CAR) is the primary receptor for many adenoviruses. We hypothesized that cigarette smoke exposure increases epithelial susceptibility to adenovirus infection by increasing the abundance of apical CAR. METHODOLOGY AND

findingsCultured human airway epithelial cells (CaLu-3) were used as a model to investigate the effect of sidestream cigarette smoke (SSS), mainstream cigarette smoke (MSS), or control air exposure on the susceptibility of polarized respiratory epithelia to adenoviral infection. Using a Cultex air-liquid interface exposure system, we have discovered novel differences in epithelial susceptibility between SSS and MSS exposures. SSS exposure upregulates an eight-exon isoform of CAR and increases adenoviral entry from the apical surface whilst MSS exposure is similar to control air exposure. Additionally, the level of cellular glycogen synthase kinase 3β (GSK3β) is downregulated by SSS exposure and treatment with a specific GSK3β inhibitor recapitulates the effects of SSS exposure on CAR expression and viral infection.

conclusionsThis is the first time that SSS exposure has been shown to directly enhance the susceptibility of a polarized epithelium to infection by a common respiratory viral pathogen. This work provides a novel understanding of the impact of SSS on the burden of respiratory viral infections and may lead to new strategies to alter viral infections. Moreover, since GSK3β inhibitors are under intense clinical investigation as therapeutics for a diverse range of diseases, studies such as these might provide insight to extend the use of clinically relevant therapeutics and increase the understanding of potential side effects.

Indexed as

Adenoviridae InfectionsBlotting, WesternCells, CulturedCoxsackie and Adenovirus Receptor-Like Membrane ProteinDisease SusceptibilityDNA PrimersElectric ImpedanceGene Expression RegulationGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHumansImmunohistochemistryReal-Time Polymerase Chain ReactionRespiratory MucosaReverse Transcriptase Polymerase Chain ReactionTobacco Smoke PollutionCLMP protein, humanCoxsackie and Adenovirus Receptor-Like Membrane ProteinDNA PrimersGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGSK3B protein, humanTobacco Smoke Pollution

Identifiers

PMID23166798
PMCPMC3499494
OpenAlexW2078810737

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.