Evidence map›Paper›PMID 30125617›Full record

ArticleAntiviral research2018

Transient inhibition of sphingosine kinases confers protection to influenza A virus infected mice.

Chuan Xia, Young-Jin Seo, Caleb J Studstill, Madhuvanthi Vijayan, Jennifer J Wolf, Bumsuk Hahm

Open access · greenAbstract read
In one paragraph

Article in Antiviral research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
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    Article
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  19. Article
  20. Ceramide and Related Molecules in Viral Infections.International journal of molecular sciences · 2021
    Review
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

6 authors at 3 institutions in 2 countries.

Chuan XiaDepartment of Surgery, University of Missouri, Columbia, MO, 65212, USA; Department of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA.
Young-Jin SeoDepartment of Life Science, Chung-Ang University, Seoul, 06974, Republic of Korea.
Caleb J StudstillDepartment of Surgery, University of Missouri, Columbia, MO, 65212, USA; Department of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA.
Madhuvanthi VijayanDepartment of Surgery, University of Missouri, Columbia, MO, 65212, USA; Department of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA.
Jennifer J WolfDepartment of Surgery, University of Missouri, Columbia, MO, 65212, USA; Department of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA.
Bumsuk HahmDepartment of Surgery, University of Missouri, Columbia, MO, 65212, USA; Department of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA. Electronic address: hahmb@health.missouri.edu.
University of Missouri · USChung-Ang University · KRUniversity of Missouri Health System · US

Funding

T cell suppression caused by persistent virus infectionR21AI127404 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI HAHM, BUMSUK · 2017 to 2018
$418k
NIAID NIH HHS R21 AI127404
6 · The paper itself

Abstract

Influenza continues to pose a threat to public health by causing illness and mortality in humans. Discovering host factors that regulate influenza virus propagation is vital for the development of novel drugs. We have previously reported that sphingosine kinase (SphK) 1 promotes influenza A virus (IAV) replication in vitro. Here we demonstrate that the other isoform of SphK, SphK2 promotes the replication of influenza A virus (IAV) in cultured cells, and temporary inhibition of SphK1 or SphK2 enhances the host defense against influenza in mice. IAV infection led to an increased expression and phosphorylation of SphK2 in host cells. Furthermore, pharmacologic inhibition or siRNA-based knockdown of SphK2 attenuated IAV replication in vitro. Notably, oral administration of an SphK2-specific inhibitor substantially improved the viability of mice following IAV infection. In addition, the local instillation of an SphK1-specific inhibitor or an inhibitor that globally blocks SphK1 and SphK2 provided protection to IAV-infected mice. Collectively, our results indicate that both SphK1 and SphK2 function as proviral factors during IAV infection in vivo. Therefore, SphK1 and SphK2 represent potential host targets for therapeutics against influenza.

Indexed as

A549 CellsAdamantaneAdministration, OralAmino AlcoholsAminophenolsAnimalsCell LineDisease Models, AnimalFemaleGene Knockdown TechniquesHEK293 CellsHumansInfluenza A virusMiceMice, Inbred C57BLOrthomyxoviridae Infections3-(4-chlorophenyl)-adamantane-1-carboxylic acid (pyridin-4-ylmethyl)amide4-((4-(4-chlorophenyl)-2-thiazolyl)amino)phenolAdamantaneAmino AlcoholsAminophenolsN-methyl-5-(4'-pentylphenyl)-2-aminopent-4-ene-1,3-diolN,N-dimethylsphingosinePhosphotransferases (Alcohol Group Acceptor)Protein IsoformsPyridinesRNA, Small InterferingSphingosineSphingosine Kinasesphingosine kinase 2, mouseThiazolesInfluenza virusSphingosine kinase 1Sphingosine kinase 2

Identifiers

PMID30125617
PMCPMC6190705
OpenAlexW2885322130

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.