Evidence map›Paper›PMID 30282713›Full record

ArticleJournal of virology2018

Salinomycin Inhibits Influenza Virus Infection by Disrupting Endosomal Acidification and Viral Matrix Protein 2 Function.

Yejin Jang, Jin Soo Shin, Yi-Seul Yoon, Yun Young Go, Hye Won Lee, Oh Seung Kwon, Sehee Park, Man-Seong Park, Meehyein Kim

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
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  6. Review
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  8. Virus infection and vesicle trafficking.Frontiers in immunology · 2025
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  15. Review
  16. Review
  17. Ionophore Toxicity in Animals: A Review of Clinical and Molecular Aspects.International journal of molecular sciences · 2023
    Review
  18. CRISPR/Cas9-mediated gene editing ofFrontiers in plant science · 2023
    Article
  19. Article
  20. 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

9 authors at 4 institutions in 1 country.

Yejin JangVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Jin Soo ShinVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Yi-Seul YoonVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Yun Young GoVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Hye Won LeeVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Oh Seung KwonVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Sehee ParkDepartment of Microbiology, Institute for Viral Diseases, College of Medicine, Korea University, Seoul, Republic of Korea.
Man-Seong ParkDepartment of Microbiology, Institute for Viral Diseases, College of Medicine, Korea University, Seoul, Republic of Korea.
Meehyein KimVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea mkim@krict.re.kr.
Korea Research Institute of Chemical Technology · KRKorea University · KRKorea Advanced Institute of Science and Technology · KRKorea University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Screening of chemical libraries with 2,000 synthetic compounds identified salinomycin as a hit against influenza A and B viruses, with 50% effective concentrations ranging from 0.4 to 4.3 μM in cells. This compound is a carboxylic polyether ionophore that exchanges monovalent ions for protons across lipid bilayer membranes. Monitoring the time course of viral infection showed that salinomycin blocked nuclear migration of viral nuclear protein (NP), the most abundant component of the viral ribonucleoprotein (vRNP) complex. It caused cytoplasmic accumulation of NP, particularly within perinuclear endosomes, during virus entry. This was primarily associated with failure to acidify the endosomal-lysosomal compartments. Similar to the case with amantadine (AMT), proton channel activity of viral matrix protein 2 (M2) was blocked by salinomycin. Using purified retroviral Gag-based virus-like particles (VLPs) with M2, it was proved that salinomycin directly affects the kinetics of a proton influx into the particles but in a manner different from that of AMT. Notably, oral administration of salinomycin together with the neuraminidase inhibitor oseltamivir phosphate (OSV-P) led to enhanced antiviral effect over that with either compound used alone in influenza A virus-infected mouse models. These results provide a new paradigm for developing antivirals and their combination therapy that control both host and viral factors.

Indexed as

Administration, OralAnimalsDisease Models, AnimalDrug Evaluation, PreclinicalEndosomesGene Expression Regulation, NeoplasticInfluenza A virusMiceNucleocapsid ProteinsOrthomyxoviridae InfectionsOseltamivirPolyether PolyketidesProtein TransportPyransRNA-Binding ProteinsViral Core ProteinsM2 protein, Influenza A virusNP protein, Influenza A virusNucleocapsid ProteinsOseltamivirPolyether PolyketidesPyransRNA-Binding ProteinssalinomycinViral Core ProteinsViral Matrix ProteinsViroporin Proteinsantiviral agentcombination treatmentinfluenza virusionophoreM2 ion channelsalinomycin

Identifiers

PMID30282713
PMCPMC6258947
OpenAlexW2894970413

What OpenQuestion holds

Textmetadata
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.