Evidence map›Paper›PMID 28187149›Full record

ArticlePloS one2017

Inhibition of influenza A virus infection by ginsenosides.

Wei Dong, Amber Farooqui, Alberto J Leon, David J Kelvin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Cheminformatics-Based Study Identifies Potential Ebola VP40 Inhibitors.International journal of molecular sciences · 2023
    Article
  5. Article
  6. Antiviral Potential of the GenusJournal of ginseng research · 2023
    Review
  7. Review
  8. Article
  9. Review
  10. Recent Advances in Antiviral Activities of Triterpenoids.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  11. Article
  12. Usefulness of ginseng in management of dengue: a bioinformatics pathway interrelationship analysis.International journal of physiology, pathophysiology and pharmacology · 2022
    Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
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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

4 authors at 3 institutions in 2 countries.

Wei DongDivision of Immunology, International Institute of Infection and Immunity, University Health Network & Shantou University Medical College, Shantou, China.
Amber FarooquiDivision of Immunology, International Institute of Infection and Immunity, University Health Network & Shantou University Medical College, Shantou, China.
Alberto J LeonDivision of Immunology, International Institute of Infection and Immunity, University Health Network & Shantou University Medical College, Shantou, China.
David J KelvinDivision of Immunology, International Institute of Infection and Immunity, University Health Network & Shantou University Medical College, Shantou, China.
Shantou University · CNKey Laboratory of Guangdong Province · CNUniversity Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Influenza viruses cause mild to severe respiratory infections in humans. Due to efficient means of transmission, the viruses infect human population on a large scale. Apart from vaccines, antiviral drugs are used to control infection; neuraminidase inhibitors are thought to be the first choice of treatment, particularly for severe cases. Rapidly evolving and emerging influenza viruses with increased frequency of viral resistance to these drugs stress the need to explore novel antiviral compounds. In this study, we investigated antiviral activity of ginseng extract and ginsenosides, the ginseng-derived triterpene and saponin compounds, against 2009 pandemic H1N1 virus in vitro and in vivo. Our data showed that treatment of mice with ginsenosides protected the animals from lethal 2009 pandemic H1N1 infection and lowered viral titers in animal lungs. Mechanistic studies revealed that ginsenosides interact with viral hemagglutinin protein and prevent the attachment of virus with α 2-3' sialic acid receptors present on host cell surfaces. The interference in the viral attachment process subsequently minimizes viral entry into the cells and decreases the severity of the viral infection. We also describe that sugar moieties present in ginsenosides are indispensible for their attachment with viral HA protein. On the basis of our observations, we can say that ginsenosides are promising candidates for the development of antiviral drugs for influenza viruses.

Indexed as

AnimalsAntiviral AgentsCHO CellsCricetinaeCricetulusDogsFemaleGinsenosidesHemagglutinin Glycoproteins, Influenza VirusInfluenza A virusMadin Darby Canine Kidney CellsMiceMice, Inbred BALB COrthomyxoviridae InfectionsProtein BindingAntiviral AgentsGinsenosidesHemagglutinin Glycoproteins, Influenza Virus

Identifiers

PMID28187149
PMCPMC5302443
OpenAlexW2586506094

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.