Evidence map›Paper›PMID 31213630›Full record

ArticleScientific reports2019

Neutralization of Acidic Intracellular Vesicles by Niclosamide Inhibits Multiple Steps of the Dengue Virus Life Cycle In Vitro.

Eunhye Jung, Sangwoo Nam, Hyeryeon Oh, Sangmi Jun, Hyun-Joo Ro, Baek Kim, Meehyein Kim, Yun Young Go

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. Review
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  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Niclosamide-A promising treatment for COVID-19.British journal of pharmacology · 2022
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Host directed therapies: COVID-19 and beyond.Current research in pharmacology and drug discovery · 2021
    Review
  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

8 authors.

Eunhye JungVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Sangwoo NamVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Hyeryeon OhVirus Research Group, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Sangmi JunConvergent Research Center for Emerging Virus Infection, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Hyun-Joo RoConvergent Research Center for Emerging Virus Infection, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.
Baek KimCenter for Drug Discovery, Department of Pediatrics, School of Medicine, Emory University, Atlanta, GA, 30322, USA.
Meehyein KimVirus 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. yygo@krict.re.kr.ORCID http://orcid.org/0000-0003-0907-2265

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue fever is one of the most important mosquito-borne viral infections in large parts of tropical and subtropical countries and is a significant public health concern and socioeconomic burden. There is an urgent need to develop antivirals that can effectively reduce dengue virus (DENV) replication and decrease viral load. Niclosamide, an antiparasitic drug approved for human use, has been recently identified as an effective antiviral agent against a number of pH-dependent viruses, including flaviviruses. Here, we reveal that neutralization of low-pH intracellular compartments by niclosamide affects multiple steps of the DENV infectious cycle. Specifically, niclosamide-induced endosomal neutralization not only prevents viral RNA replication but also affects the maturation of DENV particles, rendering them non-infectious. We found that niclosamide-induced endosomal neutralization prevented E glycoprotein conformational changes on the virion surface of flaviviruses, resulting in the release of non-infectious immature virus particles with uncleaved pr peptide from host cells. Collectively, our findings support the potential application of niclosamide as an antiviral agent against flavivirus infection and highlight a previously uncharacterized mechanism of action of the drug.

Indexed as

AnimalsAntiviral AgentsCell LineCell Line, TumorChlorocebus aethiopsCytoplasmic VesiclesDengue VirusEndosomesHumansHydrogen-Ion ConcentrationIntracellular SpaceLife Cycle StagesNiclosamideVero CellsViral Envelope ProteinsVirionAntiviral AgentsE protein TH Sman, Dengue virusNiclosamideViral Envelope Proteins

Identifiers

PMID31213630
PMCPMC6582152

What OpenQuestion holds

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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.