Evidence map›Paper›PMID 19851456›Full record

ArticlePLoS pathogens2009

Dengue virus capsid protein usurps lipid droplets for viral particle formation.

Marcelo M Samsa, Juan A Mondotte, Nestor G Iglesias, Iranaia Assunção-Miranda, Giselle Barbosa-Lima, Andrea T Da Poian, Patricia T Bozza, Andrea V Gamarnik

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 319 papers.

0numbers the graph read from it
0cells of the map it votes in
319citing papers in PubMed
27.2field-weighted citation impact, top 1% 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

319 citing papers in PubMed, 565 citations in OpenAlex.

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  11. Measles virus reprograms CD4Frontiers in cell and developmental biology · 2026
    Article
  12. Antiviral agents for dengue virus.Virologica Sinica · 2025
    Review
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  14. Review
  15. Article
  16. Article
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  19. Article
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259 more citing papers are in PubMed but not listed here.

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 at 4 institutions in 2 countries.

Marcelo M SamsaFundación Instituto Leloir-CONICET, Buenos Aires, Argentina.
Juan A Mondotte
Nestor G Iglesias
Iranaia Assunção-Miranda
Giselle Barbosa-Lima
Andrea T Da Poian
Patricia T Bozza
Andrea V Gamarnik
Consejo Nacional de Investigaciones Científicas y Técnicas · ARFundação Oswaldo Cruz · BRFundación Instituto Leloir · ARUniversidade Federal do Rio de Janeiro · BR

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Dengue virus is responsible for the highest rates of disease and mortality among the members of the Flavivirus genus. Dengue epidemics are still occurring around the world, indicating an urgent need of prophylactic vaccines and antivirals. In recent years, a great deal has been learned about the mechanisms of dengue virus genome amplification. However, little is known about the process by which the capsid protein recruits the viral genome during encapsidation. Here, we found that the mature capsid protein in the cytoplasm of dengue virus infected cells accumulates on the surface of ER-derived organelles named lipid droplets. Mutagenesis analysis using infectious dengue virus clones has identified specific hydrophobic amino acids, located in the center of the capsid protein, as key elements for lipid droplet association. Substitutions of amino acid L50 or L54 in the capsid protein disrupted lipid droplet targeting and impaired viral particle formation. We also report that dengue virus infection increases the number of lipid droplets per cell, suggesting a link between lipid droplet metabolism and viral replication. In this regard, we found that pharmacological manipulation of the amount of lipid droplets in the cell can be a means to control dengue virus replication. In addition, we developed a novel genetic system to dissociate cis-acting RNA replication elements from the capsid coding sequence. Using this system, we found that mislocalization of a mutated capsid protein decreased viral RNA amplification. We propose that lipid droplets play multiple roles during the viral life cycle; they could sequester the viral capsid protein early during infection and provide a scaffold for genome encapsidation.

Indexed as

Amino Acid MotifsAnimalsBiological TransportCapsid ProteinsCells, CulturedCricetinaeDengueDengue VirusHost-Pathogen InteractionsHumansLipid MetabolismMembrane LipidsModels, BiologicalModels, MolecularMutant ProteinsProtein MultimerizationCapsid ProteinsMembrane LipidsMutant ProteinsRNA, Viral

Identifiers

PMID19851456
PMCPMC2760139
OpenAlexW2023422813

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.