Evidence map›Paper›PMID 24828333›Full record

ArticleThe Journal of general virology2014

Delivery of antiviral small interfering RNA with gold nanoparticles inhibits dengue virus infection in vitro.

Amber M Paul, Yongliang Shi, Dhiraj Acharya, Jessica R Douglas, Amanda Cooley, John F Anderson, Faqing Huang, Fengwei Bai

Open access · greenAbstract read
In one paragraph

Article in The Journal of general virology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 101 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Amber M PaulDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Yongliang ShiDepartment of Chemistry and Biochemistry, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Dhiraj AcharyaDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Jessica R DouglasDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Amanda CooleyDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
John F AndersonDepartment of Entomology, Connecticut Agricultural Experiment Station, New Haven, CT 06504, USA.
Faqing HuangDepartment of Chemistry and Biochemistry, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
Fengwei BaiDepartment of Biological Sciences, University of Southern Mississippi, Hattiesburg, MS 39406, USA.
University of Southern Mississippi · USConnecticut Agricultural Experiment Station · US

Funding

Training and Mentoring Core P20GM103476 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI MICHAEL R GARRETT · 2012 to 2026
$60.2M
Cancer Cell-Targeted siRNA Delivery by Folate-Conjugated Gold-siRNA-PEG/PEI NanopR15CA152822 · NCI · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI HUANG, FAQING · 2010 to 2010
$435k
NCI NIH HHS R15 CA152822NCI NIH HHS R15CA152822NIGMS NIH HHS P20 GM103476NIGMS NIH HHS P20GM103476
6 · The paper itself

Abstract

Dengue virus (DENV) infection in humans can cause flu-like illness, life-threatening haemorrhagic fever or even death. There is no specific anti-DENV therapeutic or approved vaccine currently available, partially due to the possibility of antibody-dependent enhancement reaction. Small interfering RNAs (siRNAs) that target specific viral genes are considered a promising therapeutic alternative against DENV infection. However, in vivo, siRNAs are vulnerable to degradation by serum nucleases and rapid renal excretion due to their small size and anionic character. To enhance siRNA delivery and stability, we complexed anti-DENV siRNAs with biocompatible gold nanoparticles (AuNPs) and tested them in vitro. We found that cationic AuNP-siRNA complexes could enter Vero cells and significantly reduce DENV serotype 2 (DENV-2) replication and infectious virion release under both pre- and post-infection conditions. In addition, RNase-treated AuNP-siRNA complexes could still inhibit DENV-2 replication, suggesting that AuNPs maintained siRNA stability. Collectively, these results demonstrated that AuNPs were able to efficiently deliver siRNAs and control infection in vitro, indicating a novel anti-DENV strategy.

Indexed as

Virus ReleaseVirus ReplicationAnimalsAntiviral AgentsChlorocebus aethiopsDengue VirusDrug CarriersGoldNanoparticlesRNA, Small InterferingVero CellsAntiviral AgentsDrug CarriersGoldRNA, Small Interfering

Identifiers

PMID24828333
PMCPMC4103068
OpenAlexW2041517581

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.