Evidence map›Paper›PMID 40938858›Full record

ArticlePloS one2025

Dissecting the dynamics of virus-derived DNA of dengue virus 2 (DENV-2) in Aedes mosquitoes.

Hiroka Aonuma, Aboubacar Sombié, Jian-Chiuan Li, Manabu Ote, Erisha Saiki, Hidetoshi Ichimura, Itoe Iizuka, Taichi Odagawa, Tatsuya Sakurai, Kayoko Yamaji and 4 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Hiroka AonumaDepartment of Tropical Medicine, The Jikei University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0009-0000-2244-4292
Aboubacar SombiéLaboratoire d'Entomologie Fondamentale et Appliquée, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso.
Jian-Chiuan LiNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan, Taiwan.
Manabu OteDepartment of Tropical Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Erisha SaikiCenter for Medical Entomology, The Jikei University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0003-2844-9582
Hidetoshi IchimuraDepartment of Tropical Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Itoe IizukaDepartment of Tropical Medicine, The Jikei University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-5454-6661
Taichi OdagawaDepartment of Tropical Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Tatsuya SakuraiCenter for Medical Entomology, The Jikei University School of Medicine, Tokyo, Japan.
Kayoko YamajiDepartment of Tropical Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Masayuki SaijoDepartment of Virology 1, National Institute of Infectious Diseases, Tokyo, Japan.
Chun-Hong ChenNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan, Taiwan.
Athanase BadoloLaboratoire d'Entomologie Fondamentale et Appliquée, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso.
Hirotaka KanukaDepartment of Tropical Medicine, The Jikei University School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0003-0432-6510

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue is one of the neglected tropical diseases (NTDs) transmitted by Aedes mosquitoes and continues to spread globally. When mosquitoes are infected with dengue virus (DENV), virus-derived DNA (vDNA) is generated in mosquitoes, which subsequently contributes to their immune response. We traced the generation and presence of dengue virus type 2 (DENV-2) vDNA in experimentally infected cultured mosquito cells and Aedes mosquitoes, and notably, in wild mosquitoes collected in Burkina Faso. Detection of vDNA was achieved using a method incorporating loop-mediated isothermal amplification (LAMP), specifically, a LAMP-based vDNA detection method (vDNA-LAMP). The LAMP reaction, using primers targeting a segment of the NS5 region of DENV-2, detected vDNA from crude DNA extracted from experimentally infected cultured cells and Aedes mosquitoes. Detection revealed that the amount of DENV-2 vDNA generated in infected cells was relatively low; nevertheless, vDNA-LAMP enabled successful detection. The timing and quantity of vDNA generation in cultured cells were associated with the initial number of viral particles introduced during infection. Furthermore, vDNA-LAMP was applied to detect dengue virus vDNA in wild mosquitoes in dengue-endemic regions. This resulted in the successful detection of DENV-2 vDNA in field-collected mosquitoes, indicating that a proportion of wild mosquitoes in Burkina Faso harbored DENV-2 vDNA. Mapping these vDNA-positive mosquitoes allowed the identification of areas where infected mosquitoes and/or their progeny were likely present. These findings provide insights into the dynamics of DENV-2 vDNA in natural environments and underscore the potential of vDNA-LAMP as a tool for tracing vDNA in wild mosquitoes, which are responsible for transmitting viral infections.

Indexed as

AedesDengue VirusDNA, ViralMosquito VectorsAnimalsBurkina FasoDengueMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesDNA, Viral

Identifiers

PMID40938858
PMCPMC12431436

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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.