Evidence map›Paper›PMID 35947597›Full record

ArticlePloS one2022

Detection and persistence of environmental DNA (eDNA) of the different developmental stages of a vector mosquito, Culex pipiens pallens.

Masayuki K Sakata, Megumi Sato, Marcello Otake Sato, Tomoe Watanabe, Honami Mitsuishi, Tomoyuki Hikitsuchi, Jun Kobayashi, Toshifumi Minamoto

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed, 10 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 4 institutions in 1 country.

Masayuki K SakataGraduate School of Human Development and Environment, Kobe University, Kobe City, Japan.ORCID 0000-0003-4837-854X
Megumi SatoGraduate School of Health Sciences, Niigata University, Niigata, Japan.
Marcello Otake SatoLaboratory of Tropical Medicine and Parasitology, Dokkyo Medical University, Tochigi, Japan.ORCID 0000-0002-9204-0602
Tomoe WatanabeDainihon Jochugiku Co., Ltd Research & Development Laboratory Biological Research Section 1-11, Osaka, Japan.
Honami MitsuishiDainihon Jochugiku Co., Ltd Research & Development Laboratory Biological Research Section 1-11, Osaka, Japan.
Tomoyuki HikitsuchiDainihon Jochugiku Co., Ltd Research & Development Laboratory Biological Research Section 1-11, Osaka, Japan.
Jun KobayashiGraduate School of Health Sciences, University of the Ryukyus, Okinawa, Japan.
Toshifumi MinamotoGraduate School of Human Development and Environment, Kobe University, Kobe City, Japan.
Sumitomo Dainippon Pharma (Japan) · JPKobe University · JPNiigata University · JPUniversity of the Ryukyus · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preventing mosquito-borne infectious diseases requires that vector mosquitoes are monitored and controlled. Targeting immature mosquitoes (eggs, larvae, and pupae), which have less mobility than adults, is an effective management approach. However, conducting these surveys is often difficult due to the limitations of morphological classification and survey costs. The application of environmental DNA (eDNA) analysis can solve these issues because it allows easy estimation of species distribution and morphology-independent species identification. Although a few previous studies have reported mosquito eDNA detection, there is a gap in knowledge regarding the dynamics related to the persistence of immature mosquito eDNA. We used Culex pipiens pallens, a vector of West Nile fever, as a model species. First, we developed a species-specific detection assay and confirmed its specificity using in silico and in vitro tests. Next, we conducted laboratory experiments using breeding tanks. Water samples were collected at each developmental stage. In addition, water samples were collected daily until the seventh day after emergence from the pupae. We quantified eDNA using real-time PCR with the developed assay to investigate the dynamics of mosquito eDNA. The specificity of the developed assay was confirmed by in silico and in vitro tests. Mosquito eDNA was detected at all developmental stages and detected up to seven days after emergence of pupae. In particular, high concentrations of eDNA were detected immediately after hatching from eggs and after emergence from pupae. Highly frequent positive eDNA signals were continuously detected between egg hatching and pupa hatching. Mosquito eDNA was detected immediately after the eggs were introduced, and eDNA-positive detections continued until pupae emergence, suggesting that eDNA analysis is useful for monitoring mosquito larvae. In the future, monitoring immature mosquitoes using eDNA analysis will contribute to prevent mosquito-borne infectious diseases.

Indexed as

Communicable DiseasesCulexCulicidaeDNA, EnvironmentalAnimalsLarvaMosquito VectorsPupaWaterDNA, EnvironmentalWater

Identifiers

PMID35947597
PMCPMC9365122
OpenAlexW4291676261

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.