Evidence map›Paper›PMID 36430340›Full record

ArticleInternational journal of molecular sciences2022

Development of a Molecular Aptamer Beacon Applied to Magnetic-Assisted RNA Extraction for Detection of Dengue and Zika Viruses Using Clinical Samples.

Amanda Gabrielle da Silva, Luiz Ricardo Goulart, Philipp Löffler, Christian Code, Adriana Freitas Neves

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Aptamers: Functional-Structural Studies and Biomedical Applications 2.0.International journal of molecular sciences · 2024
    Article
  3. Review
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

5 authors at 3 institutions in 2 countries.

Amanda Gabrielle da SilvaInstitute of Physics, Postgraduate Program in Exact and Technological Sciences, Universidade Federal de Catalão, Catalão 75704-020, Brazil.ORCID 0000-0003-1794-5660
Luiz Ricardo GoulartNanobiotechnology Laboratory, Institute of Biotechnology, Universidade Federal de Uberlândia, Uberlândia 38402-022, Brazil.ORCID 0000-0002-1803-4861
Philipp LöfflerDepartment of Physics, Chemistry and Pharmacy, University of Southern Denmark, Campusvej 55, 5230 Odense, Denmark.ORCID 0000-0002-8995-6783
Christian CodeDianox ApS, Fruebjergvej 3, 2100 København, Denmark.
Adriana Freitas NevesInstitute of Biotechnology, Molecular Biology Laboratory, Universidade Federal de Catalão, Catalão 75704-020, Brazil.ORCID 0000-0002-2299-2114
Universidade Federal de Catalão · BRUniversity of Southern Denmark · DKUniversidade Federal de Uberlândia · BR

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior/ Fundação de Amparo à Pesquisa do Estado de Goiás 2017102670026024Fundação de Amparo à Pesquisa do Estado de Goiás (FAPEG) )/Ministério da Saúde - Depar-tamento de Ciência e Tecnologia da Secretaria de Ciência, Tecnologia, Inovação e Insumos Estratégicos em Saúde (Decit/SCTIE/MS) 201810267000103Fundação de Amparo à Pesquisa do Estado de Minas Gerais CBB - APQ-03613-17National Council for Scientific and Technological Development 485463/2012-1National Institute of Science & Technology in Theranostics and Nanobiotechnology 403193/2022-2National Institute of Science & Technology in Theranostics and Nanobiotechnology 465669/2014-0
6 · The paper itself

Abstract

Limitations in the detection of cocirculating flaviviruses such as Dengue and Zika lead us to propose the use of aptameric capture of the viral RNA in combination with RT-PCR (APTA-RT-PCR). Aptamers were obtained via SELEX and next-generation sequencing, followed by colorimetric and fluorescent characterizations. An APTA-RT-PCR assay was developed, optimized, and tested against the viral RNAs in 108 serum samples. After selection, sequence APTAZC10 was designed as a bifunctional molecular beacon (APTAZC10-MB), exhibiting affinity for the viral targets. APTA-RT-PCR was able to detect Dengue and Zika RNA in 43% and 8% of samples, respectively. Our results indicate that APTAZC10-MB and APTA-RT-PCR will be useful to improve the detection of Dengue and Zika viruses in a fast molecular assay for the improvement of infectious disease surveillance.

Indexed as

DengueZika VirusZika Virus InfectionHumansMagnetic PhenomenaOligonucleotidesRNA, ViralOligonucleotidesRNA, ViraldiagnosisflavivirushybridizationoligonucleotidesRT-PCR

Identifiers

PMID36430340
PMCPMC9693377
OpenAlexW4308695696

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.