Evidence map›Paper›PMID 40507847›Full record

ArticleInternational journal of molecular sciences2025

Screening out microRNAs and Their Molecular Pathways with a Potential Role in the Regulation of Parvovirus B19 Infection Through In Silico Analysis.

Vívian de Almeida Salvado, Arthur Daniel Rocha Alves, Wagner Luis da Costa Nunes Pimentel Coelho, Mayla Abrahim Costa, Alexandro Guterres, Luciane Almeida Amado

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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. 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

6 authors.

Vívian de Almeida SalvadoLaboratory of Technological Development in Virology, Oswaldo Cruz Institute (IOC), FIOCRUZ, Rio de Janeiro 21040-360, Brazil.
Arthur Daniel Rocha AlvesLaboratory of Technological Development in Virology, Oswaldo Cruz Institute (IOC), FIOCRUZ, Rio de Janeiro 21040-360, Brazil.ORCID 0000-0002-6371-6482
Wagner Luis da Costa Nunes Pimentel CoelhoLaboratory of Technological Development in Virology, Oswaldo Cruz Institute (IOC), FIOCRUZ, Rio de Janeiro 21040-360, Brazil.ORCID 0000-0001-8654-839X
Mayla Abrahim CostaCompetitive Intelligence Office, Institute of Immunobiological Technology (Bio-Manguinhos), FIOCRUZ, Rio de Janeiro 21040-360, Brazil.
Alexandro GuterresLaboratory of Technological Development in Virology, Oswaldo Cruz Institute (IOC), FIOCRUZ, Rio de Janeiro 21040-360, Brazil.ORCID 0000-0001-8323-1477
Luciane Almeida AmadoLaboratory of Technological Development in Virology, Oswaldo Cruz Institute (IOC), FIOCRUZ, Rio de Janeiro 21040-360, Brazil.ORCID 0000-0002-7919-8915

Funding

Coordination for the Improvement of Higher Education Personnel 001FAPERJ-JCM e-26/210.058/2024FAPERJ-JCNE e-26/201.406/2021FAPERJ-PDR10 e-26/205.975/2022Oswaldo Cruz Institute 001
6 · The paper itself

Abstract

Parvovirus B19 (B19V) infection in healthy individuals is commonly asymptomatic or has non-specific symptoms, such as fever, headache, chills, myalgia, rash, and arthralgia. However, some groups of individuals, such as pregnant women, patients with hemolytic disorders, and immunocompromised individuals, may present severe forms of the infection, which may even lead to a negative outcome. To better understand what leads to this divergence of outcomes in different populational groups, this study sought to analyze the role of miRNAs in the pathogenesis of B19V infection. The miRNAs that potentially bind to the B19V transcripts were identified using complete genomic sequences retrieved from Genbank and miRNAs cataloged in miRbase. The results of this alignment between the seed region of the miRNAs with the B19V complete genome identified 1517 miRNAs that showed 100% identity, of which 412 are bound to NS1, VP1, and VP2 transcripts. Based on the number of total binds to the genome, these miRNAs were ranked, and the top five, miR-4799-5p, miR-5690, miR-335-3p, miR-193b-5p, and miR-6771-3p, were selected to evaluate the target genes and signaling pathways in which they act. We identified 214 common genes among the top five miRNAs, and five of these genes bind to at least two of these miRNAs. Based on WikiPathways and KEGG, these 214 genes act on 29 statistically significant pathways, and the three main pathways were selected. Our results revealed some miRNAs that may be involved in regulating B19V replication and that can act as potential biomarkers for the prognosis of infection.

Indexed as

Erythema InfectiosumMicroRNAsParvoviridae InfectionsParvovirus B19, HumanComputational BiologyComputer SimulationHumansMicroRNAsin silicomicroRNAsParvovirus B19pathwaytarget gene

Identifiers

PMID40507847
PMCPMC12155502

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Registered trials

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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.