Evidence map›Paper›PMID 40143275›Full record

ArticleViruses2025

Utilizing Viral Metagenomics to Characterize Pathogenic and Commensal Viruses in Pediatric Patients with Febrile Neutropenia.

Anielly Sarana da Silva, Gabriel Montenegro de Campos, Gabriela Marengone Altizani, Enéas de Carvalho, Alice Chagas Barros, Eleonora Cella, Simone Kashima, Sandra Coccuzzo Sampaio, Maria Carolina Elias, Marta Giovanetti and 2 more

Abstract read
In one paragraph

Article in Viruses, 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

12 authors.

Anielly Sarana da SilvaBlood Center of Ribeirão Preto, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto 14051-140, Brazil.
Gabriel Montenegro de CamposBlood Center of Ribeirão Preto, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto 14051-140, Brazil.ORCID 0000-0001-5181-415X
Gabriela Marengone AltizaniDepartment of Puericulture and Pediatrics, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto 14049-900, Brazil.
Enéas de CarvalhoButantan Institute, Avenida Vital Brasil, 1500, São Paulo 05503-001, Brazil.
Alice Chagas BarrosCentral Laboratory, University Hospital of the Faculty of Medicine in Ribeirão Preto, University of São Paulo, Ribeirão Preto 14040-030, Brazil.
Eleonora CellaBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Simone KashimaBlood Center of Ribeirão Preto, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto 14051-140, Brazil.ORCID 0000-0002-1487-0141
Sandra Coccuzzo SampaioButantan Institute, Avenida Vital Brasil, 1500, São Paulo 05503-001, Brazil.
Maria Carolina EliasButantan Institute, Avenida Vital Brasil, 1500, São Paulo 05503-001, Brazil.ORCID 0000-0002-0501-8280
Marta GiovanettiSciences and Technologies for Sustainable Development and One Health, Università Campus Bio-Medico di Roma, 00128 Rome, Italy.ORCID 0000-0002-5849-7326
Carlos Alberto ScrideliDepartment of Puericulture and Pediatrics, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto 14049-900, Brazil.ORCID 0000-0001-6618-789X
Svetoslav Nanev SlavovButantan Institute, Avenida Vital Brasil, 1500, São Paulo 05503-001, Brazil.ORCID 0000-0003-0805-6140

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 403075/2023-8; 305111/2022-1Fundação de Amparo à Pesquisa do Estado de São Paulo 17/23205-8; 21/11944-6; 2022/10278-5
6 · The paper itself

Abstract

Febrile neutropenia (FN) is one of the most common complications in pediatric oncology patients. It has a complex etiologic nature, which in the majority of cases remains unclear. Intervention often follows empirical treatment protocols, mainly using broad-spectrum antibiotics. To evaluate potential viral etiologic agents, this study applied viral metagenomics to paired plasma and oropharyngeal samples obtained from pediatric patients with oncological diseases diagnosed with FN. Metagenomic sequencing was performed on 15 pediatric patients with oncological diseases and FN at the outpatient clinic of Pediatric Oncology at the University Hospital of the Faculty of Medicine of Ribeirão Preto, University of São Paulo. As a control group, we included 15 pediatric patients with oncological diseases in remission or undergoing treatment. Clinically relevant viruses identified by metagenomics in FN patients predominantly included herpesviruses and viruses found in the respiratory tract, like adenoviruses. Direct molecular confirmation was performed on all of them. Anelloviruses, represented by various genera and species in all groups, were also highly prevalent. The data obtained in this study show that viruses might also have possible implications for the etiology of FN. However, due to the complex nature of this disease, more studies are necessary to evaluate their causal relationship. The results obtained in our study may serve to improve patient treatment and ensure adequate management.

Indexed as

Febrile NeutropeniaMetagenomicsVirus DiseasesVirusesAdolescentChildChild, PreschoolFemaleHumansInfantMaleOropharynxfebrile neutropeniaherpesvirusesmetagenomicsoncologypediatricsvirome

Identifiers

PMID40143275
PMCPMC11946616

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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.