Evidence map›Paper›PMID 41128638›Full record

ArticleJournal of medical virology2025

Respiratory Syncytial Virus (RSV) in an Italian Pediatric Cohort: Genomic Analysis and Circulation Pattern in the Season 2022-2023.

Alessia Lai, Annalisa Bergna, Valentina Fabiano, Carla Della Ventura, Hanin Chmes, Alice Romero, Martina Loiodice, Angela Maria Dolores Boria, Alessandro Campagnoli, Felicia Stefania Falvella and 3 more

Abstract read
In one paragraph

Article in Journal of medical virology, 2025. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

13 authors.

Alessia LaiDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.ORCID 0000-0002-3174-5721
Annalisa BergnaDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.ORCID 0000-0003-1653-1917
Valentina FabianoDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Carla Della VenturaDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Hanin ChmesDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Alice RomeroDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Martina LoiodiceDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Angela Maria Dolores BoriaSC Patologia Clinica ASST Fatebenefratelli-Sacco, Milan, Italy.
Alessandro CampagnoliSC Patologia Clinica ASST Fatebenefratelli-Sacco, Milan, Italy.
Felicia Stefania FalvellaSC Patologia Clinica ASST Fatebenefratelli-Sacco, Milan, Italy.
Alberto DolciDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Gian Vincenzo ZuccottiDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Gianguglielmo ZehenderDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.ORCID 0000-0002-1886-2915

Funding

This study was supported by the EU funding within the NextGeneration EU-MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases (Project no. PE00000007, INF-ACT).
6 · The paper itself

Abstract

There is growing interest in the molecular surveillance of the respiratory syncytial virus (RSV) and data concerning the virus molecular epidemiology in high-risk pediatric patients in Italy are still limited. A total of 127 RSV-positive swabs collected in 2022-2023 season were analyzed. Whole genomes were obtained by next-generation sequencing and used for phylogenetic and phylodynamic analyses. A large proportion of the subjects had required hospitalization (78%) and age of hospitalized subjects was significantly lower than that of nonhospitalized (69 vs. 129 days; p < 0.0001). Genomic analysis suggested a significant increase in nucleotide variability in recent samples compared to previous waves and especially in subtype A. Phylogenetic analysis identified 14 and 16 clades including Italian strains in RSV-A and B, respectively. Italian strains tended to group together forming monophyletic groups, 9 in RSV-A and 13 in RSV-B, probably representing local chains of transmission. A few of those pure Italian subclades began in 21-22 wave and persisted for more than 1 year. For both subtypes the skyline plot showed two peaks in transmissions, the first between 2017 and 2019, followed by a temporary reduction in 2021 coinciding with the widespread use of control measures against COVID-19 and the second at the beginning of 2023. Accordingly, the Re estimates showed fluctuating values. This study suggests that the large circulation of RSV following pandemic restrictions is partly due to the introduction of viral strains already circulating across Europe, and partly to strains that persist in our region from one season to the next.

Indexed as

Respiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsChildChild, PreschoolCohort StudiesCOVID-19FemaleGenome, ViralGenomicsHigh-Throughput Nucleotide SequencingHospitalizationHumansInfantInfant, NewbornItalyMalegenomic epidemiologypediatric cohortrespiratory syncytial viruswhole‐genome sequencing

Identifiers

PMID41128638
PMCPMC12548520

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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.