Evidence map›Paper›PMID 41078243›Full record

ArticleInfluenza and other respiratory viruses2025

Genetic and Epidemiological Insights Into Respiratory Syncytial Virus Infections: A Comparative Study of Hospitalized Versus Community Cases in Portugal (2021-2023).

Miguel Lança, Vânia Gaio, Ana Paula Rodrigues, Camila Henriques, Licínia Gomes, Daniela Dias, Maria de Jesus Chasqueira, Raquel Guiomar, Aryse Melo

Abstract readComparative Study
In one paragraph

Article in Influenza and other respiratory viruses, 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

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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.

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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

9 authors.

Miguel LançaNational Reference Laboratory for Influenza Virus and Other Respiratory Virus, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.ORCID 0000-0003-0376-2572
Vânia GaioDepartment of Epidemiology, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.ORCID 0000-0001-7626-4991
Ana Paula RodriguesDepartment of Epidemiology, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.ORCID 0000-0003-2264-4723
Camila HenriquesNational Reference Laboratory for Influenza Virus and Other Respiratory Virus, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.ORCID 0000-0002-3654-4929
Licínia GomesNational Reference Laboratory for Influenza Virus and Other Respiratory Virus, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.ORCID 0009-0009-0214-9646
Daniela DiasNational Reference Laboratory for Influenza Virus and Other Respiratory Virus, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.ORCID 0009-0006-6744-0571
Maria de Jesus ChasqueiraComprehensive Health Research Center, NOVA Medical School, Universidade NOVA de Lisboa, Lisboa, Portugal.ORCID 0000-0002-8015-7109
Raquel GuiomarNational Reference Laboratory for Influenza Virus and Other Respiratory Virus, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.ORCID 0000-0002-4563-6315
Aryse MeloNational Reference Laboratory for Influenza Virus and Other Respiratory Virus, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.ORCID 0000-0002-6655-8715

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRespiratory syncytial virus (RSV) is the leading cause of acute respiratory infection (ARI) in young children, but its genetic diversity requires ongoing surveillance.

methodsFrom 2021 to 2023, a total of 619 and 94 RSV-positive samples from the National Respiratory Syncytial Virus Surveillance Network (VigiRSV) and the Sentinel Influenza and other respiratory viruses surveillance network (Sentinel ISN), respectively, were analysed. The RSV A and RSV B typing was assessed by a multiplex real-time RT-PCR. Sanger sequencing was performed on a subset of samples (n = 495). Phylogenetic analysis was carried out on partial glycoprotein G sequences. Clinical and epidemiological data were compared through Pearson Chi-Square tests.

resultsRSV Subgroup A was more prevalent (53.5%, 85/159) in the 2021/2022 season, whereas in the 2022/2023 season, it was RSV Subgroup B (82.1%, 435/530) in both networks. RSV A strains in VigiRSV clustered mainly to A.D.1 (39.0%, 39/100), whereas in Sentinel ISN, they clustered in A.D.5 (30.0%, 3/10). RSV Type B clustered mainly to B.D.E.1 (96.6%, 372/385) in both networks. All lineages cocirculated during the study period and in both surveillance networks. Regional clusters were identified for both subgroups.

conclusionsThis study provides new insights into RSV genetic variability in Portugal, namely, the cocirculation of lineages and intravariability among lineages within both subgroups during the study period and in all Portuguese regions. However, our study is based on partial sequencing of the G gene, and because of this limitation, our results should be considered with great caution.

Indexed as

Respiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsAdolescentChildChild, PreschoolCommunity-Acquired InfectionsFemaleGenetic VariationHospitalizationHumansInfantInfant, NewbornMalePhylogenyPortugalRespiratory Tract InfectionschildrenEuropemolecular characterizationrespiratory virusesRSVsurveillance

Identifiers

PMID41078243
PMCPMC12516350

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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.