Evidence map›Paper›PMID 40096248›Full record

ArticleMicrobial genomics2025

Human respiratory syncytial virus genetic diversity and lineage replacement in Ireland pre- and post-COVID-19 pandemic.

Alan Rice, Gabriel Gonzalez, Michael Carr, Jonathan Dean, Emer O'Byrne, Lynn Aarts, Harry Vennema, Weronika Banka, Charlene Bennett, Siobhán Cleary and 11 more

Abstract read
In one paragraph

Article in Microbial genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 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

21 authors.

Alan RiceUCD National Virus Reference Laboratory, University College Dublin, Dublin, Belfield, D04 E1W1, Ireland.
Gabriel GonzalezInstitute for Vaccine Research and Development, Hokkaido University, Sapporo, Hokkaido 001-0021, Japan.
Michael CarrUCD National Virus Reference Laboratory, University College Dublin, Dublin, Belfield, D04 E1W1, Ireland.
Jonathan DeanUCD National Virus Reference Laboratory, University College Dublin, Dublin, Belfield, D04 E1W1, Ireland.
Emer O'ByrneUCD National Virus Reference Laboratory, University College Dublin, Dublin, Belfield, D04 E1W1, Ireland.
Lynn AartsCentre for Infectious Disease Control, National Institute for Public Health and Environment, Bilthoven, Netherlands.
Harry VennemaCentre for Infectious Disease Control, National Institute for Public Health and Environment, Bilthoven, Netherlands.
Weronika BankaUCD National Virus Reference Laboratory, University College Dublin, Dublin, Belfield, D04 E1W1, Ireland.
Charlene BennettUCD National Virus Reference Laboratory, University College Dublin, Dublin, Belfield, D04 E1W1, Ireland.
Siobhán ClearyUCD National Virus Reference Laboratory, University College Dublin, Dublin, Belfield, D04 E1W1, Ireland.
Lisa DomeganHealth Protection Surveillance Centre, Dublin, Ireland.
Joan O'DonnellHealth Protection Surveillance Centre, Dublin, Ireland.
Maureen O'LearyHealth Protection Surveillance Centre, Dublin, Ireland.
Stephanie GoyaDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, USA.
Lance PresserCentre for Infectious Disease Control, National Institute for Public Health and Environment, Bilthoven, Netherlands.
Adam MeijerCentre for Infectious Disease Control, National Institute for Public Health and Environment, Bilthoven, Netherlands.
Greg MartinHealth Improvement, Health Service Executive, Dublin, Ireland.
Hirofumi SawaInstitute for Vaccine Research and Development, Hokkaido University, Sapporo, Hokkaido 001-0021, Japan.
Allison WatersIrish Blood Transfusion Service, National Blood Centre, Dublin, Ireland.
Cillian De GascunUCD National Virus Reference Laboratory, University College Dublin, Dublin, Belfield, D04 E1W1, Ireland.
Daniel HareUCD National Virus Reference Laboratory, University College Dublin, Dublin, Belfield, D04 E1W1, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human respiratory syncytial virus (HRSV) is a common cause of lower respiratory tract infections globally, and changes in viral epidemiology have been observed in many jurisdictions following the coronavirus disease 2019 (COVID-19) pandemic. Newly licensed vaccines and monoclonal antibodies are anticipated to alleviate the burden on healthcare systems, though such interventions may exert selective pressures on viral evolution. To evaluate the diversity of HRSV in Ireland pre- and post-COVID-19 pandemic, whole-genome sequencing was performed on HRSV-A (

Indexed as

COVID-19Genetic VariationRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsGenome, ViralHumansIrelandPandemicsPhylogenySARS-CoV-2Whole Genome Sequencinggenetic diversityhuman respiratory syncytial viruslineagesorthopneumoviruswhole-genome sequencing

Identifiers

PMID40096248
PMCPMC11914048

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.