Evidence map›Paper›PMID 41157588›Full record

ArticleViruses2025

Monopoly of Minor Group Rhinovirus Infections in Hospitalised Children in Hong Kong During the SARS-CoV-2 Pandemic.

Jason Chun Sang Pun, Kin Pong Tao, Shaojun Liu, Ben Kam San Wong, Tony Chun Hei Lei, Lucky Lu Yi Tsoi, Joseph Gar Shun Tsun, Agnes Sze Yin Leung, Paul Kay Sheung Chan, Renee Wan Yi Chan

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. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jason Chun Sang PunDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, 6/F Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.ORCID 0000-0003-2650-922X
Kin Pong TaoDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, 6/F Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.ORCID 0009-0003-7843-1740
Shaojun LiuDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, 6/F Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.
Ben Kam San WongDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, 6/F Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.
Tony Chun Hei LeiDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, 6/F Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.
Lucky Lu Yi TsoiDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, 6/F Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.
Joseph Gar Shun TsunDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, 6/F Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.ORCID 0000-0003-1853-5348
Agnes Sze Yin LeungDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, 6/F Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.ORCID 0000-0001-8249-4478
Paul Kay Sheung ChanSH Ho Research Centre for Infectious Diseases Faculty of Medicine, Rm 207, 2/F, S.H. Ho Research Centre for Infectious Diseases, JC School of Public Health Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.ORCID 0000-0002-6360-4608
Renee Wan Yi ChanDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, 6/F Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, China.ORCID 0000-0001-6485-0926

Funding

CUHK Research Committee Direct Grants 2017.61CUHK Research Committee Direct Grants 2019.073Hong Kong RGC - Early Career Scheme 24107017Hong Kong RGC - General Research Fund 14103119
6 · The paper itself

Abstract

backgroundWhile rhinoviruses (RVs) typically cause mild respiratory infections, their persistence during the SARS-CoV-2 pandemic, particularly in Hong Kong's strict zero-coronavirus disease 2019 policy, revealed unexpected epidemiological patterns. Two distinct RV surges emerged despite stringent public health measures, suggesting unique transmission advantages among circulating strains. We hypothesised that RV persistence during pandemic restrictions reflected strain-specific adaptations in respiratory tract replication efficiency and/or immune evasion.

methodsWe analysed RV genotypes and conducted blinded clinical severity assessment for 96 paediatric hospitalisations during 2020-2021 outbreaks, compared with 180 age- and sex-matched control subjects from the corresponding weeks in pre-pandemic years (2018-2019). RV isolates from 2020 to 2021 outbreaks were characterised for their replication competence and transcriptomic responses in primary human nasal epithelial cell (HNEC) and environmental stability assays, using RV-A16 and RV-A1B as controls.

resultMinor group genotypes RV-A47 and RV-A49 were overrepresented during these two outbreaks. RV-A49 exhibited comparable replication efficiency to RV-A16 but induced significantly stronger transcriptomic responses, notably enhanced TNF and IL-1 signalling, in HNECs, alongside robust replication competence. Our data also suggests the association of RV-A49 with tachypnoea in 2021, particularly in younger males, though limited by a small sample size and single-centre design.

conclusionThe predominance of RV-A49 in hospitalised children during the SARS-CoV-2 pandemic potentially driven by its replication competence in HNECs and its capacity to enhanced inflammatory responses. The result is hypothesis-generating, warranting further studies with historical strains and broader populations to confirm strain-specific severity.

Indexed as

COVID-19Picornaviridae InfectionsRhinovirusAdolescentChildChild, HospitalizedChild, PreschoolFemaleGenotypeHong KongHospitalizationHumansInfantMalePandemicsSARS-CoV-2air–liquid interfaceenvironmental stabilityHong KongrhinovirusRV-A49transmissibility

Identifiers

PMID41157588
PMCPMC12567708

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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.