Evidence map›Paper›PMID 41787562›Full record

ArticleGenome medicine2026

Identifying intra-hospital Norovirus GII transmission using whole-genome sequencing.

Logan Grimes, Jeffrey Fink, Michael Elkan, Jessica Llewellyn, Rose C Patrick, Ana Luiza Araújo Jernigan, Benjamin M Liu, Kenneth P Smith, Rebecca M Harris, Ericka Hayes and 1 more

Abstract read
In one paragraph

Article in Genome medicine, 2026. 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
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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

11 authors.

Logan Grimes *Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States of America.
Jeffrey Fink *Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Michael ElkanDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Jessica LlewellynDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Rose C PatrickDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Ana Luiza Araújo JerniganDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Benjamin M LiuDivision of Pathology and Laboratory Medicine, Children's National Hospital, Washington, DC, United States of America.ORCID 0000-0003-1225-9936
Kenneth P SmithDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Rebecca M HarrisDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America.
Ericka HayesDepartment of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States of America.
Robert Fredrick PotterDepartment of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, United States of America. potterr1@chop.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNorovirus genogroup II (GII) is a common gastrointestinal pathogen that can cause spatially and temporally linked outbreaks due to its resistance to disinfectants and desiccation. Despite this threat, routine whole-genome sequencing has rarely been systematically applied to Norovirus.

methodsWe performed whole-genome amplification of Norovirus GII from 665 clinical stool specimens collected between 2019 and 2025 at Children’s Hospital of Philadelphia (CHOP), and 47 samples from Children’s National Hospital, using a modified PCR protocol and Oxford Nanopore Technologies (ONT) sequencing. Viral genomes were assembled using long-read sequencing and paired with clinical metadata from the electronic medical record to identify suspected transmission events.

resultsOur assay improves on previous methods and achieved an 84% success rate in assembling CHOP samples into near-complete genomes. Genotyping analysis showed dominance of GII.4 Sydney [P16] from 2019 to 2024, with recent emergence of GII.17 [P17]. We identified multiple cliques (n = 44) of genetically indistinguishable or near-identical (≤ 5 SNP) strains. 32% (14/44) of these cliques were from patients on the same units and are considered “Likely” Norovirus GII transmission events. 20% (9/44) of the cliques are from different units or inpatient and emergency department and are “Possible” transmission events. All “Likely” Norovirus GII transmission events have a confirmed epidemiological link or occurred entirely within unit and 56% (5/9) of the “Possible” transmission events have an epidemiological link - either a shared clinician or shared off unit location or both.

conclusionsThis study demonstrates that whole-genome sequencing of Norovirus GII is a powerful tool for high-resolution viral surveillance. Prospective genomic monitoring combined with informatics enables detection of nosocomial outbreaks and reveals hidden transmission chains. Routine implementation of this platform could facilitate earlier implementation of containment measures that may ultimately reduce healthcare-associated Norovirus transmission.

Indexed as

Caliciviridae InfectionsCross InfectionGenome, ViralNorovirusWhole Genome SequencingFecesGastroenteritisGenotypeHumansPhylogenyGenomic SurveillanceNorovirus GIIViral GastroenteritisWhole-Genome Sequencing

Identifiers

PMID41787562
PMCPMC13077947

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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.