Evidence map›Paper›PMID 39599573›Full record

ArticlePathogens (Basel, Switzerland)2024

Coxsackievirus A6 U.K. Genetic and Clinical Epidemiology Pre- and Post-SARS-CoV-2 Emergence.

Alice M Joyce, Jack D Hill, Theocharis Tsoleridis, Stuart Astbury, Louise Berry, Hannah C Howson-Wells, Nancy Allen, Ben Canning, Carl B Jones, Gemma Clark and 3 more

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Serial passagingFrontiers in cellular and infection microbiology · 2026
    Article
  5. Article
  6. 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.

Alice M JoyceSchool of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Jack D HillSchool of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Theocharis TsoleridisSchool of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0000-0002-9685-6318
Stuart AstburyNottingham Digestive Diseases Centre, Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham NG7 2UH, UK.
Louise BerryClinical Microbiology, Nottingham University Hospitals NHS Trust, Nottingham NG7 2UH, UK.
Hannah C Howson-WellsClinical Microbiology, Nottingham University Hospitals NHS Trust, Nottingham NG7 2UH, UK.
Nancy AllenClinical Microbiology, Nottingham University Hospitals NHS Trust, Nottingham NG7 2UH, UK.
Ben CanningClinical Microbiology, Nottingham University Hospitals NHS Trust, Nottingham NG7 2UH, UK.
Carl B JonesClinical Microbiology, Nottingham University Hospitals NHS Trust, Nottingham NG7 2UH, UK.
Gemma ClarkClinical Microbiology, Nottingham University Hospitals NHS Trust, Nottingham NG7 2UH, UK.
William L IrvingSchool of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Alexander W TarrSchool of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0000-0003-1009-0823
C Patrick McClureSchool of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0000-0002-1710-1049

Funding

Clinical Virology Network N/A
6 · The paper itself

Abstract

Coxsackievirus A6 (CVA6) has become increasingly clinically relevant as a cause of Hand, Foot and Mouth Disease (HFMD) globally since 2008. However, most laboratories do not routinely determine the enteroviral type of positive samples. The non-pharmaceutical measures introduced to curb transmission during the COVID-19 pandemic may also have perturbed CVA6 epidemiology. We thus aimed to determine the prevalence, clinical presentation and genetic relationship of CVA6 across three complete epidemic seasons: one pre-SARS-CoV-2 emergence and two post-SARS-CoV-2 emergence in our regional healthcare setting. Surplus diagnostic nucleic acid from diagnosed enteroviral positives diagnosed between September and December of 2018 and between May 2021 and April of 2023 was subject to VP1 gene sequencing to determine the CVA6 cases and interrogate their phylogenetic relationship. The confirmed CVA6 cases were also retrospectively clinically audited. CVA6 infections were identified in 33 and 69 individuals pre- and post-pandemic, respectively, with cases peaking in November of 2018 and 2022, but in October of 2021. HFMD was the primary diagnosis in 85.5% of the post-pandemic cases, but only 69.7% of the pre-pandemic cases, where respiratory and neurological symptoms (45.5% and 12.1%, respectively) were significantly elevated. A complete VP1 sequence was retrieved for 94% of the CVA6 cases, revealing that studied infections were genetically diverse and suggestive of multiple local and international transmission chains. CVA6 presented a significant clinical burden in our regional U.K. hospital setting both pre- and post-pandemic and was subject to dynamic clinical and genetic epidemiology.

Indexed as

COVID-19Hand, Foot and Mouth DiseasePhylogenySARS-CoV-2AdolescentAdultChildChild, PreschoolEnterovirusEnterovirus A, HumanFemaleHumansInfantMaleMiddle AgedPandemicscoxsackievirus A6CVA6enterovirusgenetic epidemiologyhand, foot and mouth diseaseHFMD

Identifiers

PMID39599573
PMCPMC11597771

What OpenQuestion holds

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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.