Evidence map›Paper›PMID 40225905›Full record

ArticleWellcome open research2025

Identification of coxsackievirus A24 variant during an acute hemorrhagic conjunctivitis outbreak in coastal Kenya, 2024.

Arnold W Lambisia, John Mwita Morobe, Edidah Moraa, Salim Mwarumba, Fredrick K N Korir, Raila Seif Athman, Rebecca Kiptui, Micheal Mbee, Nelly Mugo, Patrick Amoth and 8 more

Abstract read
In one paragraph

Article in Wellcome open research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

18 authors.

Arnold W LambisiaKenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0001-5312-0960
John Mwita MorobeKenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0003-2398-6717
Edidah MoraaKenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Salim MwarumbaKenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Fredrick K N KorirLighthouse for Christ Eye Centre, Mombasa, Kenya.
Raila Seif AthmanCoast General Teaching and Referral Hospital, Mombasa, Kenya.
Rebecca KiptuiMinistry of Health, Nairobi, Kenya.
Micheal MbeeMinistry of Health, Nairobi, Kenya.ORCID https://orcid.org/0000-0002-7655-3416
Nelly MugoKenya Medical Research Institute, Nairobi, Kenya.
Patrick AmothMinistry of Health, Nairobi, Kenya.
Penny MuangeMinistry of Health, Nairobi, Kenya.
Charlotte J HouldcroftDepartment of Genetics, University of Cambridge, Cambridge, England, UK.
Edwine BarasaKenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Joseph MwangangiKenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
George GithinjiKenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0001-9640-7371
Edward C HolmesThe University of Sydney School of Medical Sciences, Sydney, Australia.ORCID https://orcid.org/0000-0001-9596-3552
Lynette Isabella Ochola-OyierKenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Charles N AgotiKenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0002-2160-567X

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: In early 2024, a surge in acute hemorrhagic conjunctivitis (AHC), also referred as "red eye" disease, was observed in coastal Kenya, prompting the Ministry of Health to issue an outbreak alert. Herein, we investigated the etiology of this outbreak. Methods: Ocular swabs were obtained from 13 individuals presenting with AHC at a Mombasa clinic in early February 2024. Ten of these were analyzed using bacterial cultures, and all 13 using a pan-adenovirus quantitative PCR (qPCR) and metagenomic sequencing. Potential viral etiology was confirmed by a specific qPCR, amplicon sequencing and phylogenetic analysis. Results: Bacterial cultures yielded no growth except in three samples where non-pathogenic bacteria were detected. All 13 samples were adenovirus qPCR negative. Metagenomic sequencing detected coxsackievirus A24 variant (CA24v) in three of the 13 samples. CV-A24v detections were confirmed by both CV-A24v specific qPCR and amplicon sequencing of an approximately 450 nucleotide long VP4/2 junction genomic region. Phylogenetic analysis of the VP4/2 sequences showed that they were closely related to CV-A24v genotype IV. Conclusion: The AHC epidemic in coastal Kenya in early 2024 was likely caused by CA24v. Metagenomic sequencing is a powerful tool for identifying potential causative agents of new disease outbreaks.

Indexed as

AfricaConjuctivitisCoxsackievirus A24 variantEnterovirusKenyaRed eye

Identifiers

PMID40225905
PMCPMC11992516

What OpenQuestion holds

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LicenceCC BY
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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.