Evidence map›Paper›PMID 42378230›Full record

ArticlePloS one2026

Whole-genome sequencing reveals a previously unrecognized measles virus cluster in Burundi.

Néhémie Nzoyikorera, David F Nieuwenhuijse, Leonard Schuele, Cassien Nduwimana, Armstrong Ndihokubwayo, Théogène Ihorimbere, Denis Niyomwungere, Hayley Cassidy, Marjan Boter, Celestin Nibogora and 11 more

Abstract read
In one paragraph

Article in PloS one, 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
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

21 authors.

Néhémie NzoyikoreraNational Reference Laboratory, National Public Health Institute, Bujumbura, Burundi.ORCID https://orcid.org/0000-0002-0971-2245
David F NieuwenhuijseDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, the Netherlands.
Leonard SchueleDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, the Netherlands.
Cassien NduwimanaNational Reference Laboratory, National Public Health Institute, Bujumbura, Burundi.ORCID https://orcid.org/0000-0001-5514-3656
Armstrong NdihokubwayoNational Reference Laboratory, National Public Health Institute, Bujumbura, Burundi.
Théogène IhorimbereNational Reference Laboratory, National Public Health Institute, Bujumbura, Burundi.
Denis NiyomwungereNational Reference Laboratory, National Public Health Institute, Bujumbura, Burundi.
Hayley CassidyDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, the Netherlands.
Marjan BoterDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, the Netherlands.
Celestin NibogoraNational Reference Laboratory, National Public Health Institute, Bujumbura, Burundi.
Richard MolenkampDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, the Netherlands.
Alexis NiyomwungereOrganisation Mondiale de la Santé, Bujumbura, Burundi.
Dionis NizigiyimanaNational Public Health Institute, Ministry of Public Health, Bujumbura, Burundi.
Marie Noelle UwinezaNational Reference Laboratory, National Public Health Institute, Bujumbura, Burundi.
Idrissa DiawaraResearch Laboratory of Microbiology, Infectious Diseases, Allergology and Pathogen Surveillance (LARMIAS), Mohammed VI Faculty of Medicine, Mohammed VI University of Sciences and Health (UM6SS), Casablanca, Morocco.
Saria OtaniResearch Group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Kgs. Lyngby, Denmark.
Rogier BodewesCentre for Infectious Disease Control, National Institute for Public Health, and the Environment (RIVM), Bilthoven, The Netherlands.ORCID https://orcid.org/0000-0002-0689-7889
Frank M AarestrupResearch Group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Kgs. Lyngby, Denmark.
Marion KoopmansDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, the Netherlands.
Joseph NyandwiNational Public Health Institute, Ministry of Public Health, Bujumbura, Burundi.
Bas B Oude MunninkDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-9394-1189

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite remarkable progress towards measles elimination in Burundi, the country has seen a resurge in cases since 2019. Epidemiological investigations have been performed; however, it remained unclear if all measles cases involved in recent outbreaks were linked or caused by multiple independent events including introductions from other countries. Therefore, the objective of this study is to investigate the genetic diversity and evolution of measles virus (MeV) during the last large MeV outbreak in Burundi in 2024. The study was carried out on oropharyngeal swab samples collected from four neighboring health districts. Amplicon-based MeV sequencing was performed on the MinION Mk1D. Consensus sequences were generated from 18 isolates and phylogenetic and Bayesian evolution analysis including 152 closely related public genomes were performed. Results showed that all 18 newly generated whole-genome sequences belonged to the genotype B3. Phylogenetic analysis revealed a diverse population of MeV circulating in Burundi, with sequences divided into two separate clusters. The first cluster consisted of two sequences and was most closely related to Italian sequences, while the second cluster was more related to local transmission in the Great-Lakes region based on the N450 region. Based on whole-genome sequences, the remaining 16 whole-genome sequences from Burundi clustered with one sequence from the Netherlands. The most recent common ancestor of the sequences in the second cluster was estimated to be around the beginning of 2023 (between the end of 2022 and the end of 2023 using the 95% confidence intervals) by using Bayesian evolutionary analysis. Here, we provide the first batch of MeV whole-genome sequences generated on the African continent of the ongoing MeV outbreak in the Great Lakes region of Africa. Using these whole genome sequences, we demonstrated that measles viruses genotype B3 were already circulating in Burundi since the beginning of 2023 well before the outbreak in 2024 was noted. We also showed that the recurrent measles outbreaks in Burundi are ignited from different sources, showing that measles in Burundi is sustained by multiple introductions and emphasizing the importance of ongoing molecular surveillance for elimination efforts.

Indexed as

Genome, ViralMeaslesMeasles virusWhole Genome SequencingBayes TheoremBurundiDisease OutbreaksGenetic VariationGenotypeHumansPhylogeny

Identifiers

PMID42378230
PMCPMC13317999

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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.