Evidence map›Paper›PMID 42045835›Full record

SynthesisBMC infectious diseases2026

Prevalence and genetic diversity of enteric viruses in Sub-Saharan Africa: a systematic review and meta-analysis.

Ange Oho Roseline Badjo, Nongodo Firmin Kabore, Arsène Zongo, Justice Agbadu, Essia Belarbi, Abdoul-Salam Ouedraogo

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Ange Oho Roseline BadjoLaboratory of Emerging and Re-emerging Pathogens, Nazi Boni University, Bobo Dioulasso, 01 BP 1091, Burkina Faso. angebadjo@yahoo.fr.
Nongodo Firmin KaboreCentre MURAZ, Institut National de Santé Publique, Bobo-Dioulasso, Burkina Faso.
Arsène ZongoCentre for International Health Protection, Public Health Laboratory Support, Robert Koch Institute, Unit 4, Berlin, Germany.
Justice AgbaduCharité - Universitätsmedizin Berlin, Berlin, Germany.
Essia BelarbiCentre for International Health Protection, Public Health Laboratory Support, Robert Koch Institute, Unit 4, Berlin, Germany.
Abdoul-Salam OuedraogoLaboratory of Emerging and Re-emerging Pathogens, Nazi Boni University, Bobo Dioulasso, 01 BP 1091, Burkina Faso.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRotavirus A (RVA), norovirus (NoV), human astrovirus (HAstV), and sapovirus (SaV) are the main viruses responsible for acute gastroenteritis worldwide. Among them, RVA is generally the most prevalent, predominantly in Sub-Saharan Africa. With the introduction of RVA vaccines, several epidemiological changes have been reported in cases of viral gastroenteritis, particularly in Sub-Saharan Africa. Therefore, it is essential to understand the current burden and diversity of these viruses in order to guide public health interventions and vaccination strategies in the region.

objectiveOur objective was to examine changes in prevalence data and circulating genotypes of RVA, NoV, SaV, and HAstV associated with acute gastrointestinal infections in both adults and children in Sub-Saharan Africa, based on studies published between 2010 and 2023.

methodsA systematic search was conducted in PubMed and Google Scholar to identify relevant studies published between 2010 and 2023, focusing exclusively on Sub-Saharan Africa. No restrictions were applied in terms of language or age group. Study selection, data extraction, and methodological quality assessment were performed using standardized procedures. Heterogeneity between studies was assessed using Cochrane’s Q test and the I² statistic in a random-effects model. Combined prevalence estimates for RVA, NoV, SaV, and HAstV were calculated using Comprehensive Meta-Analysis software.

resultsA total of 55 studies from 19 countries in Sub-Saharan Africa were included. The combined prevalence was 31% for RVA, 14% for NoV, 12% for SaV, and 5% for HAstV. Overall, enteric viruses accounted for a combined prevalence of 22%. High heterogeneity (I² > 73%) was observed for most viruses. Genotyping data from 27 studies conducted in 13 countries showed high genetic diversity. RVA had 33 G/P combinations, the most common being G1P[8] and for NoV the GII.4 and GII.6 genotypes predominated. The high prevalence and genetic diversity of enteric viruses observed in this study underscore the continuing burden of viral gastroenteritis on public health in sub-Saharan Africa and confirm the need for ongoing surveillance to inform vaccination and control strategies.

Indexed as

GastroenteritisGenetic VariationAfrica South of the SaharaGenotypeHumansNorovirusPrevalenceRotavirusSapovirusAstrovirusGastroenteritisMolecular epidemiologyNorovirusPrevalenceRotavirusSapovirusSub-Saharan Africa

Identifiers

PMID42045835
PMCPMC13262512

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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.