Evidence map›Paper›PMID 42281482›Full record

ArticleInfluenza and other respiratory viruses2026

Genomic Surveillance of SARS-CoV-2 in Senegal (2020-2024): Variant Turnover, Omicron Introductions, and Interregional Spread.

Ndeye Awa Ndiaye, Safiétou Sankhe, Mamadou Malado Jallow, Mouhamed Kane, Khadidiatou Ndour, Amadou Diallo, Maimouna Mbanne, Ndeye Marième Top, Seynabou Mbaye Ba Souna Diop, Madeleine Dieng and 12 more

Abstract read
In one paragraph

Article in Influenza and other respiratory viruses, 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

22 authors.

Ndeye Awa NdiayeVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0009-0006-0819-194X
Safiétou SankheVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0001-8559-2161
Mamadou Malado JallowVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0002-9815-4563
Mouhamed KaneVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0009-0009-6489-7244
Khadidiatou NdourVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.
Amadou DialloVaccine Research Center, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0002-8584-9972
Maimouna MbanneVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.
Ndeye Marième TopEpidemiology, Clinical Research and Data Science Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0002-8626-4140
Seynabou Mbaye Ba Souna DiopVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.
Madeleine DiengVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0009-0004-1302-4762
Issa GnasseVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0009-0006-0980-9086
Debora GoudiabyVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.
Cheikh TallaVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0003-0678-1226
Mamadou Aliou BarryPublic Health Direction, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0002-3956-8782
Oumar FayeVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0002-3478-1322
Ousmane FayePublic Health Direction, Institut Pasteur de Dakar, Dakar, Senegal.
Cheikh LoucoubarEpidemiology, Clinical Research and Data Science Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0002-9582-4197
Amadou Alpha SallVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.
Gamou FallVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0001-5035-1325
Marie Henriette Dior NdioneVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0002-5613-4521
Moussa Moïse DiagneVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0001-5461-5623
Ndongo DiaVirology Department, Institut Pasteur de Dakar, Dakar, Senegal.ORCID https://orcid.org/0000-0002-4051-3797

Funding

Agence Française de Développement CZZ3209French Ministry for Europe and Foreign AffairsGates Foundation INV-018278Gates Foundation INV-018978Gates Foundation INV-036379Gates Foundation INV-036413NIH HHS NIH3U01AI151758-02S1
6 · The paper itself

Abstract

backgroundGenomic surveillance is central to tracking SARS-CoV-2 evolution, variant replacement, and transmission dynamics. In Senegal, the Institut Pasteur de Dakar generated one of the largest national longitudinal SARS-CoV-2 genomic datasets, offering a unique view of viral spread from the first pandemic wave to the post-Omicron period.

aimsThis study aimed to reconstruct SARS-CoV-2 evolution and dissemination in Senegal from March 2020 to September 2024, assess variant and Omicron sublineage dynamics, infer introduction and interregional spread patterns, and describe the national mutational landscape. MATERIAL AND

methodsA total of 4820 SARS-CoV-2 genomes generated by the Institut Pasteur de Dakar were analyzed. Lineage assignment, temporal and regional distribution, time-scaled phylogenetics, discrete phylogeographic reconstruction, and mutation profiling were used to assess variant turnover, international seeding, intranational dissemination, and genomic diversification.

resultsAncestral A/B lineages predominated in 2020 before replacement by Alpha and Beta in early 2021, followed by Delta in mid-2021, which coincided with the highest case burden. From late 2021, Omicron became dominant, with rapid turnover of BA.1/BA.2, BA.4/BA.5, BQ.1.1, XBB, and BA.2.86, while later waves were smaller. Dakar contributed 64.7% of genomes and emerged as the main hub for inferred introductions and interregional spread, with Kaolack and Diourbel as secondary hubs. Major Omicron sublineages resulted from multiple introductions, mainly from Africa and Europe, with BA.1/BA.2 seeded from a broader range of continents than later lineages. Mutation profiling showed strong enrichment in Spike, with recurrent changes in ORF1a/ORF1b and nucleocapsid. DISCUSSION: The findings reveal repeated variant replacement, shifting international seeding routes, and a hub-and-spoke pattern of national dissemination centered on Dakar. Declining later waves may reflect increasing hybrid population immunity, although interpretation remains influenced by heterogeneous sequencing intensity.

conclusionsThis study provides an integrated national picture of SARS-CoV-2 evolution in Senegal and supports decentralized sequencing, stronger metadata capture, and routine use of genomic evidence for public health decision-making.

Indexed as

COVID-19Genome, ViralSARS-CoV-2Evolution, MolecularGenomicsHumansMutationPhylogenyPhylogeographySenegalgenomic surveillanceomicronphylogeographySARS‐CoV‐2Senegalviral evolution

Identifiers

PMID42281482
PMCPMC13261306

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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.