Evidence map›Paper›PMID 41840518›Full record

ArticleBMC infectious diseases2026

Genome characterization of the SARS-CoV-2 omicron in Cameroon.

Chavely Gwladys Monamele, Loique Landry Messanga Essengue, Moïse Henri Moumbeket-Yifomnjou, Pauliana Vanessa Ilouga, Aristide Mounchili-Njifon, Ibrahim Pascal Touoyem, Estelle Madaha Longla, Ripa Mohamadou Njankouo, Abdou Fatawou Modiyinji, Ifeanyi F Omah and 1 more

Abstract read
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Article 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

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

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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

11 authors.

Chavely Gwladys Monamele *Virology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon.
Loique Landry Messanga Essengue *Virology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon.
Moïse Henri Moumbeket-Yifomnjou *Virology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon.
Pauliana Vanessa IlougaVirology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon.
Aristide Mounchili-NjifonVirology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon.
Ibrahim Pascal TouoyemVirology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon.
Estelle Madaha LonglaVirology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon.
Ripa Mohamadou NjankouoVirology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon.
Abdou Fatawou ModiyinjiVirology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon.
Ifeanyi F OmahInstitute of Ecology and Evolution, University of Edinburgh, The King's Buildings, Edinburgh, EH9 3FL, UK.
Richard NjouomVirology Department, Centre Pasteur Cameroon, PO Box 1274, Yaoundé, Cameroon. njouom@pasteur-yaounde.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe omicron lineage has been declared the fifth variant of concern (VOC) by the World Health Organization (WHO). This study aims to describe the genomic characteristics of omicron sequences from Cameroon and to discuss the potential implications of identified mutations for viral evolution and immune escape, based on existing literature.

methodsThis study is a retrospective analysis of publicly available SARS-CoV-2 sequences from Cameroon submitted to GISAID (Global Initiative on Sharing Avian Influenza Data). Full-length omicron sequences from across Cameroon were retrieved from the GISAID database. Phylogenetic analyses were conducted using Nextstrain SARS-CoV-2 Workflow version 8.2.0, and mutation analysis was performed using the Nextstrain web tool, with the Wuhan-Hu-1/2019 strain as a reference.

resultsA total of 1,428 omicron sequences were analyzed, revealing eleven variants: BA.1 lineage (45.0%), B.1.1.529 (0.2%), BA.2 (7.7%), BA.4 (6.5%), BA.5 (16.3%), BE (12.2%), BF (6.3%), BN.2 (0.1%), BQ.1 (3.7%), XBB (0.5%) and JN.1 (1.5%). The sequences exhibited high number of mutations in the spike gene, with the JN.1 lineage showing the highest mutation count. All lineages contained mutations associated with neutralizing antibody evasion, including R346T, K417N, G446S, E484A, or Q493R.

conclusionsOngoing monitoring of omicron lineages is crucial to detect emerging variants and adapt vaccine strategies. The significant mutations, particularly in the JN.1 lineage warrant further investigation to assess their potential impact on transmissibility or immune escape. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

COVID-19Genome, ViralSARS-CoV-2CameroonHumansMutationPhylogenyRetrospective StudiesGenetic variabilityMutation analysisOmicronSARS-CoV-2

Identifiers

PMID41840518
PMCPMC13104191

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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.