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Review of genomic surveillance finds concurrent Mpox subclade circulation across Africa

Review of genomic surveillance finds concurrent Mpox subclade circulation across Africa
Photo by National Institute of Allergy and Infectious Diseases / Unsplash
Key Takeaway
Consider harmonized genomic surveillance and One Health strategies to track Mpox subclade transmission across Africa.

This is a review and synthesis of genomic surveillance data for Mpox across Africa. The scope covers 24 African Union Member States, using 3,450 high-quality MPXV virus whole genomes to analyze viral diversity and transmission dynamics.

The authors synthesize findings on concurrent circulation of Subclades Ia, Ib, IIa, and IIb. Subclade Ia shows high virus diversity in reservoir hosts in Central Africa, detected through zoonotic transmission and some sustained human outbreak. Subclade Ib demonstrates sustained human-to-human transmission across Eastern and Southern Africa. Subclade IIa is largely zoonotic in West Africa, while Subclade IIb involves continued zoonotic transmission and a sustained human outbreak linked to lineage G1 and G2 circulation.

Additional findings include frequent cross-border transmission aligned with human mobility corridors, with Democratic Republic of the Congo or Sierra Leone emerging as sources of regional exportation. Ongoing cross-border zoonotic spillovers are noted at interfaces such as Cameroon and Nigeria, and CAR with Cameroon or DRC.

The authors acknowledge gaps in the evidence, though specific limitations are not detailed in this synthesis. Practice relevance highlights the need for harmonized genomic surveillance, APOBEC3-aware triage, and integrated One Health strategies to prevent local outbreaks from escalating into regional epidemics and to inform vaccine deployment and public health preparedness.

Study Details

EvidenceLevel 5
PublishedApr 2026
View Original Abstract ↓
The recent MPXV epidemic across Africa revealed extensive viral diversity and complex transmission dynamics, prompting a continent-wide genomic investigation. We analysed 3,450 high-quality MPXV virus whole genomes from 24 African Union Member States, revealing the complex and concurrent circulation of Subclades Ia, Ib, IIa, and IIb. Subclade Ia showed high levels of virus diversity in reservoir hosts in Central Africa, detected through zoonotic transmission and some sustained human outbreak lastly detected. In contrast, Clade Ib exhibited signatures of sustained human to human transmission across Eastern and Southern Africa. Clade IIa remains largely zoonotic in West Africa. Like Ia, IIb shows continued zoonotic transmission, and sustained human outbreak linked to lineage G1 and G2 circulation. Phylogeographic analyses revealed frequent cross border transmission and interconnectedness, which was aligned with both human mobility corridors and international boundaries. For instance, the Democratic Republic of the Congo or Sierra Leone seems to emerge as a source of regional exportation, while the Cameroon and Nigeria, CAR and Cameroon or CAR and DRC interfaces reflected ongoing cross border zoonotic spillovers. These findings underscore the need for harmonised genomic surveillance, APOBEC3-aware triage, and integrated One Health strategies to prevent local outbreaks from escalating into regional epidemics and to inform vaccine deployment and public health preparedness.
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