Sustained human outbreak of a new MPXV clade I lineage in eastern Democratic Republic of the Congo
- PMID: 38871006
- PMCID: PMC11485229
- DOI: 10.1038/s41591-024-03130-3
Sustained human outbreak of a new MPXV clade I lineage in eastern Democratic Republic of the Congo
Abstract
Outbreaks of monkeypox (mpox) have historically resulted from zoonotic spillover of clade I monkeypox virus (MPXV) in Central Africa and clade II MPXV in West Africa. In 2022, subclade IIb caused a global epidemic linked to transmission through sexual contact. Here we describe the epidemiological and genomic features of an mpox outbreak in a mining region in eastern Democratic Republic of the Congo, caused by clade I MPXV. Surveillance data collected between September 2023 and January 2024 identified 241 suspected cases. Genomic analysis demonstrates a distinct clade I lineage divergent from previously circulating strains in the Democratic Republic of the Congo. Of the 108 polymerase chain reaction-confirmed mpox cases, the median age of individuals was 22 years, 51.9% were female and 29% were sex workers, suggesting a potential role for sexual transmission. The predominance of APOBEC3-type mutations and the estimated emergence time around mid-September 2023 imply recent sustained human-to-human transmission.
© 2024. The Author(s).
Conflict of interest statement
None of the authors declare competing interests.
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References
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- Van Dijck, C. et al. Emergence of mpox in the post-smallpox era—a narrative review on mpox epidemiology. Clin. Microbiol Infect.29, 1487–1492 (2023). - PubMed
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- 2022–24 mpox (monkeypox) outbreak: global trends. World Health Organization (2024); https://worldhealthorg.shinyapps.io/mpx_global/
MeSH terms
Grants and funding
- U01 AI096299/AI/NIAID NIH HHS/United States
- 5U01AI096299-13/U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID)
- R21 TW011706/TW/FIC NIH HHS/United States
- R25TW011217/U.S. Department of Health & Human Services | NIH | Fogarty International Center (FIC)
- D43 TW010937/TW/FIC NIH HHS/United States