# From forest to frontline: A comprehensive review of Mpox's global leap and viral evolution (2022–2024)

**Authors:** Baylor Akhavan, Abu-Bakr Ahmed, Wilson To, Samir Alkhouri, Kavita Batra

PMC · DOI: 10.1016/j.onehlt.2025.101232 · One Health · 2025-10-03

## TL;DR

This paper reviews the global spread and evolution of Mpox virus from 2022 to 2024, highlighting how two virus clades have affected different regions and populations.

## Contribution

The study provides a comprehensive synthesis of Mpox outbreaks, emphasizing genomic changes and disparities in public health responses.

## Key findings

- Clade IIb caused widespread transmission in non-endemic regions, mainly affecting men who have sex with men.
- Clade I resurged in Central Africa with high mortality among children under five.
- APOBEC3 mutations were linked to increased transmissibility of Clade I.

## Abstract

Since 2022, the global epidemiology of Mpox (MPXV) has transformed, with Clade IIb driving widespread transmission in non-endemic regions and Clade I resurging across Central Africa. Genomic adaptations, such as APOBEC3 mutations, and increasing human-to-human transmission have raised public health alarms. This review synthesizes the latest evidence on Clade I and Clade II MPXV outbreaks from 2022 to 2024, with an emphasis on geographic expansion, demographic disparities, and systemic response gaps.

A comprehensive literature search was conducted between September and December 2024 using PubMed, CDC, WHO, and ECDC databases. Studies were included if they reported primary data on Clade I or Clade II MPXV epidemiology. Gray literature, including public health reports and situation summaries, was also analyzed. Data extraction focused on demographic trends, transmission modes, genomic mutations, and public health responses.

Fifty-one sources were reviewed, including 14 peer-reviewed articles and 37 Gy literature reports. Clade IIb accounted for 117,000+ cases across 123 countries, primarily affecting men who have sex with men (MSM). Clade I resurged in the Democratic Republic of the Congo (DRC) with over 19,000 confirmed cases and 975 deaths, disproportionately affecting children under five. APOBEC3-type mutations were linked to increased Clade I transmissibility. International spread of Clade I was reported in the U.S., Europe, and Asia. Diagnostic limitations, especially in the DRC, and gaps in pediatric vaccine access remain major challenges.

MPXV's global trajectory now includes sustained transmission of both Clades I and II. Expanded genomic surveillance, pediatric-focused outbreak response, and equitable diagnostic and vaccine access are urgently needed. A One Health approach is essential to address evolving viral behavior and health disparities in endemic and non-endemic regions.

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•Clade IIb remained dominant in global spread, especially among MSM populations.•Clade I Mpox resurged in 2024 with sustained human transmission across Central Africa.•Genomic data revealed APOBEC3 mutations linked to Clade I transmission shifts.•Children under five faced the highest mortality rates in Clade I outbreaks in the DRC.•Diagnostic access remained below 20 % in the DRC, and children lacked adequate vaccine coverage and treatment access.

Clade IIb remained dominant in global spread, especially among MSM populations.

Clade I Mpox resurged in 2024 with sustained human transmission across Central Africa.

Genomic data revealed APOBEC3 mutations linked to Clade I transmission shifts.

Children under five faced the highest mortality rates in Clade I outbreaks in the DRC.

Diagnostic access remained below 20 % in the DRC, and children lacked adequate vaccine coverage and treatment access.

## Linked entities

- **Genes:** Apobec3 (apolipoprotein B mRNA editing enzyme, catalytic polypeptide 3) [NCBI Gene 80287]

## Full-text entities

- **Diseases:** deaths (MESH:D003643), I (MESH:D006969)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12538092/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12538092/full.md

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Source: https://tomesphere.com/paper/PMC12538092