Article Text
Abstract
Objectives The 2022 global outbreak of monkeypox virus (MPXV), previously confined to Central and West Africa, necessitates an enhanced understanding of its spread. Comprehensive genomic surveillance to understand the virus’s evolution and spread is needed, particularly in Asia.
Methods Genomic data from 169 MPXV genome sequences in Asia were analysed. Through advanced genomic sequencing of clinical samples, we analysed the distribution and mutations of MPXV lineages in Asia.
Results Phylogenetic analysis revealed a distinct clustering of C.1 strains rise in Northeast Asia in 2023, while genomic examination identified specific consensus mutations like R84K, R665C and L16F in C.1 strains. The mutations, coupled with an increased rate of apolipoprotein B mRNA-editing catalytic polypeptide-like 3 motif G-to-A mutations in C.1 (OR 24.87±8.81), indicate a potential adaptation mechanism.
Conclusions Our findings underscore the need for ongoing surveillance and provide vital insights into MPXV’s evolving dynamics, aiding in public health strategy formulation against this emerging infectious threat.
- Epidemiology
- VIROLOGY
- SEXUAL HEALTH
Statistics from Altmetric.com
Footnotes
Handling editor Apostolos Beloukas
Y-CC and Y-CL contributed equally.
Contributors Y-CC: conceptualisation, methodology, data curation, investigation, writing—original draft. Y-CL: conceptualisation, methodology, data curation, writing—original draft, writing—review and editing. Y-CM: conceptualisation, methodology, data curation, investigation. T-KY: writing—review and editing. P-YL: conceptualisation, methodology, data curation, investigation, writing—original draft, writing—review and editing.
Funding This work was supported by grant from National Health Research Institutes (PH-112-PP05) to Y-CL. National Science and Technology Council grant 112-2314-B-075A-006, Taichung Veterans General Hospital: TCVGH-1123901C, TCVGH-1123901D; TCVGH-PU1128105 to P-YL.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.