Nationwide Mpox Genomic Surveillance Reveals Clade Ib Introductions, APOBEC3-Driven Evolution, and Terminal Deletions
Brochu, H. N.; Shi, Q.; Song, K.; Zhang, Q.; Munroe, J.; Harris, N. J.; Britt, N.; Zeng, Q.; Kapuria, K.; Chappell, J.; Norvell, B. M.; Peavy, L.; Williams, J. D.; Harris, A. B.; Chaitram, J.; Hutson, C. L.; Deng, J.; McGrath, D.; Boles, D.; Dale, S. E.; Gigante, C. M.; Iyer, L. K.
Show abstract
Background The 2022-2023 global mpox outbreak highlighted the critical need for robust genomic surveillance capabilities to track mpox virus (MPXV) evolution and transmission dynamics. Methods Building upon our established SARS-CoV-2 sequencing infrastructure, we implemented a Molecular Loop probe-based long-read sequencing approach using Pacific Biosciences Sequel II technology for comprehensive MPXV genomic surveillance across the United States (US). From August 2024 to June 2025, we generated 326 high-quality whole genome sequences from residual mpox-positive clinical specimens collected by Labcorp across all 10 US Department of Health and Human Services regions. Results Our analysis identified two samples containing clade Ib MPXV in January and June 2025 and captured shifting trends in clade IIb diversity, with 13 distinct lineages observed. We also identified multiple instances of large (~1.6-17.6kb) deletions proximal to the inverted terminal repeats in clade IIb genomes. APOBEC3 mutation analysis indicated substantial evidence of human-to-human transmission among both clades. Further, we observed significantly higher APOBEC3-associated SNPs per kilobase (P<0.001) in clade IIb genomic variable regions relative to their central conserved region. Our assay exhibited strong reproducibility across biological replicates from individual patients and accuracy was confirmed via parallel sequencing of select specimens by US Centers for Disease Control and Prevention (CDC) using metagenomic sequencing. We also demonstrated via custom simulation that our assay discriminates all known MPXV clades and lineages, including those we have not observed in the US. Conclusions Our integrated nationwide surveillance system facilitates real-time genomic tracking of outbreak evolution, with demonstrated capacity across SARS-CoV-2 and MPXV, positioning this platform for rapid deployment during future pathogen emergence.
Matching journals
The top 11 journals account for 50% of the predicted probability mass.