Author:
Ndodo Nnaemeka,Ashcroft Jonathan,Lewandowski Kuiama,Yinka-Ogunleye Adesola,Chukwu Chimaobi,Ahmad Adama,King David,Akinpelu Afolabi,de Motes Carlos Maluquer,Ribeca Paolo,Sumner Rebecca P.,Rambaut Andrew,Chester Michael,Maishman Tom,Bamidele Oluwafemi,Mba Nwando,Babatunde Olajumoke,Aruna Olusola,Pullan Steven T.,Gannon Benedict,Brown Colin,Ihekweazu Chikwe,Adetifa Ifedayo,Ulaeto David O.
Abstract
AbstractThe origin and hazardous potential of human mpox is obscured by a lack of genomic data between the 2018, when exportations from Nigeria were recorded, and 2022 when the global outbreak started. Here, 18 genomes from patients across southern Nigeria in 2019/20 reveal multiple lineages of Monkeypox virus have achieved sustained human-to-human transmission, co-existing in humans for several years and accumulating mutations consistent with APOBEC3 activity suggesting the virus in humans is now segregated from its natural reservoir. Remarkably, three genomes have disruptions in the A46R gene, which contributes to innate immune modulation. The data demonstrates that the A.2 lineage, multiply exported to North America since 2021 independently of the global outbreak, has persisted in Nigeria for more than two years prior to its latest exportation.One-Sentence SummaryMpox is now a human diseae evolving in humans with multiple variants taking separate paths towards adaptation, some analogous to those ofVariola
Publisher
Cold Spring Harbor Laboratory
Cited by
2 articles.
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