Parker Edyth, Omah Ifeanyi F, Varilly Patrick, Magee Andrew, Ayinla Akeemat Opeyemi, Sijuwola Ayotunde E, Ahmed Muhammad I, Ope-Ewe Oludayo O, Ogunsanya Olusola Akinola, Olono Alhaji, Eromon Philomena, Tomkins-Tinch Christopher H, Otieno James Richard, Akanbi Olusola, Egwuenu Abiodun, Ehiakhamen Odianosen, Chukwu Chimaobi, Suleiman Kabiru, Akinpelu Afolabi, Ahmad Adama, Imam Khadijah Isa, Ojedele Richard, Oripenaye Victor, Ikeata Kenneth, Adelakun Sophiyah, Olajumoke Babatunde, Djuicy Delia Doreen, Essengue Loique Landry Messanga, Yifomnjou Moïse Henri Moumbeket, Zeller Mark, Gangavarapu Karthik, O'Toole Áine, Park Daniel J, Mboowa Gerald, Tessema Sofonias Kifle, Tebeje Yenew Kebede, Folarin Onikepe, Happi Anise, Lemey Philippe, Suchard Marc A, Andersen Kristian G, Sabeti Pardis, Rambaut Andrew, Njoum Richard, Ihekweazu Chikwe, Jide Idriss, Adetifa Ifedayo, Happi Christian T
African Center of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA.
medRxiv. 2024 Jun 19:2024.06.18.24309104. doi: 10.1101/2024.06.18.24309104.
Five years before the 2022-2023 global mpox outbreak Nigeria reported its first cases in nearly 40 years, with the ongoing epidemic since driven by sustained human-to-human transmission. However, limited genomic data has left questions about the timing and origin of the mpox virus' (MPXV) emergence. Here we generated 112 MPXV genomes from Nigeria from 2021-2023. We identify the closest zoonotic outgroup to the human epidemic in southern Nigeria, and estimate that the lineage transmitting from human-to-human emerged around July 2014, circulating cryptically until detected in September 2017. The epidemic originated in Southern Nigeria, particularly Rivers State, which also acted as a persistent and dominant source of viral dissemination to other states. We show that APOBEC3 activity increased MPXV's evolutionary rate twenty-fold during human-to-human transmission. We also show how Delphy, a tool for near-real-time Bayesian phylogenetics, can aid rapid outbreak analytics. Our study sheds light on MPXV's establishment in West Africa before the 2022-2023 global outbreak and highlights the need for improved pathogen surveillance and response.
在2022 - 2023年全球猴痘疫情爆发的五年前,尼日利亚报告了近40年来的首例病例,此后持续的人际传播导致了疫情的蔓延。然而,有限的基因组数据使得关于猴痘病毒(MPXV)出现的时间和起源存在疑问。在此,我们从2021年至2023年期间在尼日利亚生成了112个MPXV基因组。我们确定了尼日利亚南部人类疫情最接近的人畜共患病外类群,并估计人际传播的谱系大约在2014年7月出现,隐秘传播直至2017年9月被发现。疫情起源于尼日利亚南部,特别是河流州,该州也是病毒传播到其他州的持续且主要的源头。我们表明,APOBEC3活性在人际传播过程中将MPXV的进化速率提高了20倍。我们还展示了Delphy(一种用于近实时贝叶斯系统发育分析的工具)如何有助于快速的疫情分析。我们的研究揭示了MPXV在2022 - 2023年全球疫情爆发之前在西非的传播情况,并强调了加强病原体监测和应对的必要性。