Nyathi Sindiso, Rezende Izabela M, Walter Katharine S, Thongsripong Panpim, Mutuku Francis, Ndenga Bryson, Mbakaya Joel O, Agola Gladys, Vu David M, Bennett Shannon, Mordecai Erin A, Andrews Jason R, LaBeaud A Desiree
Department of Epidemiology and Population Health, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, United States.
Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, United States.
Virus Evol. 2024 Dec 30;11(1):veae116. doi: 10.1093/ve/veae116. eCollection 2025.
Despite the increasing burden of dengue in Kenya and Africa, the introduction and expansion of the virus in the region remain poorly understood. The objective of this study is to examine the genetic diversity and evolutionary histories of dengue virus (DENV) serotypes 1 and 3 in Kenya and contextualize their circulation within circulation dynamics in the broader African region. Viral RNA was extracted from samples collected from a cohort of febrile patients recruited at clinical sites in Kenya from 2013 to 2022. Samples were tested by polymerase chain reaction (PCR) for DENV presence. Five DENV-positive samples were serotyped, and complete viral genomes for phylogenetic inference were obtained via sequencing on Illumina platforms. Sequences generated in our study were combined with global datasets of sequences, and Bayesian and maximum likelihood methods were used to infer phylogenetic trees and geographic patterns of spread with a focus on Kenya and Africa as a whole. Four new DENV-1 and one new DENV-3 genomes were successfully sequenced and combined with 328 DENV-1 and 395 DENV-3 genomes from elsewhere for phylogenetic analyses. The DENV-1 sequences from our study formed a monophyletic cluster with an inferred common ancestor in 2019 (most recent common ancestor 2019 and 95% high posterior density 2018-19), which was closely related to sequences from Tanzania. The single DENV-3 sequence clustered with sequences from Tanzania and Kenya, was collected between 2017 and 2019 and was related to recent outbreaks in the region. Phylogenetic trees resolved multiple clades of DENV-1 and DENV-3 concurrently circulating in Africa, introduced in the early-to mid-2000s. Three DENV-1 and four DENV-3 clades are highlighted, introduced between 2000 and 2015. Phylogeographic models suggest frequent, independent importations of DENV lineages into Kenya and Africa from East and South-East Asia via distinct geographic pathways. DENV-1 and DENV-3 evolutionary dynamics in Africa are characterized by the cocirculation of multiple recently introduced lineages. Circulating lineages are introduced via distinct geographic pathways that may be centered around regional nexus locations. Increased surveillance is required to identify key regional locations that drive spread, and dengue interventions should focus on interrupting spread at these locations.
尽管登革热在肯尼亚和非洲造成的负担日益加重,但该病毒在该地区的传入和传播情况仍鲜为人知。本研究的目的是研究肯尼亚登革热病毒(DENV)1型和3型的遗传多样性和进化史,并将它们在更广泛的非洲地区的传播动态背景下进行分析。从2013年至2022年在肯尼亚临床地点招募的一组发热患者采集的样本中提取病毒RNA。通过聚合酶链反应(PCR)检测样本中是否存在登革热病毒。对5份登革热病毒阳性样本进行血清分型,并通过Illumina平台测序获得用于系统发育推断的完整病毒基因组。将我们研究中生成的序列与全球序列数据集相结合,使用贝叶斯方法和最大似然方法推断系统发育树和传播的地理模式,重点关注肯尼亚和整个非洲。成功测序了4个新的DENV-1和1个新的DENV-3基因组,并与来自其他地方的328个DENV-1和395个DENV-3基因组相结合进行系统发育分析。我们研究中的DENV-1序列形成了一个单系簇,推断其共同祖先为2019年(最近共同祖先为2019年,95%的高后验密度为2018 - 2019年),与来自坦桑尼亚的序列密切相关。单一的DENV-3序列与来自坦桑尼亚和肯尼亚的序列聚类,于2017年至2019年期间采集,与该地区最近的疫情有关。系统发育树解析了21世纪初至中期传入非洲并同时传播的多个DENV-1和DENV-3分支。突出显示了2000年至2015年期间引入的3个DENV-1和4个DENV-3分支。系统地理学模型表明,DENV谱系通过不同的地理路径频繁、独立地从东亚和东南亚传入肯尼亚和非洲。非洲的DENV-1和DENV-3进化动态的特点是多个最近引入的谱系同时传播。传播的谱系通过可能以区域枢纽地点为中心的不同地理路径引入。需要加强监测以确定推动传播的关键区域地点,登革热干预措施应侧重于在这些地点阻断传播。