The Re-Emergence of Bundibugyo Ebolavirus in Uganda and the Democratic Republic of Congo: Epidemiological Drivers, Response Strategies, and Implications for Global Health Security.

IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES
Infection and Drug Resistance Pub Date : 2026-09-03 eCollection Date: 2026-01-01 DOI:10.2147/IDR.S632723
Gerald Olwit, Ivy Bochaberi Ombongi, Henon Ataryeba, Andrea Nantongo, Babirye Shamim
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引用次数: 0

Abstract

Bundibugyo ebolavirus (BDBV) is one of the least studied species within the genus Orthoebolavirus (family Filoviridae), despite its capacity to cause severe Ebola virus disease (EVD) with substantial mortality. First identified during a 2007-2008 outbreak in Bundibugyo District, western Uganda (149 reported cases, 37 deaths; case-fatality rate [CFR] approximately 25-36%), BDBV re-emerged in 2012 in Orientale Province, Democratic Republic of the Congo (DRC) (57-59 cases, 29-34 deaths; CFR 34-58%), before resurfacing in Ituri Province, DRC, in April-May 2026. By 11 August 2026, this third outbreak had grown to 4566 laboratory-confirmed cases and 2128 deaths (CFR ≈ 47%) across five DRC provinces and Uganda, becoming the largest, fastest-growing BDBV epidemic on record and the second-largest Ebola-family outbreak overall. This narrative review, not a systematic review or meta-analysis, summarizes peer-reviewed literature, preprints, and official situation reports from WHO, Africa CDC, US CDC, ECDC, and national health ministries, identified through PubMed, Scopus, Web of Science, Google Scholar, and Embase from inception to 12 August 2026, to examine BDBV historical evolution, virology and pathogenesis, drivers of re-emergence, surveillance and response, therapeutic and vaccine gaps, and global health security implications. The 2026 outbreak, unfolding amid conflict and mass displacement in eastern DRC, has been marked by an estimated basic reproduction number of 1.4-2.1 (central estimate 1.71), disproportionate infection among healthcare workers (7.2% of confirmed cases in DRC, 20% in Uganda), and the continued absence of licensed BDBV-specific vaccines or therapeutics. Findings underscore the need for sustained genomic and ecological surveillance, decentralized rapid diagnostics, broadly protective pan-filovirus vaccines, conflict-sensitive response strategies, and strengthened Uganda-DRC collaboration. Because the evidence base for the ongoing outbreak remains preliminary, findings should be interpreted cautiously and revisited as further peer-reviewed data emerge.

本迪布焦埃博拉病毒在乌干达和刚果民主共和国的重新出现:流行病学驱动因素、应对战略和对全球卫生安全的影响。
本迪布焦埃博拉病毒(BDBV)是正埃博拉病毒属(丝状病毒科)中研究最少的物种之一,尽管它能够引起严重的埃博拉病毒病(EVD)并造成大量死亡率。在2007-2008年乌干达西部本迪布乔区暴发期间首次发现BDBV(149例报告病例,37例死亡;病死率[CFR]约为25-36%),2012年在刚果民主共和国东方省再次出现(57-59例,29-34例死亡;CFR 34-58%),然后于2026年4月至5月在刚果民主共和国伊图里省重新出现。到2026年8月11日,第三次疫情在刚果民主共和国5个省和乌干达已发展到4566例实验室确诊病例和2128例死亡(病死率≈47%),成为有记录以来规模最大、增长最快的BDBV疫情和总体上第二大埃博拉家族疫情。本叙述性综述(不是系统综述或荟萃分析)总结了从成立到2026年8月12日期间通过PubMed、Scopus、Web of Science、谷歌Scholar和Embase确定的来自世卫组织、非洲疾病预防控制中心、美国疾病预防控制中心、ECDC和各国卫生部的同行评审文献、预印本和官方情况报告,以检查BDBV的历史演变、病毒学和发病机制、再次出现的驱动因素、监测和反应、治疗和疫苗差距。以及全球卫生安全影响。在刚果民主共和国东部的冲突和大规模流离失所中爆发的2026年疫情的特点是,估计基本繁殖数为1.4-2.1(中央估计为1.71),卫生保健工作者感染比例过高(刚果民主共和国确诊病例占7.2%,乌干达占20%),以及持续缺乏获得许可的bdbv特异性疫苗或治疗方法。调查结果强调需要持续的基因组和生态监测、分散的快速诊断、广泛保护性的泛丝状病毒疫苗、对冲突敏感的应对战略以及加强乌干达与刚果民主共和国的合作。由于目前疫情的证据基础仍然是初步的,因此应谨慎解释调查结果,并随着进一步同行评议数据的出现而重新审视。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infection and Drug Resistance
Infection and Drug Resistance Medicine-Pharmacology (medical)
CiteScore
5.60
自引率
7.70%
发文量
826
审稿时长
16 weeks
期刊介绍: About Journal Editors Peer Reviewers Articles Article Publishing Charges Aims and Scope Call For Papers ISSN: 1178-6973 Editor-in-Chief: Professor Suresh Antony An international, peer-reviewed, open access journal that focuses on the optimal treatment of infection (bacterial, fungal and viral) and the development and institution of preventative strategies to minimize the development and spread of resistance.
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