从乌干达塞姆利基森林的伊蚊中检测到的韦塞尔布隆病毒流行前变种的基因型和系统地理学见解。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-11-12 DOI:10.1128/spectrum.00914-24
Georg Joachim Eibner, Selina Laura Graff, Christian Hieke, James Robert Ochieng, Anne Kopp, Christian Drosten, Julius Lutwama, Innocent Bidason Rwego, Sandra Junglen
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引用次数: 0

摘要

韦塞尔布隆病毒(Wesselsbron virus,WSLV)是一种被忽视的蚊媒病毒,属于黄热病亚群,属于黄热病病毒科正黄热病病毒属。尽管 WSLV 主要是一种可导致反刍动物死胎、先天性畸形和死亡的兽用病原体,但它也会感染人类,导致通常是自限性的发热性疾病,或在极少数情况下导致神经系统并发症。WSLV 在南部非洲零星爆发,但在其他非洲国家的蚊子身上发现的结果表明其分布范围更广。在此,我们报告了从乌干达西部塞穆利基国家公园内的原始生态系统中采集的伊蚊中检测并分离出 WSLV 的情况。与流行病参考毒株 SA H177 相比,检测到的毒株 M5937-UG-2018 在不同宿主的细胞系中的感染性、复制和传染性颗粒的产生都受到了影响。通过对蚊子匀浆进行下一代全基因组测序,发现该病毒与 1996 年从南非采集的人类样本中分离出的 WSLV 的核苷酸最大同一性为 98.1%。在系统发育分析中,M5937-UG-2018 与来自南非和塞内加尔的菌株进行了分组。对 WSLV 在非洲的时间和空间传播进行的重建估计,WSLV 可能于 19 世纪初起源于南非,并在随后的几十年中在南部非洲传播。根据模型,向非洲西部和东部的长距离迁移发生在 21 世纪初。然而,改变 M5937-UG-2018 的来源并没有降低模型支持 WSLV 广泛分布于非洲这一假设的可能性。WSLV 主要流行于南部非洲,但在其他地区的发现表明它在非洲大陆分布更广。由于很少对出现与 WSLV 感染相符的症状的家畜和人类进行鉴别诊断,因此对 WSLV 分布情况的了解很有限。我们对偏远热带雨林地区蚊子的病毒感染进行了调查,结果表明 WSLV 在乌干达流行。与来自南非的流行病分离物相比,分离出的病毒传染性较弱,体外复制能力也较低。空间和时间移动的系统地理学重建,以及新检测到的毒株起源地的位移,表明 WSLV 可能广泛分布于非洲各地。我们的数据表明,WSLV 的地理分布及其对人类和动物健康的影响很可能被低估了。
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Genotypic and phylogeographic insights into a pre-epidemic variant of Wesselsbron virus detected in sylvatic Aedes mcintoshi from Semuliki Forest, Uganda.

Wesselsbron virus (WSLV) is a neglected mosquito-borne virus within the yellow fever subgroup in the genus Orthoflavivirus of the Flaviviridae family. Despite being primarily a veterinary pathogen able to cause stillbirths, congenital malformations, and mortality in ruminants, WSLV also infects humans, causing a usually self-limiting febrile illness, or may lead to neurological complications in rare cases. WSLV causes sporadic outbreaks in Southern Africa, but findings in mosquitoes from other African countries suggest a wider distribution. Here, we report the detection and isolation of WSLV from an Aedes mcintoshi mosquito collected in a pristine ecosystem within Semuliki National Park, western Uganda. The detected strain M5937-UG-2018 was impaired in infectivity, replication, and production of infectious particles in cell lines derived from different hosts compared to an epidemic reference strain, SA H177. Full-genome sequencing by next-generation sequencing from the mosquito homogenate revealed a maximum nucleotide identity of 98.1% to a WSLV isolate from a human sample collected in South Africa in 1996. M5937-UG-2018 grouped in phylogenetic analyses with strains from South Africa and Senegal. Reconstruction of the temporal and spatial dispersal of WSLV across Africa estimated a likely origin of WSLV in South Africa in the early 19th century and spread in Southern Africa in the following decades. Long-distance movement toward Western and Eastern Africa was modeled to have occurred in the early 21st century. However, displacing the origin of M5937-UG-2018 did not decrease the likelihood of the model supporting the hypothesis that WSLV is widely distributed in Africa.IMPORTANCEWSLV is a neglected mosquito-borne virus causing teratogenicity in ruminants and febrile illness in humans. WSLV is mainly endemic to Southern Africa, but findings in other regions suggest a wider distribution on the continent. Knowledge of the distribution of WSLV is impaired as differential diagnostics are rarely performed in livestock and humans presenting with symptoms compatible with WSLV infection. Our work investigating viral infections in mosquitoes from a remote tropical rainforest region demonstrates that WSLV is endemic in Uganda. The isolated virus was less infective and showed lower replication ability in vitro compared to an epidemic isolate from South Africa. Phylogeographic reconstruction of spatial and temporal movements, along with the displacement of the origin of the newly detected strain, suggests that WSLV may be widely distributed across Africa. Our data show that the geographic distribution of WSLV and its impact on human and animal health are likely underestimated.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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