Exploring the transmission modalities of Bunyamwera virus

IF 2.8 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Erik A Turner, R. Christofferson
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Abstract

Bunyamwera virus (BUNV) (Bunyamwera orthobunyavirus) has been found in Sub-Saharan Africa and demonstrated recently as cocirculating with Rift Valley Fever Virus (RVFV). Little is known regarding the breadth of transmission modalities of Bunyamwera. Given its co-occurence with RVFV, we hypothesized the transmission system of BUNV shared similarities to the RVFV system including transmission by Ae. aegypti mosquitoes and environmentally mediated transmission through fomites and environmental contamination. We exposed Ae. aegypti mosquitoes to BUNV and evaluated their ability to transmit both vertically and horizontally. Further, we investigated the potential for a novel transmission modality via environmental contamination. We found that the LSU colony of Ae. aegypti was not competent for the virus for either horizontal or vertical transmission; but, 20% of larva exposed to virus via contaminated aquatic habitat were positive. However, transstadial clearance of the virus was absolute. Finally, under simulated temperature conditions that matched peak transmission in Rwanda, we found that BUNV was stable in both whole blood and serum for up to 28 days at higher total volume in tubes at moderate quantities (103–5 genome copies/mL). In addition, infectiousness of these samples was demonstrated in 80% of the replicates. At lower volume samples (in plates), infectiousness was retained out to 6–8 days with a maximum infectious titer of 104 PFU/mL. Thus, the potential for contamination of the environment and/or transmission via contaminated fomites exists. Our findings have implications for biosafety and infection control, especially in the context of food animal production.
探索布尼亚姆韦拉病毒的传播方式
布尼亚姆韦拉病毒(BUNV)(布尼亚姆韦拉正圆病毒)已在撒哈拉以南非洲发现,最近被证实与裂谷热病毒(RVFV)共同传播。人们对 Bunyamwera 传播方式的广度知之甚少。鉴于布尼亚姆韦拉病毒与 RVFV 病毒共存,我们假设布尼亚姆韦拉病毒的传播系统与 RVFV 病毒的传播系统有相似之处,包括通过埃及姬蚊传播,以及通过寄生虫和环境污染在环境中传播。我们让埃及姬蚊接触 BUNV,并评估了它们垂直和水平传播的能力。此外,我们还研究了通过环境污染进行新型传播的可能性。我们发现,埃及伊蚊的 LSU 群体不具备水平或垂直传播病毒的能力;但是,通过受污染的水生栖息地接触病毒的幼虫中有 20% 呈阳性。不过,病毒的横向清除率是绝对的。最后,在与卢旺达传播高峰期相匹配的模拟温度条件下,我们发现在中等数量(103-5 基因组拷贝/毫升)的试管中,全血和血清中的 BUNV 在较高的总体积下可稳定长达 28 天。此外,这些样本在 80% 的重复样本中都具有传染性。在低容量样本(平板)中,感染性可保持 6-8 天,最大感染滴度为 104 PFU/mL。因此,存在污染环境和/或通过受污染的寄生体传播的可能性。我们的研究结果对生物安全和感染控制,尤其是食用动物生产中的生物安全和感染控制具有重要意义。
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来源期刊
Experimental Biology and Medicine
Experimental Biology and Medicine 医学-医学:研究与实验
CiteScore
6.00
自引率
0.00%
发文量
157
审稿时长
1 months
期刊介绍: Experimental Biology and Medicine (EBM) is a global, peer-reviewed journal dedicated to the publication of multidisciplinary and interdisciplinary research in the biomedical sciences. EBM provides both research and review articles as well as meeting symposia and brief communications. Articles in EBM represent cutting edge research at the overlapping junctions of the biological, physical and engineering sciences that impact upon the health and welfare of the world''s population. Topics covered in EBM include: Anatomy/Pathology; Biochemistry and Molecular Biology; Bioimaging; Biomedical Engineering; Bionanoscience; Cell and Developmental Biology; Endocrinology and Nutrition; Environmental Health/Biomarkers/Precision Medicine; Genomics, Proteomics, and Bioinformatics; Immunology/Microbiology/Virology; Mechanisms of Aging; Neuroscience; Pharmacology and Toxicology; Physiology; Stem Cell Biology; Structural Biology; Systems Biology and Microphysiological Systems; and Translational Research.
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