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以布尼亚姆韦拉病毒和巴泰病毒为模型探究正布尼亚病毒的重配现象。

Probing orthobunyavirus reassortment using Bunyamwera and Batai viruses as models.

作者信息

Bowen James M, Gunter Krista, Lunel Andrew M, Omoga Dorcus C A, Jones Jennifer E, Giesel Henry, Duprex W Paul, Tilston Natasha L

机构信息

Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.

Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.

出版信息

PLoS Negl Trop Dis. 2025 May 30;19(5):e0013120. doi: 10.1371/journal.pntd.0013120. eCollection 2025 May.

DOI:10.1371/journal.pntd.0013120
PMID:40445997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12169594/
Abstract

Reassortment is a critical evolutionary mechanism for segmented viruses, enabling the exchange of intact genome segments during co-infection and driving orthobunyavirus evolution; however, the molecular mechanisms underpinning this process remain unclear. With over 100 orthobunyavirus species, many of which are significant human and veterinary pathogens, understanding how reassortment influences transmissibility and virulence is essential for preempting the emergence of novel pathogens. Here, we use Bunyamwera virus (BUNV) and Batai virus (BATV) as models to explore orthobunyavirus reassortment through reverse genetics. We established the first reverse genetics system for BATV, generated reassortants, and employed minigenome assays to assess replication machinery compatibility. Additionally, we developed a novel hybridization chain reaction assay for high-resolution visualization of viral RNA segments. Our findings revealed that all six reassortants between BUNV and BATV are viable, exhibiting notable phenotypic differences in interferon-deficient (IFNAR-/-) mice. This work introduces essential tools and new insights into orthobunyavirus reassortment and pathogenesis, laying the groundwork for understanding this critical evolutionary process.

摘要

重配是分节段病毒的一种关键进化机制,能在共感染期间实现完整基因组节段的交换,推动正布尼亚病毒进化;然而,支撑这一过程的分子机制仍不清楚。正布尼亚病毒有100多个种,其中许多是重要的人类和兽医病原体,了解重配如何影响传播性和毒力对于预防新型病原体的出现至关重要。在此,我们以布尼亚姆韦拉病毒(BUNV)和巴泰病毒(BATV)为模型,通过反向遗传学探索正布尼亚病毒的重配。我们建立了首个BATV反向遗传学系统,产生了重配体,并采用微型基因组试验评估复制机制的兼容性。此外,我们开发了一种新型杂交链式反应试验,用于高分辨率可视化病毒RNA节段。我们的研究结果表明,BUNV和BATV之间的所有六种重配体都是可行的,在干扰素缺陷(IFNAR-/-)小鼠中表现出显著的表型差异。这项工作为正布尼亚病毒的重配和发病机制引入了重要工具和新见解,为理解这一关键进化过程奠定了基础。

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