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用博尔纳病病毒1对鼩鼱进行实验性感染:对病毒传播和脱落的见解

Experimental infection of shrews () with Borna disease virus 1: Insights into viral spread and shedding.

作者信息

Nobach Daniel, Raeder Leif, Müller Jana, Herzog Sibylle, Eickmann Markus, Herden Christiane

机构信息

Institute of Veterinary Pathology, Justus-Liebig-University, Giessen 35392, Germany.

Chemical and Veterinary Analysis Agency Stuttgart (CVUAS), Schaflandstraße 3/2, Fellbach 70736, Germany.

出版信息

PNAS Nexus. 2025 May 6;4(5):pgaf144. doi: 10.1093/pnasnexus/pgaf144. eCollection 2025 May.

DOI:10.1093/pnasnexus/pgaf144
PMID:40375974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12080549/
Abstract

Numbers of human encephalitis cases caused by infection with Borna disease virus 1 (BoDV1) increase continuously in endemic areas. The reservoir host of BoDV1 is the bicolored white-toothed shrew, albeit few naturally infected individuals of other shrew species have been detected. To establish a reliable experimental reservoir model, 15 greater white-toothed shrews were infected with a shrew-derived BoDV1 isolate by different inoculation routes (intracerebral, intranasal, oral, subcutaneous, and intraperitoneal) and monitored up to 41 days. Except for the oral route, all other animals (12/15) were successfully infected, and the majority of them displayed temporarily reduced feed intake and loss of body weight but no inflammatory lesions. Infectious virus was isolated from 11/12 infected animals. Viral RNA was demonstrated by qRT-PCR in the central nervous system (CNS) and the majority of organs. Immunohistochemistry demonstrated BoDV1 antigen in neurons and astrocytes in the CNS and peripheral nerves. High viral loads in the CNS and the spinal cord points towards spread from periphery to the CNS to enhance viral replication and subsequent centrifugal spread to organs capable of secretion and excretions. In general, successful experimental BoDV1 infection of shrews proves their usefulness as animal model, enabling further studies on maintenance, transmission, pathogenesis, and risk assessment for human spillover infections.

摘要

在流行地区,由博尔纳病病毒1(BoDV1)感染引起的人类脑炎病例数量持续增加。BoDV1的储存宿主是双色白齿鼩,尽管已检测到其他鼩鼱物种中自然感染的个体很少。为了建立一个可靠的实验储存宿主模型,15只大白齿鼩通过不同的接种途径(脑内、鼻内、口服、皮下和腹腔内)感染了一种源自鼩鼱的BoDV1分离株,并监测长达41天。除口服途径外,所有其他动物(12/15)均成功感染,其中大多数表现出暂时的采食量减少和体重减轻,但无炎症病变。从11/12只感染动物中分离出传染性病毒。通过qRT-PCR在中枢神经系统(CNS)和大多数器官中检测到病毒RNA。免疫组织化学显示CNS和外周神经中的神经元和星形胶质细胞中有BoDV1抗原。CNS和脊髓中的高病毒载量表明病毒从外周扩散到CNS,以增强病毒复制,随后离心扩散到能够分泌和排泄的器官。总体而言,鼩鼱成功的实验性BoDV1感染证明了它们作为动物模型的有用性,能够进一步研究病毒的维持、传播、发病机制以及人类溢出感染的风险评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/ad4322f14a6d/pgaf144f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/0f786185f903/pgaf144f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/17a5bb88c367/pgaf144f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/d2b3ed34a7db/pgaf144f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/ca2435555017/pgaf144f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/ad4322f14a6d/pgaf144f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/0f786185f903/pgaf144f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/17a5bb88c367/pgaf144f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/d2b3ed34a7db/pgaf144f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/ca2435555017/pgaf144f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbb/12080549/ad4322f14a6d/pgaf144f5.jpg

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本文引用的文献

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Lethal Borna disease virus 1 infections of humans and animals - in-depth molecular epidemiology and phylogeography.致死性博尔纳病病毒 1 感染人类和动物的深入分子流行病学和系统地理学研究。
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Disease tolerance as immune defense strategy in bats: One size fits all?
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Detection of novel orthoparamyxoviruses, orthonairoviruses and an orthohepevirus in European white-toothed shrews.在欧洲白齿鼩鼱中检测新型正粘病毒、正布尼亚病毒和正肝病毒。
Microb Genom. 2024 Aug;10(8). doi: 10.1099/mgen.0.001275.
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One Health in action: Investigation of the first detected local cluster of fatal borna disease virus 1 (BoDV-1) encephalitis, Germany 2022.行动中的One Health:德国 2022 年首例致命博尔纳病病毒 1(BoDV-1)脑炎局部聚集性病例的调查。
J Clin Virol. 2024 Apr;171:105658. doi: 10.1016/j.jcv.2024.105658. Epub 2024 Feb 23.
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