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建立一种使用表达尼帕病毒糖蛋白和荧光蛋白的水疱性口炎病毒的中和测定法。

Development of a neutralization assay using a vesicular stomatitis virus expressing Nipah virus glycoprotein and a fluorescent protein.

机构信息

Viral Special Pathogens Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, 30329, USA.

Viral Special Pathogens Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, 30329, USA.

出版信息

Virology. 2023 Oct;587:109858. doi: 10.1016/j.virol.2023.109858. Epub 2023 Aug 2.

Abstract

Nipah virus (NiV) is a highly pathogenic paramyxovirus with a high case fatality rate. Due to its high pathogenicity, pandemic potential, and lack of therapeutics or approved vaccines, its study requires biosafety level 4 (BSL4) containment. In this report, we developed a novel neutralization assay for use in biosafety level 2 laboratories. The assay uses a recombinant vesicular stomatitis virus expressing NiV glycoprotein and a fluorescent protein. The recombinant virus propagates as a replication-competent virus in a cell line constitutively expressing NiV fusion protein, but it is restricted to a single round of replication in wild-type cells. We used this system to evaluate the neutralization activity of monoclonal and polyclonal antibodies, plasma from NiV-infected hamsters, and serum from human patients. Therefore, this recombinant virus could be used as a surrogate for using pathogenic NiV and may constitute a powerful tool to develop therapeutics in low containment laboratories.

摘要

尼帕病毒(NiV)是一种高致病性副粘病毒,病死率很高。由于其高致病性、大流行潜力以及缺乏治疗方法或批准的疫苗,因此需要在生物安全 4 级(BSL4)条件下进行研究。在本报告中,我们开发了一种新的中和测定法,可在生物安全 2 级实验室中使用。该测定法使用表达 NiV 糖蛋白和荧光蛋白的重组水疱性口炎病毒。重组病毒在稳定表达 NiV 融合蛋白的细胞系中以复制型病毒形式繁殖,但在野生型细胞中只能进行单轮复制。我们使用该系统评估了单克隆和多克隆抗体、来自 NiV 感染的仓鼠的血浆以及人类患者的血清的中和活性。因此,这种重组病毒可用作致病性 NiV 的替代物,并且可能成为在低隔离实验室中开发治疗方法的有力工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfeb/11539236/7132d5aaaf52/nihms-2032928-f0001.jpg

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