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利用假型病毒建立新型 SARS-CoV-2 呼吸道感染仓鼠模型。

A novel hamster model of SARS-CoV-2 respiratory infection using a pseudotyped virus.

机构信息

Department of Microbiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.

Section of Host Defences, Institute of Natural Medicine, University of Toyama, Toyama, Japan.

出版信息

Sci Rep. 2022 Jul 1;12(1):11125. doi: 10.1038/s41598-022-15258-8.

DOI:10.1038/s41598-022-15258-8
PMID:35778450
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9247941/
Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a biosafety level (BSL)-3 pathogen; therefore, its research environment is limited. Pseudotyped viruses that mimic the infection of SARS-CoV-2 have been widely used for in vitro evaluation because they are available in BSL-2 containment laboratories. However, in vivo application is inadequate. Therefore, animal models instigated with animal BSL-2 will provide opportunities for in vivo evaluation. Hamsters (6-10-week-old males) were intratracheally inoculated with luciferase-expressing vesicular stomatitis virus (VSV)-based SARS-CoV-2 pseudotyped virus. The lungs were harvested 24-72 h after inoculation and luminescence was measured using an in vivo imaging system. Lung luminescence after inoculation with the SARS-CoV-2 pseudotyped virus increased in a dose-dependent manner and peaked at 48 h. The VSV-G (envelope G) pseudotyped virus also induced luminescence; however, a 100-fold concentration was required to reach a level similar to that of the SARS-CoV-2 pseudotyped virus. The SARS-CoV-2 pseudotyped virus is applicable to SARS-CoV-2 respiratory infections in a hamster model. Because of the single-round infectious virus, the model can be used to study the steps from viral binding to entry, which will be useful for future research on SARS-CoV-2 entry without using live SARS-CoV-2 or transgenic animals.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是一种生物安全级别 3(BSL-3)病原体;因此,其研究环境受到限制。模拟 SARS-CoV-2 感染的假型病毒已被广泛用于体外评估,因为它们可在 BSL-2 控制实验室中获得。然而,其体内应用仍不够充分。因此,使用动物 BSL-2 引发的动物模型将为体内评估提供机会。用表达荧光素酶的基于水疱性口炎病毒(VSV)的 SARS-CoV-2 假型病毒经气管内接种 6-10 周龄雄性仓鼠。接种后 24-72 小时收获肺部,并使用活体成像系统测量发光。接种 SARS-CoV-2 假型病毒后,肺部发光呈剂量依赖性增加,并在 48 小时达到峰值。VSV-G(包膜 G)假型病毒也诱导发光;然而,需要 100 倍的浓度才能达到与 SARS-CoV-2 假型病毒相似的水平。SARS-CoV-2 假型病毒适用于仓鼠模型中的 SARS-CoV-2 呼吸道感染。由于该病毒为单轮感染性病毒,因此该模型可用于研究从病毒结合到进入的步骤,这对于未来研究 SARS-CoV-2 进入而不使用活 SARS-CoV-2 或转基因动物将非常有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5230/9249834/df447b85e6cf/41598_2022_15258_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5230/9249834/eab05f97ec78/41598_2022_15258_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5230/9249834/28283705d298/41598_2022_15258_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5230/9249834/df447b85e6cf/41598_2022_15258_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5230/9249834/eab05f97ec78/41598_2022_15258_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5230/9249834/28283705d298/41598_2022_15258_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5230/9249834/df447b85e6cf/41598_2022_15258_Fig3_HTML.jpg

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