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仓鼠和雪貂经鼻腔感染低剂量单株 SARS-CoV-2 的实验感染。

Hamster and ferret experimental infection with intranasal low dose of a single strain of SARS-CoV-2.

机构信息

Nancy laboratory for rabies and wildlife, ANSES, Malzéville, France.

Nancy laboratory for rabies and wildlife, ANSES, Atton experimental facility, Atton France, France.

出版信息

J Gen Virol. 2021 Mar;102(3). doi: 10.1099/jgv.0.001567. Epub 2021 Feb 19.

Abstract

Understanding the pathogenesis of the SARS-CoV-2 infection is key to developing preventive and therapeutic strategies against COVID-19, in the case of severe illness but also when the disease is mild. The use of appropriate experimental animal models remains central in the exploration of the physiopathology of infection and antiviral strategies. This study describes SARS-CoV-2 intranasal infection in ferrets and hamsters with low doses of low-passage SARS-CoV-2 clinical French isolate UCN19, describing infection levels, excretion, immune responses and pathological patterns in both animal species. Individual infection with 10 p.f.u. SARS-CoV-2 induced a more severe disease in hamsters than in ferrets. Viral RNA was detected in the lungs of hamsters but not of ferrets and in the brain (olfactory bulb and/or medulla oblongata) of both species. Overall, the clinical disease remained mild, with serological responses detected from 7 days and 10 days post-inoculation in hamsters and ferrets respectively. The virus became undetectable and pathology resolved within 14 days. The kinetics and levels of infection can be used in ferrets and hamsters as experimental models for understanding the pathogenicity of SARS-CoV-2, and testing the protective effect of drugs.

摘要

了解 SARS-CoV-2 感染的发病机制是开发针对 COVID-19 的预防和治疗策略的关键,无论是在严重疾病的情况下还是疾病较轻时。使用适当的实验动物模型仍然是探索感染和抗病毒策略的病理生理学的核心。本研究描述了低传代 SARS-CoV-2 临床法国分离株 UCN19 以低剂量经鼻腔感染雪貂和仓鼠,描述了两种动物物种的感染水平、排泄、免疫反应和病理模式。10 p.f.u. SARS-CoV-2 的个体感染在仓鼠中引起的疾病比在雪貂中更为严重。在仓鼠的肺部而不是在雪貂的肺部以及在两种动物的大脑(嗅球和/或延髓)中检测到病毒 RNA。总体而言,临床疾病仍然较轻,分别在仓鼠和雪貂感染后 7 天和 10 天检测到血清学反应。病毒在 14 天内消失,病理学得到解决。感染的动力学和水平可用于雪貂和仓鼠作为理解 SARS-CoV-2 致病性和测试药物保护作用的实验模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c27/8515860/697477c5db04/jgv-102-1567-g001.jpg

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