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Infection with MERS-CoV causes lethal pneumonia in the common marmoset.中东呼吸综合征冠状病毒(MERS-CoV)感染可导致普通狨猴患致死性肺炎。
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2
Severe acute respiratory syndrome-coronavirus infection in aged nonhuman primates is associated with modulated pulmonary and systemic immune responses.严重急性呼吸系统综合症冠状病毒感染老年非人类灵长类动物与肺部和全身免疫反应的调节有关。
Immun Ageing. 2014 Mar 19;11(1):4. doi: 10.1186/1742-4933-11-4.
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Rapid generation of a mouse model for Middle East respiratory syndrome.快速建立中东呼吸综合征小鼠模型。
Proc Natl Acad Sci U S A. 2014 Apr 1;111(13):4970-5. doi: 10.1073/pnas.1323279111. Epub 2014 Mar 5.
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The pathology and pathogenesis of experimental severe acute respiratory syndrome and influenza in animal models.实验性严重急性呼吸综合征和流感在动物模型中的病理学及发病机制
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Adenosine deaminase acts as a natural antagonist for dipeptidyl peptidase 4-mediated entry of the Middle East respiratory syndrome coronavirus.腺苷脱氨酶可作为二肽基肽酶 4 介导的中东呼吸综合征冠状病毒进入的天然拮抗剂。
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Wild-type and innate immune-deficient mice are not susceptible to the Middle East respiratory syndrome coronavirus.野生型和先天性免疫缺陷型小鼠不易感染中东呼吸综合征冠状病毒。
J Gen Virol. 2014 Feb;95(Pt 2):408-412. doi: 10.1099/vir.0.060640-0. Epub 2013 Nov 6.
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Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor.一种使用 ACE2 受体的蝙蝠 SARS 样冠状病毒的分离与鉴定
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Middle East respiratory syndrome coronavirus (MERS-CoV) causes transient lower respiratory tract infection in rhesus macaques.中东呼吸综合征冠状病毒(MERS-CoV)可导致恒河猴一过性下呼吸道感染。
Proc Natl Acad Sci U S A. 2013 Oct 8;110(41):16598-603. doi: 10.1073/pnas.1310744110. Epub 2013 Sep 23.
10
Reverse genetics with a full-length infectious cDNA of the Middle East respiratory syndrome coronavirus.中东呼吸综合征冠状病毒全长感染性 cDNA 的反向遗传学。
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冠状病毒诱导的重症肺炎分析的遗传方法和模型综述

A review of genetic methods and models for analysis of coronavirus-induced severe pneumonitis.

作者信息

McGruder Brenna, Leibowitz Julian L

机构信息

Department of Microbial Pathogenesis and Immunology, Texas A & M University Health Science Center, Bryan, TX 77807, USA.

出版信息

J Gen Virol. 2015 Mar;96(Pt 3):494-506. doi: 10.1099/vir.0.069732-0. Epub 2014 Sep 24.

DOI:10.1099/vir.0.069732-0
PMID:25252685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4811657/
Abstract

Coronaviruses (CoVs) have been studied for over 60 years, but have only recently gained notoriety as deadly human pathogens with the emergence of severe respiratory syndrome CoV and Middle East respiratory syndrome virus. The rapid emergence of these viruses has demonstrated the need for good models to study severe CoV respiratory infection and pathogenesis. There are, currently, different methods and models for the study of CoV disease. The available genetic methods for the study and evaluation of CoV genetics are reviewed here. There are several animal models, both mouse and alternative animals, for the study of severe CoV respiratory disease that have been examined, each with different pros and cons relative to the actual pathogenesis of the disease in humans. A current limitation of these models is that no animal model perfectly recapitulates the disease seen in humans. Through the review and analysis of the available disease models, investigators can employ the most appropriate available model to study various aspects of CoV pathogenesis and evaluate possible antiviral treatments that may potentially be successful in future treatment and prevention of severe CoV respiratory infections.

摘要

冠状病毒(CoVs)已经被研究了60多年,但直到严重急性呼吸综合征冠状病毒和中东呼吸综合征病毒出现,它们才作为致命的人类病原体而声名狼藉。这些病毒的迅速出现表明需要良好的模型来研究严重冠状病毒呼吸道感染和发病机制。目前,有不同的方法和模型用于研究冠状病毒疾病。本文综述了用于研究和评估冠状病毒遗传学的现有遗传方法。有几种动物模型,包括小鼠和其他动物,用于研究严重冠状病毒呼吸道疾病,每种模型相对于人类疾病的实际发病机制都有不同的优缺点。这些模型目前的一个局限性是没有动物模型能完美再现人类所见的疾病。通过对现有疾病模型的综述和分析,研究人员可以采用最合适的现有模型来研究冠状病毒发病机制的各个方面,并评估可能在未来治疗和预防严重冠状病毒呼吸道感染中取得成功的抗病毒治疗方法。