COVID-19 的动物模型。I. 比较病毒学和疾病发病机制。

IF 3.1 3区 农林科学 Q1 VETERINARY SCIENCES
Ilar Journal Pub Date : 2021-12-31 DOI:10.1093/ilar/ilab007
Caroline J Zeiss, Susan Compton, Rebecca Terilli Veenhuis
{"title":"COVID-19 的动物模型。I. 比较病毒学和疾病发病机制。","authors":"Caroline J Zeiss, Susan Compton, Rebecca Terilli Veenhuis","doi":"10.1093/ilar/ilab007","DOIUrl":null,"url":null,"abstract":"<p><p>The Coronavirus Disease 2019 (COVID-19) pandemic has fueled unprecedented development of animal models to understand disease pathogenesis, test therapeutics, and support vaccine development. Models previously developed to study severe acute respiratory syndrome coronavirus (SARS-CoV) have been rapidly deployed to study SARS-CoV-2. However, it has become clear that despite the common use of ACE2 as a receptor for both viruses, the host range of the 2 viruses does not entirely overlap. Distinct ACE2-interacting residues within the receptor binding domain of SARS-CoV and SARS-CoV-2, as well as species differences in additional proteases needed for activation and internalization of the virus, are likely sources of host differences between the 2 viruses. Spontaneous models include rhesus and cynomolgus macaques, African Green monkeys, hamsters, and ferrets. Viral shedding and transmission studies are more frequently reported in spontaneous models. Mice can be infected with SARS-CoV; however, mouse and rat ACE2 does not support SARS-CoV-2 infection. Murine models for COVID-19 are induced through genetic adaptation of SARS-CoV-2, creation of chimeric SARS-CoV and SARS-CoV-2 viruses, use of human ACE2 knock-in and transgenic mice, and viral transfection of wild-type mice with human ACE2. Core aspects of COVID-19 are faithfully reproduced across species and model. These include the acute nature and predominantly respiratory source of viral shedding, acute transient and nonfatal disease with a largely pulmonary phenotype, similar short-term immune responses, and age-enhanced disease. Severity of disease and tissue involvement (particularly brain) in transgenic mice varies by promoter. To date, these models have provided a remarkably consistent template on which to test therapeutics, understand immune responses, and test vaccine approaches. The role of comorbidity in disease severity and the range of severe organ-specific pathology in humans remains to be accurately modeled.</p>","PeriodicalId":56299,"journal":{"name":"Ilar Journal","volume":"62 1-2","pages":"35-47"},"PeriodicalIF":3.1000,"publicationDate":"2021-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083356/pdf/ilab007.pdf","citationCount":"0","resultStr":"{\"title\":\"Animal Models of COVID-19. I. Comparative Virology and Disease Pathogenesis.\",\"authors\":\"Caroline J Zeiss, Susan Compton, Rebecca Terilli Veenhuis\",\"doi\":\"10.1093/ilar/ilab007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The Coronavirus Disease 2019 (COVID-19) pandemic has fueled unprecedented development of animal models to understand disease pathogenesis, test therapeutics, and support vaccine development. Models previously developed to study severe acute respiratory syndrome coronavirus (SARS-CoV) have been rapidly deployed to study SARS-CoV-2. However, it has become clear that despite the common use of ACE2 as a receptor for both viruses, the host range of the 2 viruses does not entirely overlap. Distinct ACE2-interacting residues within the receptor binding domain of SARS-CoV and SARS-CoV-2, as well as species differences in additional proteases needed for activation and internalization of the virus, are likely sources of host differences between the 2 viruses. Spontaneous models include rhesus and cynomolgus macaques, African Green monkeys, hamsters, and ferrets. Viral shedding and transmission studies are more frequently reported in spontaneous models. Mice can be infected with SARS-CoV; however, mouse and rat ACE2 does not support SARS-CoV-2 infection. Murine models for COVID-19 are induced through genetic adaptation of SARS-CoV-2, creation of chimeric SARS-CoV and SARS-CoV-2 viruses, use of human ACE2 knock-in and transgenic mice, and viral transfection of wild-type mice with human ACE2. Core aspects of COVID-19 are faithfully reproduced across species and model. These include the acute nature and predominantly respiratory source of viral shedding, acute transient and nonfatal disease with a largely pulmonary phenotype, similar short-term immune responses, and age-enhanced disease. Severity of disease and tissue involvement (particularly brain) in transgenic mice varies by promoter. To date, these models have provided a remarkably consistent template on which to test therapeutics, understand immune responses, and test vaccine approaches. The role of comorbidity in disease severity and the range of severe organ-specific pathology in humans remains to be accurately modeled.</p>\",\"PeriodicalId\":56299,\"journal\":{\"name\":\"Ilar Journal\",\"volume\":\"62 1-2\",\"pages\":\"35-47\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2021-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083356/pdf/ilab007.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ilar Journal\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1093/ilar/ilab007\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"VETERINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ilar Journal","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1093/ilar/ilab007","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

冠状病毒疾病 2019(COVID-19)大流行推动了动物模型的空前发展,以了解疾病发病机制、测试治疗方法并支持疫苗开发。以前为研究严重急性呼吸系统综合症冠状病毒(SARS-CoV)而开发的模型已被迅速用于研究 SARS-CoV-2 。然而,尽管两种病毒共同使用 ACE2 作为受体,但这两种病毒的宿主范围并不完全重叠,这一点已变得很清楚。SARS-CoV 和 SARS-CoV-2 受体结合域内不同的 ACE2 相互作用残基,以及病毒激活和内化所需的其他蛋白酶的物种差异,可能是这两种病毒宿主差异的来源。自发模型包括恒河猴和猕猴、非洲绿猴、仓鼠和雪貂。自发模型的病毒脱落和传播研究报告较多。小鼠可感染 SARS-CoV,但小鼠和大鼠 ACE2 不支持 SARS-CoV-2 感染。COVID-19 的小鼠模型是通过对 SARS-CoV-2 进行基因改造、创建嵌合型 SARS-CoV 和 SARS-CoV-2 病毒、使用人类 ACE2 基因敲入小鼠和转基因小鼠以及用人类 ACE2 病毒转染野生型小鼠来诱导的。COVID-19 的核心内容在不同物种和模型中都得到了忠实再现。这些方面包括病毒脱落的急性性质和主要呼吸道来源、急性一过性和非致命性疾病(主要是肺表型)、类似的短期免疫反应和年龄增强型疾病。转基因小鼠的疾病严重程度和受累组织(尤其是大脑)因启动子而异。迄今为止,这些模型为测试疗法、了解免疫反应和测试疫苗方法提供了非常一致的模板。合并症在疾病严重程度中的作用以及人类严重器官特异性病变的范围仍有待精确建模。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Animal Models of COVID-19. I. Comparative Virology and Disease Pathogenesis.

Animal Models of COVID-19. I. Comparative Virology and Disease Pathogenesis.

The Coronavirus Disease 2019 (COVID-19) pandemic has fueled unprecedented development of animal models to understand disease pathogenesis, test therapeutics, and support vaccine development. Models previously developed to study severe acute respiratory syndrome coronavirus (SARS-CoV) have been rapidly deployed to study SARS-CoV-2. However, it has become clear that despite the common use of ACE2 as a receptor for both viruses, the host range of the 2 viruses does not entirely overlap. Distinct ACE2-interacting residues within the receptor binding domain of SARS-CoV and SARS-CoV-2, as well as species differences in additional proteases needed for activation and internalization of the virus, are likely sources of host differences between the 2 viruses. Spontaneous models include rhesus and cynomolgus macaques, African Green monkeys, hamsters, and ferrets. Viral shedding and transmission studies are more frequently reported in spontaneous models. Mice can be infected with SARS-CoV; however, mouse and rat ACE2 does not support SARS-CoV-2 infection. Murine models for COVID-19 are induced through genetic adaptation of SARS-CoV-2, creation of chimeric SARS-CoV and SARS-CoV-2 viruses, use of human ACE2 knock-in and transgenic mice, and viral transfection of wild-type mice with human ACE2. Core aspects of COVID-19 are faithfully reproduced across species and model. These include the acute nature and predominantly respiratory source of viral shedding, acute transient and nonfatal disease with a largely pulmonary phenotype, similar short-term immune responses, and age-enhanced disease. Severity of disease and tissue involvement (particularly brain) in transgenic mice varies by promoter. To date, these models have provided a remarkably consistent template on which to test therapeutics, understand immune responses, and test vaccine approaches. The role of comorbidity in disease severity and the range of severe organ-specific pathology in humans remains to be accurately modeled.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Ilar Journal
Ilar Journal 农林科学-兽医学
CiteScore
5.10
自引率
20.00%
发文量
8
审稿时长
>18 weeks
期刊介绍: The ILAR Journal is the peer-reviewed, theme-oriented publication of the Institute for Laboratory Animal Research (ILAR), which provides timely information for all who study, use, care for, and oversee the use of animals in research. The journal publishes original articles that review research on animals either as direct subjects or as surrogates for humans. According to policy, any previously unpublished animal research reported in the ILAR Journal will have been conducted according to the scientific, technical, and humanely appropriate guidelines current at the time the research was conducted in accordance with the Guide for the Care and Use of Laboratory Animals or other guidance provided by taxonomically-oriented professional societies (e.g., American Society of Mammalogy) as referenced in the Guide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信