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小型动物模型在丝状病毒发病机制研究中的应用。

Small Animal Models for Studying Filovirus Pathogenesis.

机构信息

Department of Molecular Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, 59840, USA.

出版信息

Curr Top Microbiol Immunol. 2017;411:195-227. doi: 10.1007/82_2017_9.

Abstract

Filovirus small animal disease models have so far been developed in laboratory mice, guinea pigs, and hamsters. Since immunocompetent rodents do not exhibit overt signs of disease following infection with wild-type filoviruses isolated from humans, rodent models have been established using adapted viruses produced through sequential passage in rodents. Rodent-adapted viruses target the same cells/tissues as the wild-type viruses, making rodents invaluable basic research tools for studying filovirus pathogenesis. Moreover, comparative analyses using wild-type and rodent-adapted viruses have provided beneficial insights into the molecular mechanisms of pathogenicity and acquisition of species-specific virulence. Additionally, wild-type filovirus infections in immunodeficient rodents have provided a better understanding of the host factors required for resistance to filovirus infection and of the immune response against the infection. This chapter provides comprehensive information on the filovirus rodent models and rodent-adapted filoviruses. Specifically, we summarize the clinical and pathological features of filovirus infections in all rodent models described to date, including the recently developed humanized and collaborative cross (CC) resource recombinant inbred (RI) intercrossed (CC-RIX) mouse models. We also cover the molecular determinants responsible for adaptation and virulence acquisition in a number of rodent-adapted filoviruses. This chapter clearly defines the characteristic and advantages/disadvantages of rodent models, helping to evaluate the practical use of rodent models in future filovirus studies.

摘要

丝状病毒小动物疾病模型迄今为止是在实验小鼠、豚鼠和仓鼠中建立的。由于免疫功能正常的啮齿动物在感染源自人类的野生型丝状病毒后不会出现明显的疾病迹象,因此通过在啮齿动物中连续传代建立了使用适应性病毒的啮齿动物模型。适应啮齿动物的病毒针对与野生型病毒相同的细胞/组织,使啮齿动物成为研究丝状病毒发病机制的宝贵基础研究工具。此外,使用野生型和适应啮齿动物的病毒进行的比较分析为致病性和获得物种特异性毒力的分子机制提供了有益的见解。此外,免疫缺陷啮齿动物中的野生型丝状病毒感染为抵抗丝状病毒感染所需的宿主因素以及针对感染的免疫反应提供了更好的理解。本章提供了关于丝状病毒啮齿动物模型和适应啮齿动物的丝状病毒的全面信息。具体而言,我们总结了迄今为止在所有描述的啮齿动物模型中丝状病毒感染的临床和病理特征,包括最近开发的人源化和合作交叉(CC)资源重组近交系(RI)杂交(CC-RIX)小鼠模型。我们还涵盖了许多适应啮齿动物的丝状病毒中负责适应和获得毒力的分子决定因素。本章清楚地定义了啮齿动物模型的特征和优缺点,有助于评估啮齿动物模型在未来丝状病毒研究中的实际用途。

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