Rodriguez Laura, Nogales Aitor, Martínez-Sobrido Luis
Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry.
Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry;
J Vis Exp. 2017 Sep 7(127):55898. doi: 10.3791/55898.
Influenza viruses cause over 500,000 deaths worldwide and are associated with an annual cost of 12 - 14 billion USD in the United States alone considering direct medical and hospitalization expenses and work absenteeism. Animal models are crucial in Influenza A virus (IAV) studies to evaluate viral pathogenesis, host-pathogen interactions, immune responses, and the efficacy of current and/or novel vaccine approaches as well as antivirals. Mice are an advantageous small animal model because their immune system is evolutionarily similar to that found in humans, they are available from commercial vendors as genetically identical subjects, there are multiple strains that can be exploited to evaluate the genetic basis of infections, and they are relatively inexpensive and easy to manipulate. To recapitulate IAV infection in humans via the airways, mice are first anesthetized prior to intranasal inoculation with infectious IAVs under proper biosafety containment. After infection, the pathogenesis of IAVs is determined by monitoring daily the morbidity (body weight loss) and mortality (survival) rate. In addition, viral pathogenesis can also be evaluated by assessing virus replication in the upper (nasal mucosa) or lower (lungs) respiratory tract of infected mice. Humoral responses upon IAV infection can be rapidly evaluated by non-invasive bleeding and secondary antibody detection assays aimed at detecting the presence of total or neutralizing antibodies. Here, we describe the common methods used to infect mice intranasally (i.n) with IAV and evaluate pathogenesis, humoral immune responses and protection efficacy.
流感病毒在全球范围内导致超过50万人死亡,仅在美国,考虑到直接医疗费用、住院费用以及旷工造成的损失,每年的花费就达120亿至140亿美元。动物模型在甲型流感病毒(IAV)研究中至关重要,可用于评估病毒发病机制、宿主与病原体的相互作用、免疫反应以及现有和/或新型疫苗方法及抗病毒药物的疗效。小鼠是一种优势小型动物模型,因为其免疫系统在进化上与人类相似,可从商业供应商处获得基因相同的个体,有多种品系可用于评估感染的遗传基础,而且相对便宜且易于操作。为了通过呼吸道模拟人类的IAV感染,在适当的生物安全防护下,先对小鼠进行麻醉,然后经鼻接种传染性IAV。感染后,通过每天监测发病率(体重减轻)和死亡率(存活率)来确定IAV的发病机制。此外,还可通过评估感染小鼠上呼吸道(鼻黏膜)或下呼吸道(肺)中的病毒复制来评估病毒发病机制。IAV感染后的体液免疫反应可通过非侵入性采血以及旨在检测总抗体或中和抗体的二抗检测试验快速评估。在此,我们描述经鼻(i.n.)用IAV感染小鼠并评估发病机制、体液免疫反应和保护效果的常用方法。