Department of Infection Genetics, Helmholtz Centre for Infection Research and University of Veterinary Medicine Hannover, Inhoffenstr. 7, D-38124 Braunschweig, Germany.
Virol J. 2012 Sep 19;9:212. doi: 10.1186/1743-422X-9-212.
The mouse represents an important model system to study the host response to influenza A infections and to evaluate new prevention or treatment strategies. We and others reported that the susceptibility to influenza A virus infections strongly varies among different inbred mouse strains. In particular, DBA/2J mice are highly susceptible to several influenza A subtypes, including human isolates and exhibit severe symptoms after infection with clinical isolates.
Upon intra-muscular immunization with live H1N1 influenza A virus (mouse-adapted PR8M, and 2009 pandemic human HA04), DBA/2J mice mounted virus-specific IgG responses and were protected against a subsequent lethal challenge. The immune response and rescue from death after immunization in DBA/2J was similar to those observed for C57BL/6J mice.
DBA/2J mice represent a suitable mouse model to evaluate virulence and pathogenicity as well as immunization regimes against existing and newly emerging human influenza strains without the need for prior adaptation of the virus to the mouse.
小鼠是研究宿主对甲型流感感染反应和评估新的预防或治疗策略的重要模型系统。我们和其他人报告说,不同近交系小鼠对甲型流感病毒感染的易感性差异很大。特别是 DBA/2J 小鼠对几种甲型流感亚型(包括人类分离株)高度易感,并且在感染临床分离株后表现出严重的症状。
通过肌肉内接种活 H1N1 流感病毒(鼠适应株 PR8M 和 2009 年大流行的人 HA04),DBA/2J 小鼠产生了病毒特异性 IgG 反应,并能抵抗随后的致死性挑战。DBA/2J 免疫后的免疫反应和免于死亡与 C57BL/6J 小鼠观察到的相似。
DBA/2J 小鼠是一种合适的小鼠模型,可用于评估现有和新出现的人类流感株的毒力和致病性以及免疫方案,而无需事先使病毒适应小鼠。