Julander Justin G, Siddharthan Venkatraman, Blatt Lawrence M, Schafer Kristiina, Sidwell Robert W, Morrey John D
Institute for Antiviral Research, Utah State University, Logan, UT 84322-5600, USA.
Virology. 2007 Apr 10;360(2):454-60. doi: 10.1016/j.virol.2006.10.031. Epub 2006 Nov 21.
Mice are used as models for western equine encephalitis virus (WEEV) infection, but high mortality is generally only seen with intracranial or intranasal challenge, while peripheral inoculation results in approximately 50% mortality and is not dose-dependent. Hamsters were therefore studied as a model for WEEV infection. Hamsters were highly sensitive to intraperitoneal (i.p.) infection with WEEV. Disease progression was rapid, and virus titers in serum, brain, liver, and kidney of infected hamsters peaked between 2 and 4 days post-virus inoculation (dpi). Foci of virus infection were detected in neurons of the cerebral cortex and midbrain. Pre-treatment i.p. with either interferon alfacon-1 (5 microg/kg/day) or with Ampligen (3.2 mg/kg/day) resulted in complete survival, reduced brain titers, and improved weight gain. This model of WEEV infection in hamsters appears to serve as a suitable model for the evaluation of potential therapeutic agents for the treatment of WEE disease.
小鼠被用作西部马脑炎病毒(WEEV)感染的模型,但通常只有在颅内或鼻内接种时才会出现高死亡率,而外周接种的死亡率约为50%,且不依赖剂量。因此,对仓鼠作为WEEV感染模型进行了研究。仓鼠对WEEV腹腔内(i.p.)感染高度敏感。疾病进展迅速,感染仓鼠血清、脑、肝和肾中的病毒滴度在病毒接种后(dpi)2至4天达到峰值。在大脑皮层和中脑的神经元中检测到病毒感染灶。腹腔内预先给予干扰素α-1(5微克/千克/天)或Ampligen(3.2毫克/千克/天)可导致完全存活、降低脑内病毒滴度并改善体重增加。仓鼠的这种WEEV感染模型似乎可作为评估治疗WEE疾病潜在治疗药物的合适模型。