Browning Shawn R, Mason Gary L, Seward Tanya, Green Mike, Eliason Gwyneth A J, Mathiason Candace, Miller Michael W, Williams Elizabeth S, Hoover Ed, Telling Glenn C
Department of Microbiology, University of Kentucky, 800 Rose St., Lexington, KY 40536, USA.
J Virol. 2004 Dec;78(23):13345-50. doi: 10.1128/JVI.78.23.13345-13350.2004.
We generated mice expressing cervid prion protein to produce a transgenic system simulating chronic wasting disease (CWD) in deer and elk. While normal mice were resistant to CWD, these transgenic mice uniformly developed signs of neurological dysfunction approximately 230 days following intracerebral inoculation with four CWD isolates. Inoculated transgenic mice homozygous for the transgene array developed disease after approximately 160 days. The brains of sick transgenic mice exhibited widespread spongiform degeneration and contained abnormal prion protein and abundant amyloid plaques, many of which were florid plaques. Transmission studies indicated that the same prion strain caused CWD in the analyzed mule deer and elk. These mice provide a new and reliable tool for detecting CWD prions.
我们培育了表达鹿朊病毒蛋白的小鼠,以建立一个模拟鹿和麋鹿慢性消耗病(CWD)的转基因系统。正常小鼠对CWD具有抗性,而这些转基因小鼠在脑内接种四种CWD分离株后约230天均出现神经功能障碍症状。转基因阵列纯合的接种转基因小鼠在约160天后发病。患病转基因小鼠的大脑表现出广泛的海绵状变性,含有异常朊病毒蛋白和大量淀粉样斑块,其中许多是典型斑块。传播研究表明,相同的朊病毒株在分析的骡鹿和麋鹿中引起CWD。这些小鼠为检测CWD朊病毒提供了一种新的可靠工具。