Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO 80523-1619, USA.
J Gen Virol. 2010 Jun;91(Pt 6):1651-8. doi: 10.1099/vir.0.017335-0. Epub 2010 Feb 17.
Little is known regarding the potential risk posed by aerosolized prions. Chronic wasting disease (CWD) is transmitted horizontally, almost surely by mucosal exposure, and CWD prions are present in saliva and urine of infected animals. However, whether CWD may be transmissible by the aerosol or nasal route is not known. To address this question, FVB mice transgenetically expressing the normal cervid PrP(C) protein [Tg(cerPrP) mice] were exposed to CWD prions by either nose-only aerosol exposure or by drop-wise instillation into the nostrils. Mice were monitored for signs of disease for up to 755 days post-inoculation (p.i.) and by examination of tissues for lesions and PrP(CWD) after necropsy. In particular, nasal mucosa, vomeronasal organ, lungs, lymphoid tissue and the brain were assessed for PrP(CWD) by Western blotting and immunohistochemistry. Six of seven aerosol-exposed Tg(cerPrP) mice developed clinical signs of neurological dysfunction mandating euthanasia between 411 and 749 days p.i. In all these mice, CWD infection was confirmed by detection of spongiform lesions and PrP(CWD) in the brain. Two of nine intranasally inoculated Tg(cerPrP) mice also developed transmissible spongiform encephalopathy associated with PrP(CWD) between 417 and 755 days p.i. No evidence of PrP(CWD) was detected in CWD-inoculated Tg(cerPrP) mice examined at pre-terminal time points. These results demonstrate that CWD can be transmitted by aerosol (as well as nasal) exposure and suggest that exposure via the respiratory system merits consideration for prion disease transmission and biosafety.
关于气溶胶化朊病毒可能带来的风险,目前知之甚少。慢性消耗病(CWD)通过水平传播,几乎可以肯定是通过黏膜暴露传播,感染动物的唾液和尿液中存在 CWD 朊病毒。然而,CWD 是否可以通过气溶胶或鼻内途径传播尚不清楚。为了解决这个问题,我们使用转染了正常鹿朊病毒(PrP(C))蛋白的 FVB 小鼠[Tg(cerPrP)小鼠],通过鼻内仅吸入气溶胶或滴注到鼻腔的方式,使它们暴露于 CWD 朊病毒之下。我们监测了这些小鼠的疾病迹象,最长可达接种后 755 天(p.i.),并在解剖后通过检查组织中的病变和 PrP(CWD)来评估它们。特别是,我们通过 Western blot 和免疫组化评估了鼻腔黏膜、犁鼻器、肺、淋巴组织和大脑中的 PrP(CWD)。在 7 只接受气溶胶暴露的 Tg(cerPrP)小鼠中,有 6 只在接种后 411 至 749 天之间出现了神经功能障碍的临床症状,需要安乐死。在所有这些小鼠中,通过检测大脑中的海绵状病变和 PrP(CWD),证实了 CWD 感染。在接受鼻内接种的 9 只 Tg(cerPrP)小鼠中,也有 2 只在接种后 417 至 755 天之间出现了与 PrP(CWD)相关的传染性海绵状脑病。在预先设定的终点时间点检查的 CWD 接种的 Tg(cerPrP)小鼠中,没有检测到 PrP(CWD)。这些结果表明,CWD 可以通过气溶胶(以及鼻内)暴露传播,并提示通过呼吸系统暴露应考虑用于朊病毒疾病传播和生物安全。