Honnold Shelley P, Mossel Eric C, Bakken Russell R, Lind Cathleen M, Cohen Jeffrey W, Eccleston Lori T, Spurgers Kevin B, Erwin-Cohen Rebecca, Glass Pamela J, Maheshwari Radha K
Virology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD, 21702, USA.
Department of Pathology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Virol J. 2015 Sep 30;12:154. doi: 10.1186/s12985-015-0385-2.
Eastern equine encephalitis virus (EEEV) is an alphavirus with a case fatality rate estimated to be as high as 75 % in humans and 90 % in horses. Surviving patients often have long-lasting and severe neurological sequelae. At present, there is no licensed vaccine or therapeutic for EEEV infection. This study completes the clinical and pathological analysis of mice infected with a North American strain of EEEV by three different routes: aerosol, intranasal, and subcutaneous. Such an understanding is imperative for use of the mouse model in vaccine and antiviral drug development.
Twelve-week-old female BALB/c mice were infected with EEEV strain FL93-939 by the intranasal, aerosol, or subcutaneous route. Mice were euthanized 6 hpi through 8 dpi and tissues were harvested for histopathological and immunohistochemical analysis.
Viral antigen was detected in the olfactory bulb as early as 1-2 dpi in aerosol and intranasal infected mice. However, histologic lesions in the brain were evident about 24 hours earlier (3 dpi vs 4 dpi), and were more pronounced following aerosol infection relative to intranasal infection. Following subcutaneous infection, viral antigen was also detected in the olfactory bulb, though not as routinely or as early. Significant histologic lesions were not observed until 6 dpi.
These pathologic studies suggest EEEV enters the brain through the olfactory system when mice are exposed via the intranasal and aerosol routes. In contrast, the histopathologic lesions were delayed in the subcutaneous group and it appears the virus may utilize both the vascular and olfactory routes to enter the brain when mice are exposed to EEEV subcutaneously.
东部马脑炎病毒(EEEV)是一种甲病毒,据估计其在人类中的病死率高达75%,在马匹中为90%。幸存患者往往有长期严重的神经后遗症。目前,尚无针对EEEV感染的许可疫苗或治疗方法。本研究完成了对感染北美株EEEV的小鼠通过三种不同途径(气溶胶、鼻内和皮下)感染后的临床和病理分析。对于在疫苗和抗病毒药物开发中使用小鼠模型而言,这种认识至关重要。
12周龄雌性BALB/c小鼠通过鼻内、气溶胶或皮下途径感染EEEV株FL93 - 939。在感染后6小时至8天对小鼠实施安乐死,并采集组织进行组织病理学和免疫组织化学分析。
在气溶胶和鼻内感染的小鼠中,早在感染后1 - 2天就在嗅球中检测到病毒抗原。然而,脑部的组织学病变在大约24小时前就很明显(分别为感染后3天和4天),并且相对于鼻内感染,气溶胶感染后的病变更明显。皮下感染后,也在嗅球中检测到病毒抗原,不过不如前两者常规和早。直到感染后6天才观察到明显的组织学病变。
这些病理学研究表明,当小鼠通过鼻内和气溶胶途径暴露时,EEEV通过嗅觉系统进入大脑。相比之下,皮下组的组织病理学病变出现延迟,并且当小鼠皮下暴露于EEEV时,病毒似乎可能利用血管和嗅觉途径进入大脑。