Eastern equine encephalitis virus in mice II: pathogenesis is dependent on route of exposure. Issue 1 (December 2015)

• Record Type: Journal Article
• Authors: Honnold, Shelley; Mossel, Eric; Bakken, Russell; Lind, Cathleen; Cohen, Jeffrey; Eccleston, Lori; Spurgers, Kevin; Erwin-Cohen, Rebecca; Glass, Pamela; Maheshwari, Radha
• Is Part Of: Virology journal. Volume 12:Issue 1(2015)
• Page Start: 1
• Page End: 23
• Publication Date: 2015-12
• Subjects: Alphavirus -- Eastern equine encephalitis virus -- Neuroinvasion -- Mice; Virology -- Periodicals; 579.2
• DOI: 10.1186/s12985-015-0385-2
• Languages: English
• ISSNs: 1743-422X

Abstract

Abstract Background 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. Methods 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. Results 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. Conclusion 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.