Publication Date

2016

Document Type

Thesis

Committee Members

Nancy Bigley (Advisor), Barbara Hull (Committee Member), Dawn Wooley (Committee Member)

Degree Name

Master of Science (MS)

Abstract

Herpes simplex virus type 1 (HSV-1) is a worldwide pathogen that affects humans and has the ability to establish a latent state of infection in the sensory nerve ganglia after primary infection of epithelial cells (Boutell and Everett, 2003). HSV-1 is a very contagious virus, which can be transmitted from person to person and cause cold sores in the infected person. Rarely, infection can lead to more serious complications, such as encephalitis. Most HSV-1 infections usually occur in childhood with lifelong potential for symptomatic or asymptomatic viral shedding episodes (Looker et al., 2015). HSV- 1 infects 60%-80% of people throughout the world (Cunningham et al., 2006). The purpose of this study was to examine the anti-apoptotic effect of HSV-1 on polarized and un-polarized RAW 246.7 murine at 4, 12, and 24 hours. We found that viability of M1 macrophages was significantly decreased compared to control cells at 4 hours (p-value<0.016), 12 hours (p-value<0.001), and 24 hours (p-value<0.001). Virus-infected M1 macrophages showed a significant increase in cell viability compare to uninfected M1 macrophages at 24 hours (P = 0.025). The percentage of late apoptotic cells in all cell groups (M0, M1, and M2) exhibited a significant decrease after infection with HSV-1 at 4 and 24 hours.

Page Count

47

Department or Program

Microbiology and Immunology

Year Degree Awarded

2016

Creative Commons License

Creative Commons Attribution-Noncommercial-Share Alike 3.0 License
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 License.


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