The overall goal of this project is to understand how retroviruses adversely affect the central nervous system and the nature of the role of macrophages in disease pathogenesis. We are utilizing the mouse as an animal model and are investigating two types of neurovirulent viruses that cause different brain diseases. We have studied the host and viral factors which control neuroinvasiveness (the capacity of these viruses to enter the brain), and the determinants of neurovirulence (induction of brain disease) after these viruses have entered the brain. Our work on neuroinvasiveness has uncovered a viral protein that has been known to exist for many years, but its function in the virus life cycle is unknown. We are interested in understanding the function of this protein since it appears to be an accessory protein of the virus that promotes virus dissemination in the host. Our work on neurovirulence has focused on the role of the viral envelope protein and its interaction with microglial cells (brain macrophages). Although these viruses interfere with normal neuronal function and in some cases actually result in neuronal death, they do not infect the neurons they damage. Instead, it is infection of microglial cells that is responsible for the neurovirulence of these viruses. Furthermore, neurovirulence has been mapped to the viral envelope protein (coat protein of the virus) and we are interested in understanding the nature of the interaction between this protein and microglial cells, which appears to play such an important role in disease pathogenesis. - Retrovirus, brain, spongiform, neurodegeneration, oncornavirus, microgila, macrophage, mouse, envelope gene, gag gene

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000086-22
Application #
6288793
Study Section
Special Emphasis Panel (LPVD)
Project Start
Project End
Budget Start
Budget End
Support Year
22
Fiscal Year
1999
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code
Portis, J L; Askovich, P; Austin, J et al. (2009) The degree of folding instability of the envelope protein of a neurovirulent murine retrovirus correlates with the severity of the neurological disease. J Virol 83:6079-86
Clase, Amanda C; Dimcheff, Derek E; Favara, Cynthia et al. (2006) Oligodendrocytes are a major target of the toxicity of spongiogenic murine retroviruses. Am J Pathol 169:1026-38
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Dimcheff, Derek E; Portis, John L; Caughey, Byron (2003) Prion proteins meet protein quality control. Trends Cell Biol 13:337-40
Dimcheff, Derek E; Askovic, Srdjan; Baker, Audrey H et al. (2003) Endoplasmic reticulum stress is a determinant of retrovirus-induced spongiform neurodegeneration. J Virol 77:12617-29
Portis, John L (2002) Perspectives on the role of endogenous human retroviruses in autoimmune diseases. Virology 296:1-5
Askovic, S; Favara, C; McAtee, F J et al. (2001) Increased expression of MIP-1 alpha and MIP-1 beta mRNAs in the brain correlates spatially and temporally with the spongiform neurodegeneration induced by a murine oncornavirus. J Virol 75:2665-74
Peterson, K E; Robertson, S J; Portis, J L et al. (2001) Differences in cytokine and chemokine responses during neurological disease induced by polytropic murine retroviruses Map to separate regions of the viral envelope gene. J Virol 75:2848-56
Fujisawa, R; McAtee, F J; Favara, C et al. (2001) N-terminal cleavage fragment of glycosylated Gag is incorporated into murine oncornavirus particles. J Virol 75:11239-43

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