The aim of this program project is to continue to study the interaction of reovirus and its individual components with the nervous system. In addition, we will begin to extend these studies using poliovirus. Reovirus has been chosen because it is one of the best understood viruses in terms of understanding the function of several of the viral genes in viral host interactions. The program project will extend this knowledge base by continuing our studies with reovirus involving primary injury to muscle, spread of virus to the central nervous system (CNS) by blood or neural transport, trans-synaptic spread, spread within the CNS, characterization of the reovirus T3 receptor and identification of the reovirus T1 receptor. In addition, the cloning and expression of several reovirus genes will provide insights into the function of reovirus genes separate from their role in complex particles. Studies with polioviruses will be initiated utilizing the approaches shown to be fruitful ones for the reoviruses. Extensive collaboration will be carried out between the five participating investigators as well as a number of collaborators. The studies involve the following interdisciplinary areas: viral genetics and molecular biology, neuropathology, developmental neurobiology, and neuroimmunology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center (P50)
Project #
5P50NS016998-11
Application #
3107734
Study Section
Neurological Disorders Program Project Review A Committee (NSPA)
Project Start
1981-04-01
Project End
1992-03-31
Budget Start
1991-04-01
Budget End
1992-03-31
Support Year
11
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
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Li, Q; Yafal, A G; Lee, Y M et al. (1994) Poliovirus neutralization by antibodies to internal epitopes of VP4 and VP1 results from reversible exposure of these sequences at physiological temperature. J Virol 68:3965-70

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