Visna is a slow infection of sheep primarily affecting the lungs and nervous system. We propose to continue our investigations of the molecular basis for the slowness of infection, and for the tissue lesions. We will examine two hypotheses, gene dosage and integration, that have been advanced as explanations for slowness, using in situ hybridization and other methods for this purpose in a new model of visna. We also will map gene functions on the viral genome and use probes to regions of known function, to try to correlate viral gene products with demyelination.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS021423-04
Application #
3402528
Study Section
Virology Study Section (VR)
Project Start
1984-03-01
Project End
1988-11-30
Budget Start
1986-12-01
Budget End
1987-11-30
Support Year
4
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Staskus, K A; Retzel, E F; Lewis, E D et al. (1991) Isolation of replication-competent molecular clones of visna virus. Virology 181:228-40
Haase, A T; Retzel, E F; Staskus, K A (1990) Amplification and detection of lentiviral DNA inside cells. Proc Natl Acad Sci U S A 87:4971-5