Accession Number : ADA191993
Title : Molecular Mechanisms of Cytopathogenicity of Primate Lymphotropic Retroviruses: Relevance to Treatment and Vaccine for AIDS.
Descriptive Note : Annual rept. 29 Sep 86-28 Sep 87,
Corporate Author : BIOTECH RESEARCH LABS INC ROCKVILLE MD
Personal Author(s) : Manak, Mark M ; Jagodzinski, Linda L
PDF Url : ADA191993
Report Date : 28 Oct 1987
Pagination or Media Count : 72
Abstract : The molecular basis of infectivity, cytopathogenicity and genomic activation of Human Immunodeficiency Virus Type 1(HIV-1) was investigated by generating deletion mutations in sor, 3'orf, 5' region, and LTR. These studies show that the sor gene is crucial for the generation of infectious virus. Analysis of 3'orf indicate that deletions in the amino terminus (which overlaps the carboxy terminus of gp41) result in significant reduction in viral propagation. Studies with the LTR sequency have delineated an enhancer activity, an sp-1 bending site, and a tat response region (TAR). Genomic clones containing the integrated provirus of Simian T-Cell Lymphotorpic Virus Type III(African Green Monkey) (STLV-II(AGM)) and HIV-2(NIH-Z) have been isolated. Their nucleic acid sequence has been determined and subjected to computer analysis. A Comparison of the nucleotide sequences of these two new viral isolates with HIV-1 indicates that these new retroviruses are structurally similar to HIV-1 and belong to the same class of viruses as HIV-1. STLV-III and HIV-2(NIH-Z) exhibit a greater homology among themselves than with HIV-1. A study of biologically active forms of these viruses will aid in understanding why these new viruses are non-pathogenic. Keywords: Vaccines, Acquired immune deficiency syndrome, Virus diseases, Immunosuppression, Deoxyribonucleic acids.
Descriptors : *VIRUSES, *IMMUNOSUPPRESSION, *VACCINES, *PATHOGENESIS, *CYTOPATHOLOGY, DEOXYRIBONUCLEIC ACIDS, MOLECULAR PROPERTIES, NUCLEOTIDES, SEQUENCES, COMPUTER APPLICATIONS, DEFICIENCIES, IMMUNITY, SIGNS AND SYMPTOMS, INFECTIOUS DISEASES, RESPONSE, PROPAGATION, RESPONSE(BIOLOGY), MOLECULE MOLECULE INTERACTIONS, CHEMOTHERAPY
Subject Categories : Microbiology
Genetic Engineering and Molecular Biology
Distribution Statement : APPROVED FOR PUBLIC RELEASE