Document 0623 DOCN M94A0623 TI Surface protein analysis of a non-syncytium inducing HIV-1 isolate. DT 9412 AU Fryer KM; Deacon NJ; Land SA; McPhee DA; Macfarlane Burnet Centre for Medical Research, Fairfield, Vic. SO Annu Conf Australas Soc HIV Med. 1993 Oct 28-30;5:72 (abstract no. SB3). Unique Identifier : AIDSLINE ASHM5/94349032 AB An Australian HIV-1 isolate that is non-syncytium inducing (NSI), and has reduced cytopathic effect on peripheral blood mononuclear cells (PBMCs) has been characterised. The biochemical properties and DNA sequence of this isolate (243925) were compared with a typical syncytium inducing (SI) isolate 228200. Both isolates replicate well in PBMCs and are neutralised by similar concentrations of sCD4 and OKT4a, but the NSI isolate does not down-modulate CD4 from the surface of infected cells. Phylogeny analysis based on envelope protein DNA sequence has mapped both to clade B, with North American isolates. The nucleotide sequences of the V3 loop of envelope of the two viruses correlate with published syncytium and non-syncytium inducing virus sequences (Fouchier et al., 1992). Western blot analysis has demonstrated greater heterogeneity in the envelope protein on the surface of cells infected with 243925 compared with infection by the NSI isolate. The surface glycoprotein gp 120 was detected on the viral particles of the NSI isolate only, suggesting that the protein is shed from the surface of the SI isolate. These studies confirm the similarity of Australian HIV-1 isolates to American isolates, and suggest a role for the stability of the envelope protein in HIV-1 syncytium formation. DE Australia Cell Line Cytopathogenic Effect, Viral/GENETICS DNA, Viral/*GENETICS Gene Expression Regulation, Viral/PHYSIOLOGY Giant Cells/*MICROBIOLOGY Human HIV Envelope Protein gp120/GENETICS HIV-1/*GENETICS Monocytes/*MICROBIOLOGY T4 Lymphocytes/MICROBIOLOGY MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).