Document 3298 DOCN M94A3298 TI Proviral DNA in virions from primary isolates. DT 9412 AU Asjo B; Sommerfelt M; National Virus Center, University of Bergen, Norway. SO Int Conf AIDS. 1994 Aug 7-12;10(1):108 (abstract no. PA0052). Unique Identifier : AIDSLINE ICA10/94369277 AB OBJECTIVE: To determine whether proviral DNA is present in HIV virions of primary isolates grown in primary cells. MATERIALS AND METHODS: Patient isolates with slow/low and rapid/high type characteristics were used to infect PHA blasts. Virions were collected by ultracentrifugation and subjected to three different treatments prior to PCR amplification using primers hybridizing with U5 and R regions in the LTR (recognizing strong-stop DNA) and the pol region. Negative control consisted of pelleted disrupted virions treated with DNAse to remove adherent contaminating proviral DNA from disrupted cells. RESULTS: Proviral DNA corresponding to strong-stop DNA was demonstrated in virions from primary isolates of both slow/low and rapid/high phenotype. No signal could be detected with primers to the pol region which is in agreement with previous data that only partial reverse transcription takes place within the virion. CONCLUSION: Our data show that strong-stop DNA synthesis is not only a phenomenon associated with laboratory adapted strains of HIV but is also present in primary isolates grown in primary cells. It most likely represents a phenomenon common to the retrovirus family. DE Cells, Cultured Deoxyribonucleases DNA, Viral/BIOSYNTHESIS/GENETICS/*ISOLATION & PURIF Genes, pol Human HIV/GENETICS/*ISOLATION & PURIF HIV Long Terminal Repeat Phenotype Polymerase Chain Reaction Proviruses/GROWTH & DEVELOPMENT/GENETICS/*ISOLATION & PURIF Virus Cultivation MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).