Document 0097 DOCN M9580097 TI Identification of HTLV-I- or HTLV-II-producing cells by cocultivation with BHK-21 cells stably transfected with a LTR-lacZ gene construct. DT 9506 AU Astier-Gin T; Portail JP; Lafond F; Guillemain B; INSERM Unite 328, Bordeaux, France. SO J Virol Methods. 1995 Jan;51(1):19-29. Unique Identifier : AIDSLINE MED/95247866 AB The Syrian Hamster kidney cell line (BHK-21) was stably transfected with a plasmid vector containing the lacZ bacterial gene under the control of a HTLV-I-LTR promoter. In these cells termed pA18G-BHK-21, this lacZ construct is inducible by the tax protein produced by a tax expression vector. It was also shown that beta-galactosidase synthesis was detected within 48 h after cocultivation of pA18G-BHK-21 cells with HTLV-I (HUT-102, MT2, C91/PL, 2060) or HTLV-II (MoT strain) -producing cells. The number of positive cells was directly related to the number of HTLV-I or -II-infected cells seeded. In addition, the LTR transactivation observed in coculture with HTLV-I-infected cells was specifically inhibited by sera containing antibodies directed against HTLV-I proteins, but not, or only weakly, by sera containing HTLV-II antibodies. Conversely, beta-galactosidase expression induced by HTLV-II-infected cells was inhibited by sera of HTLV-II-infected individuals, but not, or only weakly, by HTLV-I-positive sera. Irrespective of the inducer cell, sera from uninfected people did not inhibit LTR-driven expression of the lacZ gene in pA18G-BHK-21 cells cocultivated with HTLV-producing cells. This assay may thus be employed profitably for the detection and quantification of both HTLV-producing cells and HTLV-specific antibodies. DE beta-Galactosidase/BIOSYNTHESIS/GENETICS Animal Cell Line Genetic Vectors Hamsters Human HTLV-I/*GENETICS/*PHYSIOLOGY HTLV-I Antibodies/BLOOD HTLV-II/*PHYSIOLOGY HTLV-II Antibodies/BLOOD Lac Operon Neutralization Tests Plasmids/GENETICS Promoter Regions (Genetics) Repetitive Sequences, Nucleic Acid Support, Non-U.S. Gov't Trans-Activation (Genetics) Transfection Virology/METHODS Virus Replication JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).