New soluble-formazan assay for HIV-1 cytopathic effects: application to high-flux screening of synthetic and natural products for AIDS-antiviral activity

OS Weislow, R Kiser, DL Fine, J Bader… - JNCI: Journal of the …, 1989 - academic.oup.com
OS Weislow, R Kiser, DL Fine, J Bader, RH Shoemaker, MR Boyd
JNCI: Journal of the National Cancer Institute, 1989academic.oup.com
We have developed an effective and optimally safe microculture method for rapid and
convenient assay of the in vitro cytopathic effects of human immunodeficiency virus (HIV-1)
on human lymphoblastoid or other suitable host cells. The assay procedure is applicable to
the evaluation of drug effects on in vitro infections Induced directly in cultured host cells by
cell-free HIV-1 or by coculture with H9 cells chronically infected with HIV-1. The assay uses
a newly developed tetrazolium reagent that is metabolically reduced by viable cells to yield …
Abstract
We have developed an effective and optimally safe microculture method for rapid and convenient assay of the in vitro cytopathic effects of human immunodeficiency virus (HIV-1) on human lymphoblastoid or other suitable host cells. The assay procedure is applicable to the evaluation of drug effects on in vitro infections Induced directly in cultured host cells by cell-free HIV-1 or by coculture with H9 cells chronically infected with HIV-1. The assay uses a newly developed tetrazolium reagent that is metabolically reduced by viable cells to yield a soluble, colored formazan product measurable by conventional colorimetric techniques. This simple microassay minimizes the number of plate manipulations typically required with other assay methods and, coupled with computerized data collection and analysis, facilitates large-scale screening of agents for potential antiviral activity. To support and enhance the discovery of new anti-HIV-1 agents, the National Cancer Institute is offering investigators worldwide the opportunity to submit new candidate agents for anti-HIV-1 screening with this method. [J Nati Cancer Inst 81:577–586, 1989]
Oxford University Press