Recombinant Green Fluorescent Protein-Expressing Human Cytomegalovirus as a Tool for Screening Antiviral Agents

Manfred Marschall, Martina Freitag, Sigrid Weiler, Gabriele Sorg, Thomas Stamminger

Antimicrobial Agents and Chemotherapy · 2000 · 139 citations · 28 references

TL;DR

A recombinant human cytomegalovirus (AD169‑GFP) expressing green fluorescent protein was generated by homologous recombination. The study aimed to evaluate antiviral activities of reference and novel cytomegalovirus inhibitors using the AD169‑GFP virus. Antiviral effects were quantified by automated fluorometry, flow cytometry, and microscopy of infected fibroblasts, and virus variants derived from AD169‑GFP were used to probe drug‑resistance characteristics. The GFP‑based assay yielded stable, highly sensitive, and reproducible signals, matched reference compound profiles, uncovered distinct activities of new inhibitors, and proved reliable for concentration‑ and time‑dependent measurements, making it suitable for high‑throughput screening.

Abstract

ABSTRACT A recombinant human cytomegalovirus (AD169-GFP) expressing green fluorescent protein was generated by homologous recombination. Infection of human fibroblast cultures with AD169-GFP virus produced stable and readily detectable amounts of GFP signals which were quantitated by automated fluorometry. Hereby, high levels of sensitivity and reproducibility could be achieved, compared to those with the conventional plaque reduction assay. Antiviral activities were determined for four reference compounds as well as a set of putative novel cytomegalovirus inhibitors. The results obtained were exactly in line with the known characteristics of reference compounds and furthermore revealed distinct antiviral activities of novel in vitro inhibitors. The fluorometric data could be confirmed by GFP-based flow cytometry and fluorescence microscopy. In addition, laboratory virus variants derived from the recombinant AD169-GFP virus provided further possibilities for study of the characteristics of drug resistance. The GFP-based antiviral assay appeared to be very reliable for measuring virus-inhibitory effects in concentration- and time-dependent fashions and might also be adaptable for high-throughput screenings of cytomegalovirus-specific antiviral agents.

References

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