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Assay development and high-throughput antiviral drug screening against Bluetongue virus
被引:37
|作者:
Li, Qianjun
[1
,2
]
Maddox, Clinton
[3
]
Rasmussen, Lynn
[3
]
Hobrath, Judith V.
[4
]
White, Lucile E.
[3
]
机构:
[1] Univ Alabama, Dept Med, Div Infect Dis, Birmingham, AL 35294 USA
[2] So Res Inst, Dept Biochem & Mol Biol, Birmingham, AL 35205 USA
[3] So Res Inst, High Throughput Screening Ctr, Birmingham, AL 35205 USA
[4] So Res Inst, Dept Med Chem, Birmingham, AL 35205 USA
关键词:
Bluetongue virus;
Antiviral;
Assay development;
Cytopathic effect;
High-throughput screening;
100,000-COMPOUND LIBRARY;
MEDITERRANEAN BASIN;
MAMMALIAN-CELLS;
APOPTOSIS;
VALIDATION;
INHIBITORS;
EUROPE;
D O I:
10.1016/j.antiviral.2009.06.004
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Bluetongue virus (BTV) infection is one of the most important diseases of domestic livestock. There are no antivirals available against BTV disease. In this paper, we present the development, optimization and validation of an in vitro cell-based high-throughput screening (HTS) assay using the luminescent-based CellTiter-Glo reagent to identify novel antivirals against BTV. Conditions of the cytopathic effect (CPE)-based assay were optimized at cell density of 5000 cells/well in medium containing 1% FBS and a multiplicity of infection at 0.01 in 384-well plate, with Z'-values >= 0.70, Coefficient of Variations >= 5.68 and signal-to-background ratio >= 7.10. This assay was further validated using a 9532 compound library. The fully validated assay was then used to screen the 194950 compound collection, which identified 693 compounds with >30% CPE inhibition. The 10-concentration dose response assay identified 185 structures with IC(50) <= 100 mu M, out of which 42 compounds were grouped into six analog series corresponding to six scaffolds enriched within the active set compared to their distribution in the library. The CPE-based assay development demonstrated its robustness and reliability, and its application in the PITS campaign will make significant contribution to the antiviral drug discovery against BTV disease. (C) 2009 Elsevier B.V. All rights reserved.
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页码:267 / 273
页数:7
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