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JoVE Journal > Immunology and Infection
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Summary
Abstract
Introduction
Protocol
Results
Discussion
Disclosures
Acknowledgements
Materials
References
Immunology and Infection
为检验新型抗病毒药物的鉴定对蓝舌病病毒
Published: October 11, 2013
doi:
10.3791/50820
Please note that all translations are automatically generated.
Click here for the English version.
Linlin Gu
1
,
Stewart W. Schneller
2
,
Qianjun Li
1
1
Division of Infectious Diseases, Department of Medicine
,
University of Alabama at Birmingham
2
Molette Laboratory for Drug Discovery, Department of Chemistry and Biochemistry
,
Auburn University
Summary
Abstract
Introduction
Protocol
Representative Results
Discussion
Disclosures
The authors have nothing to disclose.
Acknowledgements
Materials
DMEM medium
Gibco
1134218
For cell culture
FBS
Gibco
16000044
For cell culture
0.05% Trypsin-EDTA
Gibco
1000185
For cell culture
DPBS
Gbico
1049769
For cell culture
CellTiter-Glo (CTG) kit
Promega
TB288
For cell viability measurement
70% ethanol
Fisher
S25309B
Diluted from 95%
Antiviral huashilcompounds
NIH MLSMR and de novo synthesis
BTV-10
ATCC
VR-187
BSR cell
Developed in house
Synergy-II multi-mode microplate reader
BioTek
For luminescent signal reading
MicroFlo select dispenser
BioTek
Adding cells, virus, and reagents
384-well flat-bottom microplate
CORNING
28908031
For cell culture
Gen. 5 software
BioTek
For analysis of reading outputs from Synergy-II multi-mode microplate reader
GraphPad Prism 5
GraphPad
Version 5
For biostatic analysis and plot
DOWNLOAD MATERIALS LIST
References
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Bluetongue virus targets conventional dendritic cells in skin lymph.
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Mortality and case fatality during the recurrence of BTV-8 in northern Europe in 2007.
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Assay development and high throughput antiviral drug screening against Bluetongue virus.
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A cell-based luminescence assay is effective for high-throughput screening of potential influenza antivirals.
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The development, optimization and validation of an assay for high throughput antiviral drug screening against Dengue virus.
Int. J. Clin. Exp. Med
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The Aedes albopictus inhibitor of apoptosis 1 gene protects vertebrate cells from bluetongue virus-induced apoptosis.
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Development of a high-throughput human rhinovirus infectivity cell-based assay for identifying antiviral compounds.
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Tetracycline-inducible packaging cell line for production of flavivirus replicon particles.
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High-throughput assays using a luciferase-expressing replicon, virus-like particles, and full-length virus for West Nile virus drug discovery.
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Puig-Basagoiti, F., et al.
Triaryl pyrazoline compound inhibits flavivirus RNA replication.
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In vitro and in vivo protection against the highly pathogenic H5N1 influenza virus by an antisense phosphorothioate oligonucleotide.
Antivir. Ther
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Ray, D., Shi, P. Y.
Recent advances in flavivirus antiviral drug discovery and vaccine development.
Recent Pat. Antiinfect. Drug Discov
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1
, 45-55 (2006).
Severson, W. E., et al.
High-throughput screening of a 100,000-compound library for inhibitors of influenza A virus (H3N2).
J. Biomol. Screen
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13
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Severson, W. E., et al.
Development and validation of a high-throughput screen for inhibitors of SARS CoV and its application in screening of a 100,000-compound library.
J. Biomol. Screen
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Tags
Antiviral Assays
BTV Antivirals
Cytopathic Effect (CPE) Assay
Dose-response Assay
Mechanism Of Action (ToA) Assay
Antiviral Screening
Viral Lifecycle
Cell Culture System
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Cite This Article
Gu, L., Schneller, S. W., Li, Q. Assays for the Identification of Novel Antivirals against Bluetongue Virus.
J. Vis. Exp.
(80), e50820, doi:10.3791/50820 (2013).
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