Species-independent bioassay for sensitive quantification of antiviral type I interferons

<p>Abstract</p> <p>Background</p> <p>Studies of the host response to infection often require quantitative measurement of the antiviral type I interferons (IFN-α/β) in biological samples. The amount of IFN is either determined via its ability to suppress a sensitive indi...

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Main Authors: Penski Nicola, Habjan Matthias, Kuri Thomas, Weber Friedemann
Format: Article
Language:English
Published: BMC 2010-02-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/7/1/50
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spelling doaj-f95a5c64bebc42e2a5683333bb4791aa2020-11-24T21:11:50ZengBMCVirology Journal1743-422X2010-02-01715010.1186/1743-422X-7-50Species-independent bioassay for sensitive quantification of antiviral type I interferonsPenski NicolaHabjan MatthiasKuri ThomasWeber Friedemann<p>Abstract</p> <p>Background</p> <p>Studies of the host response to infection often require quantitative measurement of the antiviral type I interferons (IFN-α/β) in biological samples. The amount of IFN is either determined via its ability to suppress a sensitive indicator virus, by an IFN-responding reporter cell line, or by ELISA. These assays however are either time-consuming and lack convenient readouts, or they are rather insensitive and restricted to IFN from a particular host species.</p> <p>Results</p> <p>An IFN-sensitive, <it>Renilla </it>luciferase-expressing Rift Valley fever virus (RVFV-Ren) was generated using reverse genetics. Human, murine and avian cells were tested for their susceptibility to RVFV-Ren after treatment with species-specific IFNs. RVFV-Ren was able to infect cells of all three species, and IFN-mediated inhibition of viral reporter activity occurred in a dose-dependent manner. The sensitivity limit was found to be 1 U/ml IFN, and comparison with a standard curve allowed to determine the activity of an unknown sample.</p> <p>Conclusions</p> <p>RVFV-Ren replicates in cells of several species and is highly sensitive to pre-treatment with IFN. These properties allowed the development of a rapid, sensitive, and species-independent antiviral assay with a convenient luciferase-based readout.</p> http://www.virologyj.com/content/7/1/50
collection DOAJ
language English
format Article
sources DOAJ
author Penski Nicola
Habjan Matthias
Kuri Thomas
Weber Friedemann
spellingShingle Penski Nicola
Habjan Matthias
Kuri Thomas
Weber Friedemann
Species-independent bioassay for sensitive quantification of antiviral type I interferons
Virology Journal
author_facet Penski Nicola
Habjan Matthias
Kuri Thomas
Weber Friedemann
author_sort Penski Nicola
title Species-independent bioassay for sensitive quantification of antiviral type I interferons
title_short Species-independent bioassay for sensitive quantification of antiviral type I interferons
title_full Species-independent bioassay for sensitive quantification of antiviral type I interferons
title_fullStr Species-independent bioassay for sensitive quantification of antiviral type I interferons
title_full_unstemmed Species-independent bioassay for sensitive quantification of antiviral type I interferons
title_sort species-independent bioassay for sensitive quantification of antiviral type i interferons
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2010-02-01
description <p>Abstract</p> <p>Background</p> <p>Studies of the host response to infection often require quantitative measurement of the antiviral type I interferons (IFN-α/β) in biological samples. The amount of IFN is either determined via its ability to suppress a sensitive indicator virus, by an IFN-responding reporter cell line, or by ELISA. These assays however are either time-consuming and lack convenient readouts, or they are rather insensitive and restricted to IFN from a particular host species.</p> <p>Results</p> <p>An IFN-sensitive, <it>Renilla </it>luciferase-expressing Rift Valley fever virus (RVFV-Ren) was generated using reverse genetics. Human, murine and avian cells were tested for their susceptibility to RVFV-Ren after treatment with species-specific IFNs. RVFV-Ren was able to infect cells of all three species, and IFN-mediated inhibition of viral reporter activity occurred in a dose-dependent manner. The sensitivity limit was found to be 1 U/ml IFN, and comparison with a standard curve allowed to determine the activity of an unknown sample.</p> <p>Conclusions</p> <p>RVFV-Ren replicates in cells of several species and is highly sensitive to pre-treatment with IFN. These properties allowed the development of a rapid, sensitive, and species-independent antiviral assay with a convenient luciferase-based readout.</p>
url http://www.virologyj.com/content/7/1/50
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AT habjanmatthias speciesindependentbioassayforsensitivequantificationofantiviraltypeiinterferons
AT kurithomas speciesindependentbioassayforsensitivequantificationofantiviraltypeiinterferons
AT weberfriedemann speciesindependentbioassayforsensitivequantificationofantiviraltypeiinterferons
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