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Development of a high-throughput colorimetric Zika virus infection assay

Zika virus (ZIKV) is an emerging pathogen that causes congenital infections which may result in birth defects, such as microcephaly. Currently, no approved treatment or vaccination is available. ZIKV can be readily detected in cell culture where virally infected cells are normally stained by specifi...

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Autores principales: Müller, Janis A., Harms, Mirja, Schubert, Axel, Mayer, Benjamin, Jansen, Stephanie, Herbeuval, Jean-Philippe, Michel, Detlef, Mertens, Thomas, Vapalahti, Olli, Schmidt-Chanasit, Jonas, Münch, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357303/
https://www.ncbi.nlm.nih.gov/pubmed/28176006
http://dx.doi.org/10.1007/s00430-017-0493-2
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author Müller, Janis A.
Harms, Mirja
Schubert, Axel
Mayer, Benjamin
Jansen, Stephanie
Herbeuval, Jean-Philippe
Michel, Detlef
Mertens, Thomas
Vapalahti, Olli
Schmidt-Chanasit, Jonas
Münch, Jan
author_facet Müller, Janis A.
Harms, Mirja
Schubert, Axel
Mayer, Benjamin
Jansen, Stephanie
Herbeuval, Jean-Philippe
Michel, Detlef
Mertens, Thomas
Vapalahti, Olli
Schmidt-Chanasit, Jonas
Münch, Jan
author_sort Müller, Janis A.
collection PubMed
description Zika virus (ZIKV) is an emerging pathogen that causes congenital infections which may result in birth defects, such as microcephaly. Currently, no approved treatment or vaccination is available. ZIKV can be readily detected in cell culture where virally infected cells are normally stained by specific antibodies. As ZIKV regularly causes a cytopathic effect, we were wondering whether this viral property can be used to quantitatively determine viral infectivity. We here describe the use of an 3-[4,5-dimethyl-2-thiazolyl]-2,5-diphenyl-2H-tetrazolium bromide-(MTT)-based cell viability assay that allows to determine ZIKV-induced cell death. We show that this colorimetric assay quantifies ZIKV infection over a broad range of viral dilutions in both monkey and human cells. It allows to determine inhibitory activities of antivirals that block ZIKV or to define the neutralizing antibody titers of ZIKV antisera. This MTT-based ZIKV detection assay can be evaluated by naked eye or computational tools, has a broad linear range, does not require large equipment or costly reagents, and thus represents a promising alternative to antibody-based assays, in particular in resource-poor settings. We propose to use this simple, fast, and cheap method for quantification of ZIKV neutralizing antibodies and testing of antiviral compounds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00430-017-0493-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-53573032017-03-30 Development of a high-throughput colorimetric Zika virus infection assay Müller, Janis A. Harms, Mirja Schubert, Axel Mayer, Benjamin Jansen, Stephanie Herbeuval, Jean-Philippe Michel, Detlef Mertens, Thomas Vapalahti, Olli Schmidt-Chanasit, Jonas Münch, Jan Med Microbiol Immunol Rapid Communication Zika virus (ZIKV) is an emerging pathogen that causes congenital infections which may result in birth defects, such as microcephaly. Currently, no approved treatment or vaccination is available. ZIKV can be readily detected in cell culture where virally infected cells are normally stained by specific antibodies. As ZIKV regularly causes a cytopathic effect, we were wondering whether this viral property can be used to quantitatively determine viral infectivity. We here describe the use of an 3-[4,5-dimethyl-2-thiazolyl]-2,5-diphenyl-2H-tetrazolium bromide-(MTT)-based cell viability assay that allows to determine ZIKV-induced cell death. We show that this colorimetric assay quantifies ZIKV infection over a broad range of viral dilutions in both monkey and human cells. It allows to determine inhibitory activities of antivirals that block ZIKV or to define the neutralizing antibody titers of ZIKV antisera. This MTT-based ZIKV detection assay can be evaluated by naked eye or computational tools, has a broad linear range, does not require large equipment or costly reagents, and thus represents a promising alternative to antibody-based assays, in particular in resource-poor settings. We propose to use this simple, fast, and cheap method for quantification of ZIKV neutralizing antibodies and testing of antiviral compounds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00430-017-0493-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-02-07 2017 /pmc/articles/PMC5357303/ /pubmed/28176006 http://dx.doi.org/10.1007/s00430-017-0493-2 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Rapid Communication
Müller, Janis A.
Harms, Mirja
Schubert, Axel
Mayer, Benjamin
Jansen, Stephanie
Herbeuval, Jean-Philippe
Michel, Detlef
Mertens, Thomas
Vapalahti, Olli
Schmidt-Chanasit, Jonas
Münch, Jan
Development of a high-throughput colorimetric Zika virus infection assay
title Development of a high-throughput colorimetric Zika virus infection assay
title_full Development of a high-throughput colorimetric Zika virus infection assay
title_fullStr Development of a high-throughput colorimetric Zika virus infection assay
title_full_unstemmed Development of a high-throughput colorimetric Zika virus infection assay
title_short Development of a high-throughput colorimetric Zika virus infection assay
title_sort development of a high-throughput colorimetric zika virus infection assay
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357303/
https://www.ncbi.nlm.nih.gov/pubmed/28176006
http://dx.doi.org/10.1007/s00430-017-0493-2
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