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Titration and neutralizing antibody quantification by focus forming assay for Powassan virus

The development of high-throughput assays measuring Powassan virus (POWV) lineage I and II represents an important step in virological and immunological studies. By adapting focus-forming assays previously optimized for West Nile virus and Zika virus, this protocol is able to determine viral load, e...

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Autores principales: Stone, E. Taylor, Hirsch, Alec J., Smith, Jessica L., Brien, James D., Pinto, Amelia K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218233/
https://www.ncbi.nlm.nih.gov/pubmed/35755126
http://dx.doi.org/10.1016/j.xpro.2022.101473
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author Stone, E. Taylor
Hirsch, Alec J.
Smith, Jessica L.
Brien, James D.
Pinto, Amelia K.
author_facet Stone, E. Taylor
Hirsch, Alec J.
Smith, Jessica L.
Brien, James D.
Pinto, Amelia K.
author_sort Stone, E. Taylor
collection PubMed
description The development of high-throughput assays measuring Powassan virus (POWV) lineage I and II represents an important step in virological and immunological studies. By adapting focus-forming assays previously optimized for West Nile virus and Zika virus, this protocol is able to determine viral load, evaluate antivirals, and measure neutralizing antibodies. Although limited by its requirement of a detection antibody, this protocol includes a rapid and high-throughput assay for measuring viral titer. By utilizing a baby hamster kidney cell line and a 96-well plate format, this protocol allows for more sensitivity in the detection of POWV lineage I. For complete details on the use and execution of this protocol, please refer to Stone et al. (2022).
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spelling pubmed-92182332022-06-24 Titration and neutralizing antibody quantification by focus forming assay for Powassan virus Stone, E. Taylor Hirsch, Alec J. Smith, Jessica L. Brien, James D. Pinto, Amelia K. STAR Protoc Protocol The development of high-throughput assays measuring Powassan virus (POWV) lineage I and II represents an important step in virological and immunological studies. By adapting focus-forming assays previously optimized for West Nile virus and Zika virus, this protocol is able to determine viral load, evaluate antivirals, and measure neutralizing antibodies. Although limited by its requirement of a detection antibody, this protocol includes a rapid and high-throughput assay for measuring viral titer. By utilizing a baby hamster kidney cell line and a 96-well plate format, this protocol allows for more sensitivity in the detection of POWV lineage I. For complete details on the use and execution of this protocol, please refer to Stone et al. (2022). Elsevier 2022-06-17 /pmc/articles/PMC9218233/ /pubmed/35755126 http://dx.doi.org/10.1016/j.xpro.2022.101473 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Stone, E. Taylor
Hirsch, Alec J.
Smith, Jessica L.
Brien, James D.
Pinto, Amelia K.
Titration and neutralizing antibody quantification by focus forming assay for Powassan virus
title Titration and neutralizing antibody quantification by focus forming assay for Powassan virus
title_full Titration and neutralizing antibody quantification by focus forming assay for Powassan virus
title_fullStr Titration and neutralizing antibody quantification by focus forming assay for Powassan virus
title_full_unstemmed Titration and neutralizing antibody quantification by focus forming assay for Powassan virus
title_short Titration and neutralizing antibody quantification by focus forming assay for Powassan virus
title_sort titration and neutralizing antibody quantification by focus forming assay for powassan virus
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218233/
https://www.ncbi.nlm.nih.gov/pubmed/35755126
http://dx.doi.org/10.1016/j.xpro.2022.101473
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