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A High-Throughput Yellow Fever Neutralization Assay

Quick and accurate detection of neutralizing antibodies (nAbs) against yellow fever is essential in serodiagnosis during outbreaks for surveillance and to evaluate vaccine efficacy in population-wide studies. All of this requires serological assays that can process a large number of samples in a hig...

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Autores principales: Rasulova, Madina, Vercruysse, Thomas, Paulissen, Jasmine, Coun, Catherina, Suin, Vanessa, Heyndrickx, Leo, Ma, Ji, Geerts, Katrien, Timmermans, Jolien, Mishra, Niraj, Li, Li-Hsin, Kum, Dieudonné Buh, Coelmont, Lotte, Van Gucht, Steven, Karimzadeh, Hadi, Thorn-Seshold, Julia, Rothenfußer, Simon, Ariën, Kevin K., Neyts, Johan, Dallmeier, Kai, Thibaut, Hendrik Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241659/
https://www.ncbi.nlm.nih.gov/pubmed/35670599
http://dx.doi.org/10.1128/spectrum.02548-21
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author Rasulova, Madina
Vercruysse, Thomas
Paulissen, Jasmine
Coun, Catherina
Suin, Vanessa
Heyndrickx, Leo
Ma, Ji
Geerts, Katrien
Timmermans, Jolien
Mishra, Niraj
Li, Li-Hsin
Kum, Dieudonné Buh
Coelmont, Lotte
Van Gucht, Steven
Karimzadeh, Hadi
Thorn-Seshold, Julia
Rothenfußer, Simon
Ariën, Kevin K.
Neyts, Johan
Dallmeier, Kai
Thibaut, Hendrik Jan
author_facet Rasulova, Madina
Vercruysse, Thomas
Paulissen, Jasmine
Coun, Catherina
Suin, Vanessa
Heyndrickx, Leo
Ma, Ji
Geerts, Katrien
Timmermans, Jolien
Mishra, Niraj
Li, Li-Hsin
Kum, Dieudonné Buh
Coelmont, Lotte
Van Gucht, Steven
Karimzadeh, Hadi
Thorn-Seshold, Julia
Rothenfußer, Simon
Ariën, Kevin K.
Neyts, Johan
Dallmeier, Kai
Thibaut, Hendrik Jan
author_sort Rasulova, Madina
collection PubMed
description Quick and accurate detection of neutralizing antibodies (nAbs) against yellow fever is essential in serodiagnosis during outbreaks for surveillance and to evaluate vaccine efficacy in population-wide studies. All of this requires serological assays that can process a large number of samples in a highly standardized format. Albeit being laborious, time-consuming, and limited in throughput, the classical plaque reduction neutralization test (PRNT) is still considered the gold standard for the detection and quantification of nAbs due to its sensitivity and specificity. Here, we report the development of an alternative fluorescence-based serological assay (SNT(FLUO)) with an equally high sensitivity and specificity that is fit for high-throughput testing with the potential for automation. Finally, our novel SNT(FLUO) was cross-validated in several reference laboratories and against international WHO standards, showing its potential to be implemented in clinical use. SNT(FLUO) assays with similar performance are available for the Japanese encephalitis, Zika, and dengue viruses amenable to differential diagnostics. IMPORTANCE Fast and accurate detection of neutralizing antibodies (nAbs) against yellow fever virus (YFV) is key in yellow fever serodiagnosis, outbreak surveillance, and monitoring of vaccine efficacy. Although classical PRNT remains the gold standard for measuring YFV nAbs, this methodology suffers from inherent limitations such as low throughput and overall high labor intensity. We present a novel fluorescence-based serum neutralization test (SNT(FLUO)) with equally high sensitivity and specificity that is fit for processing a large number of samples in a highly standardized manner and has the potential to be implemented for clinical use. In addition, we present SNT(FLUO) assays with similar performance for Japanese encephalitis, Zika, and dengue viruses, opening new avenues for differential diagnostics.
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spelling pubmed-92416592022-06-30 A High-Throughput Yellow Fever Neutralization Assay Rasulova, Madina Vercruysse, Thomas Paulissen, Jasmine Coun, Catherina Suin, Vanessa Heyndrickx, Leo Ma, Ji Geerts, Katrien Timmermans, Jolien Mishra, Niraj Li, Li-Hsin Kum, Dieudonné Buh Coelmont, Lotte Van Gucht, Steven Karimzadeh, Hadi Thorn-Seshold, Julia Rothenfußer, Simon Ariën, Kevin K. Neyts, Johan Dallmeier, Kai Thibaut, Hendrik Jan Microbiol Spectr Methods and Protocols Quick and accurate detection of neutralizing antibodies (nAbs) against yellow fever is essential in serodiagnosis during outbreaks for surveillance and to evaluate vaccine efficacy in population-wide studies. All of this requires serological assays that can process a large number of samples in a highly standardized format. Albeit being laborious, time-consuming, and limited in throughput, the classical plaque reduction neutralization test (PRNT) is still considered the gold standard for the detection and quantification of nAbs due to its sensitivity and specificity. Here, we report the development of an alternative fluorescence-based serological assay (SNT(FLUO)) with an equally high sensitivity and specificity that is fit for high-throughput testing with the potential for automation. Finally, our novel SNT(FLUO) was cross-validated in several reference laboratories and against international WHO standards, showing its potential to be implemented in clinical use. SNT(FLUO) assays with similar performance are available for the Japanese encephalitis, Zika, and dengue viruses amenable to differential diagnostics. IMPORTANCE Fast and accurate detection of neutralizing antibodies (nAbs) against yellow fever virus (YFV) is key in yellow fever serodiagnosis, outbreak surveillance, and monitoring of vaccine efficacy. Although classical PRNT remains the gold standard for measuring YFV nAbs, this methodology suffers from inherent limitations such as low throughput and overall high labor intensity. We present a novel fluorescence-based serum neutralization test (SNT(FLUO)) with equally high sensitivity and specificity that is fit for processing a large number of samples in a highly standardized manner and has the potential to be implemented for clinical use. In addition, we present SNT(FLUO) assays with similar performance for Japanese encephalitis, Zika, and dengue viruses, opening new avenues for differential diagnostics. American Society for Microbiology 2022-06-07 /pmc/articles/PMC9241659/ /pubmed/35670599 http://dx.doi.org/10.1128/spectrum.02548-21 Text en Copyright © 2022 Rasulova et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Methods and Protocols
Rasulova, Madina
Vercruysse, Thomas
Paulissen, Jasmine
Coun, Catherina
Suin, Vanessa
Heyndrickx, Leo
Ma, Ji
Geerts, Katrien
Timmermans, Jolien
Mishra, Niraj
Li, Li-Hsin
Kum, Dieudonné Buh
Coelmont, Lotte
Van Gucht, Steven
Karimzadeh, Hadi
Thorn-Seshold, Julia
Rothenfußer, Simon
Ariën, Kevin K.
Neyts, Johan
Dallmeier, Kai
Thibaut, Hendrik Jan
A High-Throughput Yellow Fever Neutralization Assay
title A High-Throughput Yellow Fever Neutralization Assay
title_full A High-Throughput Yellow Fever Neutralization Assay
title_fullStr A High-Throughput Yellow Fever Neutralization Assay
title_full_unstemmed A High-Throughput Yellow Fever Neutralization Assay
title_short A High-Throughput Yellow Fever Neutralization Assay
title_sort high-throughput yellow fever neutralization assay
topic Methods and Protocols
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241659/
https://www.ncbi.nlm.nih.gov/pubmed/35670599
http://dx.doi.org/10.1128/spectrum.02548-21
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