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A Novel Pan-Flavivirus Detection and Identification Assay Based on RT-qPCR and Microarray

The genus Flavivirus includes arthropod-borne viruses responsible for a large number of infections in humans and economically important animals. While RT-PCR protocols for specific detection of most Flavivirus species are available, there has been also a demand for a broad-range Flavivirus assay cov...

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Autores principales: Vina-Rodriguez, Ariel, Sachse, Konrad, Ziegler, Ute, Chaintoutis, Serafeim C., Keller, Markus, Groschup, Martin H., Eiden, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463098/
https://www.ncbi.nlm.nih.gov/pubmed/28626758
http://dx.doi.org/10.1155/2017/4248756
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author Vina-Rodriguez, Ariel
Sachse, Konrad
Ziegler, Ute
Chaintoutis, Serafeim C.
Keller, Markus
Groschup, Martin H.
Eiden, Martin
author_facet Vina-Rodriguez, Ariel
Sachse, Konrad
Ziegler, Ute
Chaintoutis, Serafeim C.
Keller, Markus
Groschup, Martin H.
Eiden, Martin
author_sort Vina-Rodriguez, Ariel
collection PubMed
description The genus Flavivirus includes arthropod-borne viruses responsible for a large number of infections in humans and economically important animals. While RT-PCR protocols for specific detection of most Flavivirus species are available, there has been also a demand for a broad-range Flavivirus assay covering all members of the genus. It is particularly challenging to balance specificity at genus level with equal sensitivity towards each target species. In the present study, a novel assay combining a SYBR Green-based RT-qPCR with a low-density DNA microarray has been developed. Validation experiments confirmed that the RT-qPCR exhibited roughly equal sensitivity of detection and quantification for all flaviviruses tested. These PCR products are subjected to hybridization on a microarray carrying 84 different oligonucleotide probes that represent all known Flavivirus species. This assay has been used as a screening and confirmation tool for Flavivirus presence in laboratory and field samples, and it performed successfully in international External Quality Assessment of NAT studies. Twenty-six Flavivirus strains were tested with the assay, showing equivalent or superior characteristics compared with the original or even with species-specific RT-PCRs. As an example, test results on West Nile virus detection in a panel of 340 mosquito pool samples from Greece are presented.
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spelling pubmed-54630982017-06-18 A Novel Pan-Flavivirus Detection and Identification Assay Based on RT-qPCR and Microarray Vina-Rodriguez, Ariel Sachse, Konrad Ziegler, Ute Chaintoutis, Serafeim C. Keller, Markus Groschup, Martin H. Eiden, Martin Biomed Res Int Research Article The genus Flavivirus includes arthropod-borne viruses responsible for a large number of infections in humans and economically important animals. While RT-PCR protocols for specific detection of most Flavivirus species are available, there has been also a demand for a broad-range Flavivirus assay covering all members of the genus. It is particularly challenging to balance specificity at genus level with equal sensitivity towards each target species. In the present study, a novel assay combining a SYBR Green-based RT-qPCR with a low-density DNA microarray has been developed. Validation experiments confirmed that the RT-qPCR exhibited roughly equal sensitivity of detection and quantification for all flaviviruses tested. These PCR products are subjected to hybridization on a microarray carrying 84 different oligonucleotide probes that represent all known Flavivirus species. This assay has been used as a screening and confirmation tool for Flavivirus presence in laboratory and field samples, and it performed successfully in international External Quality Assessment of NAT studies. Twenty-six Flavivirus strains were tested with the assay, showing equivalent or superior characteristics compared with the original or even with species-specific RT-PCRs. As an example, test results on West Nile virus detection in a panel of 340 mosquito pool samples from Greece are presented. Hindawi 2017 2017-05-24 /pmc/articles/PMC5463098/ /pubmed/28626758 http://dx.doi.org/10.1155/2017/4248756 Text en Copyright © 2017 Ariel Vina-Rodriguez et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Vina-Rodriguez, Ariel
Sachse, Konrad
Ziegler, Ute
Chaintoutis, Serafeim C.
Keller, Markus
Groschup, Martin H.
Eiden, Martin
A Novel Pan-Flavivirus Detection and Identification Assay Based on RT-qPCR and Microarray
title A Novel Pan-Flavivirus Detection and Identification Assay Based on RT-qPCR and Microarray
title_full A Novel Pan-Flavivirus Detection and Identification Assay Based on RT-qPCR and Microarray
title_fullStr A Novel Pan-Flavivirus Detection and Identification Assay Based on RT-qPCR and Microarray
title_full_unstemmed A Novel Pan-Flavivirus Detection and Identification Assay Based on RT-qPCR and Microarray
title_short A Novel Pan-Flavivirus Detection and Identification Assay Based on RT-qPCR and Microarray
title_sort novel pan-flavivirus detection and identification assay based on rt-qpcr and microarray
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463098/
https://www.ncbi.nlm.nih.gov/pubmed/28626758
http://dx.doi.org/10.1155/2017/4248756
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