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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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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. |
format | Online Article Text |
id | pubmed-5463098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
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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