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Internally Controlled, Generic Real-Time PCR for Quantification and Multiplex Real-Time PCR with Serotype-Specific Probes for Serotyping of Dengue Virus Infections
Dengue has become a global public health problem and a sensitive diagnostic test for early phase detection can be life saving. An internally controlled, generic real-time PCR was developed and validated by testing serial dilutions of a DENV positive control RNA in the presence of a fixed amount of I...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263855/ https://www.ncbi.nlm.nih.gov/pubmed/22312344 http://dx.doi.org/10.1155/2011/514681 |
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author | Menting, Sandra Thai, Khoa T. D. Nga, Tran T. T. Phuong, Hoang L. Klatser, Paul Wolthers, Katja C. Binh, Tran Q. de Vries, Peter J. Beld, Marcel |
author_facet | Menting, Sandra Thai, Khoa T. D. Nga, Tran T. T. Phuong, Hoang L. Klatser, Paul Wolthers, Katja C. Binh, Tran Q. de Vries, Peter J. Beld, Marcel |
author_sort | Menting, Sandra |
collection | PubMed |
description | Dengue has become a global public health problem and a sensitive diagnostic test for early phase detection can be life saving. An internally controlled, generic real-time PCR was developed and validated by testing serial dilutions of a DENV positive control RNA in the presence of a fixed amount of IC with results showing a good linearity (R (2) = 0.9967) and a LOD of at least 1.95 × 10(4) copies/mL. Application of the generic PCR on 136 patient samples revealed a sensitivity of 95.8% and specificity of 100%. A newly developed multiplex real-time PCR with serotype-specific probes allowed the serotyping of DENV for 80 out of 92 (87%) generic real-time PCR positive patients. Combined these real-time PCRs offer a convenient diagnostic tool for the sensitive and specific quantification of DENV in clinical specimens with the possibility for serotyping. |
format | Online Article Text |
id | pubmed-3263855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32638552012-02-06 Internally Controlled, Generic Real-Time PCR for Quantification and Multiplex Real-Time PCR with Serotype-Specific Probes for Serotyping of Dengue Virus Infections Menting, Sandra Thai, Khoa T. D. Nga, Tran T. T. Phuong, Hoang L. Klatser, Paul Wolthers, Katja C. Binh, Tran Q. de Vries, Peter J. Beld, Marcel Adv Virol Research Article Dengue has become a global public health problem and a sensitive diagnostic test for early phase detection can be life saving. An internally controlled, generic real-time PCR was developed and validated by testing serial dilutions of a DENV positive control RNA in the presence of a fixed amount of IC with results showing a good linearity (R (2) = 0.9967) and a LOD of at least 1.95 × 10(4) copies/mL. Application of the generic PCR on 136 patient samples revealed a sensitivity of 95.8% and specificity of 100%. A newly developed multiplex real-time PCR with serotype-specific probes allowed the serotyping of DENV for 80 out of 92 (87%) generic real-time PCR positive patients. Combined these real-time PCRs offer a convenient diagnostic tool for the sensitive and specific quantification of DENV in clinical specimens with the possibility for serotyping. Hindawi Publishing Corporation 2011 2011-12-05 /pmc/articles/PMC3263855/ /pubmed/22312344 http://dx.doi.org/10.1155/2011/514681 Text en Copyright © 2011 Sandra Menting et al. https://creativecommons.org/licenses/by/3.0/ 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 Menting, Sandra Thai, Khoa T. D. Nga, Tran T. T. Phuong, Hoang L. Klatser, Paul Wolthers, Katja C. Binh, Tran Q. de Vries, Peter J. Beld, Marcel Internally Controlled, Generic Real-Time PCR for Quantification and Multiplex Real-Time PCR with Serotype-Specific Probes for Serotyping of Dengue Virus Infections |
title | Internally Controlled, Generic Real-Time PCR for Quantification and Multiplex Real-Time PCR with Serotype-Specific Probes for Serotyping of Dengue Virus Infections |
title_full | Internally Controlled, Generic Real-Time PCR for Quantification and Multiplex Real-Time PCR with Serotype-Specific Probes for Serotyping of Dengue Virus Infections |
title_fullStr | Internally Controlled, Generic Real-Time PCR for Quantification and Multiplex Real-Time PCR with Serotype-Specific Probes for Serotyping of Dengue Virus Infections |
title_full_unstemmed | Internally Controlled, Generic Real-Time PCR for Quantification and Multiplex Real-Time PCR with Serotype-Specific Probes for Serotyping of Dengue Virus Infections |
title_short | Internally Controlled, Generic Real-Time PCR for Quantification and Multiplex Real-Time PCR with Serotype-Specific Probes for Serotyping of Dengue Virus Infections |
title_sort | internally controlled, generic real-time pcr for quantification and multiplex real-time pcr with serotype-specific probes for serotyping of dengue virus infections |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263855/ https://www.ncbi.nlm.nih.gov/pubmed/22312344 http://dx.doi.org/10.1155/2011/514681 |
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