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Development of three multiplex RT-PCR assays for the detection of 12 respiratory RNA viruses
Three multiplex hemi-nested RT-PCR assays were developed to detect simultaneously 12 RNA respiratory viruses: influenza viruses A, B and C, human respiratory syncytial virus (hRSV), human metapneumovirus (hMPV), parainfluenza virus types 1–4 (PIV-1, -2, -3 and -4), human coronavirus OC43 and 229E (H...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112904/ https://www.ncbi.nlm.nih.gov/pubmed/15847919 http://dx.doi.org/10.1016/j.jviromet.2005.01.020 |
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author | Bellau-Pujol, S. Vabret, A. Legrand, L. Dina, J. Gouarin, S. Petitjean-Lecherbonnier, J. Pozzetto, B. Ginevra, C. Freymuth, F. |
author_facet | Bellau-Pujol, S. Vabret, A. Legrand, L. Dina, J. Gouarin, S. Petitjean-Lecherbonnier, J. Pozzetto, B. Ginevra, C. Freymuth, F. |
author_sort | Bellau-Pujol, S. |
collection | PubMed |
description | Three multiplex hemi-nested RT-PCR assays were developed to detect simultaneously 12 RNA respiratory viruses: influenza viruses A, B and C, human respiratory syncytial virus (hRSV), human metapneumovirus (hMPV), parainfluenza virus types 1–4 (PIV-1, -2, -3 and -4), human coronavirus OC43 and 229E (HCoV) and rhinovirus (hRV). An internal amplification control was included in one of the RT-PCR assays. The RT-PCR multiplex 1 and the hemi-nested multiplex 1 detected 1 and 0.1 TCID50 of RSV A, respectively, and 0.01 and 0.001 TCID50 of influenza virus A/H3N2, respectively. Two hundred and three nasal aspirates from hospitalised children were retrospectively tested in comparison with two conventional methods: direct immunofluorescence assay and viral isolation technique. Almost all samples (89/91) that were positive by immunofluorescence assay and/or viral isolation technique were detected by the multiplex assay. This method also detected an additional 85 viruses and 33 co-infections. The overall sensitivity (98%), rapidity and enhanced efficiency of these multiplex hemi-nested RT-PCR assays suggest that they would be a significant improvement over conventional methods for the detection of a broad spectrum of respiratory viruses. |
format | Online Article Text |
id | pubmed-7112904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71129042020-04-02 Development of three multiplex RT-PCR assays for the detection of 12 respiratory RNA viruses Bellau-Pujol, S. Vabret, A. Legrand, L. Dina, J. Gouarin, S. Petitjean-Lecherbonnier, J. Pozzetto, B. Ginevra, C. Freymuth, F. J Virol Methods Article Three multiplex hemi-nested RT-PCR assays were developed to detect simultaneously 12 RNA respiratory viruses: influenza viruses A, B and C, human respiratory syncytial virus (hRSV), human metapneumovirus (hMPV), parainfluenza virus types 1–4 (PIV-1, -2, -3 and -4), human coronavirus OC43 and 229E (HCoV) and rhinovirus (hRV). An internal amplification control was included in one of the RT-PCR assays. The RT-PCR multiplex 1 and the hemi-nested multiplex 1 detected 1 and 0.1 TCID50 of RSV A, respectively, and 0.01 and 0.001 TCID50 of influenza virus A/H3N2, respectively. Two hundred and three nasal aspirates from hospitalised children were retrospectively tested in comparison with two conventional methods: direct immunofluorescence assay and viral isolation technique. Almost all samples (89/91) that were positive by immunofluorescence assay and/or viral isolation technique were detected by the multiplex assay. This method also detected an additional 85 viruses and 33 co-infections. The overall sensitivity (98%), rapidity and enhanced efficiency of these multiplex hemi-nested RT-PCR assays suggest that they would be a significant improvement over conventional methods for the detection of a broad spectrum of respiratory viruses. Elsevier B.V. 2005-06 2005-02-24 /pmc/articles/PMC7112904/ /pubmed/15847919 http://dx.doi.org/10.1016/j.jviromet.2005.01.020 Text en Copyright © 2005 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Bellau-Pujol, S. Vabret, A. Legrand, L. Dina, J. Gouarin, S. Petitjean-Lecherbonnier, J. Pozzetto, B. Ginevra, C. Freymuth, F. Development of three multiplex RT-PCR assays for the detection of 12 respiratory RNA viruses |
title | Development of three multiplex RT-PCR assays for the detection of 12 respiratory RNA viruses |
title_full | Development of three multiplex RT-PCR assays for the detection of 12 respiratory RNA viruses |
title_fullStr | Development of three multiplex RT-PCR assays for the detection of 12 respiratory RNA viruses |
title_full_unstemmed | Development of three multiplex RT-PCR assays for the detection of 12 respiratory RNA viruses |
title_short | Development of three multiplex RT-PCR assays for the detection of 12 respiratory RNA viruses |
title_sort | development of three multiplex rt-pcr assays for the detection of 12 respiratory rna viruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112904/ https://www.ncbi.nlm.nih.gov/pubmed/15847919 http://dx.doi.org/10.1016/j.jviromet.2005.01.020 |
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