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Development of real-time fluorescent reverse transcription loop-mediated isothermal amplification assay with quenching primer for influenza virus and respiratory syncytial virus
Influenza virus and respiratory syncytial virus cause acute upper and lower respiratory tract infections, especially in children and the elderly. Early treatment for these infections is thought to be important, so simple and sensitive detection methods are needed for use at clinical sites. Therefore...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier B.V.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113748/ https://www.ncbi.nlm.nih.gov/pubmed/30831121 http://dx.doi.org/10.1016/j.jviromet.2019.02.010 |
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author | Takayama, Ikuyo Nakauchi, Mina Takahashi, Hitoshi Oba, Kunihiro Semba, Shohei Kaida, Atsushi Kubo, Hideyuki Saito, Shinji Nagata, Shiho Odagiri, Takato Kageyama, Tsutomu |
author_facet | Takayama, Ikuyo Nakauchi, Mina Takahashi, Hitoshi Oba, Kunihiro Semba, Shohei Kaida, Atsushi Kubo, Hideyuki Saito, Shinji Nagata, Shiho Odagiri, Takato Kageyama, Tsutomu |
author_sort | Takayama, Ikuyo |
collection | PubMed |
description | Influenza virus and respiratory syncytial virus cause acute upper and lower respiratory tract infections, especially in children and the elderly. Early treatment for these infections is thought to be important, so simple and sensitive detection methods are needed for use at clinical sites. Therefore, in this study, real-time reverse transcription loop-mediated isothermal amplification assays with quenching primer for influenza virus and respiratory syncytial virus were developed. Evaluation of a total of 113 clinical specimens compared to real-time RT-PCR assays showed that the novel assays could distinguish between the types and subtypes of influenza virus and respiratory syncytial virus and had 100% diagnostic specificity. The diagnostic sensitivity of each assay exceeded 85.0% and the assays showed sufficient clinical accuracy. Furthermore, positive results could be obtained in around 15 min using the novel assays in cases with high concentrations of virus. The developed assays should be useful for identifying influenza virus and respiratory syncytial virus cases not only in experimental laboratories but also in hospital and quarantine laboratories. |
format | Online Article Text |
id | pubmed-7113748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Authors. Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71137482020-04-02 Development of real-time fluorescent reverse transcription loop-mediated isothermal amplification assay with quenching primer for influenza virus and respiratory syncytial virus Takayama, Ikuyo Nakauchi, Mina Takahashi, Hitoshi Oba, Kunihiro Semba, Shohei Kaida, Atsushi Kubo, Hideyuki Saito, Shinji Nagata, Shiho Odagiri, Takato Kageyama, Tsutomu J Virol Methods Article Influenza virus and respiratory syncytial virus cause acute upper and lower respiratory tract infections, especially in children and the elderly. Early treatment for these infections is thought to be important, so simple and sensitive detection methods are needed for use at clinical sites. Therefore, in this study, real-time reverse transcription loop-mediated isothermal amplification assays with quenching primer for influenza virus and respiratory syncytial virus were developed. Evaluation of a total of 113 clinical specimens compared to real-time RT-PCR assays showed that the novel assays could distinguish between the types and subtypes of influenza virus and respiratory syncytial virus and had 100% diagnostic specificity. The diagnostic sensitivity of each assay exceeded 85.0% and the assays showed sufficient clinical accuracy. Furthermore, positive results could be obtained in around 15 min using the novel assays in cases with high concentrations of virus. The developed assays should be useful for identifying influenza virus and respiratory syncytial virus cases not only in experimental laboratories but also in hospital and quarantine laboratories. The Authors. Published by Elsevier B.V. 2019-05 2019-03-01 /pmc/articles/PMC7113748/ /pubmed/30831121 http://dx.doi.org/10.1016/j.jviromet.2019.02.010 Text en © 2019 The Authors 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 Takayama, Ikuyo Nakauchi, Mina Takahashi, Hitoshi Oba, Kunihiro Semba, Shohei Kaida, Atsushi Kubo, Hideyuki Saito, Shinji Nagata, Shiho Odagiri, Takato Kageyama, Tsutomu Development of real-time fluorescent reverse transcription loop-mediated isothermal amplification assay with quenching primer for influenza virus and respiratory syncytial virus |
title | Development of real-time fluorescent reverse transcription loop-mediated isothermal amplification assay with quenching primer for influenza virus and respiratory syncytial virus |
title_full | Development of real-time fluorescent reverse transcription loop-mediated isothermal amplification assay with quenching primer for influenza virus and respiratory syncytial virus |
title_fullStr | Development of real-time fluorescent reverse transcription loop-mediated isothermal amplification assay with quenching primer for influenza virus and respiratory syncytial virus |
title_full_unstemmed | Development of real-time fluorescent reverse transcription loop-mediated isothermal amplification assay with quenching primer for influenza virus and respiratory syncytial virus |
title_short | Development of real-time fluorescent reverse transcription loop-mediated isothermal amplification assay with quenching primer for influenza virus and respiratory syncytial virus |
title_sort | development of real-time fluorescent reverse transcription loop-mediated isothermal amplification assay with quenching primer for influenza virus and respiratory syncytial virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113748/ https://www.ncbi.nlm.nih.gov/pubmed/30831121 http://dx.doi.org/10.1016/j.jviromet.2019.02.010 |
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