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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...

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Autores principales: Takayama, Ikuyo, Nakauchi, Mina, Takahashi, Hitoshi, Oba, Kunihiro, Semba, Shohei, Kaida, Atsushi, Kubo, Hideyuki, Saito, Shinji, Nagata, Shiho, Odagiri, Takato, Kageyama, Tsutomu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier B.V. 2019
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.
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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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