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A Two-Tube Multiplex Reverse Transcription PCR Assay for Simultaneous Detection of Sixteen Human Respiratory Virus Types/Subtypes

There is a need for the development of a rapid and sensitive diagnosis of respiratory viral pathogens. With an intended application in provincial Centers for Diseases Control and Prevention, in this study, we present a two-tube multiplex RT-PCR assay (two-tube assay) using automatic electrophoresis...

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Detalles Bibliográficos
Autores principales: Li, Jin, Qi, Shunxiang, Zhang, Chen, Hu, Xiumei, Shen, Hongwei, Yang, Mengjie, Wang, Ji, Wang, Miao, Xu, Wenbo, Ma, Xuejun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3747601/
https://www.ncbi.nlm.nih.gov/pubmed/23984344
http://dx.doi.org/10.1155/2013/327620
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author Li, Jin
Qi, Shunxiang
Zhang, Chen
Hu, Xiumei
Shen, Hongwei
Yang, Mengjie
Wang, Ji
Wang, Miao
Xu, Wenbo
Ma, Xuejun
author_facet Li, Jin
Qi, Shunxiang
Zhang, Chen
Hu, Xiumei
Shen, Hongwei
Yang, Mengjie
Wang, Ji
Wang, Miao
Xu, Wenbo
Ma, Xuejun
author_sort Li, Jin
collection PubMed
description There is a need for the development of a rapid and sensitive diagnosis of respiratory viral pathogens. With an intended application in provincial Centers for Diseases Control and Prevention, in this study, we present a two-tube multiplex RT-PCR assay (two-tube assay) using automatic electrophoresis to simultaneously detect sixteen common respiratory viruses. The specificity and the sensitivity of the assay were tested. The assay could detect 20–200 copies per reaction when each viral type was assayed individually, 2000 copies with 9 premixed viral targets in the multiplexed assay in tube 1, and 200 copies with 8 premixed templates in tube 2. A total of 247 specimens were used to evaluate the two-tube assay, and the results were compared with those obtained from the Luminex xTAG RVP Fast assay. The discordant results were confirmed by sequencing or by the Seeplex RV15 ACE detection kit. There were no false positives, but six false negatives occurred with the two-tube assay. In conclusion, the two-tube assay is demonstrated to have great potential for routine surveillance of respiratory virus infection in China.
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spelling pubmed-37476012013-08-27 A Two-Tube Multiplex Reverse Transcription PCR Assay for Simultaneous Detection of Sixteen Human Respiratory Virus Types/Subtypes Li, Jin Qi, Shunxiang Zhang, Chen Hu, Xiumei Shen, Hongwei Yang, Mengjie Wang, Ji Wang, Miao Xu, Wenbo Ma, Xuejun Biomed Res Int Research Article There is a need for the development of a rapid and sensitive diagnosis of respiratory viral pathogens. With an intended application in provincial Centers for Diseases Control and Prevention, in this study, we present a two-tube multiplex RT-PCR assay (two-tube assay) using automatic electrophoresis to simultaneously detect sixteen common respiratory viruses. The specificity and the sensitivity of the assay were tested. The assay could detect 20–200 copies per reaction when each viral type was assayed individually, 2000 copies with 9 premixed viral targets in the multiplexed assay in tube 1, and 200 copies with 8 premixed templates in tube 2. A total of 247 specimens were used to evaluate the two-tube assay, and the results were compared with those obtained from the Luminex xTAG RVP Fast assay. The discordant results were confirmed by sequencing or by the Seeplex RV15 ACE detection kit. There were no false positives, but six false negatives occurred with the two-tube assay. In conclusion, the two-tube assay is demonstrated to have great potential for routine surveillance of respiratory virus infection in China. Hindawi Publishing Corporation 2013 2013-08-05 /pmc/articles/PMC3747601/ /pubmed/23984344 http://dx.doi.org/10.1155/2013/327620 Text en Copyright © 2013 Jin Li 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
Li, Jin
Qi, Shunxiang
Zhang, Chen
Hu, Xiumei
Shen, Hongwei
Yang, Mengjie
Wang, Ji
Wang, Miao
Xu, Wenbo
Ma, Xuejun
A Two-Tube Multiplex Reverse Transcription PCR Assay for Simultaneous Detection of Sixteen Human Respiratory Virus Types/Subtypes
title A Two-Tube Multiplex Reverse Transcription PCR Assay for Simultaneous Detection of Sixteen Human Respiratory Virus Types/Subtypes
title_full A Two-Tube Multiplex Reverse Transcription PCR Assay for Simultaneous Detection of Sixteen Human Respiratory Virus Types/Subtypes
title_fullStr A Two-Tube Multiplex Reverse Transcription PCR Assay for Simultaneous Detection of Sixteen Human Respiratory Virus Types/Subtypes
title_full_unstemmed A Two-Tube Multiplex Reverse Transcription PCR Assay for Simultaneous Detection of Sixteen Human Respiratory Virus Types/Subtypes
title_short A Two-Tube Multiplex Reverse Transcription PCR Assay for Simultaneous Detection of Sixteen Human Respiratory Virus Types/Subtypes
title_sort two-tube multiplex reverse transcription pcr assay for simultaneous detection of sixteen human respiratory virus types/subtypes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3747601/
https://www.ncbi.nlm.nih.gov/pubmed/23984344
http://dx.doi.org/10.1155/2013/327620
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