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Development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection of novel avian influenza A (H7N9) virus

BACKGROUND: The emerged human infection with avian influenza A (H7N9) virus in China since 2013 has aroused global concerns. There is great demand for simple and rapid diagnostic method for early detection of H7N9 to provide timely treatment and disease control. The aim of the current study was to d...

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Autores principales: Liu, Juan, Nian, Qing-Gong, Li, Jing, Hu, Yi, Li, Xiao-Feng, Zhang, Yu, Deng, Yong-Qiang, Zhu, Shun-Ya, Zhu, Qing-Yu, Qin, E-De, Jiang, Tao, Qin, Cheng-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234856/
https://www.ncbi.nlm.nih.gov/pubmed/25394781
http://dx.doi.org/10.1186/s12866-014-0271-x
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author Liu, Juan
Nian, Qing-Gong
Li, Jing
Hu, Yi
Li, Xiao-Feng
Zhang, Yu
Deng, Yong-Qiang
Zhu, Shun-Ya
Zhu, Qing-Yu
Qin, E-De
Jiang, Tao
Qin, Cheng-Feng
author_facet Liu, Juan
Nian, Qing-Gong
Li, Jing
Hu, Yi
Li, Xiao-Feng
Zhang, Yu
Deng, Yong-Qiang
Zhu, Shun-Ya
Zhu, Qing-Yu
Qin, E-De
Jiang, Tao
Qin, Cheng-Feng
author_sort Liu, Juan
collection PubMed
description BACKGROUND: The emerged human infection with avian influenza A (H7N9) virus in China since 2013 has aroused global concerns. There is great demand for simple and rapid diagnostic method for early detection of H7N9 to provide timely treatment and disease control. The aim of the current study was to develop a rapid, accurate and feasible reverse-transcription loop-mediated isothermal amplification (RT-LAMP) assay for detection of H7N9 virus. RESULTS: The detection limits of the H7- and N9-specific RT-LAMP assay were both approximately 0.2 PFU per reaction. No cross-reactivity was observed with other subtype of influenza viruses or common respiratory viral pathogens. The assay worked well with clinical specimens from patients and chickens, and exhibited high specificity and sensitivity. CONCLUSIONS: The H7/N9 specific RT-LAMP assay was sensitive and accurate, which could be a useful alternative in clinical diagnostics of influenza A (H7N9) virus, especially in the hospitals and laboratories without sophisticated diagnostic systems.
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spelling pubmed-42348562014-11-19 Development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection of novel avian influenza A (H7N9) virus Liu, Juan Nian, Qing-Gong Li, Jing Hu, Yi Li, Xiao-Feng Zhang, Yu Deng, Yong-Qiang Zhu, Shun-Ya Zhu, Qing-Yu Qin, E-De Jiang, Tao Qin, Cheng-Feng BMC Microbiol Methodology Article BACKGROUND: The emerged human infection with avian influenza A (H7N9) virus in China since 2013 has aroused global concerns. There is great demand for simple and rapid diagnostic method for early detection of H7N9 to provide timely treatment and disease control. The aim of the current study was to develop a rapid, accurate and feasible reverse-transcription loop-mediated isothermal amplification (RT-LAMP) assay for detection of H7N9 virus. RESULTS: The detection limits of the H7- and N9-specific RT-LAMP assay were both approximately 0.2 PFU per reaction. No cross-reactivity was observed with other subtype of influenza viruses or common respiratory viral pathogens. The assay worked well with clinical specimens from patients and chickens, and exhibited high specificity and sensitivity. CONCLUSIONS: The H7/N9 specific RT-LAMP assay was sensitive and accurate, which could be a useful alternative in clinical diagnostics of influenza A (H7N9) virus, especially in the hospitals and laboratories without sophisticated diagnostic systems. BioMed Central 2014-11-14 /pmc/articles/PMC4234856/ /pubmed/25394781 http://dx.doi.org/10.1186/s12866-014-0271-x Text en © Liu et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Liu, Juan
Nian, Qing-Gong
Li, Jing
Hu, Yi
Li, Xiao-Feng
Zhang, Yu
Deng, Yong-Qiang
Zhu, Shun-Ya
Zhu, Qing-Yu
Qin, E-De
Jiang, Tao
Qin, Cheng-Feng
Development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection of novel avian influenza A (H7N9) virus
title Development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection of novel avian influenza A (H7N9) virus
title_full Development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection of novel avian influenza A (H7N9) virus
title_fullStr Development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection of novel avian influenza A (H7N9) virus
title_full_unstemmed Development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection of novel avian influenza A (H7N9) virus
title_short Development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection of novel avian influenza A (H7N9) virus
title_sort development of reverse-transcription loop-mediated isothermal amplification assay for rapid detection of novel avian influenza a (h7n9) virus
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234856/
https://www.ncbi.nlm.nih.gov/pubmed/25394781
http://dx.doi.org/10.1186/s12866-014-0271-x
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