Cargando…
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...
Autores principales: | , , , , , , , , , , , |
---|---|
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 |
_version_ | 1782344922363330560 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4234856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT liujuan developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT nianqinggong developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT lijing developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT huyi developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT lixiaofeng developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT zhangyu developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT dengyongqiang developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT zhushunya developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT zhuqingyu developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT qinede developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT jiangtao developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus AT qinchengfeng developmentofreversetranscriptionloopmediatedisothermalamplificationassayforrapiddetectionofnovelavianinfluenzaah7n9virus |