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Genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray

BACKGROUND: Influenza viruses are divided into three types, A, B, and C. Human influenza A and B viruses can cause seasonal epidemics, but influenza C causes only a mild respiratory illness. Influenza A virus can infect various host species. In 2013, human-infectious avian influenza A (H7N9) was fir...

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Autores principales: Zhang, Yingjie, Liu, Qiqi, Wang, Dou, Chen, Suhong, Wang, Xiaobo, Wang, Shengqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080273/
https://www.ncbi.nlm.nih.gov/pubmed/27822445
http://dx.doi.org/10.1186/s40064-016-3482-9
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author Zhang, Yingjie
Liu, Qiqi
Wang, Dou
Chen, Suhong
Wang, Xiaobo
Wang, Shengqi
author_facet Zhang, Yingjie
Liu, Qiqi
Wang, Dou
Chen, Suhong
Wang, Xiaobo
Wang, Shengqi
author_sort Zhang, Yingjie
collection PubMed
description BACKGROUND: Influenza viruses are divided into three types, A, B, and C. Human influenza A and B viruses can cause seasonal epidemics, but influenza C causes only a mild respiratory illness. Influenza A virus can infect various host species. In 2013, human-infectious avian influenza A (H7N9) was first reported in China. By the second week of 2014, there were 210 laboratory-confirmed human cases in the country, and the mortality rate eventually reached 22 %. Rapid and accurate diagnosis of influenza viruses is important for clinical management and epidemiology. METHODS: In this assay, a cost-effective chemiluminescence (CL) detection oligonucleotide microarray was developed to genotype and detect avian influenza A (H7N9), avian influenza A (H5N1), 2009 influenza A (H1N1), seasonal influenza A (H1N1), and seasonal influenza A (H3N2). Influenza A viruses and influenza B viruses were also generally detected using this microarray. RESULTS: The results of detection of 40 cultivated influenza virus strains showed that the microarray was able to distinguish the subtypes of these influenza viruses very well. The microarray possessed similar or 10 fold higher limit of detection than the real-time RT-PCR method. Sixty-six clinical swab samples were detected using this microarray and verified with real time RT-PCR to evaluate the efficiency of this microarray for clinical testing. CONCLUSIONS: A reliable CL detection oligonucleotide microarray had been developed to genotype and detected these influenza viruses.
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spelling pubmed-50802732016-11-07 Genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray Zhang, Yingjie Liu, Qiqi Wang, Dou Chen, Suhong Wang, Xiaobo Wang, Shengqi Springerplus Research BACKGROUND: Influenza viruses are divided into three types, A, B, and C. Human influenza A and B viruses can cause seasonal epidemics, but influenza C causes only a mild respiratory illness. Influenza A virus can infect various host species. In 2013, human-infectious avian influenza A (H7N9) was first reported in China. By the second week of 2014, there were 210 laboratory-confirmed human cases in the country, and the mortality rate eventually reached 22 %. Rapid and accurate diagnosis of influenza viruses is important for clinical management and epidemiology. METHODS: In this assay, a cost-effective chemiluminescence (CL) detection oligonucleotide microarray was developed to genotype and detect avian influenza A (H7N9), avian influenza A (H5N1), 2009 influenza A (H1N1), seasonal influenza A (H1N1), and seasonal influenza A (H3N2). Influenza A viruses and influenza B viruses were also generally detected using this microarray. RESULTS: The results of detection of 40 cultivated influenza virus strains showed that the microarray was able to distinguish the subtypes of these influenza viruses very well. The microarray possessed similar or 10 fold higher limit of detection than the real-time RT-PCR method. Sixty-six clinical swab samples were detected using this microarray and verified with real time RT-PCR to evaluate the efficiency of this microarray for clinical testing. CONCLUSIONS: A reliable CL detection oligonucleotide microarray had been developed to genotype and detected these influenza viruses. Springer International Publishing 2016-10-25 /pmc/articles/PMC5080273/ /pubmed/27822445 http://dx.doi.org/10.1186/s40064-016-3482-9 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Zhang, Yingjie
Liu, Qiqi
Wang, Dou
Chen, Suhong
Wang, Xiaobo
Wang, Shengqi
Genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray
title Genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray
title_full Genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray
title_fullStr Genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray
title_full_unstemmed Genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray
title_short Genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray
title_sort genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080273/
https://www.ncbi.nlm.nih.gov/pubmed/27822445
http://dx.doi.org/10.1186/s40064-016-3482-9
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