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Development of oligonucleotide microarray for accurate and simultaneous detection of avian respiratory viral diseases

BACKGROUND: Avian influenza virus (AIV), infectious bronchitis virus (IBV), and Newcastle disease virus (NDV) are important avian pathogens that can cause enormous economic loss on the poultry industry. Different respiratory etiological agents may induce similar clinical signs that make differential...

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Autores principales: Xiao, Qian, Yan, Liping, Yao, Lu, Lei, Jing, Bi, Zhenwei, Hu, Jianhua, Chen, Yuqing, Fang, An, Li, Hui, Li, Yuan, Yan, Yan, Zhou, Jiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642548/
https://www.ncbi.nlm.nih.gov/pubmed/31324180
http://dx.doi.org/10.1186/s12917-019-1985-7
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author Xiao, Qian
Yan, Liping
Yao, Lu
Lei, Jing
Bi, Zhenwei
Hu, Jianhua
Chen, Yuqing
Fang, An
Li, Hui
Li, Yuan
Yan, Yan
Zhou, Jiyong
author_facet Xiao, Qian
Yan, Liping
Yao, Lu
Lei, Jing
Bi, Zhenwei
Hu, Jianhua
Chen, Yuqing
Fang, An
Li, Hui
Li, Yuan
Yan, Yan
Zhou, Jiyong
author_sort Xiao, Qian
collection PubMed
description BACKGROUND: Avian influenza virus (AIV), infectious bronchitis virus (IBV), and Newcastle disease virus (NDV) are important avian pathogens that can cause enormous economic loss on the poultry industry. Different respiratory etiological agents may induce similar clinical signs that make differential diagnosis difficult. Importantly, AIV brings about severe threat to human public health. Therefore, a novel method that can distinguish these viruses quickly and simultaneously is urgently needed. RESULTS: In this study, an oligonucleotide microarray system was developed. AIV, including H5, H7, and H9 subtypes; NDV; and IBV were simultaneously detected and differentiated on a microarray. Three probes specific for AIV, NDV, and IBV, as well as three other probes for differentiating H5, H7, and H9 of AIV, were first designed and jet-printed to predetermined locations of initiator-integrated poly(dimethylsiloxane) for the synchronous detection of the six pathogens. The marked multiplex reverse transcription polymerase chain reaction (PCR) products were hybridized with the specific probes, and the results of hybridization were read directly with the naked eyes. No cross-reaction was observed with 10 other subtypes of AIV and infectious bursal disease virus, indicating that the oligonucleotide microarray assay was highly specific. The sensitivity of the method was at least 100 times higher than that of the conventional PCR, and the detection limit of NDV, AIV, H5, H7, and H9 can reach 0.1 EID(50) (50% egg infective dose), except that of IBV, which was 1 EID(50) per reaction. In the validation of 93 field samples, AIV, IBV, and NDV were detected in 53 (56.99%) samples by oligonucleotide microarray and virus isolation and in 50 (53.76%) samples by conventional PCR. CONCLUSIONS: We have successfully developed an approach to differentiate AIV, NDV, IBV, H5, H7, and H9 subtypes of AIV using oligonucleotide microarray. The microarray is an accurate, high-throughput, and relatively simple method for the rapid detection of avian respiratory viral diseases. It can be used for the epidemiological surveillance and diagnosis of AIV, IBV, and NDV. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-019-1985-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-66425482019-07-29 Development of oligonucleotide microarray for accurate and simultaneous detection of avian respiratory viral diseases Xiao, Qian Yan, Liping Yao, Lu Lei, Jing Bi, Zhenwei Hu, Jianhua Chen, Yuqing Fang, An Li, Hui Li, Yuan Yan, Yan Zhou, Jiyong BMC Vet Res Methodology Article BACKGROUND: Avian influenza virus (AIV), infectious bronchitis virus (IBV), and Newcastle disease virus (NDV) are important avian pathogens that can cause enormous economic loss on the poultry industry. Different respiratory etiological agents may induce similar clinical signs that make differential diagnosis difficult. Importantly, AIV brings about severe threat to human public health. Therefore, a novel method that can distinguish these viruses quickly and simultaneously is urgently needed. RESULTS: In this study, an oligonucleotide microarray system was developed. AIV, including H5, H7, and H9 subtypes; NDV; and IBV were simultaneously detected and differentiated on a microarray. Three probes specific for AIV, NDV, and IBV, as well as three other probes for differentiating H5, H7, and H9 of AIV, were first designed and jet-printed to predetermined locations of initiator-integrated poly(dimethylsiloxane) for the synchronous detection of the six pathogens. The marked multiplex reverse transcription polymerase chain reaction (PCR) products were hybridized with the specific probes, and the results of hybridization were read directly with the naked eyes. No cross-reaction was observed with 10 other subtypes of AIV and infectious bursal disease virus, indicating that the oligonucleotide microarray assay was highly specific. The sensitivity of the method was at least 100 times higher than that of the conventional PCR, and the detection limit of NDV, AIV, H5, H7, and H9 can reach 0.1 EID(50) (50% egg infective dose), except that of IBV, which was 1 EID(50) per reaction. In the validation of 93 field samples, AIV, IBV, and NDV were detected in 53 (56.99%) samples by oligonucleotide microarray and virus isolation and in 50 (53.76%) samples by conventional PCR. CONCLUSIONS: We have successfully developed an approach to differentiate AIV, NDV, IBV, H5, H7, and H9 subtypes of AIV using oligonucleotide microarray. The microarray is an accurate, high-throughput, and relatively simple method for the rapid detection of avian respiratory viral diseases. It can be used for the epidemiological surveillance and diagnosis of AIV, IBV, and NDV. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-019-1985-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-19 /pmc/articles/PMC6642548/ /pubmed/31324180 http://dx.doi.org/10.1186/s12917-019-1985-7 Text en © The Author(s). 2019 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. 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
Xiao, Qian
Yan, Liping
Yao, Lu
Lei, Jing
Bi, Zhenwei
Hu, Jianhua
Chen, Yuqing
Fang, An
Li, Hui
Li, Yuan
Yan, Yan
Zhou, Jiyong
Development of oligonucleotide microarray for accurate and simultaneous detection of avian respiratory viral diseases
title Development of oligonucleotide microarray for accurate and simultaneous detection of avian respiratory viral diseases
title_full Development of oligonucleotide microarray for accurate and simultaneous detection of avian respiratory viral diseases
title_fullStr Development of oligonucleotide microarray for accurate and simultaneous detection of avian respiratory viral diseases
title_full_unstemmed Development of oligonucleotide microarray for accurate and simultaneous detection of avian respiratory viral diseases
title_short Development of oligonucleotide microarray for accurate and simultaneous detection of avian respiratory viral diseases
title_sort development of oligonucleotide microarray for accurate and simultaneous detection of avian respiratory viral diseases
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642548/
https://www.ncbi.nlm.nih.gov/pubmed/31324180
http://dx.doi.org/10.1186/s12917-019-1985-7
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