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A novel protein chip for simultaneous detection of antibodies against four epidemic swine viruses in China

BACKGROUND: At present, pig industry in China is faced with the complex situation of mixed infection caused by multiple pathogens. It is urgent to develop some new high-throughput molecular diagnosis assays to simultaneously detect pathogens or antibodies. Biochip array technology has made it possib...

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Autores principales: Wu, Yue, Wu, Xudan, Chen, Jing, Hu, Jingfei, Huang, Xiaobo, Zhou, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249397/
https://www.ncbi.nlm.nih.gov/pubmed/32456688
http://dx.doi.org/10.1186/s12917-020-02375-7
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author Wu, Yue
Wu, Xudan
Chen, Jing
Hu, Jingfei
Huang, Xiaobo
Zhou, Bin
author_facet Wu, Yue
Wu, Xudan
Chen, Jing
Hu, Jingfei
Huang, Xiaobo
Zhou, Bin
author_sort Wu, Yue
collection PubMed
description BACKGROUND: At present, pig industry in China is faced with the complex situation of mixed infection caused by multiple pathogens. It is urgent to develop some new high-throughput molecular diagnosis assays to simultaneously detect pathogens or antibodies. Biochip array technology has made it possible to screen thousands of samples simultaneously; it has been twice named as one of the top 10 scientific and technological breakthroughs. Studies have reported encouraging results using protein biochips for detecting antibodies against avian infectious bronchitis virus and ruminant bluetongue virus, but the research of this technology for the diagnosis of swine diseases is still sparse. RESULTS: In this study, a novel protein chip was developed that can simultaneously detect the antibodies of four important swine viruses as follow, classical swine fever virus (CSFV), porcine parvovirus (PPV), Japanese encephalitis virus (JEV), and porcine reproductive and respiratory syndrome virus (PRRSV). Four prokaryotic expression plasmids pET-32a-E2 of CSFV, −VP2 of PPV, −EDIII of JEV, and -N of PRRSV were induced by IPTG (Isopropyl β-D-1-Thiogalactopyranoside) and overexpressed in E.coli, respectively. The purified proteins were identified by Western blotting and then printed on epoxy-coated glass slides. The optimized parameters of this diagnostic chip showed that the spotting concentrations of E2、VP2、EDIII、N proteins were 0.2, 0.4, 0.4, and 0.4 mg/mL. The optimal primary and secondary antibody dilutions were 1:50 and 1: 600. Compared with the commercial ELISA (Enzyme-linked immunosorbent assay) kits, the positive and negative coincidence rates of this chip were 95.8% ~ 100 and 86.2% ~ 100%, as well as, no cross-reaction. CONCLUSION: This protein chip provided a fast, specific, and sensitive method for simultaneous detection of antibodies in clinical serum samples. Compared with traditional methods, this protein chip can monitor very small amount of serum.
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spelling pubmed-72493972020-06-04 A novel protein chip for simultaneous detection of antibodies against four epidemic swine viruses in China Wu, Yue Wu, Xudan Chen, Jing Hu, Jingfei Huang, Xiaobo Zhou, Bin BMC Vet Res Research Article BACKGROUND: At present, pig industry in China is faced with the complex situation of mixed infection caused by multiple pathogens. It is urgent to develop some new high-throughput molecular diagnosis assays to simultaneously detect pathogens or antibodies. Biochip array technology has made it possible to screen thousands of samples simultaneously; it has been twice named as one of the top 10 scientific and technological breakthroughs. Studies have reported encouraging results using protein biochips for detecting antibodies against avian infectious bronchitis virus and ruminant bluetongue virus, but the research of this technology for the diagnosis of swine diseases is still sparse. RESULTS: In this study, a novel protein chip was developed that can simultaneously detect the antibodies of four important swine viruses as follow, classical swine fever virus (CSFV), porcine parvovirus (PPV), Japanese encephalitis virus (JEV), and porcine reproductive and respiratory syndrome virus (PRRSV). Four prokaryotic expression plasmids pET-32a-E2 of CSFV, −VP2 of PPV, −EDIII of JEV, and -N of PRRSV were induced by IPTG (Isopropyl β-D-1-Thiogalactopyranoside) and overexpressed in E.coli, respectively. The purified proteins were identified by Western blotting and then printed on epoxy-coated glass slides. The optimized parameters of this diagnostic chip showed that the spotting concentrations of E2、VP2、EDIII、N proteins were 0.2, 0.4, 0.4, and 0.4 mg/mL. The optimal primary and secondary antibody dilutions were 1:50 and 1: 600. Compared with the commercial ELISA (Enzyme-linked immunosorbent assay) kits, the positive and negative coincidence rates of this chip were 95.8% ~ 100 and 86.2% ~ 100%, as well as, no cross-reaction. CONCLUSION: This protein chip provided a fast, specific, and sensitive method for simultaneous detection of antibodies in clinical serum samples. Compared with traditional methods, this protein chip can monitor very small amount of serum. BioMed Central 2020-05-26 /pmc/articles/PMC7249397/ /pubmed/32456688 http://dx.doi.org/10.1186/s12917-020-02375-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Wu, Yue
Wu, Xudan
Chen, Jing
Hu, Jingfei
Huang, Xiaobo
Zhou, Bin
A novel protein chip for simultaneous detection of antibodies against four epidemic swine viruses in China
title A novel protein chip for simultaneous detection of antibodies against four epidemic swine viruses in China
title_full A novel protein chip for simultaneous detection of antibodies against four epidemic swine viruses in China
title_fullStr A novel protein chip for simultaneous detection of antibodies against four epidemic swine viruses in China
title_full_unstemmed A novel protein chip for simultaneous detection of antibodies against four epidemic swine viruses in China
title_short A novel protein chip for simultaneous detection of antibodies against four epidemic swine viruses in China
title_sort novel protein chip for simultaneous detection of antibodies against four epidemic swine viruses in china
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249397/
https://www.ncbi.nlm.nih.gov/pubmed/32456688
http://dx.doi.org/10.1186/s12917-020-02375-7
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