A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in Plants
The threat of West Nile virus (WNV) epidemics necessitates the development of a technology platform that can produce reagents to support detection and diagnosis rapidly and inexpensively. A plant expression system is attractive for protein production due to its low-cost and high-scalability nature a...
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doaj-279d2c38def04a8eacbe70805e9c141a2020-11-25T02:08:39ZengHindawi LimitedJournal of Biomedicine and Biotechnology1110-72431110-72512012-01-01201210.1155/2012/106783106783A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in PlantsJunyun He0Huafang Lai1Christopher Brock2Qiang Chen3The Biodesign Institute, Arizona State University, Tempe, AZ 85287, USAThe Biodesign Institute, Arizona State University, Tempe, AZ 85287, USAThe Biodesign Institute, Arizona State University, Tempe, AZ 85287, USAThe Biodesign Institute, Arizona State University, Tempe, AZ 85287, USAThe threat of West Nile virus (WNV) epidemics necessitates the development of a technology platform that can produce reagents to support detection and diagnosis rapidly and inexpensively. A plant expression system is attractive for protein production due to its low-cost and high-scalability nature and its ability to make appropriate posttranslational modifications. Here, we investigated the feasibility of using plants to produce two WNV detection and diagnostic reagents to address the current cost and scalability issues. We demonstrated that WNV DIII antigen and E16 monoclonal antibody are rapidly produced at high levels in two plant species and are easily purified. Furthermore, they are effective in identifying WNV and in detecting human IgM response to WNV infection. E16 mAb does not cross-react with other flaviviruses, therefore, is valuable for improving diagnostic accuracy. This study provides a proof of principle for using plants as a robust and economical system to produce diagnostic reagents for arboviruses.http://dx.doi.org/10.1155/2012/106783 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Junyun He Huafang Lai Christopher Brock Qiang Chen |
spellingShingle |
Junyun He Huafang Lai Christopher Brock Qiang Chen A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in Plants Journal of Biomedicine and Biotechnology |
author_facet |
Junyun He Huafang Lai Christopher Brock Qiang Chen |
author_sort |
Junyun He |
title |
A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in Plants |
title_short |
A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in Plants |
title_full |
A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in Plants |
title_fullStr |
A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in Plants |
title_full_unstemmed |
A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in Plants |
title_sort |
novel system for rapid and cost-effective production of detection and diagnostic reagents of west nile virus in plants |
publisher |
Hindawi Limited |
series |
Journal of Biomedicine and Biotechnology |
issn |
1110-7243 1110-7251 |
publishDate |
2012-01-01 |
description |
The threat of West Nile virus (WNV) epidemics necessitates the development of a technology platform that can produce reagents to support detection and diagnosis rapidly and inexpensively. A plant expression system is attractive for protein production due to its low-cost and high-scalability nature and its ability to make appropriate posttranslational modifications. Here, we investigated the feasibility of using plants to produce two WNV detection and diagnostic reagents to address the current cost and scalability issues. We demonstrated that WNV DIII antigen and E16 monoclonal antibody are rapidly produced at high levels in two plant species and are easily purified. Furthermore, they are effective in identifying WNV and in detecting human IgM response to WNV infection. E16 mAb does not cross-react with other flaviviruses, therefore, is valuable for improving diagnostic accuracy. This study provides a proof of principle for using plants as a robust and economical system to produce diagnostic reagents for arboviruses. |
url |
http://dx.doi.org/10.1155/2012/106783 |
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