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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Main Authors: Junyun He, Huafang Lai, Christopher Brock, Qiang Chen
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Journal of Biomedicine and Biotechnology
Online Access:http://dx.doi.org/10.1155/2012/106783
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spelling 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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