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Multiplex Detection of Plant Pathogens Using a Microsphere Immunoassay Technology
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Metadata
Document Title
Multiplex Detection of Plant Pathogens Using a Microsphere Immunoassay Technology
Author
Charlermroj R., Himananto O., Seepiban C., Kumpoosiri M., Warin N., Oplatowska M., Gajanandana O., Grant I.R., Karoonuthaisiri N., Elliott C.T.
Name from Authors Collection
Scopus Author ID
25026853500
Scopus Author ID
36626344500
Scopus Author ID
23111597300
Scopus Author ID
23110409300
Affiliations
Institute for Global Food Security, School of Biological Sciences, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom; National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Klong Luang, Pathum Thani, Thailand
Type
Article
Source Title
PLoS ONE
ISSN
19326203
Year
2013
Volume
8
Issue
4
Open Access
Gold, Green
DOI
10.1371/journal.pone.0062344
Abstract
Plant pathogens are a serious problem for seed export, plant disease control and plant quarantine. Rapid and accurate screening tests are urgently required to protect and prevent plant diseases spreading worldwide. A novel multiplex detection method was developed based on microsphere immunoassays to simultaneously detect four important plant pathogens: a fruit blotch bacterium Acidovorax avenae subsp. citrulli (Aac), chilli vein-banding mottle virus (CVbMV, potyvirus), watermelon silver mottle virus (WSMoV, tospovirus serogroup IV) and melon yellow spot virus (MYSV, tospovirus). An antibody for each plant pathogen was linked on a fluorescence-coded magnetic microsphere set which was used to capture corresponding pathogen. The presence of pathogens was detected by R-phycoerythrin (RPE)-labeled antibodies specific to the pathogens. The assay conditions were optimized by identifying appropriate antibody pairs, blocking buffer, concentration of RPE-labeled antibodies and assay time. Once conditions were optimized, the assay was able to detect all four plant pathogens precisely and accurately with substantially higher sensitivity than enzyme-linked immunosorbent assay (ELISA) when spiked in buffer and in healthy watermelon leaf extract. The assay time of the microsphere immunoassay (1 hour) was much shorter than that of ELISA (4 hours). This system was also shown to be capable of detecting the pathogens in naturally infected plant samples and is a major advancement in plant pathogen detection. © 2013 Charlermroj et al.
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License
CC BY
Rights
Author
Publication Source
Scopus