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Development of a Direct Competitive ELISA Kit for Detecting Deoxynivalenol Contamination in Wheat

This study was conducted to develop a self-assembled direct competitive enzyme-linked immunosorbent assay (dcELISA) kit for the detection of deoxynivalenol (DON) in food and feed grains. Based on the preparation of anti-DON monoclonal antibodies, we established a standard curve with dcELISA and opti...

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Autores principales: Han, Li, Li, Yue-Tao, Jiang, Jin-Qing, Li, Ren-Feng, Fan, Guo-Ying, Lv, Jun-Mei, Zhou, Ye, Zhang, Wen-Ju, Wang, Zi-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983206/
https://www.ncbi.nlm.nih.gov/pubmed/31877851
http://dx.doi.org/10.3390/molecules25010050
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author Han, Li
Li, Yue-Tao
Jiang, Jin-Qing
Li, Ren-Feng
Fan, Guo-Ying
Lv, Jun-Mei
Zhou, Ye
Zhang, Wen-Ju
Wang, Zi-Liang
author_facet Han, Li
Li, Yue-Tao
Jiang, Jin-Qing
Li, Ren-Feng
Fan, Guo-Ying
Lv, Jun-Mei
Zhou, Ye
Zhang, Wen-Ju
Wang, Zi-Liang
author_sort Han, Li
collection PubMed
description This study was conducted to develop a self-assembled direct competitive enzyme-linked immunosorbent assay (dcELISA) kit for the detection of deoxynivalenol (DON) in food and feed grains. Based on the preparation of anti-DON monoclonal antibodies, we established a standard curve with dcELISA and optimized the detection conditions. The performance of the kit was evaluated by comparison with high-performance liquid chromatography (HPLC). The minimum detection limit of DON with the kit was 0.62 ng/mL, the linear range was from 1.0 to 113.24 ng/mL and the half-maximal inhibition concentration (IC(50)) was 6.61 ng/mL in the working buffer; there was a limit of detection (LOD) of 62 ng/g, and the detection range was from 100 to 11324 ng/g in authentic agricultural samples. We examined four samples of wheat bran, wheat flour, corn flour and corn for DON recovery. The average recovery was in the range of 77.1% to 107.0%, and the relative standard deviation (RSD) ranged from 4.2% to 11.9%. In addition, the kit has the advantages of high specificity, good stability, a long effective life and negligible sample matrix interference. Finally, wheat samples from farms in the six provinces of Henan, Anhui, Hebei, Shandong, Jiangsu and Gansu in China were analyzed by the kit. A total of 30 samples were randomly checked (five samples in each province), and the results were in good agreement with the standardized HPLC method. These tests showed that the dcELISA kit had good performance and met relevant technical requirements, and it had the characteristics of accuracy, reliability, convenience and high-throughput screening for DON detection. Therefore, the developed kit is suitable for rapid screening of DON in marketed products.
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spelling pubmed-69832062020-02-06 Development of a Direct Competitive ELISA Kit for Detecting Deoxynivalenol Contamination in Wheat Han, Li Li, Yue-Tao Jiang, Jin-Qing Li, Ren-Feng Fan, Guo-Ying Lv, Jun-Mei Zhou, Ye Zhang, Wen-Ju Wang, Zi-Liang Molecules Article This study was conducted to develop a self-assembled direct competitive enzyme-linked immunosorbent assay (dcELISA) kit for the detection of deoxynivalenol (DON) in food and feed grains. Based on the preparation of anti-DON monoclonal antibodies, we established a standard curve with dcELISA and optimized the detection conditions. The performance of the kit was evaluated by comparison with high-performance liquid chromatography (HPLC). The minimum detection limit of DON with the kit was 0.62 ng/mL, the linear range was from 1.0 to 113.24 ng/mL and the half-maximal inhibition concentration (IC(50)) was 6.61 ng/mL in the working buffer; there was a limit of detection (LOD) of 62 ng/g, and the detection range was from 100 to 11324 ng/g in authentic agricultural samples. We examined four samples of wheat bran, wheat flour, corn flour and corn for DON recovery. The average recovery was in the range of 77.1% to 107.0%, and the relative standard deviation (RSD) ranged from 4.2% to 11.9%. In addition, the kit has the advantages of high specificity, good stability, a long effective life and negligible sample matrix interference. Finally, wheat samples from farms in the six provinces of Henan, Anhui, Hebei, Shandong, Jiangsu and Gansu in China were analyzed by the kit. A total of 30 samples were randomly checked (five samples in each province), and the results were in good agreement with the standardized HPLC method. These tests showed that the dcELISA kit had good performance and met relevant technical requirements, and it had the characteristics of accuracy, reliability, convenience and high-throughput screening for DON detection. Therefore, the developed kit is suitable for rapid screening of DON in marketed products. MDPI 2019-12-22 /pmc/articles/PMC6983206/ /pubmed/31877851 http://dx.doi.org/10.3390/molecules25010050 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Han, Li
Li, Yue-Tao
Jiang, Jin-Qing
Li, Ren-Feng
Fan, Guo-Ying
Lv, Jun-Mei
Zhou, Ye
Zhang, Wen-Ju
Wang, Zi-Liang
Development of a Direct Competitive ELISA Kit for Detecting Deoxynivalenol Contamination in Wheat
title Development of a Direct Competitive ELISA Kit for Detecting Deoxynivalenol Contamination in Wheat
title_full Development of a Direct Competitive ELISA Kit for Detecting Deoxynivalenol Contamination in Wheat
title_fullStr Development of a Direct Competitive ELISA Kit for Detecting Deoxynivalenol Contamination in Wheat
title_full_unstemmed Development of a Direct Competitive ELISA Kit for Detecting Deoxynivalenol Contamination in Wheat
title_short Development of a Direct Competitive ELISA Kit for Detecting Deoxynivalenol Contamination in Wheat
title_sort development of a direct competitive elisa kit for detecting deoxynivalenol contamination in wheat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983206/
https://www.ncbi.nlm.nih.gov/pubmed/31877851
http://dx.doi.org/10.3390/molecules25010050
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