Monoclonal Antibody-Based Sandwich ELISA for the Detection of Staphylococcal Enterotoxin A

A sensitive and specific monoclonal antibody-based sandwich enzyme-linked immunosorbent assay (ELISA) was established and validated for the detection of staphylococcal enterotoxin A (SEA). After routine fusion and selection, 10 monoclonal antibodies showed high affinity for SEA. An optimal pair for...

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Main Authors: Chuanlai Xu, Libing Wang, Liqiang Liu, Liguang Xu, Wei Ma, Wenbing Wang, Hua Kuang
Format: Article
Language:English
Published: MDPI AG 2013-04-01
Series:International Journal of Environmental Research and Public Health
Subjects:
Online Access:http://www.mdpi.com/1660-4601/10/4/1598
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spelling doaj-cc32e9b04c554fb3a36e87dba8405dba2020-11-25T00:18:22ZengMDPI AGInternational Journal of Environmental Research and Public Health1660-46012013-04-011041598160810.3390/ijerph10041598Monoclonal Antibody-Based Sandwich ELISA for the Detection of Staphylococcal Enterotoxin AChuanlai XuLibing WangLiqiang LiuLiguang XuWei MaWenbing WangHua KuangA sensitive and specific monoclonal antibody-based sandwich enzyme-linked immunosorbent assay (ELISA) was established and validated for the detection of staphylococcal enterotoxin A (SEA). After routine fusion and selection, 10 monoclonal antibodies showed high affinity for SEA. An optimal pair for sandwich ELISA was selected by pairwise interaction analysis. After optimization, the limit of detection (LOD) and linear dynamic range of the method were established, and were found to be 0.0282 ng/mL and 0.06–2 ng/mL, respectively. The recovery in pure milk ranged from 82.67% to 111.95% and the intra- and inter-assay coefficients of variation ranged from 3.16% to 6.05% and from 5.16% to 10.79%, respectively. Cross-reactivity with staphylococcal enterotoxin B (SEB), staphylococcal enterotoxin C (SEC), staphylococcal enterotoxin D (SED), and staphylococcal enterotoxin E (SEE) in this method were insignificant. These results indicate that the sandwich ELISA method developed in our study is effective for routine identification of SEA in food samples.http://www.mdpi.com/1660-4601/10/4/1598staphylococcal enterotoxin A (SEA)monoclonal antibodysandwich ELISAdetection
collection DOAJ
language English
format Article
sources DOAJ
author Chuanlai Xu
Libing Wang
Liqiang Liu
Liguang Xu
Wei Ma
Wenbing Wang
Hua Kuang
spellingShingle Chuanlai Xu
Libing Wang
Liqiang Liu
Liguang Xu
Wei Ma
Wenbing Wang
Hua Kuang
Monoclonal Antibody-Based Sandwich ELISA for the Detection of Staphylococcal Enterotoxin A
International Journal of Environmental Research and Public Health
staphylococcal enterotoxin A (SEA)
monoclonal antibody
sandwich ELISA
detection
author_facet Chuanlai Xu
Libing Wang
Liqiang Liu
Liguang Xu
Wei Ma
Wenbing Wang
Hua Kuang
author_sort Chuanlai Xu
title Monoclonal Antibody-Based Sandwich ELISA for the Detection of Staphylococcal Enterotoxin A
title_short Monoclonal Antibody-Based Sandwich ELISA for the Detection of Staphylococcal Enterotoxin A
title_full Monoclonal Antibody-Based Sandwich ELISA for the Detection of Staphylococcal Enterotoxin A
title_fullStr Monoclonal Antibody-Based Sandwich ELISA for the Detection of Staphylococcal Enterotoxin A
title_full_unstemmed Monoclonal Antibody-Based Sandwich ELISA for the Detection of Staphylococcal Enterotoxin A
title_sort monoclonal antibody-based sandwich elisa for the detection of staphylococcal enterotoxin a
publisher MDPI AG
series International Journal of Environmental Research and Public Health
issn 1660-4601
publishDate 2013-04-01
description A sensitive and specific monoclonal antibody-based sandwich enzyme-linked immunosorbent assay (ELISA) was established and validated for the detection of staphylococcal enterotoxin A (SEA). After routine fusion and selection, 10 monoclonal antibodies showed high affinity for SEA. An optimal pair for sandwich ELISA was selected by pairwise interaction analysis. After optimization, the limit of detection (LOD) and linear dynamic range of the method were established, and were found to be 0.0282 ng/mL and 0.06–2 ng/mL, respectively. The recovery in pure milk ranged from 82.67% to 111.95% and the intra- and inter-assay coefficients of variation ranged from 3.16% to 6.05% and from 5.16% to 10.79%, respectively. Cross-reactivity with staphylococcal enterotoxin B (SEB), staphylococcal enterotoxin C (SEC), staphylococcal enterotoxin D (SED), and staphylococcal enterotoxin E (SEE) in this method were insignificant. These results indicate that the sandwich ELISA method developed in our study is effective for routine identification of SEA in food samples.
topic staphylococcal enterotoxin A (SEA)
monoclonal antibody
sandwich ELISA
detection
url http://www.mdpi.com/1660-4601/10/4/1598
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