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Detection of Abrin Holotoxin Using Novel Monoclonal Antibodies

Abrin, a member of the ribosome-inactivating protein family, is produced by the Abrus precatorius plant. Having the potential to pose a severe threat to both human and animal health, abrin is classified as a Select Agent by the U.S. Department of Health and Human Services. However, an immunoassay th...

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Autores principales: He, Xiaohua, Patfield, Stephanie, Cheng, Luisa W., Stanker, Larry H., Rasooly, Reuven, McKeon, Thomas A., Zhang, Yuzhu, Brandon, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744106/
https://www.ncbi.nlm.nih.gov/pubmed/29182545
http://dx.doi.org/10.3390/toxins9120386
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author He, Xiaohua
Patfield, Stephanie
Cheng, Luisa W.
Stanker, Larry H.
Rasooly, Reuven
McKeon, Thomas A.
Zhang, Yuzhu
Brandon, David L.
author_facet He, Xiaohua
Patfield, Stephanie
Cheng, Luisa W.
Stanker, Larry H.
Rasooly, Reuven
McKeon, Thomas A.
Zhang, Yuzhu
Brandon, David L.
author_sort He, Xiaohua
collection PubMed
description Abrin, a member of the ribosome-inactivating protein family, is produced by the Abrus precatorius plant. Having the potential to pose a severe threat to both human and animal health, abrin is classified as a Select Agent by the U.S. Department of Health and Human Services. However, an immunoassay that is specific for intact abrin holotoxin has not yet been reported. In this study, seven new monoclonal antibodies (mAbs), designated as Abrin-1 through Abrin-7 have been developed. Isotyping analyses indicate these mAbs have IgG1, IgG2a, or IgG2b heavy-chains and kappa light-chains. Western blot analyses identified two abrin A-chain specific mAbs, Abrin-1 and Abrin-2, and four B-chain specific mAbs (Abrin-3, -5, -6, and -7). A sandwich enzyme-linked immunosorbent assay (ELISA), capable of detecting a mixture of abrin isoforms and agglutinins was developed using B-chain specific Abrin-3 for capture and A-chain specific Abrin-2 as detector. The ELISA is highly sensitive and detects 1 ng/mL of the abrin holotoxin in phosphate-buffered saline, nonfat milk, and whole milk, significantly below concentrations that would pose a health concern for consumers. This ELISA also detects native abrin in plant extracts with a very low background signal. The new abrin mAbs and ELISA should be useful for detecting this potent toxin in the milk supply chain and other complex matrices.
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spelling pubmed-57441062017-12-31 Detection of Abrin Holotoxin Using Novel Monoclonal Antibodies He, Xiaohua Patfield, Stephanie Cheng, Luisa W. Stanker, Larry H. Rasooly, Reuven McKeon, Thomas A. Zhang, Yuzhu Brandon, David L. Toxins (Basel) Article Abrin, a member of the ribosome-inactivating protein family, is produced by the Abrus precatorius plant. Having the potential to pose a severe threat to both human and animal health, abrin is classified as a Select Agent by the U.S. Department of Health and Human Services. However, an immunoassay that is specific for intact abrin holotoxin has not yet been reported. In this study, seven new monoclonal antibodies (mAbs), designated as Abrin-1 through Abrin-7 have been developed. Isotyping analyses indicate these mAbs have IgG1, IgG2a, or IgG2b heavy-chains and kappa light-chains. Western blot analyses identified two abrin A-chain specific mAbs, Abrin-1 and Abrin-2, and four B-chain specific mAbs (Abrin-3, -5, -6, and -7). A sandwich enzyme-linked immunosorbent assay (ELISA), capable of detecting a mixture of abrin isoforms and agglutinins was developed using B-chain specific Abrin-3 for capture and A-chain specific Abrin-2 as detector. The ELISA is highly sensitive and detects 1 ng/mL of the abrin holotoxin in phosphate-buffered saline, nonfat milk, and whole milk, significantly below concentrations that would pose a health concern for consumers. This ELISA also detects native abrin in plant extracts with a very low background signal. The new abrin mAbs and ELISA should be useful for detecting this potent toxin in the milk supply chain and other complex matrices. MDPI 2017-11-28 /pmc/articles/PMC5744106/ /pubmed/29182545 http://dx.doi.org/10.3390/toxins9120386 Text en © 2017 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
He, Xiaohua
Patfield, Stephanie
Cheng, Luisa W.
Stanker, Larry H.
Rasooly, Reuven
McKeon, Thomas A.
Zhang, Yuzhu
Brandon, David L.
Detection of Abrin Holotoxin Using Novel Monoclonal Antibodies
title Detection of Abrin Holotoxin Using Novel Monoclonal Antibodies
title_full Detection of Abrin Holotoxin Using Novel Monoclonal Antibodies
title_fullStr Detection of Abrin Holotoxin Using Novel Monoclonal Antibodies
title_full_unstemmed Detection of Abrin Holotoxin Using Novel Monoclonal Antibodies
title_short Detection of Abrin Holotoxin Using Novel Monoclonal Antibodies
title_sort detection of abrin holotoxin using novel monoclonal antibodies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744106/
https://www.ncbi.nlm.nih.gov/pubmed/29182545
http://dx.doi.org/10.3390/toxins9120386
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