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Toxins 2013, 5(11), 2212-2226; doi:10.3390/toxins5112212

A Monoclonal Antibody Based Capture ELISA for Botulinum Neurotoxin Serotype B: Toxin Detection in Food

1
Foodborne Toxin Detection and Prevention Unit, United States Department of Agriculture, Agricultural Research Service, 800 Buchanan Street, Albany, CA 94510, USA
2
DuPont Industrial Biosciences, Palo Alto, CA 94304, USA
3
United States Department of Homeland Security, Washington, DC 20528, USA
*
Author to whom correspondence should be addressed.
Received: 6 September 2013 / Revised: 30 October 2013 / Accepted: 7 November 2013 / Published: 18 November 2013
(This article belongs to the Special Issue Advances in Toxin Detection)
View Full-Text   |   Download PDF [496 KB, 19 November 2013; original version 18 November 2013]   |  

Abstract

Botulism is a serious foodborne neuroparalytic disease, caused by botulinum neurotoxin (BoNT), produced by the anaerobic bacterium Clostridium botulinum. Seven toxin serotypes (A–H) have been described. The majority of human cases of botulism are caused by serotypes A and B followed by E and F. We report here a group of serotype B specific monoclonal antibodies (mAbs) capable of binding toxin under physiological conditions. Thus, they serve as capture antibodies for a sandwich (capture) ELISA. The antibodies were generated using recombinant peptide fragments corresponding to the receptor-binding domain of the toxin heavy chain as immunogen. Their binding properties suggest that they bind a complex epitope with dissociation constants (KD’s) for individual antibodies ranging from 10 to 48 × 10−11 M. Assay performance for all possible combinations of capture-detector antibody pairs was evaluated and the antibody pair resulting in the lowest level of detection (L.O.D.), ~20 pg/mL was determined. Toxin was detected in spiked dairy samples with good recoveries at concentrations as low as 0.5 pg/mL and in ground beef samples at levels as low as 2 ng/g. Thus, the sandwich ELISA described here uses mAb for both the capture and detector antibodies (binding different epitopes on the toxin molecule) and readily detects toxin in those food samples tested.
Keywords: monoclonal antibodies; botulinum neurotoxin serotype B; capture ELISA; toxin detection in food monoclonal antibodies; botulinum neurotoxin serotype B; capture ELISA; toxin detection in food
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Stanker, L.H.; Scotcher, M.C.; Cheng, L.; Ching, K.; McGarvey, J.; Hodge, D.; Hnasko, R. A Monoclonal Antibody Based Capture ELISA for Botulinum Neurotoxin Serotype B: Toxin Detection in Food. Toxins 2013, 5, 2212-2226.

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