Development of an in Vitro Bioassay for Clostridium Botulinum Type B Neurotoxin in Foods That is More Sensitive Than the Mouse Bioassay

Overview

Journal Appl Environ Microbiol

Specialties Environmental Health
Microbiology

Date 1999 Sep 3

PMID 10473376

Citations 28

Authors

M Wictome

K Newton

K Jameson

B Hallis

P Dunnigan

E Mackay

S Clarke

R Taylor

J Gaze

K Foster

C Shone

Affiliations

Soon will be listed here.

Abstract

A novel, in vitro bioassay for detection of the botulinum type B neurotoxin in a range of media was developed. The assay is amplified by the enzymic activity of the neurotoxin's light chain and includes the following three stages: first, a small, monoclonal antibody-based immunoaffinity column captures the toxin; second, a peptide substrate is cleaved by using the endopeptidase activity of the type B neurotoxin; and finally, a modified enzyme-linked immunoassay system detects the peptide cleavage products. The assay is highly specific for type B neurotoxin and is capable of detecting type B toxin at a concentration of 5 pg ml(-1) (0.5 mouse 50% lethal dose ml(-1)) in approximately 5 h. The format of the test was found to be suitable for detecting botulinum type B toxin in a range of foodstuffs with a sensitivity that exceeds the sensitivity of the mouse assay. Using highly specific monoclonal antibodies as the capture phase, we found that the endopeptidase assay was capable of differentiating between the type B neurotoxins produced by proteolytic and nonproteolytic strains of Clostridium botulinum type B.

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