Abstract

Botulinum neurotoxins (BoNT) are the most potent toxins, which are produced by Clostridium bacteria and cause the life-threatening disease of botulism in all vertebrates. Specifically, animal botulism represents a serious environmental and economic concern in animal production due to the high mortality rates observed during outbreaks. Despite the availability of vaccines against BoNT, there are still many outbreaks of botulism worldwide. Alternative assays capable of replacing the conventional in vivo assay in terms of rapid and sensitive quantification, and the applicability for on-site analysis, have long been perused. Herein, we present a simple, highly sensitive and label-free optical biosensor for real-time detection of BoNT serotype C using a porous silicon Fabry–Pérot interferometer. A competitive immunoassay coupled to a biochemical cascade reaction was adapted for optical signal amplification. The resulting insoluble precipitates accumulated within the nanostructure changed the reflectivity spectra by alternating the averaged refractive index. The augmented optical performance allowed for a linear response within the range of 10 to 10,000 pg mL−1 while presenting a detection limit of 4.8 pg mL−1. The practical aspect of the developed assay was verified using field BoNT holotoxins to exemplify the potential use of the developed optical approach for rapid bio-diagnosis of BoNT. The specificity and selectivity of the assay were successfully validated using an adjacent holotoxin relevant for farm animals (BoNT serotype D). Overall, this work sets the foundation for implementing a miniaturized interferometer for routine on-site botulism diagnosis, thus significantly reducing the need for animal experimentation and shortening analysis turnaround for early evidence-based therapy.

Highlights

  • Botulinum neurotoxins (BoNT) are the strongest toxins known in nature, causing the severe neurological disease of botulism [1,2]

  • BoNT is produced by spore-forming anaerobic bacterial strains of Clostridium botulinum (C. botulinum) and several other clostridial species [3]

  • The significant conditions omitting BoNT-C from the assay (0 pg mL−1 ), in which pronounced insoluble at 20 min is ascribed to the absence of competing or interrelative intensity value were of 2.88 products entrapped within the PSiO

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Summary

Introduction

Botulinum neurotoxins (BoNT) are the strongest toxins known in nature, causing the severe neurological disease of botulism [1,2]. The endopep-mass spectrometry assay allows for high confidence and enhanced sensitivity detection of all known serotypes by typing their proteolytic activity products [5,18]. This technique is limited to explicit laboratories due to the high level of expertise and complex instrumentation needed for the analysis [19]. The porous nanostructure owes several beneficial features for the design and development of a sophisticated sensing platform This includes a rapid and tunable fabrication process resulting in high surface area, various photonic structures, enhanced sensitivity, and label-free practical detection of any biorecognition event occurring within the porous void [32,33].

Schematic
Materials
Porous
Interferometer Biofunctionalization
Optical Studies
Surface Functionalization Characterization
BoNT-C Detection Using Immunorecognition
Detection of BoNT-C in Field Samples
Interferometer Design and Characterization
BoNT-C toxoid biofunctionalization characterization using
O2 to the buffer by the addition ofare
Field Samples BoNT-C Detection
Conclusions
A Quantum Dot Nanobiosensor for Rapid Detection of Botulinum Neurotoxin
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