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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Veterinary Recordarrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Veterinary Record
Article . 2012 . Peer-reviewed
License: Wiley Online Library User Agreement
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A novel gold nanoparticles‐based assay for rapid detection of Melissococcus plutonius, the causative agent of European foulbrood

Authors: M, Saleh; H, Soliman; H, Sørum; A K, Fauske; M, El-Matbouli;

A novel gold nanoparticles‐based assay for rapid detection of Melissococcus plutonius, the causative agent of European foulbrood

Abstract

European foulbrood (EFB) is a severe bacterial brood disease of honey bees ( Apis mellifera ) caused by Melissococcus plutonius . Diagnosis of EFB in the field is based on visual inspection of brood‐combs and detection of diseased larvae. However, symptoms of EFB may be easily obscured by other diseases or abnormalities in the brood, making definitive diagnosis difficult. Hence, confirmatory laboratory assays, such as PCR and real‐time PCR, are used to verify the presence of M plutonius in suspected colonies. While these methods are accurate and specific, they are time consuming and labour intensive. Herein, we report development of a label‐free colorimetric nanodiagnostic method for direct detection of unamplified M plutonius DNA using unmodified gold nanoparticles. Under appropriate conditions, the DNA probes hybridised with their complementary target sequences in the sample DNA, which resulted in aggregation of the gold nanoparticles and a concomitant red to blue colour change, which was observed visually. The assay could detect as few as 25 copies of the M plutonius cell wall‐associated protease gene within 20 minutes. The assay results were in 100 per cent concordance with real‐time PCR‐positive and PCR‐negative samples. Our study demonstrated that the gold nanoparticles‐based assay is a specific and sensitive tool for rapid detection of M plutonius .

Keywords

DNA, Bacterial, Time Factors, Animals, Metal Nanoparticles, Colorimetry, Honey, Bees, Gram-Positive Bacteria

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
17
Top 10%
Average
Top 10%
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