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J Fluoresc ; 25(1): 173-83, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25511112

ABSTRACT

A fluorescent DNA aptamer-magnetic bead sandwich assay was developed to detect listeriolysin O (LLO) protein from pathogenic Listeria bacteria using a peroxidase-linked system, Amplex Ultra Red (AUR; derivatized resazurin) substrate, and a custom-designed handheld fluorometer. The assay is highly sensitive with demonstrated limits of detection (LODs) in the range of 4 to 61 L. monocytogenes cells or the equivalent LLO produced by 4 to 61 cells on average in separate titration trials. Total assay processing and analysis time was approximately 30 mins. The assay has demonstrated the ability to detect 6 species of Listeria as desired by the USDA's Food Safety Inspection Service (FSIS). The portable system was designed to be used primarily with surface swab samples from fomites, but it can also be used to assess enrichment cultures. The minimal time to detect a positive enrichment culture in our hands from an initial 10 cell inoculum in 200 ml of broth has been 8 h post-incubation at 37 °C in shaker flask cultures. An optional automated magnetic bead assay processing and wash device capable of simultaneously processing 6 samples with low and consistent fluorescence background for higher volume central laboratories is also described.


Subject(s)
Aptamers, Nucleotide/metabolism , Enzyme-Linked Immunosorbent Assay/methods , Fluorometry/instrumentation , Listeria monocytogenes/isolation & purification , Magnets/chemistry , Microspheres , Aptamers, Nucleotide/genetics , Bacterial Toxins/analysis , Base Sequence , Enzyme-Linked Immunosorbent Assay/instrumentation , Heat-Shock Proteins/analysis , Hemolysin Proteins/analysis , Time Factors
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