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A self-luminous bifunctional bacteria directed fluorescent immunosensor for the simultaneous detection and quantification of three pathogens in milk

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TLDR
A novel multiplex fluorescent competitive immunosensor using self-luminous bacteria as a bifunctional probe for the simultaneous detection and quantification of multiple pathogens and provides an alternative multiplexing analytical platform as a powerful and rapid diagnostic tool for monitoring foodborne pathogen contamination.
Abstract
Herein, we report a novel multiplex fluorescent competitive immunosensor using self-luminous bacteria as a bifunctional probe for the simultaneous detection and quantification of multiple pathogens. The self-luminous bacteria are prepared through the facile one-step co-culture of bacteria and organic fluorescent dyes. Cronobacter muytjensii, Listeria monocytogenes, and Escherichia coli O157:H7 are fluorescently labelled with 7-hydroxycoumarin, fluorescein isothiocyanate, and rhodamine B, respectively, due to the dyes small spectral overlap in excitation/emission. The obtained fluorescent bacteria retain specific immunorecognition activity, but exhibit excellent fluorescent sensing ability. By using these fluorescent bacteria as bifunctional probes for competitive recognition and optical sensing, we achieved the sensitive and simultaneous quantitative determination of three pathogens with sensitivities of below 8.6 × 103 CFU/mL. The sensitivities can be significantly enhanced to 1 CFU/mL in real milk by integrating with a pre-incubation step, showing great potential for the ultrasensitive determination of trace bacteria and even single colony with the overall detection time of less than 10 h. In summary, this work provides an alternative multiplexing analytical platform as a powerful and rapid diagnostic tool for monitoring foodborne pathogen contamination.

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Enzyme-free catalytic hairpin assembly reaction-mediated micro-orifice resistance assay for the ultrasensitive and low-cost detection of Listeria monocytogenes

TL;DR: In this paper , a micro-orifice resistance technique combined with the aggregation of polystyrene (PS) microspheres constructed by the catalytic hairpin assembly reaction (CHA) was used to detect L. monocytogenes.
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Enzyme-free catalytic hairpin assembly reaction-mediated micro-orifice resistance assay for the ultrasensitive and low-cost detection of Listeria monocytogenes.

TL;DR: A novel, enzyme-free, dual-signal amplification approach to detect L. monocytogenes based on the micro-orifice resistance technique combined with the aggregation of polystyrene microspheres constructed by the catalytic hairpin assembly reaction (CHA).
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Advantages of aggregation-induced luminescence microspheres compared with fluorescent microspheres in immunochromatography assay with sandwich format.

TL;DR: In this paper , two green emitted fluorescent microspheres (AIEFMs) and fluorescein isothiocyanate FMs (FITCFMs) were used as the labeling markers of ICA for procalcitonin (PCT) detection with the sandwich format.
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Multiplex Detection of Infectious Diseases on Microfluidic Platforms

TL;DR: In this paper , the authors present the recent advances in microfluidic platforms used for multiplex detection of infectious diseases, including microfluide immunosensors and microfluidity nucleic acid sensors, and discuss the current challenges, commercialization, and prospects.
References
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Biosensors based on modularly designed synthetic peptides for recognition, detection and live/dead differentiation of pathogenic bacteria.

TL;DR: The proposed methodology provides a universal platform for the detection of bacterial pathogens based on engineered peptides, as alternative to the most commonly used immunological and gene based assays.
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A Meta-Analysis of Major Foodborne Pathogens in Chinese Food Commodities Between 2006 and 2016.

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Journal ArticleDOI

Fluorescent Immunoassay for the Detection of Pathogenic Bacteria at the Single-Cell Level Using Carbon Dots-Encapsulated Breakable Organosilica Nanocapsule as Labels

TL;DR: Carbon dots-encapsulated breakable organosilica nanocapsules were facilely prepared and used as advanced fluorescent labels for ultrasensitive detection of Staphylococcus aureus and were amplified by 2 orders of magnitude.
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