In-situ immuno-gold nanoparticle network ELISA biosensors for pathogen detection

Food poisoning microorganisms that contaminate food products and compromise food safety and security have been considered a major health threat and a serious concern for food producers and processors. Developing sensor technologies that are rapid for sensitive and selective detection and quantificat...

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Veröffentlicht in:International journal of food microbiology 2013-06, Vol.164 (1), p.70-75
Hauptverfasser: Cho, Il-Hoon, Irudayaraj, Joseph
Format: Artikel
Sprache:eng
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Zusammenfassung:Food poisoning microorganisms that contaminate food products and compromise food safety and security have been considered a major health threat and a serious concern for food producers and processors. Developing sensor technologies that are rapid for sensitive and selective detection and quantification of pathogens is a high priority for scientists in academia, state and federal research institutes, and industries. In this work we propose an in-situ immuno-AuNP network-based ELISA biosensor integrated with a sample concentration step based on immuno-magnetic separation to detect pathogenic microorganisms with high sensitivity. The sensor system was optimized by the specific formation of immuno-AuNP network onto the antigenic site present at the outer membrane surface of bacteria and the analytical concept was validated by a microtiter immunoassay. The in-situ network biosensor was able to detect pathogens at extremely low numbers: 3cells/mL of Escherichia coli O157:H7 and Salmonella typhimurium in buffer and 3CFU/mL of E. coli O157:H7 and 15CFU/mL of S. typhimurium in real sample conditions within 2h of inoculation. The ability to monitor target bacteria with improved analytical sensitivity compared to the current techniques presents a unique opportunity for routine monitoring to improve the safety of foods. •Development of novel gold nanoparticle network biosensors for diagnostics.•Direct detection possible in food matrices because of a magnetic separation step.•Detection of less than 10 CFU/ml of the foodborne pathogens possible in food matrices in less than 2 h.•Enhancement of signal can be controlled to increase sensitivity.•Can be generalized to detect a variety of threat agents for biosecirity.
ISSN:0168-1605
1879-3460
DOI:10.1016/j.ijfoodmicro.2013.02.025