A rapid bioassay for single bacterial cell quantitation using bioconjugated nanoparticles
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Open Access
- 11 October 2004
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 101 (42), 15027-15032
- https://doi.org/10.1073/pnas.0404806101
Abstract
The rapid and sensitive determination of pathogenic bacteria is extremely important in biotechnology, medical diagnosis, and the current fight against bioterrorism. Current methods either lack ultrasensitivity or take a long time for analysis. Here, we report a bioconjugated nanoparticle-based bioassay for in situ pathogen quantification down to single bacterium within 20 min. The bioconjugated nanoparticle provides an extremely high fluorescent signal for bioanalysis and can be easily incorporated with biorecognition molecules, such as antibody. The antibody-conjugated nanoparticles can readily and specifically identify a variety of bacterium, such as Escherichia coli O157:H7, through antibody–antigen interaction and recognition. The single-bacterium-detection capability within 20 min has been confirmed by the plate-counting method and realized by using two independent optical techniques. The two detection methods correlated extremely well. Furthermore, we were able to detect multiple bacterial samples with high throughput by using a 384-well microplate format. To show the usefulness of this assay, we have accurately detected 1–400 E. coli O157 bacterial cells in spiked ground beef samples. Our results demonstrate the potential for a broad application of bioconjugated nanoparticles in practical biotechnological and medical applications in various biodetection systems. The ultimate power of integrating bionanotechnology into complex biological systems will emerge as a revolutionary tool for ultrasensitive detection of disease markers and infectious agents.Keywords
This publication has 26 references indexed in Scilit:
- Miniature biochip system for detection of Escherichia coli O157:H7 based on antibody-immobilized capillary reactors and enzyme-linked immunosorbent assayAnalytica Chimica Acta, 2004
- Development of Organic‐Dye‐Doped Silica Nanoparticles in a Reverse MicroemulsionAdvanced Materials, 2004
- Fabrication of a disposable biosensor for Escherichia coli O157:H7 detectionIEEE Sensors Journal, 2003
- Ultrasensitive DNA Detection Using Highly Fluorescent Bioconjugated NanoparticlesJournal of the American Chemical Society, 2003
- Procedures for Preparing Escherichia coli O157:H7 Immunoliposome and Its Application in Liposome ImmunoassayAnalytical Chemistry, 2003
- Detection ofEscherichia coli O157:H7 bacteria by a combination of immunofluorescent staining and capillary electrophoresisElectrophoresis, 2003
- THE USE OF TIME‐RESOLVED FLUOROIMMUNOASSAY TO SIMULTANEOUSLY DETECT ESCHERICHIA COLI O157:H7, SALMONELLA ENTERICA SEROVAR TYPHIMURIUM AND SALMONELLA ENTERICA SEROVAR ENTERIDITIS IN FOODS1Journal of Rapid Methods and Automation in Microbiology, 2002
- Escherichia coli O157 and Salmonella Infections Associated with Sprouts in California, 1996–1998Annals of Internal Medicine, 2001
- Solid-Phase Capture of Proteins, Spores, and BacteriaApplied and Environmental Microbiology, 2001
- OPTICAL DETECTION OF SINGLE MOLECULESAnnual Review of Biophysics, 1997