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Multiple Phage-Based Magnetoelastic Biosensors System for the Detection of Salmonella typhimurium and Bacillus anthracis Spores

Published online by Cambridge University Press:  01 February 2011

S. Huang
Affiliation:
[email protected], Auburn University, Materials Engineering, Auburn, Alabama, United States
S. Li
Affiliation:
[email protected], Auburn University, Materials Engineering, Auburn, Alabama, United States
H. Yang
Affiliation:
[email protected], Auburn University, Materials Engineering, Auburn, Alabama, United States
M. L. Johnson
Affiliation:
[email protected], Auburn University, Materials Engineering, Auburn, Alabama, United States
Ramji S Lakshmanan
Affiliation:
[email protected], Auburn University, Materials Engineering, Auburn, Alabama, United States
I.-H. Chen
Affiliation:
[email protected], Auburn University, Materials Engineering, Auburn, Alabama, United States
V. A. Petrenko
Affiliation:
[email protected], Auburn University, Materials Engineering, Auburn, Alabama, United States
J. M. Barbaree
Affiliation:
[email protected], Auburn University, Materials Engineering, Auburn, Alabama, United States
B. A. Chin
Affiliation:
[email protected], Auburn University, Materials Engineering, Auburn, Alabama, United States
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Abstract

This paper presents a multiple magnetoelastic (ME) biosensor system for in-situ detection of S. typhimurium and B. anthracis spores in a flowing bacterial/spore suspension (5 x 101 - 5 x 108 cfu/ml). The ME biosensor was formed by immobilizing filamentous phage (specific to each detection target) on the ME platforms. An alternating magnetic field was used to resonate the ME biosensor to determine its resonance frequency. When cells/spores are bound to a ME biosensor surface, the additional mass of the cells/spores causes a decrease in the resonance frequency of the biosensor. The detection system was composed of a control sensor, an E2 phage-based biosensor (specific to S. typhimurium) and a JRB7 phage-based biosensor (specific to B. anthracis spores). The frequency response curves of the ME biosensors as a function of exposure time were then measured and the detection limit of the ME biosensor was observed to be 5 x 103 cfu/ml. The results show that phage-based ME biosensors can detect multiple pathogens simultaneously and offer good performance, including good sensitivity and rapid detection.

Type
Research Article
Copyright
Copyright © Materials Research Society 2009

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References

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