Comparison of fluorescence and resonance light scattering for highly sensitive microarray detection of bacterial pathogens
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作者:
Francois, P
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Univ Hosp Geneva, Div Infect Dis, Genom Res Lab, CH-1211 Geneva 14, SwitzerlandUniv Hosp Geneva, Div Infect Dis, Genom Res Lab, CH-1211 Geneva 14, Switzerland
Francois, P
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Bento, M
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机构:Univ Hosp Geneva, Div Infect Dis, Genom Res Lab, CH-1211 Geneva 14, Switzerland
Bento, M
Vaudaux, P
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机构:Univ Hosp Geneva, Div Infect Dis, Genom Res Lab, CH-1211 Geneva 14, Switzerland
Vaudaux, P
Schrenzel, J
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机构:Univ Hosp Geneva, Div Infect Dis, Genom Res Lab, CH-1211 Geneva 14, Switzerland
Schrenzel, J
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[1] Univ Hosp Geneva, Div Infect Dis, Genom Res Lab, CH-1211 Geneva 14, Switzerland
Microarrays have emerged as potential tools for bacterial detection and identification. Given their high parallelism, they might represent a breakthrough in current diagnostic methods, provided they can be coupled to simplified labeling protocols and detected with adequate sensitivities. We describe here a technique to directly label total bacterial RNA, thus avoiding the multiple steps and possible biases associated with enzymatic amplification (e.g. PCR). We have then compared the performances of one white-light source and two laser-based fluorescence scanners for detection reliability and sensitivity. Our study reveals that nanoparticle-labeled bacterial RNA generates reproducible resonance light scattering signals that are at least 50 times more intense than state-of-the-art confocal-based fluorescence signals. (C) 2003 Elsevier B.V. All rights reserved.