On-chip microbial culture for the specific detection of very low levels of bacteria.

Abstract : Microbial culture continues to be the most common protocol for bacterial detection and identification in medicine and agronomics. Using this process may take days to identify a specific pathogen for most bacterial strains. Surface Plasmon Resonance (SPR) detection is an emerging alternative technology that can be used for the detection of bacteria using protein microarrays although typical limits of detection are in the range of 10(3)-10(6) cfu mL(-1), which is not compatible with most Food Safety regulation requirements. In this work, we combine concomitant "on-chip" microbial culture with sensitive SPR detection of bacteria thus allowing rapid specific detection of bacteria pathogens - including Salmonella enterica serovar Enteritidis, Streptococcus pneumoniae and Escherichia coli O157:H7 - cultured on a protein microarray. This Culture-Capture-Measure (CCM) approach significantly decreases both the number of processing steps and the overall assay time for bacterial detection. Signal analysis of SPR responses allowed the fast and quantitative assessment of bacterial concentrations initially present in the sample as low as 2.8 ± 19.6 cfu per milliliter. Altogether, our results show how simple, easy-to-operate, fluidic-less and lo-tec microarrays can be used with unprocessed samples and yield - in a single assay - both qualitative and quantitative information regarding bacterial contamination.
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Article dans une revue
Lab on a Chip, Royal Society of Chemistry, 2013, 13 (20), pp.4024-32
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http://hal.univ-grenoble-alpes.fr/hal-01322346
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Soumis le : vendredi 27 mai 2016 - 09:38:32
Dernière modification le : vendredi 9 mars 2018 - 16:36:02

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  • HAL Id : hal-01322346, version 1
  • PUBMED : 23912527

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Sihem Bouguelia, Yoann Roupioz, Sami Slimani, Laure Mondani, Maria G Casabona, et al.. On-chip microbial culture for the specific detection of very low levels of bacteria.. Lab on a Chip, Royal Society of Chemistry, 2013, 13 (20), pp.4024-32. 〈hal-01322346〉

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