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Biochips for Direct Detection and Identification of Bacteria in Blood Culture-Like Conditions

Bloodstream bacterial infections are life-threatening conditions necessitating prompt medical care. Rapid pathogen identification is essential for early setting of the best anti-infectious therapy. However, the bacterial load in blood samples from patients with bacteremia is too low and under the li...

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Autores principales: Templier, V., Livache, T., Boisset, S., Maurin, M., Slimani, S., Mathey, R., Roupioz, Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572712/
https://www.ncbi.nlm.nih.gov/pubmed/28842712
http://dx.doi.org/10.1038/s41598-017-10072-z
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author Templier, V.
Livache, T.
Boisset, S.
Maurin, M.
Slimani, S.
Mathey, R.
Roupioz, Y.
author_facet Templier, V.
Livache, T.
Boisset, S.
Maurin, M.
Slimani, S.
Mathey, R.
Roupioz, Y.
author_sort Templier, V.
collection PubMed
description Bloodstream bacterial infections are life-threatening conditions necessitating prompt medical care. Rapid pathogen identification is essential for early setting of the best anti-infectious therapy. However, the bacterial load in blood samples from patients with bacteremia is too low and under the limit of detection of most methods for direct identification of bacteria. Therefore, a preliminary step enabling the bacterial multiplication is required. To do so, blood cultures still remain the gold standard before bacteremia diagnosis. Bacterial identification is then usually obtained within 24 to 48 hours -at least- after blood sampling. In the present work, the fast and direct identification of bacteria present in blood cultures is completed in less than 12 hours, during bacterial growth, using an antibody microarray coupled to a Surface Plasmon Resonance imager (SPRi). Less than one bacterium (Salmonella enterica serovar Enteritidis) per milliliter of blood sample is successfully detected and identified in blood volumes similar to blood tests collected in clinics (i.e. several milliliters). This proof of concept demonstrates the workability of our method for human samples, despite the highly complex intrinsic nature of unprocessed blood. Our label-free method then opens new perspectives for direct and faster bacterial identification in a larger range of clinical samples.
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spelling pubmed-55727122017-09-01 Biochips for Direct Detection and Identification of Bacteria in Blood Culture-Like Conditions Templier, V. Livache, T. Boisset, S. Maurin, M. Slimani, S. Mathey, R. Roupioz, Y. Sci Rep Article Bloodstream bacterial infections are life-threatening conditions necessitating prompt medical care. Rapid pathogen identification is essential for early setting of the best anti-infectious therapy. However, the bacterial load in blood samples from patients with bacteremia is too low and under the limit of detection of most methods for direct identification of bacteria. Therefore, a preliminary step enabling the bacterial multiplication is required. To do so, blood cultures still remain the gold standard before bacteremia diagnosis. Bacterial identification is then usually obtained within 24 to 48 hours -at least- after blood sampling. In the present work, the fast and direct identification of bacteria present in blood cultures is completed in less than 12 hours, during bacterial growth, using an antibody microarray coupled to a Surface Plasmon Resonance imager (SPRi). Less than one bacterium (Salmonella enterica serovar Enteritidis) per milliliter of blood sample is successfully detected and identified in blood volumes similar to blood tests collected in clinics (i.e. several milliliters). This proof of concept demonstrates the workability of our method for human samples, despite the highly complex intrinsic nature of unprocessed blood. Our label-free method then opens new perspectives for direct and faster bacterial identification in a larger range of clinical samples. Nature Publishing Group UK 2017-08-25 /pmc/articles/PMC5572712/ /pubmed/28842712 http://dx.doi.org/10.1038/s41598-017-10072-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Templier, V.
Livache, T.
Boisset, S.
Maurin, M.
Slimani, S.
Mathey, R.
Roupioz, Y.
Biochips for Direct Detection and Identification of Bacteria in Blood Culture-Like Conditions
title Biochips for Direct Detection and Identification of Bacteria in Blood Culture-Like Conditions
title_full Biochips for Direct Detection and Identification of Bacteria in Blood Culture-Like Conditions
title_fullStr Biochips for Direct Detection and Identification of Bacteria in Blood Culture-Like Conditions
title_full_unstemmed Biochips for Direct Detection and Identification of Bacteria in Blood Culture-Like Conditions
title_short Biochips for Direct Detection and Identification of Bacteria in Blood Culture-Like Conditions
title_sort biochips for direct detection and identification of bacteria in blood culture-like conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572712/
https://www.ncbi.nlm.nih.gov/pubmed/28842712
http://dx.doi.org/10.1038/s41598-017-10072-z
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