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Rapid on-site monitoring of Legionella pneumophila in cooling tower water using a portable microfluidic system

Legionnaires’ disease, predominantly caused by the bacterium Legionella pneumophila, has increased in prevalence worldwide. The most common mode of transmission of Legionella is inhalation of contaminated aerosols, such as those generated by cooling towers. Simple, rapid and accurate methods to enum...

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Autores principales: Yamaguchi, Nobuyasu, Tokunaga, Yusuke, Goto, Satoko, Fujii, Yudai, Banno, Fumiya, Edagawa, Akiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465085/
https://www.ncbi.nlm.nih.gov/pubmed/28596545
http://dx.doi.org/10.1038/s41598-017-03293-9
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author Yamaguchi, Nobuyasu
Tokunaga, Yusuke
Goto, Satoko
Fujii, Yudai
Banno, Fumiya
Edagawa, Akiko
author_facet Yamaguchi, Nobuyasu
Tokunaga, Yusuke
Goto, Satoko
Fujii, Yudai
Banno, Fumiya
Edagawa, Akiko
author_sort Yamaguchi, Nobuyasu
collection PubMed
description Legionnaires’ disease, predominantly caused by the bacterium Legionella pneumophila, has increased in prevalence worldwide. The most common mode of transmission of Legionella is inhalation of contaminated aerosols, such as those generated by cooling towers. Simple, rapid and accurate methods to enumerate L. pneumophila are required to prevent the spread of this organism. Here, we applied a microfluidic device for on-chip fluorescent staining and semi-automated counting of L. pneumophila in cooling tower water. We also constructed a portable system for rapid on-site monitoring and used it to enumerate target bacterial cells rapidly flowing in the microchannel. A fluorescently-labelled polyclonal antibody was used for the selective detection of L. pneumophila serogroup 1 in the samples. The counts of L. pneumophila in cooling tower water obtained using the system and fluorescence microscopy were similar. The detection limit of the system was 10(4) cells/ml, but lower numbers of L. pneumophila cells (10(1) to 10(3) cells/ml) could be detected following concentration of 0.5–3 L of the water sample by filtration. Our technique is rapid to perform (1.5 h), semi-automated (on-chip staining and counting), and portable for on-site measurement, and it may therefore be effective in the initial screening of Legionella contamination in freshwater.
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spelling pubmed-54650852017-06-14 Rapid on-site monitoring of Legionella pneumophila in cooling tower water using a portable microfluidic system Yamaguchi, Nobuyasu Tokunaga, Yusuke Goto, Satoko Fujii, Yudai Banno, Fumiya Edagawa, Akiko Sci Rep Article Legionnaires’ disease, predominantly caused by the bacterium Legionella pneumophila, has increased in prevalence worldwide. The most common mode of transmission of Legionella is inhalation of contaminated aerosols, such as those generated by cooling towers. Simple, rapid and accurate methods to enumerate L. pneumophila are required to prevent the spread of this organism. Here, we applied a microfluidic device for on-chip fluorescent staining and semi-automated counting of L. pneumophila in cooling tower water. We also constructed a portable system for rapid on-site monitoring and used it to enumerate target bacterial cells rapidly flowing in the microchannel. A fluorescently-labelled polyclonal antibody was used for the selective detection of L. pneumophila serogroup 1 in the samples. The counts of L. pneumophila in cooling tower water obtained using the system and fluorescence microscopy were similar. The detection limit of the system was 10(4) cells/ml, but lower numbers of L. pneumophila cells (10(1) to 10(3) cells/ml) could be detected following concentration of 0.5–3 L of the water sample by filtration. Our technique is rapid to perform (1.5 h), semi-automated (on-chip staining and counting), and portable for on-site measurement, and it may therefore be effective in the initial screening of Legionella contamination in freshwater. Nature Publishing Group UK 2017-06-08 /pmc/articles/PMC5465085/ /pubmed/28596545 http://dx.doi.org/10.1038/s41598-017-03293-9 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
Yamaguchi, Nobuyasu
Tokunaga, Yusuke
Goto, Satoko
Fujii, Yudai
Banno, Fumiya
Edagawa, Akiko
Rapid on-site monitoring of Legionella pneumophila in cooling tower water using a portable microfluidic system
title Rapid on-site monitoring of Legionella pneumophila in cooling tower water using a portable microfluidic system
title_full Rapid on-site monitoring of Legionella pneumophila in cooling tower water using a portable microfluidic system
title_fullStr Rapid on-site monitoring of Legionella pneumophila in cooling tower water using a portable microfluidic system
title_full_unstemmed Rapid on-site monitoring of Legionella pneumophila in cooling tower water using a portable microfluidic system
title_short Rapid on-site monitoring of Legionella pneumophila in cooling tower water using a portable microfluidic system
title_sort rapid on-site monitoring of legionella pneumophila in cooling tower water using a portable microfluidic system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465085/
https://www.ncbi.nlm.nih.gov/pubmed/28596545
http://dx.doi.org/10.1038/s41598-017-03293-9
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