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A comparison of conventional methods for the quantification of bacterial cells after exposure to metal oxide nanoparticles
BACKGROUND: Due to potential interference of nanoparticles on bacterial quantification, there is a challenge to develop a fast, accurate and reproducible method for bacterial quantification. Currently various bacterial quantification methods are used by researchers performing nanoparticles study, bu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236543/ https://www.ncbi.nlm.nih.gov/pubmed/25138641 http://dx.doi.org/10.1186/s12866-014-0222-6 |
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author | Pan, Hongmiao Zhang, Yongbin He, Gui-Xin Katagori, Namrata Chen, Huizhong |
author_facet | Pan, Hongmiao Zhang, Yongbin He, Gui-Xin Katagori, Namrata Chen, Huizhong |
author_sort | Pan, Hongmiao |
collection | PubMed |
description | BACKGROUND: Due to potential interference of nanoparticles on bacterial quantification, there is a challenge to develop a fast, accurate and reproducible method for bacterial quantification. Currently various bacterial quantification methods are used by researchers performing nanoparticles study, but there has been no efficacy evaluation of these methods. Here we study interference of nanoparticles on three most commonly used conventional bacterial quantification methods, including colony counting to determine the colony-forming units (CFU), spectrophotometer method of optical density (OD) measurement, and flow cytometry (FCM). RESULTS: Three oxide nanoparticles including ZnO, TiO(2), and SiO(2) and four bacterial species including Salmonella enterica serovar Newport, Staphylococcus epidermidis, Enterococcus faecalis, and Escherichia coli were included in the test. Results showed that there is no apparent interference of the oxide nanoparticles on quantifications of all four bacterial species by FCM measurement; CFU counting is time consuming, less accurate and not suitable for automation; and the spectrophotometer method using OD measurement was the most unreliable method to quantify and detect the bacteria in the presence of the nanoparticles. CONCLUSION: In summary, FCM measurement proved to be the best method, which is suitable for rapid, accurate and automatic detection of bacteria in the presence of the nanoparticles. |
format | Online Article Text |
id | pubmed-4236543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42365432014-11-19 A comparison of conventional methods for the quantification of bacterial cells after exposure to metal oxide nanoparticles Pan, Hongmiao Zhang, Yongbin He, Gui-Xin Katagori, Namrata Chen, Huizhong BMC Microbiol Research Article BACKGROUND: Due to potential interference of nanoparticles on bacterial quantification, there is a challenge to develop a fast, accurate and reproducible method for bacterial quantification. Currently various bacterial quantification methods are used by researchers performing nanoparticles study, but there has been no efficacy evaluation of these methods. Here we study interference of nanoparticles on three most commonly used conventional bacterial quantification methods, including colony counting to determine the colony-forming units (CFU), spectrophotometer method of optical density (OD) measurement, and flow cytometry (FCM). RESULTS: Three oxide nanoparticles including ZnO, TiO(2), and SiO(2) and four bacterial species including Salmonella enterica serovar Newport, Staphylococcus epidermidis, Enterococcus faecalis, and Escherichia coli were included in the test. Results showed that there is no apparent interference of the oxide nanoparticles on quantifications of all four bacterial species by FCM measurement; CFU counting is time consuming, less accurate and not suitable for automation; and the spectrophotometer method using OD measurement was the most unreliable method to quantify and detect the bacteria in the presence of the nanoparticles. CONCLUSION: In summary, FCM measurement proved to be the best method, which is suitable for rapid, accurate and automatic detection of bacteria in the presence of the nanoparticles. BioMed Central 2014-08-21 /pmc/articles/PMC4236543/ /pubmed/25138641 http://dx.doi.org/10.1186/s12866-014-0222-6 Text en Copyright © 2014 Pan et al.; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Pan, Hongmiao Zhang, Yongbin He, Gui-Xin Katagori, Namrata Chen, Huizhong A comparison of conventional methods for the quantification of bacterial cells after exposure to metal oxide nanoparticles |
title | A comparison of conventional methods for the quantification of bacterial cells after exposure to metal oxide nanoparticles |
title_full | A comparison of conventional methods for the quantification of bacterial cells after exposure to metal oxide nanoparticles |
title_fullStr | A comparison of conventional methods for the quantification of bacterial cells after exposure to metal oxide nanoparticles |
title_full_unstemmed | A comparison of conventional methods for the quantification of bacterial cells after exposure to metal oxide nanoparticles |
title_short | A comparison of conventional methods for the quantification of bacterial cells after exposure to metal oxide nanoparticles |
title_sort | comparison of conventional methods for the quantification of bacterial cells after exposure to metal oxide nanoparticles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236543/ https://www.ncbi.nlm.nih.gov/pubmed/25138641 http://dx.doi.org/10.1186/s12866-014-0222-6 |
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