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Species Dependence of SYTO 9 Staining of Bacteria
SYTO 9 is a fluorescent nucleic acid stain that is widely used in microbiology, particularly for fluorescence microscopy and flow cytometry analyzes. Fluorimetry-based analysis, i.e., analysis of fluorescence intensity from a bulk sample measurement, is more cost effective, rapid and accessible than...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494787/ https://www.ncbi.nlm.nih.gov/pubmed/33013779 http://dx.doi.org/10.3389/fmicb.2020.545419 |
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author | McGoverin, Cushla Robertson, Julia Jonmohamadi, Yaqub Swift, Simon Vanholsbeeck, Frédérique |
author_facet | McGoverin, Cushla Robertson, Julia Jonmohamadi, Yaqub Swift, Simon Vanholsbeeck, Frédérique |
author_sort | McGoverin, Cushla |
collection | PubMed |
description | SYTO 9 is a fluorescent nucleic acid stain that is widely used in microbiology, particularly for fluorescence microscopy and flow cytometry analyzes. Fluorimetry-based analysis, i.e., analysis of fluorescence intensity from a bulk sample measurement, is more cost effective, rapid and accessible than microscopy or flow cytometry but requires application-specific calibration. Here we show the relevance of SYTO 9 for food safety analysis. We stained four bacterial species of relevance to food safety (Bacillus cereus, Escherichia coli, Salmonella enterica subspecies enterica ser. Typhimurium, Staphylococcus aureus) with different concentrations of SYTO 9, with and without the presence of ethylenediaminetetraacetic acid (EDTA), for varying amounts of time, to investigate the effect of these treatment parameters on fluorescence intensity. The addition of EDTA and an increased staining duration did not significantly affect fluorescence intensity, and over the bacterial cell concentration range investigated (∼10(5)–10(8) CFU/ml) there was no significant difference in using 0.5 or 1 μM SYTO 9. The effect of bacterial cell concentration on fluorescence intensity was species specific. At different bacterial cell concentrations, the effect of species on fluorescence intensity is different. This interaction complicates the development of a general fluorimetry-based protocol for the determination of bacterial cell concentration in a mixed bacterial suspension, as would be expected from samples taken from food safety settings. |
format | Online Article Text |
id | pubmed-7494787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74947872020-10-02 Species Dependence of SYTO 9 Staining of Bacteria McGoverin, Cushla Robertson, Julia Jonmohamadi, Yaqub Swift, Simon Vanholsbeeck, Frédérique Front Microbiol Microbiology SYTO 9 is a fluorescent nucleic acid stain that is widely used in microbiology, particularly for fluorescence microscopy and flow cytometry analyzes. Fluorimetry-based analysis, i.e., analysis of fluorescence intensity from a bulk sample measurement, is more cost effective, rapid and accessible than microscopy or flow cytometry but requires application-specific calibration. Here we show the relevance of SYTO 9 for food safety analysis. We stained four bacterial species of relevance to food safety (Bacillus cereus, Escherichia coli, Salmonella enterica subspecies enterica ser. Typhimurium, Staphylococcus aureus) with different concentrations of SYTO 9, with and without the presence of ethylenediaminetetraacetic acid (EDTA), for varying amounts of time, to investigate the effect of these treatment parameters on fluorescence intensity. The addition of EDTA and an increased staining duration did not significantly affect fluorescence intensity, and over the bacterial cell concentration range investigated (∼10(5)–10(8) CFU/ml) there was no significant difference in using 0.5 or 1 μM SYTO 9. The effect of bacterial cell concentration on fluorescence intensity was species specific. At different bacterial cell concentrations, the effect of species on fluorescence intensity is different. This interaction complicates the development of a general fluorimetry-based protocol for the determination of bacterial cell concentration in a mixed bacterial suspension, as would be expected from samples taken from food safety settings. Frontiers Media S.A. 2020-09-03 /pmc/articles/PMC7494787/ /pubmed/33013779 http://dx.doi.org/10.3389/fmicb.2020.545419 Text en Copyright © 2020 McGoverin, Robertson, Jonmohamadi, Swift and Vanholsbeeck. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology McGoverin, Cushla Robertson, Julia Jonmohamadi, Yaqub Swift, Simon Vanholsbeeck, Frédérique Species Dependence of SYTO 9 Staining of Bacteria |
title | Species Dependence of SYTO 9 Staining of Bacteria |
title_full | Species Dependence of SYTO 9 Staining of Bacteria |
title_fullStr | Species Dependence of SYTO 9 Staining of Bacteria |
title_full_unstemmed | Species Dependence of SYTO 9 Staining of Bacteria |
title_short | Species Dependence of SYTO 9 Staining of Bacteria |
title_sort | species dependence of syto 9 staining of bacteria |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494787/ https://www.ncbi.nlm.nih.gov/pubmed/33013779 http://dx.doi.org/10.3389/fmicb.2020.545419 |
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