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A simple viability analysis for unicellular cyanobacteria using a new autofluorescence assay, automated microscopy, and ImageJ

BACKGROUND: Currently established methods to identify viable and non-viable cells of cyanobacteria are either time-consuming (eg. plating) or preparation-intensive (eg. fluorescent staining). In this paper we present a new and fast viability assay for unicellular cyanobacteria, which uses red chloro...

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Detalles Bibliográficos
Autores principales: Schulze, Katja, López, Diana A, Tillich, Ulrich M, Frohme, Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247844/
https://www.ncbi.nlm.nih.gov/pubmed/22129198
http://dx.doi.org/10.1186/1472-6750-11-118
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author Schulze, Katja
López, Diana A
Tillich, Ulrich M
Frohme, Marcus
author_facet Schulze, Katja
López, Diana A
Tillich, Ulrich M
Frohme, Marcus
author_sort Schulze, Katja
collection PubMed
description BACKGROUND: Currently established methods to identify viable and non-viable cells of cyanobacteria are either time-consuming (eg. plating) or preparation-intensive (eg. fluorescent staining). In this paper we present a new and fast viability assay for unicellular cyanobacteria, which uses red chlorophyll fluorescence and an unspecific green autofluorescence for the differentiation of viable and non-viable cells without the need of sample preparation. RESULTS: The viability assay for unicellular cyanobacteria using red and green autofluorescence was established and validated for the model organism Synechocystis sp. PCC 6803. Both autofluorescence signals could be observed simultaneously allowing a direct classification of viable and non-viable cells. The results were confirmed by plating/colony count, absorption spectra and chlorophyll measurements. The use of an automated fluorescence microscope and a novel ImageJ based image analysis plugin allow a semi-automated analysis. CONCLUSIONS: The new method simplifies the process of viability analysis and allows a quick and accurate analysis. Furthermore results indicate that a combination of the new assay with absorption spectra or chlorophyll concentration measurements allows the estimation of the vitality of cells.
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spelling pubmed-32478442011-12-30 A simple viability analysis for unicellular cyanobacteria using a new autofluorescence assay, automated microscopy, and ImageJ Schulze, Katja López, Diana A Tillich, Ulrich M Frohme, Marcus BMC Biotechnol Methodology Article BACKGROUND: Currently established methods to identify viable and non-viable cells of cyanobacteria are either time-consuming (eg. plating) or preparation-intensive (eg. fluorescent staining). In this paper we present a new and fast viability assay for unicellular cyanobacteria, which uses red chlorophyll fluorescence and an unspecific green autofluorescence for the differentiation of viable and non-viable cells without the need of sample preparation. RESULTS: The viability assay for unicellular cyanobacteria using red and green autofluorescence was established and validated for the model organism Synechocystis sp. PCC 6803. Both autofluorescence signals could be observed simultaneously allowing a direct classification of viable and non-viable cells. The results were confirmed by plating/colony count, absorption spectra and chlorophyll measurements. The use of an automated fluorescence microscope and a novel ImageJ based image analysis plugin allow a semi-automated analysis. CONCLUSIONS: The new method simplifies the process of viability analysis and allows a quick and accurate analysis. Furthermore results indicate that a combination of the new assay with absorption spectra or chlorophyll concentration measurements allows the estimation of the vitality of cells. BioMed Central 2011-11-30 /pmc/articles/PMC3247844/ /pubmed/22129198 http://dx.doi.org/10.1186/1472-6750-11-118 Text en Copyright ©2011 Schulze et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Schulze, Katja
López, Diana A
Tillich, Ulrich M
Frohme, Marcus
A simple viability analysis for unicellular cyanobacteria using a new autofluorescence assay, automated microscopy, and ImageJ
title A simple viability analysis for unicellular cyanobacteria using a new autofluorescence assay, automated microscopy, and ImageJ
title_full A simple viability analysis for unicellular cyanobacteria using a new autofluorescence assay, automated microscopy, and ImageJ
title_fullStr A simple viability analysis for unicellular cyanobacteria using a new autofluorescence assay, automated microscopy, and ImageJ
title_full_unstemmed A simple viability analysis for unicellular cyanobacteria using a new autofluorescence assay, automated microscopy, and ImageJ
title_short A simple viability analysis for unicellular cyanobacteria using a new autofluorescence assay, automated microscopy, and ImageJ
title_sort simple viability analysis for unicellular cyanobacteria using a new autofluorescence assay, automated microscopy, and imagej
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247844/
https://www.ncbi.nlm.nih.gov/pubmed/22129198
http://dx.doi.org/10.1186/1472-6750-11-118
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