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Bacteria viability assessment after photocatalytic treatment

The aim of the present work was to evaluate several methods for analyzing the viability of bacteria after antibacterial photocatalytic treatment. Colony-forming unit (CFU) counting, metabolic activity assays based on resazurin and phenol red and the Live/Dead(®) BacLight™ bacterial viability assay (...

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Detalles Bibliográficos
Autores principales: Cai, Yanling, Strømme, Maria, Welch, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964257/
https://www.ncbi.nlm.nih.gov/pubmed/28324445
http://dx.doi.org/10.1007/s13205-013-0137-1
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author Cai, Yanling
Strømme, Maria
Welch, Ken
author_facet Cai, Yanling
Strømme, Maria
Welch, Ken
author_sort Cai, Yanling
collection PubMed
description The aim of the present work was to evaluate several methods for analyzing the viability of bacteria after antibacterial photocatalytic treatment. Colony-forming unit (CFU) counting, metabolic activity assays based on resazurin and phenol red and the Live/Dead(®) BacLight™ bacterial viability assay (Live/Dead staining) were employed to assess photocatalytically treated Staphylococcus epidermidis and Streptococcus mutans. The results showed conformity between CFU counting and the metabolic activity assays, while Live/Dead staining showed a significantly higher viability post-treatment. This indicates that the Live/Dead staining test may not be suitable for assessing bacterial viability after photocatalytic treatment and that, in general, care should be taken when selecting a method for determining the viability of bacteria subjected to photocatalysis. The present findings are expected to become valuable for the development and evaluation of photocatalytically based disinfection applications.
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spelling pubmed-39642572014-03-25 Bacteria viability assessment after photocatalytic treatment Cai, Yanling Strømme, Maria Welch, Ken 3 Biotech Original Article The aim of the present work was to evaluate several methods for analyzing the viability of bacteria after antibacterial photocatalytic treatment. Colony-forming unit (CFU) counting, metabolic activity assays based on resazurin and phenol red and the Live/Dead(®) BacLight™ bacterial viability assay (Live/Dead staining) were employed to assess photocatalytically treated Staphylococcus epidermidis and Streptococcus mutans. The results showed conformity between CFU counting and the metabolic activity assays, while Live/Dead staining showed a significantly higher viability post-treatment. This indicates that the Live/Dead staining test may not be suitable for assessing bacterial viability after photocatalytic treatment and that, in general, care should be taken when selecting a method for determining the viability of bacteria subjected to photocatalysis. The present findings are expected to become valuable for the development and evaluation of photocatalytically based disinfection applications. Springer Berlin Heidelberg 2013-05-21 2014-04 /pmc/articles/PMC3964257/ /pubmed/28324445 http://dx.doi.org/10.1007/s13205-013-0137-1 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Cai, Yanling
Strømme, Maria
Welch, Ken
Bacteria viability assessment after photocatalytic treatment
title Bacteria viability assessment after photocatalytic treatment
title_full Bacteria viability assessment after photocatalytic treatment
title_fullStr Bacteria viability assessment after photocatalytic treatment
title_full_unstemmed Bacteria viability assessment after photocatalytic treatment
title_short Bacteria viability assessment after photocatalytic treatment
title_sort bacteria viability assessment after photocatalytic treatment
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964257/
https://www.ncbi.nlm.nih.gov/pubmed/28324445
http://dx.doi.org/10.1007/s13205-013-0137-1
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