Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophila
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/1822/9713 |
Resumo: | Legionella pneumophila is an ubiquitous environmental microorganism that can cause Legionnaires’ disease or Pontiac fever. As a waterborne pathogen, it has been found to be resistant to chlorine disinfection and survive in drinking water systems, leading to potential outbreaks of waterborne disease. In this work, the effect of different concentrations of free chlorine was studied (0.2, 0.7, and 1.2 mg l−1), the cultivability of cells assessed by standard culture techniques (buffered charcoal yeast extract agar plates) and viability using the SYTO 9/propidium iodide fluorochrome uptake assay (LIVE/DEAD® BacLight™). Results demonstrate that L. pneumophila loses cultivability after exposure for 30 min to 0.7 mg l−1 of free chlorine and in 10 min when the concentration is increased to 1.2 mg l−1. However, the viability of the cells was only slightly affected even after 30 min exposure to the highest concentration of chlorine; good correlation was obtained between the rapid SYTO 9/propidium iodide fluorochrome uptake assay and a longer cocultivation with Acanthamoeba polyphaga assay, confirming that these cells could still recover their cultivability. These results raise new concerns about the assessment of drinking water disinfection efficiency and indicate the necessity of further developing new validated rapid methods, such as the SYTO 9/propidium iodide uptake assay, to assess viable but noncultivable L. pneumophila cells in the environment. |
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Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophilaScience & TechnologyLegionella pneumophila is an ubiquitous environmental microorganism that can cause Legionnaires’ disease or Pontiac fever. As a waterborne pathogen, it has been found to be resistant to chlorine disinfection and survive in drinking water systems, leading to potential outbreaks of waterborne disease. In this work, the effect of different concentrations of free chlorine was studied (0.2, 0.7, and 1.2 mg l−1), the cultivability of cells assessed by standard culture techniques (buffered charcoal yeast extract agar plates) and viability using the SYTO 9/propidium iodide fluorochrome uptake assay (LIVE/DEAD® BacLight™). Results demonstrate that L. pneumophila loses cultivability after exposure for 30 min to 0.7 mg l−1 of free chlorine and in 10 min when the concentration is increased to 1.2 mg l−1. However, the viability of the cells was only slightly affected even after 30 min exposure to the highest concentration of chlorine; good correlation was obtained between the rapid SYTO 9/propidium iodide fluorochrome uptake assay and a longer cocultivation with Acanthamoeba polyphaga assay, confirming that these cells could still recover their cultivability. These results raise new concerns about the assessment of drinking water disinfection efficiency and indicate the necessity of further developing new validated rapid methods, such as the SYTO 9/propidium iodide uptake assay, to assess viable but noncultivable L. pneumophila cells in the environment.This work was supported by the Portuguese Institute Fundacao para a Ciencia e Tecnologia (PhD grant SFRH/BD/17088/2004) and has been undertaken as part of a research project which is supported by the European Commission within the Fifth Framework Programme, "Energy, Environment and sustainable development programme", no. EVK1-CT-2002-00108. Disclaimer states that the author is solely responsible for the work; it does not represent the opinion of the Community, and the Community is not responsible for any use that might be made of data appearing therein.SpringerUniversidade do MinhoGião, M. S.Wilks, S. A.Azevedo, N. F.Vieira, M. J.Keevil, C. W.2009-072009-07-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/9713eng"Microbial Ecology". ISSN 0095-3628. 58:1 (2009) 56-62.0095-362810.1007/s00248-008-9472-x19043657info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:31:21Zoai:repositorium.sdum.uminho.pt:1822/9713Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:26:36.682070Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophila |
title |
Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophila |
spellingShingle |
Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophila Gião, M. S. Science & Technology |
title_short |
Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophila |
title_full |
Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophila |
title_fullStr |
Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophila |
title_full_unstemmed |
Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophila |
title_sort |
Validation of SYTO 9/Propidium Iodide Uptake for rapid detection of viable but noncultivable Legionella pneumophila |
author |
Gião, M. S. |
author_facet |
Gião, M. S. Wilks, S. A. Azevedo, N. F. Vieira, M. J. Keevil, C. W. |
author_role |
author |
author2 |
Wilks, S. A. Azevedo, N. F. Vieira, M. J. Keevil, C. W. |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Gião, M. S. Wilks, S. A. Azevedo, N. F. Vieira, M. J. Keevil, C. W. |
dc.subject.por.fl_str_mv |
Science & Technology |
topic |
Science & Technology |
description |
Legionella pneumophila is an ubiquitous environmental microorganism that can cause Legionnaires’ disease or Pontiac fever. As a waterborne pathogen, it has been found to be resistant to chlorine disinfection and survive in drinking water systems, leading to potential outbreaks of waterborne disease. In this work, the effect of different concentrations of free chlorine was studied (0.2, 0.7, and 1.2 mg l−1), the cultivability of cells assessed by standard culture techniques (buffered charcoal yeast extract agar plates) and viability using the SYTO 9/propidium iodide fluorochrome uptake assay (LIVE/DEAD® BacLight™). Results demonstrate that L. pneumophila loses cultivability after exposure for 30 min to 0.7 mg l−1 of free chlorine and in 10 min when the concentration is increased to 1.2 mg l−1. However, the viability of the cells was only slightly affected even after 30 min exposure to the highest concentration of chlorine; good correlation was obtained between the rapid SYTO 9/propidium iodide fluorochrome uptake assay and a longer cocultivation with Acanthamoeba polyphaga assay, confirming that these cells could still recover their cultivability. These results raise new concerns about the assessment of drinking water disinfection efficiency and indicate the necessity of further developing new validated rapid methods, such as the SYTO 9/propidium iodide uptake assay, to assess viable but noncultivable L. pneumophila cells in the environment. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-07 2009-07-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/1822/9713 |
url |
http://hdl.handle.net/1822/9713 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
"Microbial Ecology". ISSN 0095-3628. 58:1 (2009) 56-62. 0095-3628 10.1007/s00248-008-9472-x 19043657 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Springer |
publisher.none.fl_str_mv |
Springer |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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