Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal spores

Detalhes bibliográficos
Autor(a) principal: Mesquita, N.
Data de Publicação: 2013
Outros Autores: Portugal, A., Piñar, G., Loureiro, J., Coutinho, A. P., Trovão, J., Nunes, I., Botelho, M. L., Freitas, H.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/25739
https://doi.org/10.1016/j.ibiod.2012.05.008
Resumo: Flow cytometry is often used for viability and vitality assessment in bacteria and yeasts. However, its application to the study of fungal spore development is uncommon, probably due to the difficulties in successfully staining these cells. In the current study, we used flow cytometry for the first time to assess the effects of a disinfection treatment on the survival, growth and metabolic activity of fungal spores (Penicillium chrysogenum, Aspergillus nidulans and Aspergillus niger) submitted to gamma radiation (0e15 kGy). The Forward and Side-Scatter parameters of the cytometer were used to assess the differences in size and complexity of particles. Furthermore, two fluorescent dyes were used: Propidium Iodide to assess the membrane integrity and spore viability, in a culture-independent procedure; and Dihydroethidium to measure the changes in metabolic activity of irradiated spores in their first 10 h of growth in a liquid culture medium. Our results support that flow cytometry is a valuable tool in assessing different biological parameters and biocide effects, as it allowed accurate determination of the viability, growth and metabolic activity of gamma-irradiated spores. The fluorescence of Propidium Iodide was 5e7 more intense in unviable spores. The Dihydroethidium fluorescence increase was associated with faster growth. Control and low radiation doses allowed the germination and growth of spores, while higher doses led to growth inhibition and lower fluorescence.
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spelling Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal sporesFlow cytometrySpore viabilityFungal viabilityMetabolic activitySpore growthFilamentous fungiGamma radiationDihydroethidiumReactive oxygen speciesROSFlow cytometry is often used for viability and vitality assessment in bacteria and yeasts. However, its application to the study of fungal spore development is uncommon, probably due to the difficulties in successfully staining these cells. In the current study, we used flow cytometry for the first time to assess the effects of a disinfection treatment on the survival, growth and metabolic activity of fungal spores (Penicillium chrysogenum, Aspergillus nidulans and Aspergillus niger) submitted to gamma radiation (0e15 kGy). The Forward and Side-Scatter parameters of the cytometer were used to assess the differences in size and complexity of particles. Furthermore, two fluorescent dyes were used: Propidium Iodide to assess the membrane integrity and spore viability, in a culture-independent procedure; and Dihydroethidium to measure the changes in metabolic activity of irradiated spores in their first 10 h of growth in a liquid culture medium. Our results support that flow cytometry is a valuable tool in assessing different biological parameters and biocide effects, as it allowed accurate determination of the viability, growth and metabolic activity of gamma-irradiated spores. The fluorescence of Propidium Iodide was 5e7 more intense in unviable spores. The Dihydroethidium fluorescence increase was associated with faster growth. Control and low radiation doses allowed the germination and growth of spores, while higher doses led to growth inhibition and lower fluorescence.Elsevier Ltd.2013info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/25739http://hdl.handle.net/10316/25739https://doi.org/10.1016/j.ibiod.2012.05.008enghttp://www.sciencedirect.com/science/article/pii/S0964830512001084#Mesquita, N.Portugal, A.Piñar, G.Loureiro, J.Coutinho, A. P.Trovão, J.Nunes, I.Botelho, M. L.Freitas, H.info: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:RCAAP2021-08-30T10:23:25Zoai:estudogeral.uc.pt:10316/25739Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:56:05.145069Repositório 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 Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal spores
title Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal spores
spellingShingle Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal spores
Mesquita, N.
Flow cytometry
Spore viability
Fungal viability
Metabolic activity
Spore growth
Filamentous fungi
Gamma radiation
Dihydroethidium
Reactive oxygen species
ROS
title_short Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal spores
title_full Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal spores
title_fullStr Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal spores
title_full_unstemmed Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal spores
title_sort Flow cytometry as a tool to assess the effects of gamma radiation on the viability, growth and metabolic activity of fungal spores
author Mesquita, N.
author_facet Mesquita, N.
Portugal, A.
Piñar, G.
Loureiro, J.
Coutinho, A. P.
Trovão, J.
Nunes, I.
Botelho, M. L.
Freitas, H.
author_role author
author2 Portugal, A.
Piñar, G.
Loureiro, J.
Coutinho, A. P.
Trovão, J.
Nunes, I.
Botelho, M. L.
Freitas, H.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Mesquita, N.
Portugal, A.
Piñar, G.
Loureiro, J.
Coutinho, A. P.
Trovão, J.
Nunes, I.
Botelho, M. L.
Freitas, H.
dc.subject.por.fl_str_mv Flow cytometry
Spore viability
Fungal viability
Metabolic activity
Spore growth
Filamentous fungi
Gamma radiation
Dihydroethidium
Reactive oxygen species
ROS
topic Flow cytometry
Spore viability
Fungal viability
Metabolic activity
Spore growth
Filamentous fungi
Gamma radiation
Dihydroethidium
Reactive oxygen species
ROS
description Flow cytometry is often used for viability and vitality assessment in bacteria and yeasts. However, its application to the study of fungal spore development is uncommon, probably due to the difficulties in successfully staining these cells. In the current study, we used flow cytometry for the first time to assess the effects of a disinfection treatment on the survival, growth and metabolic activity of fungal spores (Penicillium chrysogenum, Aspergillus nidulans and Aspergillus niger) submitted to gamma radiation (0e15 kGy). The Forward and Side-Scatter parameters of the cytometer were used to assess the differences in size and complexity of particles. Furthermore, two fluorescent dyes were used: Propidium Iodide to assess the membrane integrity and spore viability, in a culture-independent procedure; and Dihydroethidium to measure the changes in metabolic activity of irradiated spores in their first 10 h of growth in a liquid culture medium. Our results support that flow cytometry is a valuable tool in assessing different biological parameters and biocide effects, as it allowed accurate determination of the viability, growth and metabolic activity of gamma-irradiated spores. The fluorescence of Propidium Iodide was 5e7 more intense in unviable spores. The Dihydroethidium fluorescence increase was associated with faster growth. Control and low radiation doses allowed the germination and growth of spores, while higher doses led to growth inhibition and lower fluorescence.
publishDate 2013
dc.date.none.fl_str_mv 2013
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/10316/25739
http://hdl.handle.net/10316/25739
https://doi.org/10.1016/j.ibiod.2012.05.008
url http://hdl.handle.net/10316/25739
https://doi.org/10.1016/j.ibiod.2012.05.008
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://www.sciencedirect.com/science/article/pii/S0964830512001084#
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Elsevier Ltd.
publisher.none.fl_str_mv Elsevier Ltd.
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
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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