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Persistence of Bacteroides ovatus under simulated sunlight irradiation

BACKGROUND: Bacteroides ovatus, a member of the genus Bacteroides, is considered for use in molecular-based methods as a general fecal indicator. However, knowledge on its fate and persistence after a fecal contamination event remains limited. In this study, the persistence of B. ovatus was evaluate...

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Autores principales: Dong, Shengkun, Hong, Pei-Ying, Nguyen, Thanh H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099502/
https://www.ncbi.nlm.nih.gov/pubmed/24993443
http://dx.doi.org/10.1186/1471-2180-14-178
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author Dong, Shengkun
Hong, Pei-Ying
Nguyen, Thanh H
author_facet Dong, Shengkun
Hong, Pei-Ying
Nguyen, Thanh H
author_sort Dong, Shengkun
collection PubMed
description BACKGROUND: Bacteroides ovatus, a member of the genus Bacteroides, is considered for use in molecular-based methods as a general fecal indicator. However, knowledge on its fate and persistence after a fecal contamination event remains limited. In this study, the persistence of B. ovatus was evaluated under simulated sunlight exposure and in conditions similar to freshwater and seawater. By combining propidium monoazide (PMA) treatment and quantitative polymerase chain reaction (qPCR) detection, the decay rates of B. ovatus were determined in the presence and absence of exogenous photosensitizers and in salinity up to 39.5 parts per thousand at 27°C. RESULTS: UVB was found to be important for B. ovatus decay, averaging a 4 log(10) of decay over 6 h of exposure without the presence of extracellular photosensitizers. The addition of NaNO(2), an exogenous sensitizer producing hydroxyl radicals, did not significantly change the decay rate of B. ovatus in both low and high salinity water, while the exogenous sensitizer algae organic matter (AOM) slowed down the decay of B. ovatus in low salinity water. At seawater salinity, the decay rate of B. ovatus was slower than that in low salinity water, except when both NaNO(2) and AOM were present. CONCLUSION: The results of laboratory experiments suggest that if B. ovatus is released into either freshwater or seawater environment in the evening, 50% of it may be intact by the next morning; if it is released at noon, only 50% may be intact after a mere 5 min of full spectrum irradiation on a clear day. This study provides a mechanistic understanding to some of the important environmental relevant factors that influenced the inactivation kinetics of B. ovatus in the presence of sunlight irradiation, and would facilitate the use of B. ovatus to indicate the occurrence of fecal contamination.
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spelling pubmed-40995022014-07-17 Persistence of Bacteroides ovatus under simulated sunlight irradiation Dong, Shengkun Hong, Pei-Ying Nguyen, Thanh H BMC Microbiol Research Article BACKGROUND: Bacteroides ovatus, a member of the genus Bacteroides, is considered for use in molecular-based methods as a general fecal indicator. However, knowledge on its fate and persistence after a fecal contamination event remains limited. In this study, the persistence of B. ovatus was evaluated under simulated sunlight exposure and in conditions similar to freshwater and seawater. By combining propidium monoazide (PMA) treatment and quantitative polymerase chain reaction (qPCR) detection, the decay rates of B. ovatus were determined in the presence and absence of exogenous photosensitizers and in salinity up to 39.5 parts per thousand at 27°C. RESULTS: UVB was found to be important for B. ovatus decay, averaging a 4 log(10) of decay over 6 h of exposure without the presence of extracellular photosensitizers. The addition of NaNO(2), an exogenous sensitizer producing hydroxyl radicals, did not significantly change the decay rate of B. ovatus in both low and high salinity water, while the exogenous sensitizer algae organic matter (AOM) slowed down the decay of B. ovatus in low salinity water. At seawater salinity, the decay rate of B. ovatus was slower than that in low salinity water, except when both NaNO(2) and AOM were present. CONCLUSION: The results of laboratory experiments suggest that if B. ovatus is released into either freshwater or seawater environment in the evening, 50% of it may be intact by the next morning; if it is released at noon, only 50% may be intact after a mere 5 min of full spectrum irradiation on a clear day. This study provides a mechanistic understanding to some of the important environmental relevant factors that influenced the inactivation kinetics of B. ovatus in the presence of sunlight irradiation, and would facilitate the use of B. ovatus to indicate the occurrence of fecal contamination. BioMed Central 2014-07-04 /pmc/articles/PMC4099502/ /pubmed/24993443 http://dx.doi.org/10.1186/1471-2180-14-178 Text en Copyright © 2014 Dong 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Dong, Shengkun
Hong, Pei-Ying
Nguyen, Thanh H
Persistence of Bacteroides ovatus under simulated sunlight irradiation
title Persistence of Bacteroides ovatus under simulated sunlight irradiation
title_full Persistence of Bacteroides ovatus under simulated sunlight irradiation
title_fullStr Persistence of Bacteroides ovatus under simulated sunlight irradiation
title_full_unstemmed Persistence of Bacteroides ovatus under simulated sunlight irradiation
title_short Persistence of Bacteroides ovatus under simulated sunlight irradiation
title_sort persistence of bacteroides ovatus under simulated sunlight irradiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099502/
https://www.ncbi.nlm.nih.gov/pubmed/24993443
http://dx.doi.org/10.1186/1471-2180-14-178
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