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dc.contributor.authorFykse, Else-Marie
dc.contributor.authorAarskaug, Tone
dc.contributor.authorBlatny, Janet Martha
dc.date.accessioned2017-10-31T12:01:38Z
dc.date.accessioned2017-11-01T09:03:15Z
dc.date.available2017-10-31T12:01:38Z
dc.date.available2017-11-01T09:03:15Z
dc.date.issued2014
dc.identifier.citationFykse E, Aarskaug T, Blatny JM. Detection of Legionella pneumophila in a biological treatment plant by co-cultivatiobn with Acanthamoeba castellanii. Current Environmental Engineering. 2014;1(2):91-99en_GB
dc.identifier.urihttp://hdl.handle.net/20.500.12242/768
dc.identifier.urihttps://ffi-publikasjoner.archive.knowledgearc.net/handle/20.500.12242/768
dc.descriptionFykse, Else-Marie; Aarskaug, Tone; Blatny, Janet Martha. Detection of Legionella pneumophila in a biological treatment plant by co-cultivatiobn with Acanthamoeba castellanii. Current Environmental Engineering 2014 ;Volum 1.(2) s. 91-99en_GB
dc.description.abstractLegionella pneumophila was identified in the aeration ponds of a biological wastewater treatment plant at the pulp and paper industry Borregaard, Sarpsborg, Norway. After 3 outbreaks of Legionaires’ disease reported in this area in 2005 and 2008, the aeration ponds were shut down by the Norwegian authorities in September 2008. During the shutdown of these ponds, September to December 2008, the viable counts of L. pneumophila decreased from 107 to < 10 CFU/mL measured using the International Standard growth (ISO11731) method. The aim of this work was to use amoebal coculture with Achantamoebae castellanii to recover and detect L. pneumophila from the complex microbial community in the pond during the shutdown period. This work shows that the viable counts of the environmental L. pneumophila ST 462 outbreak strain present in the pond samples during shutdown, was increased from 0-10 CFU/mL (no amoebae added) to 107 -108 CFU/mL in co-culture with A. castellanii. This indicates that pathogenic L. pneumophila isolates present in the environment may not be detected using standard culture methods. As a consequence, methodological improvements are needed to ensure more reliable detection and isolation of Legionella. By using amoebal co-culture, the concentration of L. pneumophila increased by 5-7 log units, allowing low concentrations and bacteria not detected using standard growth methods (according to the ISO11731), to be detected. Cells in the viable but non-culturable (VBNC) form will not be detected using the ISO 11731 standard culture method, and growth on agar media may be inhibited by other organisms and inhibitors present in complex environmental samples. The methodological procedure described in this paper may assist in providing a general more robust and sensitive approach to detect L. pneumophila in more complex environmental samples and may assist in providing improved hazard assessments.en_GB
dc.language.isoenen_GB
dc.titleDetection of Legionella pneumophila in a biological treatment plant by co-cultivatiobn with Acanthamoeba castellaniien_GB
dc.typeArticleen_GB
dc.date.updated2017-10-31T12:01:38Z
dc.identifier.cristinID1184610
dc.identifier.cristinID1184610
dc.identifier.doi10.2174/2212717801666140707161649#sthash.ZKqyNxkw.dpuf
dc.relation.projectIDForsvarets forskningsinstitutt: 1326
dc.source.issn2212-7178
dc.type.documentJournal article
dc.relation.journalCurrent Environmental Engineering


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