2019
DOI: 10.1186/s40168-019-0715-5
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Active eukaryotes in drinking water distribution systems of ground and surface waterworks

Abstract: Background Eukaryotes are ubiquitous in natural environments such as soil and freshwater. Little is known of their presence in drinking water distribution systems (DWDSs) or of the environmental conditions that affect their activity and survival. Methods Eukaryotes were characterized by Illumina high-throughput sequencing targeting 18S rRNA gene (DNA) that estimates the total community and the 18S rRNA gene transcript (RNA) that is more representative of the active part… Show more

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Cited by 29 publications
(53 citation statements)
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“…The nucleic acids from the water samples were extracted using a Chemagic DNA Plant Kit (Perkin Elmer, United States) as previously described in Inkinen et al (2019) . An All Prep DNA/RNA Mini Kit (Qiagen, United States) was used for RNA and DNA extraction from fecal samples according to Pitkänen et al (2013) .…”
Section: Methodsmentioning
confidence: 99%
“…The nucleic acids from the water samples were extracted using a Chemagic DNA Plant Kit (Perkin Elmer, United States) as previously described in Inkinen et al (2019) . An All Prep DNA/RNA Mini Kit (Qiagen, United States) was used for RNA and DNA extraction from fecal samples according to Pitkänen et al (2013) .…”
Section: Methodsmentioning
confidence: 99%
“…Finally, even tap water enables the dispersal of nematodes, as these and other meiobenthic organisms (e.g., rotifers, oligochaetes, gastrotrichs, flatworms, microcrustaceans) are present in drinking water distribution systems (Funch et al, 1995;Schreiber et al, 1997;Christensen, 2011;Inkinen et al, 2019). In fact, guideline values for finished water from the Netherlands (in 1993) and North America include the allowance of 0.3 and 2.5 nematodes/l (reviewed by Christensen, 2011).…”
Section: Gone With the Windmentioning
confidence: 99%
“…After incubation, the sample was centrifuged 10 000× g for 30 min at 4 °C and the pellet was suspended in PBS. Biofilm from water meters was detached and collected as previously described [34]. Before further analyses, all biofilm samples were sonicated for 1 min in 40 kHz (Branson Ultrasonics, Danbury, USA).…”
Section: Methodsmentioning
confidence: 99%
“…The nucleic acids were extracted using Chemagic DNA Plant kit (Perkin Elmer, Waltham, USA). Complementary DNA was synthesized as previously described (outbreak I) [34] or by using Superscript IV VILO (outbreak II, Thermo Fisher Scientific, Waltham, USA). MST markers (GenBac3 and HF183) were quantified using DNA-based qPCR assays and RNA-based RT-qPCR assays as described earlier by Pitkänen et al [27].…”
Section: Methodsmentioning
confidence: 99%