2022
DOI: 10.1128/spectrum.02158-22
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Exploring the Impacts of Full-Scale Distribution System Orthophosphate Corrosion Control Implementation on the Microbial Ecology of Hydrologically Connected Urban Streams

Abstract: Elevated lead levels in drinking water supplies are a public health risk. As such, it is imperative for cities to urgently address lead contamination from aging drinking water supplies by way of lead service line replacements and corrosion control methods.

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Cited by 3 publications
(3 citation statements)
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“…DNA was extracted from the stored filters using the FastDNA Spin Kit (MP Biomedicals, Solon, OH) and stored at −20 °C until use. The density (number of gene copies per unit volume of sample) of total bacteria and Cyanobacteria was determined using digital droplet PCR (ddPCR) as previously described . Additional ddPCR assays for L.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…DNA was extracted from the stored filters using the FastDNA Spin Kit (MP Biomedicals, Solon, OH) and stored at −20 °C until use. The density (number of gene copies per unit volume of sample) of total bacteria and Cyanobacteria was determined using digital droplet PCR (ddPCR) as previously described . Additional ddPCR assays for L.…”
Section: Methodsmentioning
confidence: 99%
“…The density (number of gene copies per unit volume of sample) of total bacteria and Cyanobacteria was determined using digital droplet PCR (ddPCR) as previously described. 32 Additional ddPCR assays for L. pneumophila (Lmip gene), 33 P. aeruginosa (Orpl gene), 34 and NTM (atpE gene) 35 were conducted using previously published primers ( 16S rRNA Gene Amplicon Sequencing. 16S rRNA gene amplicon (V4−V5 hypervariable region) library preparation and sequencing were performed on all samples (collected DWDS samples and negative controls) at Argonne National Laboratory following the Illumina Earth Microbiome Protocol.…”
Section: Sample Information and Orthophosphate Additionmentioning
confidence: 99%
“…Such regional differences could result in underestimating risk if the most appropriate species are not targeted (56,57). Due to the difficulties in identifying NTM to the species-or complex-level, drinking water studies often quantify total NTM, with many targeting the ATP synthase subunit c (atpE) gene (15,(58)(59)(60), or only investigating one or a few species of concern, such as M. avium or Mycobacterium intracellulare (19,22,61,62). Identification of NTM to the species level in colonies from plate culture is typically done using PCR and Sanger sequencing targeting genes such as β-subunit of RNA polymerase (rpoB) or heat shock protein 65 (hsp65) (63)(64)(65)(66).…”
Section: Introductionmentioning
confidence: 99%