2023
DOI: 10.3389/fmicb.2023.1260460
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Assessing residential activity in a home plumbing system simulator: monitoring the occurrence and relationship of major opportunistic pathogens and phagocytic amoebas

Vicente Gomez-Alvarez,
Hodon Ryu,
Min Tang
et al.

Abstract: Opportunistic premise plumbing pathogens (OPPPs) have been detected in buildings’ plumbing systems causing waterborne disease outbreaks in the United States. In this study, we monitored the occurrence of OPPPs along with free-living amoeba (FLA) and investigated the effects of residential activities in a simulated home plumbing system (HPS). Water samples were collected from various locations in the HPS and analyzed for three major OPPPs: Legionella pneumophila, nontuberculous mycobacterial species (e.g., Myco… Show more

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Cited by 4 publications
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“…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).…”
mentioning
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).…”
mentioning
confidence: 99%