Gradual Recovery of Building Plumbing-Associated Microbial Communities after Extended Periods of Altered Water Demand during the COVID-19 Pandemic.
Solize VoslooLinxuan HuoUmang ChauhanIrmarie CottoBenjamin GincleyKatherine J VilardiBryan YoonKaiqin BianMarco GabrielliKelsey J PieperAron StubbinsAmeet J PintoPublished in: Environmental science & technology (2023)
COVID-19 pandemic-related building restrictions heightened drinking water microbiological safety concerns post-reopening due to the unprecedented nature of commercial building closures. Starting with phased reopening (i.e., June 2020), we sampled drinking water for 6 months from three commercial buildings with reduced water usage and four occupied residential households. Samples were analyzed using flow cytometry and full-length 16S rRNA gene sequencing along with comprehensive water chemistry characterization. Prolonged building closures resulted in 10-fold higher microbial cell counts in the commercial buildings [(2.95 ± 3.67) × 10 5 cells mL -1 ] than in residential households [(1.11 ± 0.58) × 10 4 cells mL -1 ] with majority intact cells. While flushing reduced cell counts and increased disinfection residuals, microbial communities in commercial buildings remained distinct from those in residential households on the basis of flow cytometric fingerprinting [Bray-Curtis dissimilarity ( d BC ) = 0.33 ± 0.07] and 16S rRNA gene sequencing ( d BC = 0.72 ± 0.20). An increase in water demand post-reopening resulted in gradual convergence in microbial communities in water samples collected from commercial buildings and residential households. Overall, we find that the gradual recovery of water demand played a key role in the recovery of building plumbing-associated microbial communities as compared to short-term flushing after extended periods of reduced water demand.
Keyphrases
- drinking water
- induced apoptosis
- single cell
- cell cycle arrest
- air pollution
- health risk
- flow cytometry
- health risk assessment
- cell death
- oxidative stress
- genome wide
- copy number
- stem cells
- microbial community
- bone marrow
- risk assessment
- mesenchymal stem cells
- transcription factor
- genome wide identification
- drug induced