Pipe materials appear to play an important role in the development of biofilms in drinking water distribution systems. However, there is controversy as to whether pipe materials shape the composition and diversity of bacterial communities in biofilms. To investigate the long-term effects of pipe materials on biofilms, triplicate samples of mature biofilms on unplasticized polyvinyl chloride (PVC-U), grey cast iron and asbestos cement (pipe age > 40 years) were obtained from three areas of an unchlorinated drinking water distribution system in the Netherlands. Illumina sequencing was performed and 773 OTUs (730 OTUs-814 OTUs) were detected within the biofilms on the three pipe materials, all of which were dominated by Proteobacteria (36.2%-46.1%). Both the alpha and beta diversity results showed that the bacterial communities of the biofilms formed on different pipe materials were highly similar. The neutral community model revealed that the assembly of the biofilm communities was governed by environmental selection rather than neutral processes. Among the 142 shared OTUs between the water and biofilm samples, there were 25 enriched OTUs (e.g., OTU7, assigned as Nitrospira spp.), which accounted for 62.6% of the total sequences, while 16 OTUs were disadvantaged (e.g., OTU14 and OTU40, assigned as Hyphomicrobiaceae), accounting for 2.2% of the sequences. Based on the findings, we propose and discuss a harmonisation process by which biofilms with significant differences due to the pipe material harmonize over time resulting in biofilms with similar bacterial communities. Our findings provide valuable insights into long-term biofilm development, bridging an essential gap in our current understanding of the influence of pipe materials on biofilm communities. These findings also highlight the importance of long-term studies and point to a potentially masked harmonizing process during biofilm development over years/decades.

Drinking water quality deteriorates from treatment plant to customer taps, especially in the plumbing system. There is no direct evidence about what the differences are contributed by plumbing system. This study compared the water quality in the water main and at customer tap by preparing a sampling tap on the water main. The biomass was quantified by adenosine triphosphate (ATP) and the microbial community was profiled by 454 pyrosequencing. The results showed that in distribution pipes, biofilm contributed >94% of the total biomass, while loose deposits showed little contribution (< 2%) because of the low amount of loose deposits. The distribution of biological stable water had minor effects on the microbiocidal water quality regarding both quantity (ATP 1 ng/L vs. 1.7 ng/L) and community of the bacteria. Whereas the plumbing system has significant contribution to the increase of active biomass (1.7 ng/L vs. 2.9 ng/L) and the changes of bacterial community. The relative abundance of Sphingomonas spp. at tap (22%) was higher than that at water main (2%), while the relative abundance of Pseudomonas spp. in tap water (15%) was lower than that in the water from street water main (29%). Though only one location was prepared and studied, the present study showed that the protocol of making sampling tap on water main offered directly evidences about the impacts of plumbing system on tap water quality, which makes it possible to distinguish and study the processes in distribution system and plumbing system separately.

Slow sand filters (SSFs) are widely applied to treat potable water; the removal of contaminants (e.g., particles, organic matter, and microorganism) occurs primarily in the top layer. However, the development of the microbial community and its metabolic function is still poorly understood. In the present study, we analyzed the microbial quantity and community of the influents sampled from the effluent of the last step (rapid sand filtration) and of the top layers of SSFs (Schmutzdecke, 0–2 cm, 4–6 cm, 8–10 cm) sampled near terminal head loss when the Schmutzdecke (SCM) was most developed in two full-scale drinking water treatment plants (DWTPs). The two DWTPs use the same artificially recharged groundwater source. The biomass in the filter, quantified by flow cytometric intact cell counts (ICC) and adenosine triphosphate (ATP), decreased rapidly along the depth till 8–10 cm (>1 log TCC; >75% ATP); the decrease was most pronounced from the SCM to the surface sand layer (0–2 cm), after which the biomass stabilized quickly at lower depths (2–10 cm). Remarkably, beta diversity showed that SSFs layers of the same depth in two DWTPs with distinctive filter age and plant location clustered together, which indicated their insignificant effects in shaping microbial communities in SSFs. The alpha diversity indices followed the trend of the biomass, suggesting more active and diverse communities in SCM layer. PICRUSt-based function prediction revealed significant over-representation of metabolism and degradation of complex organic matters (e.g., butanoate, propanoate, xenobiotic, D-Alanine, chloroalkene, and bisphenol) in SCM layer, the functional importance of which was confirmed by the co-occurrence patterns of the dominant taxa and metabolic functions. Using an island biogeography model, we found that microbial communities in SSFs were strongly assembled by selection (68 OTUs, 50.0% sequences), rather than by simple accumulation of the microbial communities in the influents (120 OTUs, 44.8% sequences). Our findings enhance the understanding of microbial community assembly and of metabolic function in the top layers of SSFs, and constitute a valuable contribution to optimizing the design and operation of biofilters in full-scale DWTPs.