Efficiency of a multi-barrier household system for surface water treatment combining a household slow sand filter to a Mesita Azul® ultraviolet disinfection device.

Low-cost household technologies for water treatment are crucial to improving drinking water quality and preventing health, social and economic impacts, mostly in middle- and low-income regions. This work assessed the removal efficiency of physical-chemical and bacteriological parameters from river water by a multi-barrier household water treatment system for 113 consecutive days. This system combines a pre-treatment step through a non-woven synthetic blanket, filtration by an intermittent household slow sand filter (HSSF) and a Mesita Azul® ultraviolet disinfection device. In general, the water quality was improved by the evaluated system. Turbidity was removed by an average of 73% (ranging from 33 to 94%), total coliforms (TC) of 3.88 log10 (ranging from 2.22 to 5.16 log10) and E. coli of 2.49 log10 (ranging from 1.81 to 3.30 log10). Filtration improvement was mostly correlated to HSSF biofilm development and influent water quality. Characterisation of HSSF schmutzdecke demonstrated a predominance of organic content, and a higher presence of carbohydrates than proteins on the sand and the blanket. Ultraviolet disinfection with Mesita Azul® inactivated most of the remaining bacteria after filtration and no regrowth was observed after 15 days of disinfection. In conclusion, the multi-barrier household water treatment system was efficient in treating river water, reducing risks of microbial contamination to achieve safe drinking water.

Effect of UV light on the inactivation of recombinant human adenovirus and murine norovirus seeded in seawater in shellfish depuration tanks.

Shellfish depuration is a process that aims to eliminate pathogens from mollusk tissues. Seawater disinfection during the depuration process is important and ultraviolet (UV) light treatment is the most used method worldwide. Viral models are usually employed as surrogates of fastidious viruses in viability studies. The aim of this study was to employ methods based on green fluorescent protein (GFP) fluorescence and plaque forming units to detect, respectively, recombinant adenovirus (rAdV-GFP) and murine norovirus (MNV) artificially seeded in environmental matrices. These assays were applied to assess the inactivation of rAdV-GFP and MNV in seawater in recirculation shellfish depuration tanks with and without UV light treatment. Kinetics of rAdV GFP-expression was previously measured by UV-spectrophotometer. Flow cytometry (FC), fluorescence microscopy (FM), and plaque assay were used to determine virus titer and detection limits. The influence of the environmental matrix on the performance of the methods was prior determined using either drinking water or filtered seawater seeded with rAdV-GFP. Disinfection of seeded seawater was evaluated with and without UV treatment. The time of 24-h post-infection was established as ideal for fluorescence detection on rAdV-GFP infected cells. FC showed lower sensitivity, when compared to FM, which was similar to plaque assay. Seawater disinfection on depuration tanks was promising and rAdV-GFP declined 99.99 % after 24 and 48 h with and without UV treatment, respectively. MNV was completely inactivated after 24 h in both treatments. As conclusion, the depuration tanks were effective to inactivate rAdV-GFP and MNV and the UV disinfection treatment accelerated the process.