Adsorption of MS2 bacteriophage on ultrafiltration membrane laboratory equipments

Virus adsorption has been quantified (i) on different materials including various containers made of glass, plastic or stainless steel and hollow fiber membranes made of polyethersulfone, polysulfone, PVDF or cellulose acetate (with two configurations: in/out and out/in and various molecular weight cut-offs); and (ii) on the filtration equipment. The selected virus is MS2 bacteriophage used as a model to estimate viral survival in water or to quantify virus elimination by membrane filtration. A series of experiments have been conducted with suspensions of MS2 at different concentrations prepared in a sterilized saline solution (8 g/L of KCl) or in sterilized distilled water. This study has shown that the most appropriate material to be used as a filtration test tank is Pyrex glass. We show that an addition of a virus solution 15 min after the beginning of the experiment allows keeping the virus concentration at a high level in the system (including tank, tubing,and pump). No adsorption was observed on membrane materials tested during soaking

Role of the cell-wall structure in the retention of bacteria by microfiltration membranes

This experimental study investigates the retention of bacteria by porous membranes. The transfer of bacteria larger than the nominal pore size of microfiltration track-etched membranes has been studied for several kinds of bacterial strains. This unexpected transfer does not correlate to the hydrophobicity,neither to the surface charge of the microorganism, as suggested in previous reports. We conclude that,in our conditions, the kind of bacteria (Gram-positive or Gram-negative) is finally the most important parameter. As the distinction between those two types of bacteria is related to the cell-wall structure, we provide an experimental evidence, via the action of an antibiotic, that the cell-wall flexibility triggers the transfer of the bacteria through artificial membranes, when the pores are smaller in size than the cell

Effects of membrane alterations on bacterial retention

The study shows the respective roles of skin and support of an ultrafiltration membrane in the retention mechanisms of bacteria (Escherichia coli). For this, pinholes defects of 5–200 μm in diameter were performed through ultrafiltration polymeric membranes and their impact was assessed on bacterialretention in a stirred cell when the transmembrane pressure is set at 0.5 bars. Various techniques have been used to make the defects such as a microhardness tester or femtosecond lasers. As long as the selective skin is not altered through its whole thickness, the membrane keeps a retention efficiency equivalent to the one of an uncompromised membrane. The retention by the macroporous support is also investigated. In case of membrane with defects of cylindrical geometry, experimental results are compared to calculated data obtained with a pore flow model, and the validity of this model is discussed

Potable water production by membrane processes: membrane characterization using a series of bacterial strains

The aim of this study was to develop a method for characterizing membranes (ultrafiltration and microfiltration) used in drinking water production. The method accounts for the specific behaviour of microorganisms during filtration, namely their deformation under mechanical stress. The leaks of microorganisms are linked to the presence of a small number of defects or abnormally large pores in the membrane structure. Assuming that the defects are cylindrical capillaries, the range of pore diameters concerned by the method lies between 0.05 and 1.2mm

Protocol for the assessment of viral retention capability of membranes

A series of experiments has been carried out to determine the Log removal value (LRV) of MS2 bacteriophages suspended in various buffers (osmosed water, tap water, aqueous solutions of NaCl and phosphate buffer solution) during filtration through hollow fiber membranes made of cellulose acetate. Viral concentrations in permeate and retentate were determined using two different methods, namely plaque forming unit (PFU) counting, which reveals only infectious particles and quantitative RT-PCR which detects the total (infectious + inactivated) number of viral genomes regardless of their infectivity.From this experimental study, we propose guidelines for preparing the challenging solutions and measuring their concentration which ensure a reliable assessment of the membrane performance