L. pneumophila can remain cultivable for at least 32 days although less cultivable when associated with Acidovorax sp. and Sphingomonas sp. The experiments with H. pylori demonstrated that this pathogen loses cultivability in less than 24 hours when in mono-species or in dual-species biofilms with V. paradoxus, Acidovorax sp. and Brevundimonas sp., while retaining cultivability for at least 24 hours when biofilms are grown in the presence of M. chelonae and Sphingomonas

sp. Consequently, M. chelonae seems to have a positive effect on the cultivability of both pathogens and being a pathogen commonly found in drinking water systems [60, 61], can play an important role in the control of these two pathogens. Control of this mycobacterial opportunistic pathogen and other biofilm species that can have a LCL161 cell line synergetic effect on L. pneumophila and H. pylori might provide an important contribution towards the supply of safe drinking water as both L. pneumophila and H. pylori have been found to be chlorine resistant [62, 63]. Methods Culture maintenance In this work, L. pneumophila NCTC 12821 and H. pylori NCTC 11637 strains were used. Strains of V. paradoxus, M. chelonae, Acidovorax sp., Sphingomonas sp. and Brevundimonas sp. were isolated from drinking water biofilms [28, 29]. All strains were maintained in vials frozen at Defactinib supplier -80°C and recovered by standard plating procedures onto the appropriate media and JQEZ5 cell line subcultured

once prior to biofilm

formation experiments. L. pneumophila NCTC 12821, V. paradoxus and M. chelonae were grown on Buffered Charcoal Yeast Extract (BCYE) agar (Oxoid, UK) for 24 hours at 30°C. Acidovorax sp. and Sphingomonas sp. were grown on R2A (Oxoid, UK) for 48 hours at 22°C. H. pylori NCTC 11637 and Brevundimonas sp. were grown on Columbia Agar (Oxoid, UK) supplemented with 5% (v/v) defibrinated horse blood (CBA) (Oxoid, UK) and incubated for 48 hours at 37°C in a microaerophilic atmosphere of 10% CO2, 7% H2 and 3% O2 (the remainder being N2). Auto- and co-aggregation in Mannose-binding protein-associated serine protease test tubes Prior to the start of the experiments tap water from Southampton, UK, was collected in a transparent flask and left, loosely closed, overnight for chlorine evaporation. Then the water was sterilized by filtration through a 0.2 μm pore size Nylon filter (Pall Gelman, UK). All bacterial species were suspended in this dechlorinated and filtered tap water, with the following characteristics, provided by the water company (Southern Water, UK): pH 7.3; turbidity 0.10 FTU; conductivity 504 μS cm-1; total organic carbon 0.649 mg l-1; total iron 16 μg Fe l-1; free chlorine 0.21 mg Cl2 l-1; total chlorine 0.26 mg Cl2 l-1. The inocula had a final concentration of approximately 2 × 108 cells ml-1. For autoaggregation, 3 ml of each suspension was transferred into a sterile test tube, whereas for co-aggregation experiments 1.5 ml of either L. pneumophila or H. pylori suspension were mixed with 1.