Also, C. jejuni bacteria have been observed in the haemocoel and gut of infected larvae, and have been demonstrated to induce damage to the Selleck 17-AAG midgut [36]. In this study,

we demonstrate that G. mellonella is susceptible to infection with H. pylori and may represent a valuable model to identify virulence factors and pathogenic mechanisms of H. pylori. Methods Bacterial strains and growth conditions A total of eleven H. pylori strains were included in this study. In particular, we used: a) the wild-type H. pylori strain G27 (VacA+/cagPAI+/urease+) and its isogenic mutants in which selleck screening library the cagA (G27ΔcagA) or cagE (G27ΔcagE) gene or the entire cagPAI (G27ΔcagPAI) were disrupted by insertional mutagenesis [3,37]; b) the wild-type H. pylori strain 60190 (ATCC 49503; VacA + s1/i1/m1/cagPAI+/urease+) and its isogenic mutants in which vacA (60190ΔvacA), or cagA (60190ΔcagA), or cagE (60190ΔcagE) were disrupted by insertional mutagenesis [38,39]

as well as its urease-negative spontaneous mutant urease (60190 Urease-negative) [40]; c) the mouse-adapted H. pylori strain M5 and its GGT-defective isogenic mutant (M5ggt::aph) in which ggt was disrupted by insertional mutagenesis [8]. Bacteria were cultured on Columbia agar supplemented with 10% defibrinated horse blood, 1% Vitox and Skirrow’s supplement under microaerophilic conditions in anaerobic jars PF-6463922 price with microaerobic System CampyGen (all from Oxoid, Milan, Italy) at 37°C for 3 days. Preparation of broth culture filtrates (BCFs) BCFs were prepared as previously described [41,42]. Briefly, bacteria were grown in Brucella broth medium supplemented with 1% Vitox and Skirrow as well as 5% heat-inactivated fetal calf serum (FCS; Sigma-Aldrich, Milan, Italy) in anaerobic jars with microaerobic System CampyGen with gentle shaking (150 oscillations/min) for 24–48 h at 37°C. When bacterial suspensions reached 1.0 optical density units at 450 nm (corresponding to a bacterial concentration of 5 × 108 colony-forming units (CFUs/ml), bacteria were removed by centrifugation

(12,000 g SB-3CT for 15 min), and the supernatants were sterilized by filtering through a 0.22-μm-pore-size cellulose acetate filter (Sartorius Minisart SM 16534, Sigma-Aldrich) to obtain BCFs. Purification and use of VacA toxin VacA (s1/m1 genotype) was purified by ammonium sulphate precipitation and gel filtration chromatography from wild-type H. pylori 60190 strain grown in Brucella broth in which foetal calf serum was replaced by 0.2% β-cyclodextrins (Sigma-Aldrich) [43,44]. Purified VacA was stored in melting ice and, immediately before use on G. mellonella larvae, was activated or not by dropwise acidification to pH 3.0 with 0.2 N HCl. Vacuolating activity of purified VacA was determined by means of neutral red uptake as previously described [45].