meningitidis and this organism can

survive without LPS [23]. In E. coli, msbA was implicated in lipid A-core moiety flipping from the inner leaflet to outer leaflet of the inner membrane [24, 25], and then Imp/RlpB protein complex was responsible for transport of LPS from the periplasm to the outer leaflet of the outer membrane [17]. Here we showed that imp/ostA and msbA might be synergistic in hydrophobic drugs resistance and LPS transport in H. pylori. Methods Chemicals Glutaraldehyde was purchased from Electron Microscopy Sciences (Hatfield, PA). Chloramphenicol, erythromycin, kanamycin, novobiocin, MLN0128 molecular weight rifampicin, ethidium bromide, and carbonyl cyanide m-chlorophenylhydrazone (CCCP) were purchased from Sigma Chemical Co (St Louis, MO). Bacterial strains and culture conditions Clinical isolates were collected from National Taiwan University Hospital (NTUH) as Selleckchem MM-102 previously described [26]. H. pylori strains were grown on Columbia agar plates containing 5% sheep blood under microaerophilic conditions (5% O2, 10% CO2, and 85% N2) at 37°C. For microarray analysis, we selected a rapidly growing strain NTUH-S1 with a higher MIC (MIC = 6 μg/ml) to glutaraldehyde from a patient with gastritis to study gene expression. To screen for mutant strains, blood agar plates were supplemented with 4 μg/ml chloramphenicol or 10 μg/ml kanamycin. To screen for imp/ostA and msbA double deletion mutant or complementation strains, blood agar plates

were supplemented with 4 μg/ml chloramphenicol and 10 μg/ml kanamycin. Determination the MICs of glutaraldehyde and hydrophobic drugs in H. pylori The MICs of glutaraldehyde and hydrophobic drugs (erythromycin, novobiocin, rifampicin, and ethidium bromide) were determined by the agar dilution method. Suspension of H. pylori was adjusted to 107 cells/ml. Five

microliters of bacterial suspensions were spotted on blood agar plates supplemented with different Wee1 inhibitor concentrations of drugs. Results were observed after 72 h incubation under microaerophilic condition at 37°C. RNA slot blot hybridization Four strains with the MICs of 7–10 μg/ml glutaraldehyde (designed numbers 1~4), four with the MICs of 4–6 μg/ml glutaraldehyde (numbers 5~8), and three with the ALOX15 MICs of 1–3 μg/ml glutaraldehyde (numbers 9~11) were grown on Columbia blood agar plates for 48 h, and further passaged on Columbia blood agar plates or 0.5 μg/ml glutaraldehyde-containing blood agar plates for 48 h. Since 0.5 μg/ml was the half concentration of the minimum MIC for the 11 strains, we defined this as the induction concentration. Subsequently, RNA was extracted from the bacteria with or without glutaraldehyde treatment. Total RNA from each H. pylori clinical isolate was extracted as described previously [27]. Ten micrograms of total RNA was transferred onto a nylon membrane using a slot-blot system (Hoefer, Holliston, MA). The membrane was hybridized with DNA probes specific for 23S rRNA (0.