90%, 10.57%, I-BET-762 price and 17.68%, in LB with 0, 150, and 300 mM NaCl, respectively). While the mutant had less invasion efficiency, the result clearly demonstrated that increasing salt concentration from 0 to 150 or 300 mM NaCl led to significantly improved invasion of B. pseudomallei mutant into A549 cells as it is observed for the wild type strain (Figure 2). Figure 2 Invasion of A549 epithelial

cells by B. pseudomallei. A549 cells were infected with overnight cultures of B. pseudomallei K96243 at MOI of 100, SDO mutant, and complement strains grown in NaCl-free LB broth, LB broth with 150 mM NaCl, or LB broth with 300 mM. Intracellular bacteria were counted after lysing infected cells at 4 hrs post-infection. Asterisks indicate significant differences (p-value ≤ 0.05, t-test) between groups. Error bars represent standard errors of mean for CFTRinh-172 chemical structure experiments performed in triplicate. The ability of B. pseudomallei to survive and replicate intracellularly DMXAA may be attributable

to the successful evasion of cellular killing strategies. We next examined the intracellular survival of the B. pseudomallei wild type and the SDO mutant within macrophages. The macrophage cells were chosen for this experiment because B. pseudomallei can be uptaken and multiply within these cells, and resist their bactericidal response [21, 22]. The mutant showed fewer intracellular bacteria within the J774A.1 macrophage cell line during the initial stages of infection – up to 6 hrs (p -value ≤ 0.05) (Figure 3). The intracellular doubling time of the B. pseudomallei SDO mutant pre-exposure to 0, 150, and 300 mM NaCl was 41.83 ± 1.71, 45.41 ± 2.66, and 50.41 ±

1.33%. In contrast, the doubling time of the wild type bacteria next was 32.50 ± 4.29, 36.39 ± 1.44, and 47.23 ± 2.31% in LB with 0, 150, and 300 mM NaCl. The SDO complement strain recovered the growth of the SDO mutant with a rate similar to the wild type at an early time. Our data suggests that SDO plays an important role during the early phase of B. pseudomallei infection. It is possible the mutagenesis of SDO impaired the invasion of B. pseudomallei into A549 epithelial cells, and delayed initial multiplication within J774A.1 macrophage cells. Figure 3 Intracellular survival of B. pseudomallei in J774A.1 macrophages. J774A.1 cells were infected with overnight cultures of B. pseudomallei K96243 at MOI of 2, SDO mutant and complement strain grown in NaCl-free LB broth, LB broth with 150 mM NaCl, or LB broth with 300 mM. Intracellular bacteria were counted after lysing infected cells at 3, 6 and 9 hrs post-infection. Asterisks indicate significant differences (p-value ≤ 0.05, t-test) between groups. Error bars represent standard errors of mean for experiments performed in triplicate. SDO is not essential for B.