Similar results were obtained when studies were conducted with MH-S cells and JAWSII cells (not shown). Although the reasons underlying the greater recovery of spores from infections conducted under non-germinating www.selleckchem.com/products/VX-770.html conditions are not clear, we speculate that germinated spores might be more susceptible than dormant spores to killing after uptake from the cell surface. This potential explanation is consistent with earlier reports that spores that had been intentionally pre-germinated prior to exposure to mammalian cells were more readily killed than dormant spores upon uptake into mammalian cells [20, 22]. These results support the idea that the germination state of B. anthracis spores

SP600125 is a critical determinant of the PX-478 fate of the intracellular bacteria. Figure 6 The germination state of spores influences the viability of intracellular B. anthracis. RAW264.7 cells were incubated for 30 min with dormant B. anthracis spores

(MOI 10) in DMEM in the presence (+, black bars) or absence (-, white bars) of FBS (10%), or, with pre-germinated spores (MOI 10) in DMEM in the absence of FBS (grey bars). B. anthracis spores were pre-germinated by incubation for 30 min in PBS pH 7.2 supplemented with L-alanine and L-inosine (both at 10 mM), and then washed twice with PBS pH 7.2 to remove germinants. After 30 min, the cells were washed to remove extracellular B. anthracis, and then further incubated with cAMP FBS (10%) and, as described under “”Methods,”" with gentamicin to germinate and kill any remaining spores that had not been germinated. After 15 min, the cells were washed and then further incubated in the absence of gentamicin. At 5, 60, or 240 min after removal of gentamicin, as indicated, the RAW264.7 cells were lysed, and the lysates were evaluated for viable B. anthracis, as described under Materials and Methods. The data were rendered as the fold-change in recoverable CFU in the absence or presence of FBS, relative to cells at 5 min

post infection in the absence of FBS. The rendered data were combined from three independent experiments, each conducted in triplicate. Error bars indicate standard deviations. The P values were calculated to evaluate the statistical significance of the differences in recoverable CFU between cells infected in the absence or presence of FBS. Germination state of B. anthracis spores influences the viability of RAW264.7 cells during in vitro infection The greater number of viable, intracellular B. anthracis recovered from cells infected under non-germinating conditions (Figure 6) prompted us to examine whether the viability of infected host cells might also be influenced by the germination state of spores during uptake. To evaluate this issue, RAW264.7 cells were incubated with B. anthracis spores (MOI 10) in the presence or absence of FBS (10%). Subsequent to employing the same gentamicin-protection procedure used for monitoring intracellular B.