Addition of exogenous PLD did not enhance adhesion of the wild type (Figure 3A), suggesting that under these conditions, the effect of PLD on wild type adhesion is at saturation. As the exogenously-added

PLD is soluble and not Adriamycin bacterially-associated, this indicates that PLD cannot directly act as an adhesin. Bacterial invasion was not altered in the presence of exogenous PLD for either the wild type or pld mutant, suggesting that PLD does not play a direct role in invasion once the bacteria are adherent (Figure 3B). HeLa cell viability is reduced following invasion by PLD-expressing A. haemolyticum The viability of HeLa cells following invasion by A. haemolyticum strains was measured to determine whether PLD expressed intracellularly Selonsertib solubility dmso was cytotoxic. The viability of A. haemolyticum-inoculated HeLa cells was determined as a percentage

of uninoculated HeLa cells, which was set at 100%. Following invasion of host cells with wild type A. haemolyticum, only 15.6% of the HeLa cells remained viable after 5 h, compared with uninoculated HeLa cells (p < 0.05; Figure 4). The pld mutant displayed significantly reduced cytotoxicity with 82.3% of HeLa cells viable, as compared to the uninoculated control (p < 0.05; Figure 4). Invasion of HeLa cells with the complemented pld mutant resulted in 15.4% of HeLa cell viability, similar to that of the wild type (Figure 4). Initial measurements of HeLa viability at 2 h did not demonstrate a significant loss of host cell viability (data not shown). This is not

unexpected, as time is required for the invaded bacteria to synthesize and express PLD, and for PLD to exert its effects leading to the end-stage, measurable outcome of loss of host cell viability. Figure 4 PLD expressed inside HeLa cells is cytotoxic. HeLa cells were inoculated with A. haemolyticum strains and the bacteria were allowed Erastin research buy to adhere for 2 h and invade for 5 h prior to determination of host cell viability. Viability is shown as a percentage of that of JAK inhibition diluent-treated cells, which was set to 100%. Error bars indicate one standard deviation from the mean calculated from the averages of at least three independent experiments conducted in triplicate. These data indicated that invasion of HeLa cells by A. haemolyticum results in loss of host cell viability, with the majority of that being attributable to expression of PLD. Interestingly, when purified HIS-PLD was applied to the exterior of HeLa monolayers for 2-24 h, no HeLa cytotoxicity was detected over this time period, even at the highest concentrations of PLD (data not shown). A. haemolyticum PLD expressed inside HeLa cells results in host cell necrosis The mechanisms of host cell death following invasion of wild type A. haemolyticum were investigated. Apoptosis was determined by measurement of caspases 3/7, 8 and 9 activity, following inoculation of HeLa cells with A. haemolyticum strains. The levels of caspase 3/7, 8 or 9 activation of untreated HeLa cells were set at a nominal value of 1.