05; **, P < 0.005; ***, P < 0.0005). Error bars represent the standard error of the mean (SEM). Shown is a representative experiment BLI to identify

mutants with defects in dissemination or colonization One of the goals of this study was to determine whether mutants with a defect in colonization and/or dissemination could be identified by BLI. As proof of concept, we compared radiance from mice infected with Yplux + or YpΔcaf1ΔpsaAlux + mutant. Caf1 and PsaA previously were shown to play a role in dissemination and colonization in an additive manner [30]. The SC model of EPZ-6438 purchase infection and C57BL/6J mice were chosen for this comparison because the colonization phenotype of the Δcaf1ΔpsaA strain was originally tested using this model. BLI revealed that the Δcaf1ΔpsaA strain was attenuated in dissemination or colonization to deeper tissues from the LN, in agreement with previous work [30] (Figure 4A LGX818 cell line and B). Radiance measurements allowed us to determine that signal intensity in the neck was lower in animals infected with the double mutant strain in comparison to those infected with Yplux +, indicating that colonization of the LN by the Δcaf1ΔpsaAlux + mutant also was impaired compared to wild type, in agreement with previous work [30] (Figure 4C). Differences of radiance values from mice infected with Yplux + against Δcaf1ΔpsaAlux

+ attained statistical significance at 24, 48, 72 and 96 hpi (linear regression analysis of normalized values, P < 0.05). Mice infected

with the Δcaf1ΔpsaA strain never displayed detectible signal from the abdomen at any time point (Figure 4A). The radiance values from the abdomen of these mice were below background levels at each time point examined. These radiance values were subjected to regression analysis and determined to be significantly different from the values obtained from mice infected with Yplux + at 48, 72 and 96 hpi. To determine if the absence of signal in YpΔcaf1ΔpsaAlux +-infected mice was due to extremely low levels that were blocked by skin or other tissue, we dissected the mice and imaged isolated spleens and livers at 96 hpi. No signal was detected from the individual organs (Figure 4B). In addition, all animals infected with the Δcaf1ΔpsaA Flavopiridol (Alvocidib) mutant survived past 96 hpi and never showed any signs of disease. We continued to image these animals up to 168 hpi, and found that the signal from the neck never disappeared and that bacteria appeared to be contained at this site (data not shown). Overall, imaging from mice infected with YpΔcaf1ΔpsaAlux +confirmed previous findings in C57BL/6J where bacteria were detected in LN, but at lower numbers in comparison to mice infected with a wild type strain, and never or rarely were detected in spleens [30]. Discussion Plague is a disease with devastating effects on the host that are fatal if left untreated. These effects are the result of the FAK inhibitor ability that Y.