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. Author manuscript; available in PMC: 2019 May 1.
Published in final edited form as: J Immunol. 2018 Mar 21;200(9):3188–3200. doi: 10.4049/jimmunol.1700834

Fig. 4.

Fig. 4

S100A9 deficiency does not change survival or weight change after CLP, but does impair local bacterial clearance. There was no significant difference in survival after CLP in wild-type and S100A9−/− mice (A, Gehan-Breslow-Wilcoxon test, p=0.5). S100A9−/− mice lost and regained a similar percentage of baseline body weight after CLP as wild-type controls (B, 2-way ANOVA, p=0.0005 for effect of time, p=0.28 for effect of genotype). While there was no significant difference in intraperitoneal bacterial burden 3 days after CLP, S100A9−/− mice failed to clear intraperitoneal infection 7 days after CLP (C, 2-way ANOVA p<0.01 for interaction of time and genotype, Sidak’s p=0.003 at 7 days for differences among genotypes). Low levels of disseminated bacteria were detected in the spleen (D, 2-way ANOVA p=0.35) and brain (E, 2-way ANOVA p=0.08) but did not differ by genotype. ** p <0.01