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. Author manuscript; available in PMC: 2015 Sep 15.
Published in final edited form as: J Immunol. 2014 Aug 11;193(6):3055–3069. doi: 10.4049/jimmunol.1301548

Figure 4. Pglyrp3−/−Nod2−/− mice have changes in intestinal bacterial flora, however only Pglyrp3-dependent changes contribute to the increased sensitivity to colitis in Pglyrp3−/− Nod2−/− mice.

Figure 4

(A) Changes in the composition of bacterial flora in the stools of WT and knockout mice in all Eubacteria and the indicated bacterial groups, measured by qPCR; (B) WT germ-free mice were treated with 4% DSS and gavaged daily with stool homogenates from conventionally raised WT, Nod2−/−, Pglyrp3−/−, or Pglyrp3−/−Nod2−/− mice or (C) Nod2−/− mice were pre-treated with antibiotics for 3 weeks and then gavaged daily with stool homogenates from conventionally raised WT or Pglyrp3−/− and treated with 4% DSS. Development of colitis in B and C was evaluated by measuring survival, body weight, and stool score. Gross rectal bleeding in mice gavaged with stools from Pglyrp3−/− mice but not from WT mice is shown in (C). The results are means ± SEM of (A) 18 mice/group and (B and C) 6 mice/group from 2 experiments. Significance of differences for (A) *, knockout versus WT; (B) *, Pglyrp3−/− versus Nod2−/− and WT; #, Pglyrp3−/−Nod2−/− versus Nod2−/− and WT; ^, Pglyrp3−/−Nod2−/− versus Pglyrp3−/−; (C) *, Pglyrp3−/− versus WT; *, #, ^, P ≤ 0.05; **, ##, ^^, P ≤ 0.005.