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. 2016 Nov 21;82(24):7185–7196. doi: 10.1128/AEM.02238-16

FIG 4.

FIG 4

sEPSneg is not protective in a T cell transfer colitis model. Following receipt of CD4+ CD25 CD45RBhi T cells, C.B-17 SCID mice were orally administered B. longum 35624 (n = 8), sEPScomp (n = 8), or sEPSneg (n = 8). (A) Weight loss and disease activity were monitored over time. Statistical significance was determined using two-way ANOVA (*, P < 0.05). (B) Following euthanasia, the colon/body weight ratio was determined. A representative picture of colons from B. longum 35624- and sEPSneg-treated animals is provided. (C) The percentages of IL-17+, IFN-γ+, and IL-10+ lymphocytes from mesenteric lymph nodes are illustrated (n = 8 mice per group). Data are presented as box-and-whisker plots with the median values and maximum/minimum values illustrated. Statistical significance was determined using the Kruskal-Wallis test and Dunn's multiple-comparison test (*, P < 0.05 for sEPSneg strain versus the other strains). Error bars show standard deviations.