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. Author manuscript; available in PMC: 2018 May 10.
Published in final edited form as: Cell Host Microbe. 2017 May 10;21(5):592–602.e4. doi: 10.1016/j.chom.2017.04.002

Figure 2. ARM transplantation prevents the loss of intestinal homeostasis caused by antibiotic treatment.

Figure 2

(A) Experimental scheme for ARM administration. Three doses of PBS or ARM were administered daily by oral gavage to C57BL/6 ampicillin-treated mice beginning on day 2 of ampicillin treatment. Fecal samples were collected before antibiotics (d0) and on days 1 (prior to transplant), 4, 8 and 15 after antibiotic initiation. (B) Density of 16S rRNA gene copies in fecal samples over time (n = 5 mice per group). Box plots show the median, 25th percentile and 75th percentile; whiskers represent minimum and maximum values (*P = 0.0137, ***P = 0.0009, ****P > 0.0001, Student’s t test). (C) Difference in cecum size among the different groups. (D) Visualization of the inner mucus layer and goblet cells (Muc2) as well as all bacteria (16S rRNA gene) in colon cross-sections. Hoechst dye was used to visualize nuclei. Original magnification, 63X. Scale bars, 10μm. (E) Protein extracts from ileal tissues were analyzed by Western blotting with RegIIIγ-specific antiserum and anti-β-tubulin as loading control. (D–F) Representative images and samples from 5 mice per group are shown. See also Figure S2.