(A–B) Il1β−/− mice orally infected with ΔslrP were fed ad libitum (n=6) or given restricted amounts of food (n=6). ΔslrP-infected B6 mice (n=5) were fed ad libitum. Weight loss (A) and survival (B) were measured.
(C) Heat map of differentially expressed genes in the hypothalamus of wt (n=3) and ΔslrP (n=3) infected B6 mice 48hr post-infection.
(D) Quantitative PCR analysis of genes identified in (C) in the hypothalamus of B6 mice infected with wt (n=4) or ΔslrP (n=4) and Il1β−/− (n=10) mice infected with ΔslrP ST for 48hr.
(E) Feeding of ΔslrP-infected vagotomized or sham B6 mice. Values normalized to feeding amounts of uninfected mice. n=9–10/group. Data represent 2 independent experiments combined.
(F) Quantitative PCR analysis of genes identified in (C) in the hypothalamus of ΔslrP-infected vagotomized or sham B6 mice at 48hrs post-infection. n=4–5/group.
(G) Levels of mature IL-1β were determined by IL-1R reporter assay 48hr post-infection in SI of ΔslrP-infected vagotomized or sham B6 mice. Graph shown depicts reporter fluorescence (arbitrary units), indicative of active IL-1β. n=4–5/group.
****p<0.0001, ***<0.01, **p<0.05, *p=0.05. Unpaired student t-test, one-sample t test, or Log rank analysis for survival. Error bars indicate +/− SEM. Il1β for (D) is from hypothalamus from 48hr and 72hr. See Figure S4 and S5.