Fig. 4: Eosinophil-driven goblet cell induction promotes innate defence against enteric pathogens. | Nature

Fig. 4: Eosinophil-driven goblet cell induction promotes innate defence against enteric pathogens.

From: Eosinophils drive intestinal remodelling and innate defence in reproduction

Fig. 4: Eosinophil-driven goblet cell induction promotes innate defence against enteric pathogens.The alternative text for this image may have been generated using AI.

a, Schematic of the experiment of oral infection of lactating dams and controls with foodborne pathogens. b,c, Infection with 2 × 107 Y. pseudotuberculosis. b, Left, faecal burden at 6 h for control (n = 15) and lactating (n = 23) mice. Right, kinetics for control (n = 13, 12, 12 for days 1, 2, 3) and lactating (n = 13, 13, 20 for days 1, 2, 3) mice. c, Dissemination at day 3. Top, frequency of mice with detectable pathogen. Bottom, splenic burden. n = 24 control mice; n = 20 lactating mice. d,e, Infection with 106 L. monocytogenes. d, Left, faecal burden at 6 h (n = 9). Right, kinetics for control (n = 9, 8, 9 for days 1, 2, 3) and lactating (n = 9) mice. e, Dissemination at day 3. Top, frequency of mice with detectable pathogen. Bottom, pathogen burden (n = 9). fh, Infection with 106 S. Typhimurium. f, Left, faecal burden at 6 h (n = 15). Right, kinetics for control (n = 9, 8, 10 for days 1, 2, 5) and lactating (n = 6, 6, 12 for days 1, 2, 5) mice. g, Dissemination at day 5 for control (n = 15) and lactating (n = 14) mice. h, Survival curves. im, Eosinophil depletion using anti-CCR3 in timed-pregnant dams followed by infection with Y. pseudotuberculosis (j,k) or S. Typhimurium during lactation (l,m). j, Left, faecal burden at 6 h for control mice (n = 10) and mice given an isotype (n = 11) or anti-CCR3 (n = 12) antibody. Right, kinetics for control mice (n = 10, 5, 8 for days 1, 2, 3) and mice given an isotype (n = 11) or anti-CCR3 (n = 12, 13, 12 for days 1, 2, 3) antibody. k, Dissemination at day 3. Top, frequency of mice with detectable pathogen. Bottom, splenic burden. n = 19 for control, n = 18 for isotype, n = 24 for anti-CCR3. l, Faecal burden at 6 h for control mice (n = 15) and mice given an isotype (n = 15) or anti-CCR3 (n = 16) antibody. m, Dissemination at day 3 for control mice (n = 15) and mice given an isotype (n = 15) or anti-CCR3 (n = 16) antibody. Data are pooled from at least two independent experiments. Each dot represents an individual mouse (except kinetics). Error bars are the mean ± s.d. Significance analysis: two-tailed unpaired Student’s t-test (bh), one-way ANOVA (jm) or Fisher’s exact test for frequency (c). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. Icons in a and i created in BioRender; Huang, C. https://BioRender.com/pmrvxbl (2026).

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