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. 2020 Nov 9;9:e55615. doi: 10.7554/eLife.55615

Figure 3. Mr1-/- mice had higher sepsis-induced mortality and bacterial burden compared to wild type mice.

(A) Age-matched Mr1-/- and WT mice (n = 15 per group) underwent CLP to induce polymicrobial sepsis. Survival was recorded over a period of 4–5 days (WT versus Mr1-/- mice, ***p=0.0007). Data represent two independent experiments. Statistical analysis was performed using the Log-rank (Mantel-Cox) test. (B) Blood was collected from WT and Mr1-/- mice (n = 8–10 per group) 18 hr post-CLP, and serial dilutions were plated on Luria Broth (LB) agar plates. Colony-forming units (CFU) were determined 24 hr after plating and were expressed as CFU/mL. Statistical analysis was performed using the Mann-Whitney test. (C) The bedding transfer procedure (detailed in Materials and methods section) was used to exchange gut microbiome between age-matched Mr1-/- and WT mice (total n = 31 for Mr1-/- mice and total n = 30 for WT mice) before inducing sepsis by CLP. Survival was recorded over a period of 4–5 days (WT versus Mr1-/- mice, *p=0.03). Data represent three independent experiments. Statistical analysis was performed using the Log-rank (Mantel-Cox) test.

Figure 3.

Figure 3—figure supplement 1. Mr1-/- mice had significantly higher mortality from ExPEC sepsis, compared to WT mice.

Figure 3—figure supplement 1.

Graph shows survival curves after intraperitoneal injection with 1 × 106 CFU of extraintestinal pathogenic Escherichia coli (ExPEC) F11 strain. Statistical analysis was performed using the Log-rank (Mantel-Cox) test.