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. 2022 Feb 22;7(4):e152690. doi: 10.1172/jci.insight.152690

Figure 2. Fibrotic lung disease impairs MRSA clearance 14 and 21 days after bleomycin treatment.

Figure 2

(A) Mice were treated with bleomycin or saline 14 days prior to infection with MRSA (7 × 107 CFU/mouse). Lung bacterial burden was quantified 1–4 days after infection. (B) Lung bacterial burden from mice described in A. Bacterial burden was quantified at specified time points (n = 5 mice per group). Representative of 2 independent experiments. Data represent the means ± SD. Statistical analysis by multiple Student’s t tests. *P < 0.05, **P < 0.01, ***P < 0.001. (C) Mice were treated with saline or bleomycin and then infected with 1 × 107 CFU MRSA 14 or 20 days after bleomycin treatment. Lung bacterial burden was quantified 24 hours postinfection (day 15 or day 21). Saline-treated mice were infected on day 20 and MRSA was quantified on day 21. (D) Lung bacterial burden from mice described in C (saline + MRSA n = 5, bleomycin + MRSA day 14 n = 6, bleomycin + MRSA day 20 n = 4). Representative of 2 independent experiments. Data represent the means ± SD. Statistical analysis by Kruskal-Wallis test with Dunn’s multiple comparisons. *P < 0.05. (E) Spleen bacterial burden from mice infected with 1 × 107 CFU MRSA 20 days after bleomycin (n = 9) or saline (n = 10) treatment. CFU measured 24 hours postinfection. Data from 2 combined independent experiments. Data represent the means ± SD. Statistical analysis by Mann-Whitney U test. ****P < 0.0001. LOD, limit of detection.