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. Author manuscript; available in PMC: 2023 Sep 1.
Published in final edited form as: Mol Microbiol. 2022 Aug 15;118(3):125–144. doi: 10.1111/mmi.14968

Figure 10. l-serine catabolism provides a greater fitness advantage to P. mirabilis within the catheterized urinary tract than d-serine catabolism.

Figure 10.

Wild-type P. mirabilis, the l-serine catabolism mutant (ΔsdaAB) and the triple mutant (ΔsdaABΔdsdA) were cultured in LB broth overnight, washed once in PBS, and adjusted to 2×106 CFU/ml. (A) Female CBA/J mice were transurethrally inoculated with 50 μl containing 1×105 CFU of either WT (n=12), ΔsdaAB (n=11), or ΔsdaABΔdsdA (n=10), and a 4 mm segment of silicone catheter tubing was advanced into the bladder during inoculation. Mice were euthanized 96 hours post-inoculation (hpi), and bacterial burden was determined in the urine, bladder, kidneys, and spleen. Each symbol represents the Log10 CFU per milliliter of urine or gram of tissue from an individual mouse, gray bars represent the median, and the dashed line indicates the limit of detection. ***P<0.01 by nonparametric Mann-Whitney test. (B-D) CBA/J mice were inoculated as above with the following 50:50 mixtures and euthanized at the indicated time points: (B) WT and ΔsdaAB (n=10, 96 hpi); (C) WT and ΔsdaABΔdsdA (n=10, 48 hpi); and (D) ΔdsdA and ΔsdaAB (n=10, 96 hpi). Each symbol represents the Log10 CFU per milliliter of urine or gram of tissue from an individual mouse, with CFUs of each strain recovered from an individual mouse connected by a black line. A competitive index was also calculated for each co-challenge, in which each symbol represents the Log10 CI for an individual mouse, error bars represent the median, and the dashed line indicates Log10 CI=0 (the expected value if the ratio of the indicated strains is 1:1). *P<0.05, **P<0.01 by Wilcoxon signed-rank test.