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Image Search Results
Journal: Cell host & microbe
Article Title: Murine model of colonization with fungal pathogen Candida auris to explore skin tropism, host risk factors and therapeutic strategies.
doi: 10.1016/j.chom.2020.12.002
Figure Lengend Snippet: Figure 3. Immunodeficient Rag2–/– and Rag2–/–Il2rg–/– mice exhibit a greater propensity for C. auris skin colonization (A) IL-17A and IL-17F production by ILCs is increased in the skin of Rag2/ mice. Shown are numbers of IL-17A-producing (left panel) and IL-17F-producing (right panel) ILCs in the skin of WT and Rag2-deficient mice at steady state and 7 days after C. auris colonization. The statistics were calculated using the t test or Mann-Whitney U test, as appropriate. n = 6–9 mice for each group; two independent experiments. Data are mean ± SEM. (B) Rag2/ mice are defective in controlling C. auris colonization on the ear skin surface (CFU/swab) and within the tissue compartment (CFU/gram of tissue). The statistics were calculated using the t test or Mann-Whitney U test, as appropriate. n = 9–10 mice for each group; two independent experiments. (C) Immunodeficient Rag2/Il2rg/ mice are defective in clearing C. auris from the ear and back skin surface (CFU/swab) and tissue (CFU/gram of tissue); and intestinal compartments (CFU/gram of intestinal content) as determined by culturing from WT and Rag2/Il2rg/ mice 2 weeks after topical colonization. The statistics were calculated using the Mann-Whitney U test. n = 5 mice for each group, representative of two independent experiments. Data are shown with mean ± SEM. See also Figures S4G and S4H. (D) Longitudinally, WT and Rag2/Il2rg/ mouse skin swabs were cultured for C. auris on days 4, 10, 17, 24, and 32, and extended through days 59, 91, and 119 for Rag2/Il2rg/ mice. The Mann-Whitney U test was used to compare between WT and Rag2/Il2rg/ mice at each time point up to day 32. n = 6 mice for each group, representative of three independent experiments. Data are shown with mean ± SEM. (E) Immunodeficient Rag2/Il2rg/ mice are defective in clearing C. auris from the ear and back skin tissues (CFU/gram of tissue); and intestinal compartments (CFU/gram of intestinal content) as measured by culturing from WT and Rag2/Il2rg/ mice 208 days after topical association. No C. auris colonies were cultured from WT mice on day 208. n = 6 mice for each group, representative of three independent experiments. Data are shown with mean ± SEM. ND, not detected.
Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Yeast Extract-Peptone-Dextrose (YPD) Broth BD Bioscience Cat # 242820 eBioscience Fixation/Permeabilization Concentrate eBioscience Cat #00-5123-43 eBioscience Fixation/Permeabilization Diluent eBioscience Cat #00-5223-56 eBioscience Permeabilization Buffer (10X) eBioscience Cat #00-8333-56 Experimental Models: Organisms/Strains Diabetic mice (db/db) NIAID
Techniques: MANN-WHITNEY, Cell Culture
Journal: Cell host & microbe
Article Title: Murine model of colonization with fungal pathogen Candida auris to explore skin tropism, host risk factors and therapeutic strategies.
doi: 10.1016/j.chom.2020.12.002
Figure Lengend Snippet: Figure 4. Skin antiseptic chlorhexidine pro- tects WT mice from C. auris colonization and promotes C. auris decolonization of Rag2–/–Il2rg–/– mice (A) Schematic for experimental design to model CHG skin bathing. Wipes impregnated with CHG were used daily for 4 days to ‘‘bathe’’ the mouse skin before topical association. A cotton gauze saturated with sterile PBS was used as the proce- dural control. C. auris cells were topically associ- ated onto mouse ear pinna and dorsal back skin at two concentrations: 107 CFU as medium concen- tration, and 109 CFU as high concentration. After topical association, CHG was applied every other day for the duration of the experiment. Skin swabs were taken during the experiment and skin tissues were disaggregated at the end of the experiment and processed for C. auris culturing. (B) CHG bathing protects WT mouse skin from C. auris topical exposure (medium and high con- centrations) as measured by culturing skin swabs. n = 4 mice for each group, representative of two independent experiments. (C) CHG bathing protects WT mouse skin tissue from C. auris residence after topical exposure (me- dium and high concentrations). n = 4 mice for each group, representative of two independent experi- ments. (D) Schematic for experimental design to model CHG skin bathing to promote C. auris decoloniza- tion. After C. auris (medium and high concentra- tions) topical association, daily bathing with CHG was deployed for 1 week. Skin swabs were taken during the experiment and skin tissues were dis- aggregated at the end of the experiment for culturing. (E) CHG bathing promotes C. auris decolonization on Rag2/Il2rg/ ear skin swabs 4 and 10 days after high concentration topical exposure. The sta- tistics were calculated using the t test. n = 5 mice for each group, representative of two independent experiments. (F) CHG bathing promotes C. auris decolonization in Rag2/Il2rg/ resident skin tissue after medium and high concentration topical exposure. n = 5 mice for each group, representative of two independent experiments. See also Table S3. The statistics for (B), (C), (E), and (F) were calculated using the t test. *p < 0.05, **p < 0.01.
Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Yeast Extract-Peptone-Dextrose (YPD) Broth BD Bioscience Cat # 242820 eBioscience Fixation/Permeabilization Concentrate eBioscience Cat #00-5123-43 eBioscience Fixation/Permeabilization Diluent eBioscience Cat #00-5223-56 eBioscience Permeabilization Buffer (10X) eBioscience Cat #00-8333-56 Experimental Models: Organisms/Strains Diabetic mice (db/db) NIAID
Techniques: Sterility, Control, Concentration Assay