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Published on: August 12, 2017
Immunosuppression affects the severity of experimental Fusarium solani keratitis
Tzu G Wu1, Victor V Keasler, Bradley M Mitchell
1Sid W. Richardson Ocular Microbiology Laboratory, Cullen Eye Institute, Department of Ophthalmology, Baylor College of Medicine, Houston, Texas 77030, USA.
Abstract:
We have established a mouse model of corneal fusariosis that permits the evaluation of fungal infection and pathogenesis. Corneas of immunocompetent and cyclophosphamide-treated adult BALB/c mice were topically inoculated with Fusarium solani after corneal scarification. Eyes were scored for corneal involvement daily for 8 days and at 2 weeks after infection. Eyes were enucleated at various time points for quantitative fungal recovery and histopathological examination. An inoculum-dose response was observed in cyclophosphamide-treated mice, and fungi were recovered from the infected eyes by quantitative microbial culturing. Treatment with cyclophosphamide increased disease severity and delayed fungal clearance. Fungal hyphae, inflammatory cells, and stromal edema were histologically evident within corneal tissue and correlated with disease severity. Although the mouse cornea resists fungal infections, F. solani keratitis could be induced in immunosuppressed mice after surface scarification, which resulted in infection and clinical disease that could be evaluated both in vivo and in vitro.
Insights
This study establishes a mouse model for corneal fusariosis, demonstrating that immunosuppression enhances Fusarium solani keratitis development and progression, aiding infection evaluation.
Area of Science:
- Ophthalmology
- Mycology
- Immunology
Background:
- Corneal fusariosis is a severe fungal keratitis.
- Current models for studying Fusarium solani keratitis are limited.
- Understanding fungal pathogenesis is crucial for treatment.
Purpose of the Study:
- To establish and validate a mouse model for corneal fusariosis.
- To evaluate the role of immunosuppression in Fusarium solani keratitis.
- To enable in vivo and in vitro assessment of fungal keratitis.
Main Methods:
- BALB/c mice (immunocompetent and cyclophosphamide-treated) were inoculated with Fusarium solani after corneal scarification.
- Ocular scoring for disease severity was performed daily for 8 days and at 2 weeks.
- Fungal load was quantified via microbial culturing, and histopathology was conducted on corneal tissues.
Main Results:
- A dose-response relationship was observed in cyclophosphamide-treated mice.
- Cyclophosphamide treatment increased disease severity and delayed fungal clearance.
- Histopathology revealed fungal hyphae, inflammatory cells, and stromal edema correlating with disease severity.
Conclusions:
- A mouse model for corneal fusariosis was successfully established.
- Immunosuppression facilitates the induction and progression of Fusarium solani keratitis.
- This model allows for comprehensive evaluation of fungal keratitis in vivo and in vitro.
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