Fungal Keratitis (FK) Model

Huateng Bio offers validated Fusarium solani-induced fungal keratitis models in C57BL/6 mice. Features 48h infection progression, slit-lamp scoring, and ISO-compliant protocols. Ideal for ophthalmic drug development. Download validation data.

Model Name
Fungal Keratitis (FK) Model
Animal Strains
C57BL/6J Mice (8-month-old males, 24 ± 2 g)

Model Description

Fungal keratitis (FK), a vision-threatening corneal infection prevalent among agricultural workers, is predominantly caused by Fusarium and Aspergillus species following plant-related trauma. Our model replicates human FK pathophysiology through controlled Fusarium solani inoculation, achieving:

  • Rapid infection progression: Corneal opacity ≥Grade 2 within 48 hours
  • Stromal invasion: Fungal hyphae penetration confirmed by confocal microscopy
  • High clinical relevance: Mimics trauma-induced infections in young adults
  •  

Key Advantages:
✓ Species-specific pathogenicity: Fusarium solani (ATCC 36031)
✓ Standardized scarification protocol: 95% infection success rate
✓ Drug validation compatibility: Responsive to natamycin/voriconazole

 


Applications

• Antifungal drug efficacy testing (azoles, polyenes)
• Immune response modulation studies (neutrophil recruitment, cytokine profiling)
• Novel diagnostic tool development (PCR-based fungal detection)
• Corneal healing mechanism research

 


Modeling Protocol —— Corneal Scarification & Fungal Inoculation

1. Pre-op Screening:

Slit-lamp exam to exclude mice with pre-existing ocular abnormalities

2. Infection Induction:

  • Corneal scarification: Create 1mm-diameter cross-shaped stromal scratches with sterile blade
  • Fungal inoculation: Apply 5μL Fusarium solani conidial suspension (1×10⁶ CFU/mL)
  • Post-op ofloxacin ointment BID ×2 days

3. Monitoring:

  • Daily slit-lamp scoring (opacity/edema/ulceration)
  • Humane endpoint: Perforation risk or severe inflammation

Validation & Testing

Category

Parameters

Slit-Lamp Scoring

• Opacity: 0 (clear) - 4 (complete obscuration)
• Edema/Ulceration: 0-3 scale

In Vivo Imaging

Laser scanning confocal microscopy: Fungal hyphae density ∙ Stromal infiltration depth

Histopathology

PAS staining: Hyphal invasion ∙ H&E: Neutrophil infiltration grading

Microbiological Confirmation

Corneal culture ∙ qPCR (Fusarium 28S rRNA)


Technical Advantages

Feature

Our Model

Alternative Models

Speed

48h disease progression

5-7 day models

Pathogen Specificity

Fusarium solani (clinical isolate)

Non-specific Candida models

Ethical Compliance

AAALAC-approved endpoints

Uncontrolled ulceration risks

 


 

Send Us A Message