Morphological aspects of gastrointestinal tract invasion by Candida albicans in the infant mouse

G T Cole1, K R Seshan, L M Pope

  • 1Department of Botany, University of Texas, Austin 78713-7640.

Insights

The infant mouse model effectively simulates gastrointestinal candidosis. Candida albicans rapidly invades the jejunum, digests the mucus barrier, and enters cells with minimal host damage.

Area of Science:

  • Mycology
  • Gastroenterology
  • Infectious Diseases

Background:

  • Gastrointestinal candidosis is a significant clinical concern.
  • Infant mice offer a viable model for studying Candida albicans infections.
  • Understanding the early stages of fungal invasion is crucial for developing treatments.

Purpose of the Study:

  • To investigate the utility of the infant mouse model for studying gastrointestinal candidosis.
  • To elucidate the early mechanisms of Candida albicans invasion in the infant gastrointestinal tract.
  • To identify potential targets for therapeutic intervention.

Main Methods:

  • Oral-intragastric inoculation of 5-6-day-old mice with Candida albicans (CA30).
  • Histological and ultrastructural examinations of the gastrointestinal tract at various time points post-inoculation.
  • Assessment of fungal dissemination and host cell interaction.

Main Results:

  • Systemic spread of Candida albicans observed within 30 minutes post-inoculation.
  • Maximal mucosal invasion frequency in the jejunum 1-3 hours after inoculation.
  • Candida albicans demonstrated extracellular digestion of the mucus barrier and microvillus layer.
  • Intracellular invasion of columnar epithelial cells with minimal host cell disruption.
  • The infant mouse model is suitable for studying extracellular products of Candida albicans in vivo.

Conclusions:

  • The infant mouse model is highly effective for studying gastrointestinal candidosis.
  • Candida albicans employs a multi-step invasion strategy involving extracellular digestion and intracellular entry.
  • Further research using this model can identify key virulence factors for therapeutic targeting.