Immunostimulant (1 --> 3)-D-glucans from the cell wall of Cryphonectria parasitica (Murr.) Barr strain 263

A Molinaro1, R Lanzetta, A Mancino

  • 1Dipartimento di Chimica Organica e Biologica, Università di Napoli Federico II, Naples, Italy. molinaro@unina.it

Carbohydrate Research
|December 16, 2000
PubMed

Insights

This study identifies beta-D-glucans in the fungus Cryphonectria parasitica. These polysaccharides exhibit immunological activity, inducing tumor necrosis factor alpha and nitrite production.

Area of Science:

  • Mycology
  • Carbohydrate Chemistry
  • Immunology

Background:

  • The fungal cell wall is a complex structure crucial for fungal survival and pathogenicity.
  • Polysaccharides, particularly beta-D-glucans, are key components of fungal cell walls with diverse biological roles.
  • Cryphonectria parasitica is an important plant pathogen, and understanding its cell wall composition can reveal targets for control.

Purpose of the Study:

  • To characterize the water-soluble and water-insoluble polysaccharides from the cell wall of Cryphonectria parasitica strain 263.
  • To investigate the immunological activity of these isolated polysaccharide fractions.

Main Methods:

  • Extraction and purification of water-soluble and water-insoluble polysaccharide fractions.
  • Structural analysis of the glucans, including linkage analysis.
  • In vitro assays to assess the induction of immune mediators like tumor necrosis factor alpha (TNF-alpha) and nitrite (NO2-).

Main Results:

  • A (1 --> 3)-beta-D-glucan, with 30% beta-D-Glc-(1 --> 6) branching, was identified as the primary water-soluble component.
  • A (1 --> 3)-glucan containing both alpha and beta anomeric linkages was found in the water-insoluble fraction.
  • Both polysaccharide fractions demonstrated significant immunological activity.

Conclusions:

  • The cell wall of Cryphonectria parasitica contains distinct (1 --> 3)-beta-D-glucan structures.
  • These fungal beta-glucans can stimulate immune responses, evidenced by the induction of TNF-alpha and NO2-.
  • The identified polysaccharides represent potential targets for immunomodulatory therapies or diagnostic markers.