Pseudomonas aeruginosa alginate is a potent secretagogue in the isolated ferret trachea

C Kishioka1, K Okamoto, D J Hassett

  • 1Mie University School of Medicine, Tsu, Japan.

Pediatric Pulmonology
|April 23, 1999
PubMed

Insights

Pseudomonas aeruginosa alginate, found in cystic fibrosis (CF) airways, stimulates airway mucus and lysozyme secretion. This suggests alginate contributes to CF lung disease progression and respiratory issues.

Area of Science:

  • Pulmonary Medicine
  • Microbiology
  • Biochemistry

Background:

  • Airway mucus hypersecretion is a key response to infection and inflammation.
  • Pseudomonas aeruginosa infection, particularly mucoid strains producing alginate, is prevalent in advanced cystic fibrosis (CF).

Purpose of the Study:

  • To investigate if Pseudomonas aeruginosa alginate stimulates mucus and lysozyme secretion from ferret tracheal cells.
  • To assess alginate's effect at concentrations relevant to the CF airway environment.

Main Methods:

  • Isolated ferret tracheal segments were used.
  • Sandwich enzyme-linked lectin assay (ELLA) measured mucin secretion.
  • Spectrophotometry measured lysozyme secretion.

Main Results:

  • Purified Pseudomonas aeruginosa alginate significantly stimulated mucin secretion (+111%) and lysozyme secretion (+20%) in a dose-dependent manner.
  • Stimulation occurred at 200 microg/mL alginate concentration.
  • No proteolytic activity or ultrastructural damage was observed.

Conclusions:

  • Pseudomonas aeruginosa alginate can directly stimulate mucin and lysozyme secretion in the trachea.
  • Alginate may be a contributing factor to mucus hypersecretion and respiratory morbidity in CF patients with P. aeruginosa infection.

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