Characterization of Staphylococcus aureus isolates from pediatric patients with cystic fibrosis

Ying Liu1,2, Jiang Zhang1, Dengke Zhong1,2

  • 1Shanghai Vocational College of Agriculture and Forestry , Shanghai, China.

Insights

Staphylococcus aureus in cystic fibrosis (CF) patients shows varied antibiotic resistance and virulence. ST typing may predict the cytotoxicity and invasion potential of these respiratory pathogens.

Area of Science:

  • Medical Microbiology
  • Infectious Diseases
  • Genomics

Background:

  • Staphylococcus aureus is a significant respiratory pathogen in cystic fibrosis (CF) patients.
  • Understanding S. aureus isolate characteristics is crucial for managing CF lung infections.

Purpose of the Study:

  • To characterize S. aureus isolates from CF patients.
  • To investigate the relationship between sequence types (STs) and isolate virulence factors.

Main Methods:

  • Antibiotic susceptibility testing.
  • Cytotoxicity assays and epithelial cell invasion assays.
  • Multilocus sequence typing (MLST).

Main Results:

  • Most isolates were penicillin-resistant but sensitive to vancomycin and minocycline.
  • 90% of isolates carried enterotoxin genes (sea, hlg).
  • Distinct cytotoxic and invasion capacities were observed among isolates; specific STs (e.g., ST5, ST30) showed lower toxicity and invasion potential.

Conclusions:

  • S. aureus isolates from CF patients exhibit diverse antibiotic resistance and virulence profiles.
  • Sequence typing (ST) may serve as a predictive tool for S. aureus cytotoxicity and invasion in CF patients.

Related Concept Videos

Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
1000
Cystic Fibrosis: Management01:24

Cystic Fibrosis: Management

Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
603
Bacterial Phylum Actinobacteria01:30

Bacterial Phylum Actinobacteria

Coryneform bacteria are gram-positive, aerobic, nonmotile rods that exhibit irregular, club-shaped, or V-shaped arrangements. Their V-shape results from snapping division, where the inner cell wall layer forms the cross-wall, while the outer layer remains intact until it ruptures on one side, causing the daughter cells to bend away.The primary genera are Corynebacterium and Arthrobacter. Corynebacterium includes diverse species, ranging from saprophytes to pathogens like Corynebacterium...
806