Staphylococcus aureus Infection Reduces Nutrition Uptake and Nucleotide Biosynthesis in a Human Airway Epithelial

Philipp Gierok1, Manuela Harms2, Karen Methling3

  • 1Institute of Biochemistry, University of Greifswald, 17487 Greifswald, Germany. gierokp47@uni-greifswald.de.

Metabolites
|November 12, 2016
PubMed

Insights

Staphylococcus aureus infection restricts nutrient uptake and shuts down nucleotide synthesis in airway epithelial cells. This study reveals how the host cell metabolome is altered during bacterial pneumonia.

Area of Science:

  • Microbiology
  • Cell Biology
  • Metabolomics

Background:

  • Staphylococcus aureus is a significant cause of pneumonia, particularly in hospital-acquired infections and cystic fibrosis patients.
  • The human airway epithelium acts as a primary defense against pathogens, but the host's metabolic response to S. aureus infection remains unclear.

Purpose of the Study:

  • To investigate the metabolic alterations in human airway epithelial cells upon S. aureus infection.
  • To understand how S. aureus impacts host cell metabolism and nutrient utilization.

Main Methods:

  • Utilized a metabolomics approach on the A549 human airway epithelial cell line.
  • Monitored nutrient uptake using proton magnetic resonance spectroscopy (¹H-NMR).
  • Analyzed intracellular metabolic fingerprints via gas chromatography-mass spectrometry (GC-MS) and high-performance liquid chromatography-mass spectrometry (HPLC-MS).

Main Results:

  • S. aureus infection led to restricted uptake of essential nutrients by A549 cells.
  • The infection caused a shutdown of de novo purine and pyrimidine synthesis.
  • The hexosamine biosynthesis pathway remained active despite the infection.

Conclusions:

  • S. aureus infection negatively impacts airway epithelial cell growth and metabolic composition.
  • The study highlights a specific impact on de novo nucleotide biosynthesis in host cells during infection.
  • These findings provide insights into the host metabolic response to S. aureus pneumonia.