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Published on: February 7, 2013
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.
Abstract:
The Gram positive opportunistic human pathogen Staphylococcus aureus induces a variety of diseases including pneumonia. S. aureus is the second most isolated pathogen in cystic fibrosis patients and accounts for a large proportion of nosocomial pneumonia. Inside the lung, the human airway epithelium is the first line in defence with regard to microbial recognition and clearance as well as regulation of the immune response. The metabolic host response is, however, yet unknown. To address the question of whether the infection alters the metabolome and metabolic activity of airway epithelial cells, we used a metabolomics approach. The nutrition uptake by the human airway epithelial cell line A549 was monitored over time by proton magnetic resonance spectroscopy (¹H-NMR) and the intracellular metabolic fingerprints were investigated by gas chromatography and high performance liquid chromatography (GC-MS) and (HPLC-MS). To test the metabolic activity of the host cells, glutamine analogues and labelled precursors were applied after the infection. We found that A549 cells restrict uptake of essential nutrients from the medium after S. aureus infection. Moreover, the infection led to a shutdown of the purine and pyrimidine synthesis in the A549 host cell, whereas other metabolic routes such as the hexosamine biosynthesis pathway remained active. In summary, our data show that the infection with S. aureus negatively affects growth, alters the metabolic composition and specifically impacts the de novo nucleotide biosynthesis in this human airway epithelial cell model.
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.
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