Staphylococcus epidermidis and Staphylococcus aureus trigger different interleukin-8 and intercellular adhesion molecule-1 in lung cells: implications for inflammatory complications following neonatal sepsis

Acta Paediatr. 2013 Oct;102(10):1010-6. doi: 10.1111/apa.12350. Epub 2013 Aug 5.

Abstract

Aim: Staphylococci are a major contribution for neonatal sepsis, which is the main risk factor for bronchopulmonary dysplasia. This study investigated the expression of pro-inflammatory mediators in endothelial and respiratory cells from newborns exposed to staphylococci.

Methods: Human vascular endothelial cells and small airway epithelial cells were incubated with neonatal blood isolates of Staphylococcus epidermidis (n = 14) and Staphylococcus aureus (n = 14). The extracellular release of IL-8, IL-10, sICAM-1, ICAM-1 mRNA and the expression of membrane bound ICAM-1 were assessed by ELISA, RT-PCR and immunofluorescence microscopy.

Results: Staphylococcus epidermidis induced higher levels of IL-8 (mean 38.5 ng/mL) and ICAM-1 mRNA (mean ratio 1.037) in the small airway epithelial cells than S. aureus (IL-8 mean 22.2 ng/mL, p < 0.01 and ICAM-1 mRNA mean ratio 0.715, p < 0.01). In the endothelial cells, ICAM-1 remained more integrated in the cell membranes after exposure to S. epidermidis compared with S. aureus, which induced disintegration and release of soluble ICAM-1 into the supernatants.

Conclusion: Staphylococcus epidermidis induced a higher chemoattractive response than S. aureus. A persistent transmigration of granulocytes into the lung tissue in neonatal S. epidermidis sepsis might contribute to the development of bronchopulmonary dysplasia.

Keywords: Bronchopulmonary dysplasia; ICAM-1; Interleukin-8; Neonatal sepsis; Staphylococci.

MeSH terms

  • Biomarkers / metabolism
  • Cells, Cultured
  • Endothelial Cells / metabolism*
  • Endothelial Cells / microbiology
  • Enzyme-Linked Immunosorbent Assay
  • Fluorescent Antibody Technique
  • Humans
  • Infant, Newborn
  • Intercellular Adhesion Molecule-1 / metabolism*
  • Interleukin-10 / metabolism
  • Interleukin-8 / metabolism*
  • Real-Time Polymerase Chain Reaction
  • Respiratory Mucosa / metabolism*
  • Respiratory Mucosa / microbiology
  • Sepsis / metabolism
  • Staphylococcal Infections / metabolism*
  • Staphylococcus aureus / isolation & purification
  • Staphylococcus aureus / pathogenicity*
  • Staphylococcus epidermidis / isolation & purification
  • Staphylococcus epidermidis / pathogenicity*

Substances

  • Biomarkers
  • IL10 protein, human
  • Interleukin-8
  • Intercellular Adhesion Molecule-1
  • Interleukin-10