Bacterial pathogens activate a common inflammatory pathway through IFNλ regulation of PDCD4

PLoS Pathog. 2013;9(10):e1003682. doi: 10.1371/journal.ppat.1003682. Epub 2013 Oct 3.

Abstract

The type III interferon (IFNλ) receptor IL-28R is abundantly expressed in the respiratory tract and has been shown essential for host defense against some viral pathogens, however no data are available concerning its role in the innate immune response to bacterial pathogens. Staphylococcus aureus and Pseudomonas aeruginosa induced significant production of IFNλ in the lung, and clearance of these bacteria from the lung was significantly increased in IL-28R null mice compared to controls. Improved bacterial clearance correlated with reduced lung pathology and a reduced ratio of pro- vs anti-inflammatory cytokines in the airway. In human epithelial cells IFNλ inhibited miR-21 via STAT3 resulting in upregulation of PDCD4, a protein known to promote inflammatory signaling. In vivo 18 hours following infection with either pathogen, miR-21 was significantly reduced and PDCD4 increased in the lungs of wild type compared to IL-28R null mice. Infection of PDCD4 null mice with USA300 resulted in improved clearance, reduced pathology, and reduced inflammatory cytokine production. These data suggest that during bacterial pneumonia IFNλ promotes inflammation by inhibiting miR-21 regulation of PDCD4.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins / biosynthesis*
  • Apoptosis Regulatory Proteins / genetics
  • Cell Line
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Humans
  • Lung / metabolism
  • Lung / microbiology
  • Lung / pathology
  • Mice
  • Mice, Knockout
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Pneumonia, Staphylococcal / genetics
  • Pneumonia, Staphylococcal / metabolism*
  • Pneumonia, Staphylococcal / pathology
  • Pseudomonas Infections / genetics
  • Pseudomonas Infections / metabolism*
  • Pseudomonas Infections / pathology
  • Pseudomonas aeruginosa / genetics
  • Pseudomonas aeruginosa / metabolism*
  • RNA-Binding Proteins / biosynthesis*
  • RNA-Binding Proteins / genetics
  • Respiratory Mucosa / metabolism*
  • Respiratory Mucosa / microbiology
  • Respiratory Mucosa / pathology
  • Staphylococcus aureus / genetics
  • Staphylococcus aureus / metabolism*

Substances

  • Apoptosis Regulatory Proteins
  • Cytokines
  • MIRN21 microRNA, human
  • MIRN21 microRNA, mouse
  • MicroRNAs
  • PDCD4 protein, human
  • Pdcd4 protein, mouse
  • RNA-Binding Proteins
  • interferon-lambda protein, mouse