Rhinovirus infection induces degradation of antimicrobial peptides and secondary bacterial infection in chronic obstructive pulmonary disease

Am J Respir Crit Care Med. 2012 Dec 1;186(11):1117-24. doi: 10.1164/rccm.201205-0806OC. Epub 2012 Sep 28.

Abstract

Rationale: Chronic obstructive pulmonary disease (COPD) exacerbations are associated with virus (mostly rhinovirus) and bacterial infections, but it is not known whether rhinovirus infections precipitate secondary bacterial infections.

Objectives: To investigate relationships between rhinovirus infection and bacterial infection and the role of antimicrobial peptides in COPD exacerbations.

Methods: We infected subjects with moderate COPD and smokers and nonsmokers with normal lung function with rhinovirus. Induced sputum was collected before and repeatedly after rhinovirus infection and virus and bacterial loads measured with quantitative polymerase chain reaction and culture. The antimicrobial peptides secretory leukoprotease inhibitor (SLPI), elafin, pentraxin, LL-37, α-defensins and β-defensin-2, and the protease neutrophil elastase were measured in sputum supernatants.

Measurements and main results: After rhinovirus infection, secondary bacterial infection was detected in 60% of subjects with COPD, 9.5% of smokers, and 10% of nonsmokers (P < 0.001). Sputum virus load peaked on Days 5-9 and bacterial load on Day 15. Sputum neutrophil elastase was significantly increased and SLPI and elafin significantly reduced after rhinovirus infection exclusively in subjects with COPD with secondary bacterial infections, and SLPI and elafin levels correlated inversely with bacterial load.

Conclusions: Rhinovirus infections are frequently followed by secondary bacterial infections in COPD and cleavage of the antimicrobial peptides SLPI and elafin by virus-induced neutrophil elastase may precipitate these secondary bacterial infections. Therapy targeting neutrophil elastase or enhancing innate immunity may be useful novel therapies for prevention of secondary bacterial infections in virus-induced COPD exacerbations.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Analysis of Variance
  • Antimicrobial Cationic Peptides / metabolism*
  • Bacterial Infections / etiology
  • Bacterial Infections / physiopathology
  • C-Reactive Protein / analysis
  • C-Reactive Protein / metabolism
  • Cohort Studies
  • Coinfection / etiology*
  • Coinfection / physiopathology
  • Disease Progression
  • Elafin / analysis
  • Elafin / metabolism
  • Female
  • Humans
  • Inflammation Mediators / analysis
  • Male
  • Middle Aged
  • Picornaviridae Infections / complications*
  • Picornaviridae Infections / physiopathology
  • Polymerase Chain Reaction / methods
  • Prognosis
  • Prospective Studies
  • Pulmonary Disease, Chronic Obstructive / complications
  • Pulmonary Disease, Chronic Obstructive / microbiology*
  • Pulmonary Disease, Chronic Obstructive / virology*
  • Rhinovirus*
  • Risk Assessment
  • Secretory Leukocyte Peptidase Inhibitor / analysis
  • Secretory Leukocyte Peptidase Inhibitor / metabolism
  • Serum Amyloid P-Component / analysis
  • Serum Amyloid P-Component / metabolism
  • Severity of Illness Index
  • Smoking
  • Sputum / cytology
  • Statistics, Nonparametric

Substances

  • Antimicrobial Cationic Peptides
  • Elafin
  • Inflammation Mediators
  • Secretory Leukocyte Peptidase Inhibitor
  • Serum Amyloid P-Component
  • PTX3 protein
  • C-Reactive Protein