Nontypeable Haemophilus influenzae initiates formation of neutrophil extracellular traps

Richard A Juneau1, Bing Pang, Kristin E D Weimer

  • 1Department of Microbiology and Immunology, Wake Forest University Health Sciences, 5053 Hanes Building, 1000 Medical Center Boulevard, Winston-Salem, NC 27157, USA.

Infection and Immunity
|October 20, 2010
PubMed

Insights

Nontypeable Haemophilus influenzae (NTHI) triggers neutrophil extracellular traps (NETs) but resists killing within them. This resistance, mediated by lipooligosaccharides, allows NTHI persistence in chronic infections like otitis media.

Area of Science:

  • Microbiology
  • Immunology
  • Infectious Diseases

Background:

  • Nontypeable Haemophilus influenzae (NTHI) causes chronic and recurrent otitis media.
  • Bacterial biofilms, including host neutrophil extracellular traps (NETs), contribute to persistent infections.
  • NTHI survives within NETs, suggesting a role in disease chronicity.

Purpose of the Study:

  • To investigate how NTHI initiates NET formation.
  • To determine if NTHI components contribute to NET induction.
  • To understand NTHI resistance to NET-mediated killing.

Main Methods:

  • In vitro model system using NTHI strains and components.
  • Assessment of NET formation induced by viable/nonviable NTHI, DNA, outer membrane proteins, and lipooligosaccharide (endotoxin).
  • Evaluation of NTHI survival and killing within NETs and by phagocytic neutrophils.

Main Results:

  • Both viable and nonviable NTHI, along with bacterial DNA, outer membrane proteins, and endotoxin, induced NET formation.
  • NTHI endotoxin showed potent NET-inducing activity.
  • NTHI within NETs resisted extracellular and phagocytic killing due to lipooligosaccharide structures.

Conclusions:

  • NTHI utilizes multiple pathogen-associated molecular patterns, primarily endotoxin, to elicit NET formation.
  • NTHI's resistance to NET-mediated killing, attributed to lipooligosaccharides, is a key determinant for persistence.
  • NETs may provide a protective niche for NTHI in the middle ear, contributing to chronic otitis media.

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