Haemophilus influenzae biofilm formation in chronic otitis media with effusion

Helen Van Hoecke1, Ann-Sophie De Paepe2, Edward Lambert2

  • 1Department of Otorhinolaryngology, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium. helen.vanhoecke@ugent.be.

Insights

Chronic otitis media with effusion (COME) in children often involves bacteria in the middle ear fluid and adenoids. Biofilms, particularly Haemophilus influenzae, are present and may drive COME pathogenesis.

Area of Science:

  • Microbiology
  • Pediatric Otolaryngology
  • Infectious Diseases

Background:

  • Otitis media with effusion (OME) is common in children, but its causes and the role of bacteria remain unclear.
  • Chronic OME (COME) presents persistent challenges in pediatric ear health.
  • Understanding the bacterial presence and organization in COME is crucial for effective treatment.

Purpose of the Study:

  • To identify otopathogenic bacteria in middle ear effusion (MEE) and adenoids of children with COME.
  • To investigate the in vivo formation of bacterial biofilms, especially Haemophilus influenzae, in MEE.
  • To explore the link between adenoid bacteria and middle ear infections.

Main Methods:

  • Bacterial culturing and genotyping of MEE and adenoid samples from 21 COME patients.
  • Fluorescence in situ hybridization (FISH) and confocal laser scanning microscopy (CLSM) to visualize biofilms.
  • Analysis of bacterial species and genotype concordance between MEE and adenoid.

Main Results:

  • 64.7% of MEE samples and 100% of adenoid samples were culture-positive for otopathogens.
  • Haemophilus influenzae and Streptococcus pneumoniae were frequently detected in MEE and adenoids, respectively.
  • Biofilm structures of H. influenzae were visualized in 5 out of 8 culture-positive MEE samples.

Conclusions:

  • Adenoids serve as a reservoir for bacteria implicated in COME.
  • Bacterial biofilms, often involving H. influenzae, are present in the middle ear fluid of children with COME.
  • Biofilms likely play a significant role in COME pathogenesis, informing future therapeutic strategies.