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Published on: January 20, 2011
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.
Abstract:
Otitis media with effusion (OME) is a highly prevalent disease in children, but the exact pathogenesis and role of bacteria are still not well understood. This study aimed to investigate the presence of otopathogenic bacteria in the middle ear effusion (MEE) and adenoid of children with chronic OME (COME), and to investigate in vivo whether these bacteria, especially Haemophilus influenzae, are organized as a biofilm in the middle ear fluid. MEE and adenoid samples were collected from 21 patients with COME. Extensive bacterial culturing and genotyping was performed on all middle ear and adenoid samples. Fluorescence in situ hybridization (FISH) and confocal laser scanning microscopy (CLSM) was used to visualize possible biofilm structures for a selection of middle ear effusion samples. 34 MEE samples were collected from 21 patients of which 64.7 % were culture positive for bacteria and 47.0 % were culture positive for Haemophilus influenzae, Moraxella catarrhalis, Staphylococcus aureus and/or Streptococcus pneumoniae. All 21 adenoid samples were culture positive for one or more of these four otopathogens. H. influenzae (35.3 %) and S. pneumoniae (76.2 %) were the most frequently cultured bacteria in the MEE and adenoid samples, respectively. The same bacterial species was found in MEE and adenoid for 84.6 % of the patients and in 81.2 % of the cases where the same species was found in more than one site it involved the same bacterial genotype. FISH and CLSM demonstrated the presence of H. influenzae specific biofilm structures in five of the eight culture positive MEEs that were tested, but in none of the two culture negative MEEs. The findings in this study indicate that the adenoid acts as a reservoir for bacteria in MEE and confirms that biofilms, in at least half of the cases consisting of H. influenzae, are indeed present in the MEE of children with COME. Biofilms may thus play a crucial role in the pathogenesis of COME, which is important in the understanding of this disease and the development of potential future treatment options.
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.
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