The microbiome of pediatric patients with chronic rhinosinusitis

Amanda L Stapleton1, Amber D Shaffer1, Alison Morris2,3

  • 1Department of Otolaryngology, University of Pittsburgh Medical Center (UPMC) Children's Hospital of Pittsburgh, Pittsburgh, PA.

Insights

The nasopharynx and nasal cavity have distinct microbial communities. Chronic rhinosinusitis (CRS) patients did not show significant differences in microbiota compared to healthy controls.

Area of Science:

  • Microbiology
  • Otolaryngology
  • Pediatric Health

Background:

  • Chronic rhinosinusitis (CRS) is a common pediatric condition.
  • Adenoidectomy is a surgical procedure for CRS and obstructive sleep apnea.
  • Understanding the nasopharyngeal and sinus microbiota is crucial for pediatric respiratory health.

Purpose of the Study:

  • To compare the nasopharyngeal and sinus microbiota in pediatric patients with CRS undergoing adenoidectomy versus healthy controls.
  • To investigate the relationship between microbiota composition, diversity, and clinical factors.
  • To explore the ecological differences between the nasopharynx and nasal cavity.

Main Methods:

  • Recruitment of pediatric patients with CRS (n=37) and obstructive sleep apnea (n=50).
  • Collection of nasopharyngeal and nasal cavity samples during adenoidectomy.
  • 16S ribosomal RNA (rRNA) gene sequencing for taxonomic abundance analysis.
  • Statistical analyses including PERMANOVA and diversity measures.

Main Results:

  • Moraxella was the most abundant organism; higher alpha diversity in nasopharynx vs. nasal cavity.
  • No significant difference in microbiota diversity between CRS and control patients.
  • Age and eczema influenced diversity; medications (nasal steroids, inhaled steroids, antihistamines) impacted nasopharyngeal and nasal cavity microbiota.

Conclusions:

  • Nasopharynx and nasal cavity exhibit distinct microbial compositions and diversity.
  • No significant differences in microbiota were found between CRS patients and healthy controls.
  • Nasopharyngeal and sinus microbial shifts may play a role in adenoid hypertrophy etiology.
Abstract