Upper airway microbiota development in infants with cystic fibrosis diagnosed by newborn screen

J Kirk Harris1, Brandie D Wagner2, Charles E Robertson3

  • 1Department of Pediatrics, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, 13123 E. 16th Ave, B-395, Aurora, CO 80045, USA.

Insights

The upper airway microbiota in infants with cystic fibrosis (CF) changes significantly with age. Clinical factors like antibiotics had less impact on the oropharyngeal microbiome during the first year of life.

Area of Science:

  • Microbiology
  • Pediatrics
  • Genetics

Background:

  • Upper airway microbiota changes may influence early cystic fibrosis (CF) disease.
  • Investigating early airway microbiota in CF infants is crucial.

Purpose of the Study:

  • To assess oropharyngeal microbiota in CF infants during their first year.
  • To explore relationships between microbiota, growth, and antibiotic use.

Main Methods:

  • Longitudinal oropharyngeal swabs from 205 CF infants (1-12 months).
  • 16S rRNA gene sequencing for bacterial composition and qPCR for load.
  • Statistical analysis including mixed models and canonical correlation.

Main Results:

  • Microbiota alpha diversity increased with age, minimally affected by antibiotics.
  • Community composition strongly correlated with age, moderately with antibiotics and feeding.
  • Streptococcus decreased, while Neisseria and other taxa increased over the first year.

Conclusions:

  • Infant age is a primary driver of oropharyngeal microbiota changes in CF.
  • Clinical variables, including antibiotics, had less influence than age in the first year.
Abstract

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