Antibiotic-driven dysbiosis in early life disrupts indole-3-propionic acid production and exacerbates allergic airway inflammation in adulthood

Olaf Perdijk*, Alana Butler, Matthew Macowan, Roxanne Chatzis, Edyta Bulanda, Rhiannon D. Grant, Nicola L. Harris, Tomasz P. Wypych*, Benjamin J. Marsland

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Antibiotic use in early life disrupts microbial colonization and increases the risk of developing allergies and asthma. We report that mice given antibiotics in early life (EL-Abx), but not in adulthood, were more susceptible to house dust mite (HDM)-induced allergic airway inflammation. This susceptibility was maintained even after normalization of the gut microbiome. EL-Abx decreased systemic levels of indole-3-propionic acid (IPA), which induced long-term changes to cellular stress, metabolism, and mitochondrial respiration in the lung epithelium. IPA reduced mitochondrial respiration and superoxide production and altered chemokine and cytokine production. Consequently, early-life IPA supplementation protected EL-Abx mice against exacerbated HDM-induced allergic airway inflammation in adulthood. These results reveal a mechanism through which EL-Abx can predispose the lung to allergic airway inflammation and highlight a possible preventative approach to mitigate the detrimental consequences of EL-Abx.
Original languageEnglish
Pages (from-to)1939-1954.e7
JournalImmunity
Volume57
Issue number8
Early online date15 Jul 2024
DOIs
Publication statusPublished - 13 Aug 2024
Externally publishedYes

Keywords

  • airway epithelial cells
  • allergy
  • antibiotics
  • early life
  • gut-lung axis
  • indole-3-propionic acid
  • metabolites
  • microbiota
  • redox balance
  • window of opportunity

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