| Literature DB >> 33876729 |
Rozlyn Ct Boutin1, Charisse Petersen1, Sarah E Woodward1, Antonio Serapio-Palacios2, Tahereh Bozorgmehr2, Rachelle Loo1, Alina Chalanuchpong1, Mihai Cirstea1, Bernard Lo3, Kelsey E Huus1, Weronika Barcik2, Meghan B Azad4, Allan B Becker4, Piush J Mandhane5, Theo J Moraes6, Malcolm R Sears7, Padmaja Subbarao6, Kelly M McNagny8, Stuart E Turvey9, Brett Finlay1.
Abstract
Bacterial members of the infant gut microbiota and bacterial-derived short-chain fatty acids (SCFAs) have been shown to be protective against childhood asthma, but a role for the fungal microbiota in asthma etiology remains poorly defined. We recently reported an association between overgrowth of the yeast Pichia kudriavzevii in the gut microbiota of Ecuadorian infants and increased asthma risk. In the present study, we replicated these findings in Canadian infants and investigated a causal association between early life gut fungal dysbiosis and later allergic airway disease (AAD). In a mouse model, we demonstrate that overgrowth of P. kudriavzevii within the neonatal gut exacerbates features of type-2 and -17 inflammation during AAD later in life. We further show that P. kudriavzevii growth and adherence to gut epithelial cells are altered by SCFAs. Collectively, our results underscore the potential for leveraging inter-kingdom interactions when designing putative microbiota-based asthma therapeutics.Entities:
Keywords: human; immunology; inflammation; medicine; mouse
Year: 2021 PMID: 33876729 DOI: 10.7554/eLife.67740
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140