Bacterial–fungal interactions in the neonatal gut influence asthma outcomes later in life

Author:

Boutin Rozlyn CT12ORCID,Petersen Charisse2,Woodward Sarah E12ORCID,Serapio-Palacios Antonio2,Bozorgmehr Tahereh2,Loo Rachelle12,Chalanuchpong Alina12,Cirstea Mihai12ORCID,Lo Bernard1,Huus Kelsey E12,Barcik Weronika2,Azad Meghan B3,Becker Allan B3,Mandhane Piush J45,Moraes Theo J6,Sears Malcolm R7,Subbarao Padmaja68,McNagny Kelly M910ORCID,Turvey Stuart E111,Finlay B Brett1212ORCID

Affiliation:

1. Department of Microbiology and Immunology, University of British Columbia, Vancouver, Canada

2. Michael Smith Laboratories, University of British Columbia, Vancouver, Canada

3. Children’s Hospital Research Institute of Manitoba and Department of Pediatrics and Child Health, University of Manitoba, WinnipegMB, Canada

4. Department of Pediatrics, University of Alberta, Edmonton, Canada

5. School of Public Health, University of Alberta, Edmonton, Canada

6. The Hospital for Sick Children, Toronto, Canada

7. Department of Medicine, McMaster University, Hamilton, Canada

8. Department of Pediatrics, University of Toronto, Toronto, Canada

9. Department of Biomedical Engineering, University of British Columbia, Vancouver, Canada

10. Department of Medical Genetics University of British Columbia, Vancouver, Canada

11. Department of Pediatrics, University of British Columbia, Vancouver, Canada

12. Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, Canada

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.

Funder

Canadian Institutes of Health Research

AllerGen

Vancouver Coastal Health AND CIHR

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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