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

被引:29
|
作者
Boutin, Rozlyn C. T. [1 ,2 ]
Petersen, Charisse [2 ]
Woodward, Sarah E. [1 ,2 ]
Serapio-Palacios, Antonio [2 ]
Bozorgmehr, Tahereh [2 ]
Loo, Rachelle [1 ,2 ]
Chalanuchpong, Alina [1 ,2 ]
Cirstea, Mihai [1 ,2 ]
Lo, Bernard [1 ]
Huus, Kelsey E. [1 ,2 ]
Barcik, Weronika [2 ]
Azad, Meghan B. [3 ,4 ]
Becker, Allan B. [3 ,4 ]
Mandhane, Piush J. [5 ,6 ]
Moraes, Theo J. [7 ]
Sears, Malcolm R. [8 ]
Subbarao, Padmaja [7 ,9 ]
McNagny, Kelly M. [10 ,11 ]
Turvey, Stuart E. [1 ,12 ]
Finlay, B. Brett [1 ,2 ,13 ]
机构
[1] Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC, Canada
[2] Univ British Columbia, Michael Smith Labs, Vancouver, BC, Canada
[3] Univ Manitoba, Childrens Hosp Res Inst Manitoba, Winnipeg, MB, Canada
[4] Univ Manitoba, Dept Pediat & Child Hlth, Winnipeg, MB, Canada
[5] Univ Alberta, Dept Pediat, Edmonton, AB, Canada
[6] Univ Alberta, Sch Publ Hlth, Edmonton, AB, Canada
[7] Hosp Sick Children, Toronto, ON, Canada
[8] McMaster Univ, Dept Med, Hamilton, ON, Canada
[9] Univ Toronto, Dept Pediat, Toronto, ON, Canada
[10] Univ British Columbia, Dept Biomed Engn, Vancouver, BC, Canada
[11] Univ British Columbia, Dept Med Genet, Vancouver, BC, Canada
[12] Univ British Columbia, Dept Pediat, Vancouver, BC, Canada
[13] Univ British Columbia, Dept Biochem & Mol Biol, Vancouver, BC, Canada
来源
ELIFE | 2021年 / 10卷
基金
加拿大健康研究院;
关键词
ALLERGIC AIRWAY DISEASE; CANDIDA-ALBICANS; RECEPTOR DECTIN-1; T-CELLS; MICROBIOTA; LUNG; ACTIVATION; METABOLITES; INFECTION; CYTOKINE;
D O I
10.7554/eLife.67740
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:22
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