Epigenetic landscape links upper airway microbiota in infancy with allergic rhinitis at 6 years of age
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Epigenetic landscape links upper airway microbiota in infancy with allergic rhinitis at 6 years of age. / Morin, Andréanne; McKennan, Chris G.; Pedersen, Casper-Emil T.; Stokholm, Jakob; Chawes, Bo L.; Schoos, Ann-Marie Malby; Naughton, Katherine A.; Thorsen, Jonathan; Mortensen, Martin S.; Vercelli, Donata; Trivedi, Urvish; Sørensen, Søren J.; Bisgaard, Hans; Nicolae, Dan L.; Bønnelykke, Klaus; Ober, Carole.
I: Journal of Allergy and Clinical Immunology, Bind 146, Nr. 6, 2020, s. 1358-1366.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Epigenetic landscape links upper airway microbiota in infancy with allergic rhinitis at 6 years of age
AU - Morin, Andréanne
AU - McKennan, Chris G.
AU - Pedersen, Casper-Emil T.
AU - Stokholm, Jakob
AU - Chawes, Bo L.
AU - Schoos, Ann-Marie Malby
AU - Naughton, Katherine A.
AU - Thorsen, Jonathan
AU - Mortensen, Martin S.
AU - Vercelli, Donata
AU - Trivedi, Urvish
AU - Sørensen, Søren J.
AU - Bisgaard, Hans
AU - Nicolae, Dan L.
AU - Bønnelykke, Klaus
AU - Ober, Carole
PY - 2020
Y1 - 2020
N2 - Background The upper airways present a barrier to inhaled allergens and microbes, which alter immune responses and subsequent risk for diseases, such as allergic rhinitis (AR). Objective We tested the hypothesis that early life microbial exposures leaves a lasting signature in DNA methylation that ultimately influences the development of AR in children. Methods We studied upper airway microbiota at 1 week, 1 month and 3 months of life, and measured DNA methylation (DNAm) and gene expression profiles in upper airway mucosal cells and assessed AR at age 6 in children in the Copenhagen Prospective Studies on Asthma in Childhood (COPSAC)2010 birth cohort Results We identified 956 AR-associated differentially methylated CpGs (DMCs) in upper airway mucosal cells at age 6; 792 of which formed three modules of correlated DMCs. The eigenvector of one module was correlated with the expression of genes enriched for lysosome and bacterial invasion of epithelial cell pathways. Early life microbial diversity was lower at 1 week (richness p=0.0079) in children with AR at age 6, and reduced diversity at 1 week was also correlated with the same module’s eigenvector (rho=-0.25, p=3.3x10-5). We show that the effect of microbiota richness at 1 week on risk for AR at age 6 was mediated in part by the epigenetic signature of this module. Conclusion Our results suggest that upper airway microbial composition in infancy contributes to the development of AR during childhood, and this trajectory is mediated, at least in part, through altered DNAm patterns in upper airway mucosal cells.
AB - Background The upper airways present a barrier to inhaled allergens and microbes, which alter immune responses and subsequent risk for diseases, such as allergic rhinitis (AR). Objective We tested the hypothesis that early life microbial exposures leaves a lasting signature in DNA methylation that ultimately influences the development of AR in children. Methods We studied upper airway microbiota at 1 week, 1 month and 3 months of life, and measured DNA methylation (DNAm) and gene expression profiles in upper airway mucosal cells and assessed AR at age 6 in children in the Copenhagen Prospective Studies on Asthma in Childhood (COPSAC)2010 birth cohort Results We identified 956 AR-associated differentially methylated CpGs (DMCs) in upper airway mucosal cells at age 6; 792 of which formed three modules of correlated DMCs. The eigenvector of one module was correlated with the expression of genes enriched for lysosome and bacterial invasion of epithelial cell pathways. Early life microbial diversity was lower at 1 week (richness p=0.0079) in children with AR at age 6, and reduced diversity at 1 week was also correlated with the same module’s eigenvector (rho=-0.25, p=3.3x10-5). We show that the effect of microbiota richness at 1 week on risk for AR at age 6 was mediated in part by the epigenetic signature of this module. Conclusion Our results suggest that upper airway microbial composition in infancy contributes to the development of AR during childhood, and this trajectory is mediated, at least in part, through altered DNAm patterns in upper airway mucosal cells.
KW - Allergic rhinitis
KW - microbiota
KW - DNA methylation
KW - gene expression
KW - early life
KW - upper airways
U2 - 10.1016/j.jaci.2020.07.005
DO - 10.1016/j.jaci.2020.07.005
M3 - Journal article
C2 - 32693091
VL - 146
SP - 1358
EP - 1366
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
SN - 0091-6749
IS - 6
ER -
ID: 246637561