Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota

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作者
Lucas Moitinho-Silva
Frauke Degenhardt
Elke Rodriguez
Hila Emmert
Simonas Juzenas
Lena Möbus
Florian Uellendahl-Werth
Nicole Sander
Hansjörg Baurecht
Lukas Tittmann
Wolfgang Lieb
Christian Gieger
Annette Peters
David Ellinghaus
Corinna Bang
Andre Franke
Stephan Weidinger
Malte Christoph Rühlemann
机构
[1] Kiel University,Institute of Clinical Molecular Biology
[2] University Hospital Schleswig-Holstein,Department of Dermatology and Allergy
[3] Vilnius University,Institute of Biotechnology, Life Science Centre
[4] University of Regensburg,Department for Epidemiology and Preventive Medicine
[5] Kiel University,Biobank PopGen and Institute of Epidemiology
[6] Kiel University,Institute of Epidemiology
[7] Institute of Epidemiology,undefined
[8] Helmholtz Zentrum München – German Research Center for Environmental Health,undefined
[9] Research Unit of Molecular Epidemiology,undefined
[10] Helmholtz Zentrum München – German Research Center for Environmental Health,undefined
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摘要
Despite the increasing knowledge about factors shaping the human microbiome, the host genetic factors that modulate the skin-microbiome interactions are still largely understudied. This contrasts with recent efforts to characterize host genes that influence the gut microbiota. Here, we investigated the effect of genetics on skin microbiota across three different skin microenvironments through meta-analyses of genome-wide association studies (GWAS) of two population-based German cohorts. We identified 23 genome-wide significant loci harboring 30 candidate genes involved in innate immune signaling, environmental sensing, cell differentiation, proliferation and fibroblast activity. However, no locus passed the strict threshold for study-wide significance (P < 6.3 × 10−10 for 80 features included in the analysis). Mendelian randomization (MR) analysis indicated the influence of staphylococci on eczema/dermatitis and suggested modulating effects of the microbiota on other skin diseases. Finally, transcriptional profiles of keratinocytes significantly changed after in vitro co-culturing with Staphylococcus epidermidis, chosen as a representative of skin commensals. Seven candidate genes from the GWAS were found overlapping with differential expression in the co-culturing experiments, warranting further research of the skin commensal and host genetic makeup interaction.
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