| Literature DB >> 36261456 |
Andre Franke1, Stephan Weidinger2, Malte Christoph Rühlemann3, Lucas Moitinho-Silva3,4, Frauke Degenhardt3, Elke Rodriguez4, Hila Emmert4, Simonas Juzenas3,5, Lena Möbus4, Florian Uellendahl-Werth3, Nicole Sander4, Hansjörg Baurecht6, Lukas Tittmann7, Wolfgang Lieb8, Christian Gieger9,10, Annette Peters9, David Ellinghaus3, Corinna Bang3.
Abstract
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.Entities:
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Year: 2022 PMID: 36261456 PMCID: PMC9582029 DOI: 10.1038/s41467-022-33906-5
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 17.694