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The Skin and Nose Microbiome and Its Association with Filaggrin Gene Mutations in Pediatric Atopic Dermatitis.
van Mierlo, Minke M F; Pardo, Luba M; Fieten, Karin B; van den Broek, Tim J; Schuren, Frank H J; van Geel, Michel; Pasmans, Suzanne G M A.
Affiliation
  • van Mierlo MMF; Department of Dermatology-Center of Pediatric Dermatology, Sophia Children's Hospital, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Pardo LM; Department of Dermatology-Center of Pediatric Dermatology, Sophia Children's Hospital, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Fieten KB; Department of Dermatology and Allergology, University Medical Center, Utrecht, The Netherlands.
  • van den Broek TJ; Dutch Asthma Center Davos, Davos, Switzerland.
  • Schuren FHJ; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich, Davos, Switzerland.
  • van Geel M; Microbiology and Systems Biology, TNO Zeist, Zeist, The Netherlands.
  • Pasmans SGMA; Microbiology and Systems Biology, TNO Zeist, Zeist, The Netherlands.
Dermatology ; 238(5): 928-938, 2022.
Article de En | MEDLINE | ID: mdl-35042220
ABSTRACT

BACKGROUND:

Interactions between the skin barrier, immune system, and microbiome underlie the development of atopic dermatitis (AD).

OBJECTIVE:

To investigate the skin and nasal microbiome in relation to filaggrin gene (FLG) mutations.

METHODS:

A cross-sectional study including 77 children with difficult-to-treat AD. The entire encoding region of FLG was screened for mutations using single molecule molecular inversion probes and next-generation sequencing. Bacterial swabs from the anterior nares, lesional and nonlesional skin were analyzed using 16S rRNA sequencing. For skin samples, additional qPCR was performed for Staphylococcus aureus and Staphylococcus epidermidis.

RESULTS:

The prevalence of patients with a mutation in FLG was 40%, including 10 different mutations. Analyzing bacterial swabs from all three niches showed a significant effect for both niche and FLG mutation status on the overall microbiome composition. Using a subset analysis to test the effect of FLG mutation status per niche separately did not show a significant association to the microbiome. Shannon diversity and S. aureus abundance were significantly affected by the niche, but not by the presence of an FLG mutation.

CONCLUSIONS:

Our results suggest only a minor role for FLG mutation status on the overall microbiome, which is rather caused by differences in the present genera than by microbe richness and evenness.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Eczéma atopique / Microbiote Type d'étude: Observational_studies / Prevalence_studies / Risk_factors_studies Limites: Child / Humans Langue: En Journal: Dermatology Sujet du journal: DERMATOLOGIA Année: 2022 Type de document: Article Pays d'affiliation: Pays-Bas

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Eczéma atopique / Microbiote Type d'étude: Observational_studies / Prevalence_studies / Risk_factors_studies Limites: Child / Humans Langue: En Journal: Dermatology Sujet du journal: DERMATOLOGIA Année: 2022 Type de document: Article Pays d'affiliation: Pays-Bas
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