4.8 Article

Staphylococcus Agr virulence is critical for epidermal colonization and associates with atopic dermatitis development

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SCIENCE TRANSLATIONAL MEDICINE
卷 12, 期 551, 页码 -

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scitranslmed.aay4068

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资金

  1. JSPS KAKENHI [26713038, 16H06252, 16K15272, 18H02832]
  2. MEXT KAKENHI [16K18671, 16H06279]
  3. Naito Foundation
  4. Takeda Science Foundation
  5. AMED [JP16ek0410029h0001, JP18gm6010016h0002, 19gm0910002h0105]
  6. Intramural Research Program of the National Institute of Allergy and Infectious Diseases, NIH [ZIA AI000904-16]
  7. NIH [AR069303]
  8. University of Michigan Host Microbiome Initiative
  9. Environmental Restoration and Conservation Agency of Japan
  10. Institute for Global Prominent Research, Chiba University
  11. Joint Usage/Research Program of Medical Mycology Research Center, Chiba University [20-19]
  12. Grants-in-Aid for Scientific Research [26713038, 16K18671, 16H06252, 16K15272, 18H02832] Funding Source: KAKEN
  13. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [ZIAAI000904] Funding Source: NIH RePORTER

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Atopic dermatitis (AD) is commonly associated with colonization by Staphylococcus aureus in the affected skin. To understand the role of S. aureus in the development of AD, we performed whole-genome sequencing of S. aureus strains isolated from the cheek skin of 268 Japanese infants 1 and 6 months after birth. About 45% of infants were colonized with S. aureus at 1 month regardless of AD outcome. In contrast, skin colonization by S. aureus at 6 months of age increased the risk of developing AD. Acquisition of dysfunctional mutations in the S. aureus Agr quorum-sensing (QS) system was primarily observed in strains from 6-month-old infants who did not develop AD. Expression of a functional Agr system in S. aureus was required for epidermal colonization and the induction of AD-like inflammation in mice. Thus, retention of functional S. aureus agr virulence during infancy is associated with pathogen skin colonization and the development of AD.

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