Atopic dermatitis and skin disease
Skin microbiome before development of atopic dermatitis: Early colonization with commensal staphylococci at 2 months is associated with a lower risk of atopic dermatitis at 1 year

https://doi.org/10.1016/j.jaci.2016.07.029Get rights and content
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Background

Disease flares of established atopic dermatitis (AD) are generally associated with a low-diversity skin microbiota and Staphylococcus aureus dominance. The temporal transition of the skin microbiome between early infancy and the dysbiosis of established AD is unknown.

Methods

We randomly selected 50 children from the Cork Babies After SCOPE: Evaluating the Longitudinal Impact Using Neurological and Nutritional Endpoints (BASELINE) longitudinal birth cohort for microbiome sampling at 3 points in the first 6 months of life at 4 skin sites relevant to AD: the antecubital and popliteal fossae, nasal tip, and cheek. We identified 10 infants with AD and compared them with 10 randomly selected control infants with no AD. We performed bacterial 16S ribosomal RNA sequencing and analysis directly from clinical samples.

Results

Bacterial community structures and diversity shifted over time, suggesting that age strongly affects the skin microbiome in infants. Unlike established AD, these patients with infantile AD did not have noticeably dysbiotic communities before or with disease and were not colonized by S aureus. In comparing patients and control subjects, infants who had affected skin at month 12 had statistically significant differences in bacterial communities on the antecubital fossa at month 2 compared with infants who were unaffected at month 12. In particular, commensal staphylococci were significantly less abundant in infants affected at month 12, suggesting that this genus might protect against the later development of AD.

Conclusions

This study suggests that 12-month-old infants with AD were not colonized with S aureus before having AD. Additional studies are needed to confirm whether colonization with commensal staphylococci modulates skin immunity and attenuates development of AD.

Key words

Staphylococcus aureus
atopic dermatitis
skin
microbiome
longitudinal birth cohort
16S sequencing

Abbreviations used

AD
Atopic dermatitis
Af
Antecubital fossa
AMOVA
Analysis of molecular variance
BASELINE
Babies After SCOPE: Evaluating the Longitudinal Impact Using Neurological and Nutritional Endpoints
FLG
Filaggrin
Nt
Nasal tip
OTU
Operational taxonomic unit
Pf
Popliteal fossa

Cited by (0)

A.D.I. is funded by the National Children's Research Centre (NCRC), Dublin, Ireland. The NCRC is the primary funding source for the ongoing Cork BASELINE birth cohort. Additional support came from the UK Food Standards Agency (FSA). The work was also supported by the Intramural Research Program of the National Institutes of Health's National Cancer Institute (to E.A.K., J.-H.J., and H.H.K.) and the National Human Genome Research Institute (to J.A.S.). J.-H.J. is also supported by a grant from the Korean Health Technology R&D Project, Ministry of Health and Welfare, Republic of Korea (HI15C1095).

Disclosure of potential conflict of interest: J. O'B Hourihane receives grant support from the Food Standards Agency, United Kingdom, and the National Children's Research Centre and receives payment for lectures from DBV technologies, Nutricia, and Thermo Fisher. P. G. Fallon receives grant support from the NCRC and Wellcome Trust. A. D. Irvine receives grant support from National Children's Research Centre. The rest of the authors declare that they have no relevant conflicts of interest.

These authors contributed equally to this work.