Original Article
Clinical Research
Diverse Human Skin Fungal Communities in Children Converge in Adulthood

https://doi.org/10.1016/j.jid.2016.05.130Get rights and content
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Understanding the skin mycobiome (fungal communities) is important because both commensal and pathogenic fungi can drive cutaneous disease depending on host status and body sites, including the scalp, feet, and groin. Interestingly, age may also affect skin fungal infections as certain dermatophytoses (i.e., tinea capitis) are more frequent in children than adults. We previously described the skin mycobiomes in healthy adults, showing lipophilic fungi Malassezia predominate in most skin sites. Because children have less sebaceous skin before puberty, we compared the fungal communities of primary clinical samples from healthy children and adults, based on sequencing of a fungal phylogenetic marker. Although Malassezia predominated on the trunk, head, and arm skin of adults (age 18–39), children (age < 14) had more diverse fungal communities, for example, Eurotiomycetes, which includes common dermatophytes. Species-level classification showed that Malassezia globosa predominated in children. Collectively, our findings indicate that prepubertal skin is colonized by diverse fungi, whereas adult skin is predominantly obligatory lipophilic Malassezia, suggesting that fungal communities on skin profoundly shift during puberty. Mycobiome shifts during puberty are likely due to alterations in sebaceous gland activation and sebum composition. This study provides a foundational framework for studies investigating interactions between fungi, skin, and pediatric dermatophytosis.

Abbreviations

Ac
antecubital fossa
Ba
back
CI
confidence interval
Ea
external auditory canal
Fh
forehead
HA
healthy adults
HC
healthy children
Ic
inguinal crease
ITS1
internal transcribed spacer 1
Mb
manubrium
Oc
occiput
Ra
retroauricular crease
Vf
volar forearm

Cited by (0)

5

Current address: Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota 55905, USA

6

These authors contributed equally to this work.