TY - JOUR
T1 - Diverse Human Skin Fungal Communities in Children Converge in Adulthood
AU - NISC Comparative Sequencing Program
AU - Jo, Jay Hyun
AU - Deming, Clay
AU - Kennedy, Elizabeth A.
AU - Conlan, Sean
AU - Polley, Eric C.
AU - Ng, Weng lan
AU - Segre, Julia A.
AU - Kong, Heidi H.
N1 - Funding Information:
We thank Mark C. Udey, Keisuke Nagao, and Carmen Contreras-Sesvold for their helpful discussions; and Sheila Phang and Amynah Pradhan for their underlying efforts. This work was supported by NIH NCI/CCR and NHGRI Intramural Research Program and a grant of the Korean Health Technology R&D Project, Ministry of Health and Welfare, Republic of Korea (HI15C1095; J-HJ). Sequencing was funded by grants from the National Institutes of Health (1UH2AR057504-01 and 4UH3AR057504-02). This work utilized the computational resources of the NIH HPC Biowulf cluster ( http://hpc.nih.gov ).
Publisher Copyright:
© 2016 The Authors
PY - 2016/12/1
Y1 - 2016/12/1
N2 - 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.
AB - 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.
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U2 - 10.1016/j.jid.2016.05.130
DO - 10.1016/j.jid.2016.05.130
M3 - Article
C2 - 27476723
AN - SCOPUS:84997470882
SN - 0022-202X
VL - 136
SP - 2356
EP - 2363
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 12
ER -