TY - JOUR
T1 - Distinct skin microbiome community structures in congenital ichthyosis
AU - Tham, Khek Chian
AU - Lefferdink, Rachel
AU - Duan, Kaibo
AU - Lim, Seong Soo
AU - Wong, X. F.Colin C.
AU - Ibler, Erin
AU - Wu, Benedict
AU - Abu-Zayed, Hajar
AU - Rangel, Stephanie M.
AU - Del Duca, Ester
AU - Chowdhury, Mashkura
AU - Chima, Margot
AU - Kim, Hee Jee
AU - Lee, Bernett
AU - Guttman-Yassky, Emma
AU - Paller, Amy S.
AU - Common, John E.A.
N1 - Funding Information:
This work was supported by funding from Agency for Science, Technology and Research (A*STAR) and A*STAR BMRC EDB IAF‐PP grants – H17/01/a0/004 ‘Skin Research Institute of Singapore’ and H18/01a0/016 ‘Asian Skin Microbiome Program’ (K.‐C.T., S.S.L., X.F.C.C.W., J.E.A.C.). Although not part of the trial, some of the patients were swabbed at baseline of a clinical trial (NCT03041038), funded as an investigator‐initiated grant from Novartis CAIN457AUS05T (A.S.P., E.G.‐Y.). Biosample management of samples in this study was through NIH P30AR075049 (Northwestern’s Skin Biology and Disease Resource‐based Center/SBDRC) (A.S.P.). R.L. received partial salary funding from a National Psoriasis Foundation fellowship grant. B.L. and K.D. are part of the SIgN Immunomonitoring platform (supported by BMRC IAF 311006 grant, BMRC transition funds H16/99/b0/011, BMRC IAF‐PP H19/01/a0/024 SIGNAL grant and NRF SIS NRF2017_SISFP09 grant).
Publisher Copyright:
© 2022 British Association of Dermatologists.
PY - 2022/10
Y1 - 2022/10
N2 - Background: The ichthyoses are rare genetic keratinizing disorders that share the characteristics of an impaired epidermal barrier and increased risk of microbial infections. Although ichthyotic diseases share a T helper (Th) 17 cell immune signature, including increased expression of antimicrobial peptides, the skin microbiota of ichthyoses is virtually unexplored. Objectives: To analyse the metagenome profile of skin microbiome for major congenital ichthyosis subtypes. Methods: Body site-matched skin surface samples were collected from the scalp, upper arm and upper buttocks of 16 healthy control participants and 22 adult patients with congenital forms of ichthyosis for whole metagenomics sequencing analysis. Results: Taxonomic profiling showed significant shifts in bacteria and fungi abundance and sporadic viral increases across ichthyosis subtypes. Cutibacterium acnes and Malassezia were significantly reduced across body sites, consistent with skin barrier disruption and depletion of lipids. Microbial richness was reduced, with specific increases in Staphylococcus and Corynebacterium genera, as well as shifts in fungal species, including Malassezia. Malassezia globosa was reduced at all body sites, whereas M. sympodialis was reduced in the ichthyotic upper arm and upper buttocks. Malassezia slooffiae, by contrast, was strikingly increased at all body sites in participants with congenital ichthyosiform erythroderma (CIE) and lamellar ichthyosis (LI). A previously undescribed Trichophyton species was also detected as sporadically colonizing the skin of patients with CIE, LI and epidermolytic ichthyosis subtypes. Conclusions: The ichthyosis skin microbiome is significantly altered from healthy skin with specific changes predominating among ichthyosis subtypes. Skewing towards the Th17 pathway may represent a response to the altered microbial colonization in ichthyosis. What is already known about this topic? The skin microbiome of congenital ichthyoses is largely unexplored. Microbes play an important role in pathogenesis, as infections are common. The relative abundances of staphylococci and corynebacteria is increased in the cutaneous microbiome of patients with Netherton syndrome, but extension of these abundances to all congenital ichthyoses is unexplored. What does this study add? A common skin microbiome signature was observed across congenital ichthyoses. Distinct microbiome features were associated with ichthyosis subtypes. Changes in microbiome may contribute to T helper 17 cell immune polarization. What is the translational message? These data provide the basis for comparison of the microbiome with lipidomic and transcriptomic alterations in these forms of ichthyosis and consideration of correcting the dysbiosis as a therapeutic intervention.
AB - Background: The ichthyoses are rare genetic keratinizing disorders that share the characteristics of an impaired epidermal barrier and increased risk of microbial infections. Although ichthyotic diseases share a T helper (Th) 17 cell immune signature, including increased expression of antimicrobial peptides, the skin microbiota of ichthyoses is virtually unexplored. Objectives: To analyse the metagenome profile of skin microbiome for major congenital ichthyosis subtypes. Methods: Body site-matched skin surface samples were collected from the scalp, upper arm and upper buttocks of 16 healthy control participants and 22 adult patients with congenital forms of ichthyosis for whole metagenomics sequencing analysis. Results: Taxonomic profiling showed significant shifts in bacteria and fungi abundance and sporadic viral increases across ichthyosis subtypes. Cutibacterium acnes and Malassezia were significantly reduced across body sites, consistent with skin barrier disruption and depletion of lipids. Microbial richness was reduced, with specific increases in Staphylococcus and Corynebacterium genera, as well as shifts in fungal species, including Malassezia. Malassezia globosa was reduced at all body sites, whereas M. sympodialis was reduced in the ichthyotic upper arm and upper buttocks. Malassezia slooffiae, by contrast, was strikingly increased at all body sites in participants with congenital ichthyosiform erythroderma (CIE) and lamellar ichthyosis (LI). A previously undescribed Trichophyton species was also detected as sporadically colonizing the skin of patients with CIE, LI and epidermolytic ichthyosis subtypes. Conclusions: The ichthyosis skin microbiome is significantly altered from healthy skin with specific changes predominating among ichthyosis subtypes. Skewing towards the Th17 pathway may represent a response to the altered microbial colonization in ichthyosis. What is already known about this topic? The skin microbiome of congenital ichthyoses is largely unexplored. Microbes play an important role in pathogenesis, as infections are common. The relative abundances of staphylococci and corynebacteria is increased in the cutaneous microbiome of patients with Netherton syndrome, but extension of these abundances to all congenital ichthyoses is unexplored. What does this study add? A common skin microbiome signature was observed across congenital ichthyoses. Distinct microbiome features were associated with ichthyosis subtypes. Changes in microbiome may contribute to T helper 17 cell immune polarization. What is the translational message? These data provide the basis for comparison of the microbiome with lipidomic and transcriptomic alterations in these forms of ichthyosis and consideration of correcting the dysbiosis as a therapeutic intervention.
UR - http://www.scopus.com/inward/record.url?scp=85133403853&partnerID=8YFLogxK
U2 - 10.1111/bjd.21687
DO - 10.1111/bjd.21687
M3 - Article
C2 - 35633118
AN - SCOPUS:85133403853
SN - 0007-0963
VL - 187
SP - 557
EP - 570
JO - British Journal of Dermatology
JF - British Journal of Dermatology
IS - 4
ER -