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AuthorTricarico, Paola Maura
AuthorGratton, Rossella
AuthorSantos-Silva, Carlos André dos
AuthorMoura, Ronald Rodrigues de
AuthorUra, Blendi
AuthorSommella, Eduardo
AuthorCampiglia, Pietro
AuthorDel Vecchio, Cecilia
AuthorMoltrasio, Chiara
AuthorBerti, Irene
AuthorD’Adamo, Adamo Pio
AuthorElsherbini, Ahmed M.A.
AuthorStaudenmaier, Lena
AuthorChersi, Karin
AuthorBoniotto, Michele
AuthorKrismer, Bernhard
AuthorSchittek, Birgit
AuthorCrovella, Sergio
Available date2022-12-26T07:20:45Z
Publication Date2022-12-05
Publication NameFrontiers in Immunology
Identifierhttp://dx.doi.org/10.3389/fimmu.2022.1060547
CitationTricarico PM, Gratton R, Santos-Silva CAd, Moura RRd, Ura B, Sommella E, Campiglia P, Del Vecchio C, Moltrasio C, Berti I, D’Adamo AP, Elsherbini AMA, Staudenmaier L, Chersi K, Boniotto M, Krismer B, Schittek B and Crovella S (2022) A rare loss-of-function genetic mutation suggest a role of dermcidin deficiency in hidradenitis suppurativa pathogenesis. Front. Immunol. 13:1060547. doi: 10.3389/fimmu.2022.1060547
URIhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85144185023&origin=inward
URIhttp://hdl.handle.net/10576/37576
AbstractHidradenitis suppurativa (HS) is a chronic inflammatory skin disease with a multifactorial aetiology that involves a strict interplay between genetic factors, immune dysregulation and lifestyle. Familial forms represent around 40% of total HS cases and show an autosomal dominant mode of inheritance of the disease. In this study, we conducted a whole-exome sequence analysis on an Italian family of 4 members encompassing a vertical transmission of HS. Focusing on rare damaging variants, we identified a rare insertion of one nucleotide (c.225dupA:p.A76Sfs*21) in the DCD gene encoding for the antimicrobial peptide dermcidin (DCD) that was shared by the proband, his affected father and his 11-years old daughter. Since several transcriptome studies have shown a significantly decreased expression of DCD in HS skin, we hypothesised that the identified frameshift insertion was a loss-of-function mutation that might be associated with HS susceptibility in this family. We thus confirmed by mass spectrometry that DCD levels were diminished in the affected members and showed that the antimicrobial activity of a synthetic DCD peptide resulting from the frameshift mutation was impaired. In order to define the consequences related to a decrease in DCD activity, skin microbiome analyses of different body sites were performed by comparing DCD mutant and wild type samples, and results highlighted significant differences between the groins of mutated and wild type groups. Starting from genetic analysis conducted on an HS family, our findings showed, confirming previous transcriptome results, the potential role of the antimicrobial DCD peptide as an actor playing a crucial part in the etio-pathogenesis of HS and in the maintenance of the skin’s physiological microbiome composition; so, we can hypothesise that DCD could be used as a novel target for personalised therapeutic approach.
SponsorThis work was supported by a Biomolecular Analyses for Tailored Medicine in AcneiNversa (BATMAN) project, funded by ERA PerMed (JTC_2018), by Starting Grant (SG-2019- 12369421) founded by the Italian Ministry of Health, by grants (RC16/2018 and RC03/2020) from the Institute for Maternal and Child Health IRCCS ‘Burlo Garofolo funded by the Italian Ministry of Health. Furthermore, this work was supported (BS and BK) by the Cluster of Excellence EXC2124 project ID -390838134 of the University of Tübingen and the German Center of Infection Research (DZIF) (BK).
Languageen
PublisherFrontiers Media
Subjectantimicrobial peptides
bacteria
dermcidin
genetics
hidradenitis suppurativa
TitleA rare loss-of-function genetic mutation suggest a role of dermcidin deficiency in hidradenitis suppurativa pathogenesis
TypeArticle
Volume Number13
ESSN1664-3224
dc.accessType Open Access


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