Preprint,
Quantitative and qualitative determination of the Staphylococcus and Cutibacterium dysbiosis of the skin microbiome in acne and its decline after isotretinoin treatment
Affiliations
- [1] Aarhus University [NORA names: AU Aarhus University; University; Denmark; Europe, EU; Nordic; OECD];
- [2] University of Göttingen [NORA names: Germany; Europe, EU; OECD];
- [3] Lund University [NORA names: Sweden; Europe, EU; Nordic; OECD];
- [4] Aalborg University Hospital [NORA names: North Denmark Region; Hospital; Denmark; Europe, EU; Nordic; OECD]
Abstract
Background
Acne vulgaris is a multifactorial disease of the pilosebaceous unit of human skin. Previous studies have identified an acne-associated dysbiosis of the human skin microbiome. This dysbiosis was mainly determined for Cutibacterium acnes. However, detailed analyses combining qualitative and quantitative aspects are scarce, also regarding the possible contribution of other skin bacteria and the impact of treatment.
We conducted a culture-independent study to determine differences between the healthy skin and the acne microbiome before and after long-term isotretinoin treatment. Three amplicon-based sequencing approaches and digital droplet PCR for quantification were applied to analyze the entire bacterial community, and specifically, C. acnes and staphylococcal communities.
Results
Our results revealed a 2.2-fold reduced absolute and relative abundance of C. acnes with a reduced diversity in the acne microbiome. A phylotype switch was found, which was mainly characterized by a significant relative decrease of IB, II and type III strains in the acne microbiome. In contrast, the relative abundance of staphylococci increased significantly and the quantitative ratio staphylococci to C. acnes strongly increased from 1:34 to 1:11 in the acne cohort. The diversity of staphylococci was reduced, mainly due to the decrease of Staphylococcus hominis, and the appearance and predominance of Staphylococcus aureus in some acne patients. Isotretinoin treatment drastically depleted C. acnes (37-fold) and moderately also staphylococci (3.6-fold). Regarding the staphylococcal population, isotretinoin treatment resulted in a decrease of Staphylococcus epidermidis and a significant increase of S. aureus on forehead and cheek skin. The alpha diversity drastically increased on all examined body sites.
Conclusions
The switch from a C. acnes-dominated healthy skin microbiome towards an acne microbiome that is relatively enriched in staphylococci could indicate a stronger impact of staphylococci in the pathophysiology of acne than currently acknowledged. Our data further showed that isotretinoin largely eliminated the skin microbiome and in particular C. acnes, but also S. epidermidis. Instead, more harmful bacteria such as S. aureus could expand, which suggests that post-treatment strategies should be considered to accelerate skin microbiome recovery.
