Microbiome Modulation in Acne Patients and Clinical Correlations

Author:

Ionescu Marius-Anton1ORCID,Tatu Alin Laurentiu234ORCID,Busila Camelia25,Axente Elena Roxana6ORCID,Badalato Nelly7,Feuilloley Marc G. J.8ORCID,Asquier Estelle9,Martínez José Dario10ORCID,Lefeuvre Luc9ORCID

Affiliation:

1. Dermatology Department, University Hospital “Saint Louis”, University of Paris, 75010 Paris, France

2. Clinical Medical Department, Faculty of Medicine and Pharmacy, “Dunarea de Jos” University, 800008 Galati, Romania

3. “Sfanta Cuvioasa Parascheva” Hospital of Infectious Diseases, 800179 Galati, Romania

4. Multidisciplinary Integrated Center of Dermatological Interface Research MIC-DIR (Centrul Integrat Multidisciplinar de Cercetare de Interfata Dermatologica—CIM-CID), “Dunărea de Jos” University, 800201 Galati, Romania

5. “Sf. Ioan” Emergency Clinical Paediatric Hospital, 800487 Galati, Romania

6. Faculty of Medicine and Pharmacy, “Dunarea de Jos” University, 35 AI I Cuza St., 800010 Galati, Romania

7. GenoScreen, 59000 Lille, France

8. Research Unit UR4312 CBSA, University Rouen, 27000 Evreux, France

9. Laboratoires Dermatologiques d’Uriage, 92200 Neuilly sur-Seine, France

10. Department of Internal Medicine, Faculty of Medicine, Hospital Universitario José Eleuterio González, Universidad Autónoma de Nuevo León, Monterrey 64460, Mexico

Abstract

Background: The imbalance of skin microbiota in acne can induce changes leading to induction or to aggravation of chronic inflammatory lesions; complex mechanisms are involved. Cutibacterium acnes (C. acnes) ribotypes RT4 and RT5 express more biofilm and are associated with inflammatory acne lesions. C. acnes RT6 is a non-acne ribotype, beneficial for the skin. Objectives: In an open clinical trial, acne adults were included and assessed clinically at baseline and at month 2 using the Investigator Global Assessment of Acne (IGA) score. A topical emulsion was applied twice daily for 2 months (M2) in each included patient. In the same series of acne patients, skin swab samples were collected from acne patients at baseline and M2 from lesional and non-lesional skin; skin swabs were collected for the metagenomic long-read analysis of microbiota. Materials and Methods: Acne patients with a gravity score IGA of >1<3 were included in this pilot study. An emulsion of O/W formulated with vegetal extract of Umbelliferae associated with a polysaccharide at 1% was applied twice daily for 2 months. At baseline and M2 clinical assessments were made; skin swab samples were also taken for microbiota analysis from lesional and non-lesional skin in each included patient. Extractions of genomic DNA (gDNA) from swab samples from baseline and from M2 were made, followed by full-length (V1–V9) amplification of the 16S rDNA and sequencing of amplicon libraries for strain-level bacterial community profiling. Results: In a series of 32 adult acne patients, the mean initial IGA scale was 3.1; at M2 the IGA scale was 1.5 (p < 0.001). The mean decrease in acne lesions was by 63%. Microbiome metagenomic long-read analysis in these series was mainly dominated by C. acnes followed by Staphylococcus epidermidis (S. epidermidis). The density of C. acnes ribotypes RT6 (non-acne strain) was increased at M2 compared to baseline and the density of ribotypes C. acnes RT1 to RT5 was decreased at M2, compared to baseline (p < 0.0001). S. epidermidis ribotypes (1 to 36) were non significantly increased at M2, compared to baseline (p < 0.1). Conclusions: In a series of 32 acne patients that applied an emulsion based on vegetal extract of Umbelliferae and a polysaccharide at 1% twice daily, a significant clinical improvement in IGA scale for acne lesions was seen at M2, compared to baseline (p < 0.0001). The clinical improvement was correlated with an improvement in skin microbiome at M2 compared to baseline, indicated by the increase in the relative abundance of non-acne strain of C. acnes ribotype 6 and of the decrease in the relative abundance of acne strains ribotypes C. acnes RT1 to RT5.

Funder

Axente Elena Roxana

Laboratoires Dermatologiques d’Uriage—France

Publisher

MDPI AG

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