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Microbiome. 2018 Sep 5;6(1):154. doi: 10.1186/s40168-018-0533-1.

Alteration of the cutaneous microbiome in psoriasis and potential role in Th17 polarization.

Author information

1
Department of Dermatology, University of California, San Francisco, CA, 94115, USA.
2
Cleveland Clinic Lerner College of Medicine, Cleveland, OH, 44106, USA.
3
Department of Internal Medicine, Yale University, New Haven, CT, 06520, USA.
4
Dermatology Department, Peking University Third Hospital, Beijing, China.
5
Department of Dermatology, Dicle University School of Medicine, 21280, Diyarbakır, Turkey.
6
University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
7
Division of Gastroenterology, University of California, San Francisco, San Francisco, CA, 94143, USA.
8
Department of Dermatology, University of California, San Francisco, CA, 94115, USA. Wilson.Liao@ucsf.edu.

Abstract

BACKGROUND:

Psoriasis impacts 1-3% of the world's population and is characterized by hyper-proliferation of keratinocytes and increased inflammation. At the molecular level, psoriasis is commonly driven by a Th17 response, which serves as a major therapeutic target. Microbiome perturbations have been associated with several immune-mediated diseases such as atopic dermatitis, asthma, and multiple sclerosis. Although a few studies have investigated the association between the skin microbiome and psoriasis, conflicting results have been reported plausibly due to the lack of standardized sampling and profiling protocols, or to inherent microbial variability across human subjects and underpowered studies. To better understand the link between the cutaneous microbiota and psoriasis, we conducted an analysis of skin bacterial communities of 28 psoriasis patients and 26 healthy subjects, sampled at six body sites using a standardized protocol and higher sequencing depth compared to previous studies. Mouse studies were employed to examine dermal microbial-immune interactions of bacterial species identified from our study.

RESULTS:

Skin microbiome profiling based on sequencing the 16S rRNA V1-V3 variable region revealed significant differences between the psoriasis-associated and healthy skin microbiota. Comparing the overall community structures, psoriasis-associated microbiota displayed higher diversity and more heterogeneity compared to healthy skin bacterial communities. Specific microbial signatures were associated with psoriatic lesional, psoriatic non-lesional, and healthy skin. Specifically, relative enrichment of Staphylococcus aureus was strongly associated with both lesional and non-lesional psoriatic skin. In contrast, Staphylococcus epidermidis and Propionibacterium acnes were underrepresented in psoriatic lesions compared to healthy skin, especially on the arm, gluteal fold, and trunk. Employing a mouse model to further study the impact of cutaneous Staphylcoccus species on the skin T cell differentiation, we found that newborn mice colonized with Staphylococcus aureus demonstrated strong Th17 polarization, whereas mice colonized with Staphylococcus epidermidis or un-colonized controls showed no such response.

CONCLUSION:

Our results suggest that microbial communities on psoriatic skin is substantially different from those on healthy skin. The psoriatic skin microbiome has increased diversity and reduced stability compared to the healthy skin microbiome. The loss of community stability and decrease in immunoregulatory bacteria such as Staphylococcus epidermidis and Propionibacterium acnes may lead to higher colonization with pathogens such as Staphylococcus aureus, which could exacerbate cutaneous inflammation along the Th17 axis.

PMID:
30185226
PMCID:
PMC6125946
DOI:
10.1186/s40168-018-0533-1
[Indexed for MEDLINE]
Free PMC Article

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