ABSTRACT
Disturbance of commensal intestinal microbiota is related to chronic inflammatory dermatosis. We analyzed the diversity of the gut microbiota to characterize the biological variation of psoriasis (Ps). Significant differences of gut microbiome profiles were revealed in murine model with psoriasis by sequencing 16S rRNA V3-V4 variable region. Group comparisons included the imiquimod cream (IMQ group, n=8), the imiquimod cream and antibiotics (ATB) (PC+IMQ group, n=8) and the healthy control (CTRL group, n=8). The gut microbiota existed in Ps groups including IMQ group and PC+IMQ group encompassed less diversity than controls, which were attributed to decreased presence of several taxa. The two Ps groups were characterized by significant reduction in firmicutes. In this study, microbiota of psoriasis was defined by an increase presence of Bacteroides. After treated with ATB, we found substantial increase of Lactobacillales but significant decrease of Clostridiales and Coriobacteriales. Relative lower abundance of multiple intestinal bacteria was observed in Ps groups. Although part of genera were concomitantly reduced in both IMQ and PC+IMQ conditions, we discovered the specialty of PC+IMQ group samples was that contained lower abundance of beneficial taxa. Characteristics of gut microbiota profiles in Ps mice were comparable to profiles in patients with Ps, which were related to alteration of specific inflammatory proteins in disease groups but were significantly different from control group. Thus, this study emphasizes the role of intestinal microbiota in the pathogenesis of Ps and provides new insight for investigating association between intestinal microbes and immune inflammation.
Keywords:
intestinal microbiota; chronic inflammatory dermatosis; psoriasis; microbiome
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Group A (red) and group B (blue) samples have decreased diversity compared to controls (green). Diversity indices were evaluated by (A) OTU numbers and (B) Shannon index.
(A) Principal coordinates analysis (PCoA) based on an unweighted UniFrac analysis of intestinal microbiota. Each point represented a sample. Samples in group A (IMQ group), group B (PC+IMQ group) and group C (CTRL group) were marked as red circles, green triangles and blue crosses, respectively. The PC1 explained 39.05% of total variability and PC2 explained 9% of total variability. (B) Principal Component Analysis (PCA) of the microbiome composition comparing. PC1explained the 61.19% of the total variability found, and PC2 explained the 20.38% of the total variability.
(A) Phylum and (B) genus level compositions of skin microbiome in group A (IMQ group), group B (PC+IMQ group) and group C (CTRL group). Only the predominant taxa are shown. Other relative lower abundant taxa are not plotted. (C) Bacterial taxa enrichment at genus level was drew by barplot. Terms of group A, group B and group C were colored by blue, orange and green, respectively. Significantly enrichments were showed with LDA score (log 10) > 4.
The expression levels of IL-23, IL-17A, IL-17F, IL-4, IL-22 and IL-10 were detected by Real-Time PCR. Barplots showed the dynamic changes at (A) 5 days, (B) 7 days, (C) 9 days, (D) 11 days, and (E) 14 days. White bars represented CTRL groups, grey bars represented IMQ groups, and black bars represented PC+IMQ groups.
