Shiju Xiao1,2
Guangzhong Zhang1*Chunyan Jiang1*Xin Liu3Xiaoxu Wang1,2Yafan Li4
Meijiao Cheng5
Hongpeng Lv4Fuyang Xian4Xinwei Guo1,2,6
Yong Tan7- 1Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China
- 2Graduate School, Capital Medical University, Beijing, China
- 3Puyang Hospital of Traditional Chinese Medicine, Puyang, China
- 4Beijing University of Chinese Medicine, Beijing, China
- 5Beijing QuantiHealth Technology Co., Ltd, Beijing, China
- 6Beijing Institute of Traditional Chinese Medicine, Beijing, China
- 7Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, China
Background: Increasing evidence has shown that alterations in the intestinal microbiota play an important role in the pathogenesis of psoriasis. The existing relevant studies focus on 16S rRNA gene sequencing, but in-depth research on gene functions and comprehensive identification of microbiota is lacking.
Objectives: To comprehensively identify characteristic gut microbial compositions, genetic functions and relative metabolites of patients with psoriasis and to reveal the potential pathogenesis of psoriasis.
Methods: DNA was extracted from the faecal microbiota of 30 psoriatic patients and 15 healthy subjects, and metagenomics sequencing and bioinformatic analyses were performed. The Kyoto Encyclopedia of Genes and Genomes (KEGG) database, cluster of orthologous groups (COG) annotations, and metabolic analyses were used to indicate relative target genes and pathways to reveal the pathogenesis of psoriasis.
Results: Compared with healthy individuals, the gut microbiota of psoriasis patients displayed an alteration in microbial taxa distribution, but no significant difference in microbial diversity. A distinct gut microbial composition in patients with psoriasis was observed, with an increased abundance of the phyla Firmicutes, Actinobacteria and Verrucomicrobia and genera Faecalibacterium, Bacteroides, Bifidobacterium, Megamonas and Roseburia and a decreased abundance of the phyla Bacteroidetes, Euryarchaeota and Proteobacteria and genera Prevotella, Alistipes, and Eubacterium. A total of 134 COGs were predicted with functional analysis, and 15 KEGG pathways, including lipopolysaccharide (LPS) biosynthesis, WNT signaling, apoptosis, bacterial secretion system, and phosphotransferase system, were significantly enriched in psoriasis patients. Five metabolites, hydrogen sulfide (H2S), isovalerate, isobutyrate, hyaluronan and hemicellulose, were significantly dysregulated in the psoriatic cohort. The dysbiosis of gut microbiota, enriched pathways and dysregulated metabolites are relevant to immune and inflammatory response, apoptosis, the vascular endothelial growth factor (VEGF) signaling pathway, gut-brain axis and brain-skin axis that play important roles in the pathogenesis of psoriasis.
Conclusions: A clear dysbiosis was displayed in the gut microbiota profile, genetic functions and relative metabolites of psoriasis patients. This study is beneficial for further understanding the inflammatory pathogenesis of psoriasis and could be used to develop microbiome-based predictions and therapeutic approaches.
Introduction
Psoriasis is an immune-mediated inflammatory chronic skin disease characterized by chronic inflammation in the dermis, parakeratosis and excessive epidermal growth, and 2-3% of the population are affected by psoriasis (Parisi et al., 2013; Hidalgo-Cantabrana et al., 2019). Less attention has been focused on the relationship between intestinal microbiota dysbiosis and the pathogenesis of psoriasis (Yan et al., 2017). However, recent studies have reported an alteration in the gut microbiota in patients with psoriasis (Scher et al., 2015; Chen et al., 2018; Hidalgo-Cantabrana et al., 2019; Shapiro et al., 2019) that is related to an aberrant inflammatory response (Salem et al., 2018). The intestinal microbiota plays an important role in the maintenance of immune homeostasis, regulating both acquired and innate immune responses (Sommer and Backhed, 2013; Palm et al., 2015; Planer et al., 2016). Gut microbiota alterations may activate T cells, trigger an inflammatory process and induce immune disorders (Littman and Pamer, 2011; Collins et al., 2012; Honda and Littman, 2016). Gut microbiota dysbiosis is related to immune and autoimmune disorders such as rheumatoid arthritis (RA) (Yeoh et al., 2013), allergies (Chen et al., 2016), type 1 diabetes (de Groot et al., 2017), autism (Mangiola et al., 2016; Zhang et al., 2018), inflammatory bowel disease (IBD) (Huttenhower et al., 2014), systemic lupus erythematosus (SLE) (Edwards and Costenbader, 2014), and multiple sclerosis (Rosser and Mauri, 2016). Moreover, intestinal microbiota alteration plays a key role in psoriasis (Shamriz et al., 2016; Luo et al., 2017; Stockinger and Omenetti, 2017), as well as other skin alterations, such as atopic dermatitis and vitiligo (Penders et al., 2013). In addition, the effects of current treatments for psoriasis are limited (Torres and Puig, 2018). Thus, further research on the pathophysiology caused by gut microbiota dysbiosis in psoriasis patients, which may be a breakthrough for pathological mechanism research, is urgently required.
Gut microbiota alterations have been observed in psoriatic patients and psoriatic arthritis patients (Fry and Baker, 2007; Scher et al., 2015; Chen et al., 2018; Hidalgo-Cantabrana et al., 2019; Shapiro et al., 2019). It was also found that gut microbiota dysregulation induced by vancomycin and polymyxin exacerbated psoriasis in an imiquimod (IMQ)-induced mouse model (Zanvit et al., 2015). It has been reported that antibiotic therapy can alleviate the thickness of lesions and reduce the proportion of Th17 cells, γδT cells and IL-17 in an imiquimod-induced psoriasis mouse model (Zákostelská et al., 2016). A predisposition for intestinal bowel diseases among psoriasis patients supports the gut-skin axis theory (Kimball et al., 2014). All of these studies identified the microbiota composition using 16S rRNA sequencing. This method has limitations such as failure to determine most microbes at the strain and species level and the potential for amplification bias (Konstantinidis and Tiedje, 2007; Pinto and Raskin, 2012). In contrast, compared with 16S rRNA sequencing, metagenome sequencing can provide a higher resolution of taxonomic profiles with functional classification of the microbiome (Lee et al., 2018). Nonetheless, few studies on the relationship of the gut microbiome and psoriasis using metagenome sequencing analysis have been conducted.
In this study, to further investigate the intestinal microbiota composition, gene functions and relative metabolites predicted from the microbial composition of psoriasis patients, the profile and composition of the intestinal microbiomes from stool samples of psoriasis patients and healthy controls were compared using metagenomics sequencing analysis. Investigation of the definite role of intestinal microbiome dysbiosis in the immunopathogenesis of inflammatory diseases may boost our realization of psoriasis aetiology and pathological mechanisms and promote targeted and novel predictions and treatments.
Materials and Methods
Participants
Patients with psoriasis (n=30) were identified and collected from the Beijing Hospital of Traditional Chinese Medicine (Table 1). The control group (n=15) comprised age-, sex- and body mass index (BMI)-matched healthy donors. Patients and healthy donors who received antibiotics, probiotics, glucocorticoids, or immunosuppression during the 6 previous months were not included. People with BMI ≥ 35 or ≤ 18, and those who have been suffering from diseases of the digestive system, immune system and other severe illnesses, were excluded. They have no especially dietary habit and belong to the same ethnic’s population (Chinese). According to principle of statistics, the different sample sizes of two groups will not affect the correctness of statistical inference (Pearce, 2016). The study was approved by the Ethical Committee of the Beijing Hospital of Traditional Chinese Medicine and conformed with the Declaration of Helsinki. All study subjects signed informed consent forms. The questionnaires containing personal and clinical information were completed by the patients.
Table 1 Characteristics of the psoriasis patients and healthy individuals.
Sample Collection
Stool samples were collected in a specimen collection kit and stored at -20°C immediately after defecation and then at -80°C before further manipulation in the laboratory.
DNA Extraction and Metagenomic Analysis
DNA from stool samples was extracted using the QIAamp PowerFecal Pro DNA Kit according to the manufacturers’ instructions. DNA was resolved in 10mM Tris-cl buffer and stored at -20°C and at -80°C for short-term and long-term use, respectively. Total DNA quality was measured by using a spectrophotometer with 1% agarose gel electrophoresis. DNA was fragmented to an average size of approximately 350 bp using KAPA HyperPlus PCR-free for library construction. Subsequently, we performed metagenomic sequencing on the Illumina HiSeq platform following the manufacturer’s instructions. The quality control of all raw metagenomic sequencing data was performed using MOCAT2 software. The raw sequence reads were trimmed by SolexaQA package with a length shorter than 30 bp and a quality score lower than 20. The quality control standards are: A260/280 between 1.8-2.0, A260/280>1.5. To remove contaminated reads, the filtered reads were compared to human genome using SOAPaligner, and clean raw reads were obtained. To obtain contigs for the following annotation and prediction, we used SOAPdenovo software to assemble the clean raw reads. Afterwards, the scaftigs from each sample were predicted using MetaGeneMark.
Bioinformatics and Statistical Analysis
The relative abundances of different level of taxonomic assignment were predicted using MetaPhlAn (metagenomic phylogenetic analysis) 2.0, which includes an expanded set of ~1 million markers from >7,500 species (Truong et al., 2015). We performed all statistical analyses using R software unless otherwise specified. The Shannon indices were used to calculate the α-diversity of the samples. The β-diversity was estimated by taxon-based Bray-Curtis distance via the R package vegan, and compositional differences between psoriasis and non-psoriasis samples (β-diversity) were represented in principal coordinates analysis (PCoA) plots using the R package (Bray and Curtis, 1957; VEGAN, 2003; Dray and Dufour, 2007). The nonparametric Kruskal-Wallis test was used because some of the variables analysed lacked homogeneous variances or were not normally distributed. ANCOM analyses and permutational analysis of variance (PERMANOVA) were also performed (Mandal et al., 2015).
Linear discriminant analysis (LDA) effect size (LEfSe) was applied to identify differences in the relative abundances of genera of gut microbiota between psoriasis and healthy volunteers (Segata et al., 2011). LDA values > 2.0 with a P value < 0.05 were considered significantly enriched.
Microbial Gene Function Prediction and Metabolite Analysis
COG and KEGG pathway annotations were obtained using the DIAMOND database (Version 0.7.9.58) via BLASTP. To determine gene functions that discriminate bacterial compositions between psoriatic patients and healthy donors, the KEGG enrichment pathways were analysed with Generally Applicable Gene-set Enrichment for Pathway Analysis (GAGE) (Luo et al., 2009). The differential expressed bacteria genes were identified by comparing relative abundances between two groups using Wilcoxon test, and P values were adjusted for multiple testing with a Benjamini-Hochberg false discovery rate correction. Adjusted P value < 0.05 were considered significantly differential on gene expression.
The metabolite potential was estimated by the relative abundance of the corresponding species; values were simply added or subtracted if the species produced or consumed, respectively. The production or consumption relationships between metabolites and species were curated from the literature of Sung J et al. and Cecilia Noecker et al. (Noecker et al., 2016; Sung et al., 2017). Heatmaps were generated to represent potential metabolic differences in the gut microbiome between the 2 groups.
Results
Microbial Diversity
The species accumulation curve of each group tended to plateau, indicating that sample biodiversity was adequately covered with the applied sequencing depth (Figure 1). The α-diversity of the gut microbiota (Shannon index) in the healthy group was higher than that in the psoriasis group, but there were no significant differences between the two groups (Figure 2). Moreover, the β-diversity analyses showed through PCoA demonstrated a separate tendency, but no significant clustering of non-psoriasis controls and patients was observed based on Bray-Curtis dissimilarity, indicating that the structural diversity of the intestinal microbiota did not differ between the two groups (Figure 3).
Figure 1 Species accumulation curves. The species accumulation curve of each group tended to plateau, indicating that sample biodiversity was adequately covered with the applied sequencing depth.
Figure 2 α-Diversity based on Shannon indices displayed no significant differences in the intestinal microbiota between the two groups.
Figure 3 β-Diversity represented as a two-dimensional PCoA showed no differential clustering between the two groups. (The red dots showed the samples from psoriasis patients, whereas the green dots showed the samples from healthy individuals. The closer the dots in one group, the more similar in gut microbiota. The gut microbiota compositions are indicated with red and green circles, respectively. The smaller the overlap of two circles, the more different in the gut microbiota compositions of two groups).
Demographics of the Study Population
Forty-five faecal samples were collected: 30 (60%) samples were collected from patients suffering from psoriasis, and 15 samples were collected from healthy age-, sex-, BMI-matched individuals. The demographic characteristics details of the two groups are presented in Table 1.
Altered Gut Microbiota Composition in Psoriasis Patients
Five dominant phyla based on different relative abundances between psoriasis patients and controls were identified. The phyla Actinobacteria, Firmicutes, and Verrucomicrobia were increased, while Bacteroidetes and Proteobacteria were reduced in the psoriatic patients compared with the controls (Figure 4A, B). Moreover, at the genus level, higher proportions of Faecalibacterium, Bacteroides, Bifidobacterium, Megamonas and Roseburia and lower proportions of Prevotella, Alistipes and Eubacterium were identified in psoriatic patients (Figures 4C, D). The abundance of Faecalibacterium prausnitzii was higher in psoriasis patients than in controls (Figure 4E). It has been reported that Faecalibacterium and Prevotella are associated with anti-inflammatory properties (Shapiro et al., 2019).
Figure 4 Relative abundance (%) of the intestinal microbiota determined at the phylum (A, B) genus (C, D) and species (E) levels. The columns represent individuals in the psoriasis or control group (A, C, E).
Wilcoxon rank-sum permutation tests were performed to further compare the significant differences in the gut microbiota compositions between the 2 groups. There was a significant decrease in the phylum Euryarchaeota in the psoriasis group (0.031 vs 0.003, P < 0.05). Decreases in the families Oxalobacteraceae, Porphyromonadaceae, Pasteurellaceae, Rikenellaceae, Sphingobacteriaceae and Comamonadaceae were observed in the psoriasis patients (Table 2A). Nine genera, Butyricimonas, Oxalobacter, Actinobacillus, Odoribacter, Anaerotruncus, Alistipes, Pseudoflavonifractor, Pedobacter, and Comamonas, were significantly more abundant in the healthy control individuals than in the psoriasis patients (Table 2B).
Table 2 Taxonomic differences between the psoriasis patients and controls at the family (A) and genus (B) levels.
LEfSe was used to further determine the specific significantly different bacterial taxa between the two cohorts (Figure 5A). Several genera, including Oscillospiraceae, Oxalobacter, Haemophilus, Odoribacter, Alistipes, and Pedobacter, were significantly enriched in the faeces of controls. The identified taxa were highlighted on the cladogram to indicate significant differences in phylogenetic distributions along with their LDA scores (Figure 5B). These results represented a notable gut microbiota alteration between the 2 groups.
Figure 5 Intestinal microbiota profiles in psoriasis patients. (A) Cladogram generated from the LEfSe analysis indicating the phylogenetic distribution of the microbiota of psoriasis and control groups from phylum to genus. (B) Histogram of LDA scores to identify differentially abundant bacteria between patients and controls (LDA score > 2.0).
Gene Functions and Metabolic Variation Analysis in Psoriasis Patients
A total of 134 significantly different functional COGs between patients and controls were predicted (Table S1). Fifteen KEGG pathways (including LPS biosynthesis, WNT signaling pathway, apoptosis, bacterial secretion system, phosphotransferase system, and others) were significantly enriched in the psoriasis patient group (Table 3). Heatmaps were generated to represent the potential metabolic differences in the gut microbiome between the psoriasis and control groups. We found that 5 metabolites, H2S, isovalerate, isobutyrate, hyaluronan and hemicellulose, were significantly differentially abundant between the two cohorts (Table 4, Figure 6). Figure 6 shows that the colour of the patient individuals was different from that of the control subjects, which indicated the metabolic differences between the two groups.
Table 4 Dysregulated metabolites in psoriasis patients.
Figure 6 Faecal metabolic heatmap of samples from psoriasis patients. Hierarchical clustering showing the 5 significantly differentially abundant metabolites between the 2 groups (increased and decreased levels of metabolites are indicated by red and blue, respectively). The lines indicate specific metabolites, and the columns represent the individuals.
Discussion
Evidence linking intestinal microbiota dysbiosis to chronic inflammation and immune system-mediated diseases has been expanding. This study is the first to elucidate gut bacterial changes in patients with psoriasis by metagenomic gene profiling analysis, not 16S rRNA sequencing analysis which has limitations but has been used in most studies. For example, contributions to the metagenome by organisms such as bacteria cannot be predicted by using 16S rRNA primers (Shapiro et al., 2019). Furthermore, in this study, the target gene pathways (KEGG and COG) and metabolic function of the microbiome in patients with psoriasis compared with control subjects were also detected, which are beneficial for in depth explanation of the pathogenesis of psoriasis.
Our results indicated the gut microbiota of psoriasis patients displayed an alteration in microbial taxa distribution, but no significant difference in microbial diversity. The psoriatic patients recruited showed a microbiota profile characterized by increased proportions of the phyla Actinobacteria and Firmicutes and genera Faecalibacterium, Bacteroides, Bifidobacterium and Megamonas and a reduction in the phyla Bacteroidetes, Euryarchaeota and Proteobacteria and genera Prevotella, Alistipes and Eubacterium, which seems to be in accordance with results reported in other studies (Scher et al., 2015; Codoñer et al., 2018; Hidalgo-Cantabrana et al., 2019; Shapiro et al., 2019). Functional analysis suggested that 134 COGs were predicted, and 15 KEGG pathways, including LPS biosynthesis, WNT signaling pathway, apoptosis, bacterial secretion system, and phosphotransferase system, were significantly enriched in psoriasis patients. Five metabolites (H2S, isovalerate, isobutyrate, hyaluronan, and hemicellulose) were significantly downregulated in the psoriatic cohort.
The pathogenesis of psoriasis could be related to immune and inflammatory response due to the dysfunction of medium- and short-chain fatty acids and the compromised colonic mucosal integrity and gut inflammation (Yegorov et al., 2020). Based on these results, the Firmicutes/Bacteroidetes (F/B) ratio increased, and the abundance of Bacteroides and Prevotella was deregulated in the psoriasis group, which seems to be in accordance with results reported in other studies (Visser et al., 2019; Dei-Cas, et al., 2020; Sikora et al., 2020). It has been reported that a high F/B ratio and a deregulated abundance of Bacteroides and Prevotella alter the production of medium- and short-chain fatty acids, such as acetate and butyrate, which are essential in maintaining colonic mucosal integrity (Corrêa-Oliveira et al., 2016; Perry et al., 2016; Komaroff, 2017; Christensen et al., 2018). The compromised integrity of the mucus barrier affects gut immune homeostasis and antigen presentation, resulting in immune responses and chronic inflammation (Bischoff et al., 2014; Christensen et al., 2018). Bacteroides produce polysaccharide A, which activates regulatory T cells and plays an immunomodulatory role in the gut (Mosca et al., 2016). After the addition of arabinoxylans, an elevation in caecal Prevotella was detected; Prevotella can enhance intestinal barrier function and decrease caecal inflammatory markers (Neyrinck et al., 2011; Neyrinck et al., 2012; Hong et al., 2016). Thus, novel therapeutic approaches that lower the F/B ratio and the abundance of Bacteroides, as well higher the abundance of Prevotella may be beneficial for psoriasis.
Except for immune and inflammatory response, psoriasis aetiology and pathological mechanisms may be also related to dysfunction of gut-brain axis and brain-skin axis. The abundance of Faecalibacterium prausnitzii was higher in psoriasis patients than in controls. F. prausnitzii has been observed to be decreased in patients with major depressive diseases, RA, metabolic syndrome, Crohn’s disease and obesity (Sokol et al., 2008; Stoll et al., 2014; Jiang et al., 2015; Remely et al., 2016) and increased in children with atopic dermatitis (Song et al., 2016). It has been reported that psoriasis, associated with both a physical and a psychological burden, is closely related to chronic stress (i.e., depression and anxiety) via the hypothalamic-pituitary-adrenal (HPA) axis which secretes neuroendocrine mediators and triggers skin inflammation in psoriasis (Chen and Lyga, 2014; Alexopoulos and Chrousos, 2016; Mueller et al., 2017; Visser et al., 2019). In addition, gut-brain axis dysfunction may be associated with psoriasis and psoriatic arthritis (Lu and He, 2015; Sikora et al., 2020), and the altered gut microbiota in patients with psoriatic arthritis resembles dysbiosis in inflammatory bowel disease (Scher et al., 2015). Furthermore, F. prausnitzii has effects on cytokine production and can produce butyrate, which inhibits the NF-κB pathway, inhibiting the inflammatory response (Sokol et al., 2008; Jiang et al., 2015; Hiippala et al., 2018). The relative abundances of Alistipes and Parabacteroides were reduced in the psoriasis group. This result is consistent with studies of psoriasis (Scher et al., 2015; Hidalgo-Cantabrana et al., 2019) and Crohn’s disease (Willing et al., 2010). The abundance of members of the genus Sutterella were also found to increase. Sutterella has a potential role in immune regulation and pro-inflammatory properties (Hiippala et al., 2016). Therefore, therapies that can lower the abundance of F. prausnitzii and Sutterella, and higher the abundance of Alistipes and Parabacteroides may be effective for treating psoriasis. Further research of the role of other identified genera in psoriasis is needed in the future.
A total of 15 KEGG pathways were significantly enriched in the patients with psoriasis, including LPS biosynthesis, WNT signaling pathway, bacterial secretion system, phosphotransferase system, and apoptosis, which are relevant to inflammatory response and apoptosis. LPS has been epidemiologically relevant to psoriasis and may maintain chronic inflammation (Shapiro et al., 2007). This inflammagen will activate the production of inflammatory chemokines and cytokines, stimulating the innate and adaptive immune systems (Kell and Pretorius, 2015; Potgieter et al., 2015; Kell and Pretorius, 2018). In addition, the WNT signaling pathway, which is involved in skin inflammation in psoriasis pathogenesis, was enriched in psoriatic patients and psoriatic arthritis patients (Dolcino et al., 2015; Wang et al., 2017). It has been reported that IL-36γ promotes inflammation and suppresses the differentiation of keratinocytes in psoriasis via the WNT signaling pathway (Wang et al., 2017). Moreover, the WNT signaling pathway has been involved in synovial inflammation (Miao et al., 2013). Apoptosis plays a key role in the pathogenesis of psoriasis (Chimenti et al., 2018; Hugh and Weinberg, 2018). T cells cause chronic inflammation and apoptosis via cytokines in psoriasis (Hugh and Weinberg, 2018). It has been reported that topical sunitinib ointment can suppress the proliferation and apoptosis of keratinocytes and reduce psoriasis-like inflammation (Kuang et al., 2018). The associations of other enriched pathways and the pathogenesis of psoriasis may be the direction of further research.
Heat map and hierarchical clustering showed the 5 metabolites (H2S, isovalerate, isobutyrate, hyaluronan, and hemicellulose) that were significantly differentially abundant between psoriasis patients and controls, which are related to inflammation and the VEGF signaling pathway. Studies have shown that H2S is a novel inflammatory mediator (Bhatia, 2015). H2S has been involved in different clinical inflammatory disorders, animal models, and in vitro systems (Bhatia, 2015; Castelblanco et al., 2018). H2S can alleviate LPS-induced lung inflammation in male rats (Zhang et al., 2016; Ali et al., 2018). Remarkable elevation of 3-OH-isovalerate was confirmed in 6 patients with biotinidase deficiency, all of whom presented with some extent of neurological abnormalities and dermatological lesions, and one of them presented with generalized pustular psoriasis (Yang et al., 2003). It has been suggested that butyrate is an intermediate in the anaerobic degradation of isobutyrate (Tholozan et al., 1988). The reduced generation of butyrate in psoriasis patients may compromise the integrity of the intestinal epithelial barrier, resulting in immune responses and chronic inflammation (Bischoff et al., 2014; Christensen et al., 2018; Shapiro et al., 2019). It has been reported that hyaluronan can act as a pro-inflammatory cytokine and induce inflammatory processes in psoriatic arthritis (Hellman et al., 2019). The VEGF signaling pathway plays an important role in psoriasis, and modified hemicellulose suppresses VEGF-induced angiogenesis (Malecic and Young, 2016; Zhu et al., 2017). Chronic inflammation is relevant to alterations of the intestinal microbiota that can be modified with hemicellulose (Konkol et al., 2019).
Lower microbial diversity was detected in some studies (Scher et al., 2015; Hidalgo-Cantabrana et al., 2019), while our results were on their opposite and were consistent with the research of Codoner et al. and Tan et al. (Codoñer et al., 2018; Tan et al., 2018). Difference of those results could be due to the different algorithms used and indices used in the studies, since most studies performed 16S rRNA sequencing and considered the number of OTUs and their relative proportion.
The potential limitations of the study are as follows: (1) The sample size was too small to identify the impact of the length, severity, comorbidities and treatments of psoriasis on the microbiome. (2) The absence of stool supernatant and gut epithelium samples might be beneficial for further research. (3) The microbial metabolite profiling was inferred base on the DNA and the abundance of gut microbiota, not by metabonomics. The actual microbial metabolite profiling may be different from it in the processes of DNA transcription and translation. (4) The gut microbiota profile, genetic functions and relative metabolites of psoriasis patients were performed using metagenomics sequencing. However, the sample marker gene database may include most of the species-and strain-level information, not 100% of all existing species or organisms. (5) The dietary habits have not been screened with specific questionnaire, which may potentially influence the gut microbiota of subjects.
Conclusion
The demonstrated alterations in microbiome composition and corresponding gene function and metabolic dysregulation likely impact the regulation of inflammation and immune responses, the VEGF signaling pathway, apoptosis, gut-brain axis and brain-skin axis that lead to psoriasis. Understanding the association between the intestinal microbiome and psoriasis pathogenesis will be beneficial for the development of novel predictions and therapeutic approaches for psoriasis, including microbial administration via diet, eradication of antibiotics, addition of probiotics or faecal microbial transplantation as a substitute to shift the microbiome towards a healthy status, as has been suggested for IBD (Quraishi et al., 2017).
Data Availability Statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/sra/PRJNA688472.
Ethics Statement
The studies involving human participants were reviewed and approved by the Ethical Committee of the Beijing Hospital of Traditional Chinese Medicine. The patients/participants provided their written informed consent to participate in this study.
Author Contributions
GZ and YT designed the study. FX and YL performed the experiments. XL and XW collected and prepared samples for sequencing. MC performed sequencing and sequencing analysis with technical assistance from CJ. HL and XW performed statistical interpretation and analyses with technical assistance from XG, and SX took primary responsibility for writing the manuscript with English improved by YT and GZ. All authors discussed the results and commented on the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by grants from the National Natural Science Foundation of China (grant number 81673974, 81974572) and the Beijing Municipal Administration of Hospitals Incubating Program (grant number PZ2019024).
Conflict of Interest
MC was employed by the company Beijing QuantiHealth Technology Co., Ltd.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcimb.2021.605825/full#supplementary-material
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Keywords: gut microbiota, genetic functions, metabolites, psoriasis, metagenomics sequencing
Citation: Xiao S, Zhang G, Jiang C, Liu X, Wang X, Li Y, Cheng M, Lv H, Xian F, Guo X and Tan Y (2021) Deciphering Gut Microbiota Dysbiosis and Corresponding Genetic and Metabolic Dysregulation in Psoriasis Patients Using Metagenomics Sequencing. Front. Cell. Infect. Microbiol. 11:605825. doi: 10.3389/fcimb.2021.605825
Received: 15 September 2020; Accepted: 09 March 2021;
Published: 01 April 2021.
Edited by:
Bikash Sahay, University of Florida, United StatesReviewed by:
Simone Garcovich, Catholic University of the Sacred Heart, ItalyHung-Lin Chen, Academia Sinica, Taiwan
Copyright © 2021 Xiao, Zhang, Jiang, Liu, Wang, Li, Cheng, Lv, Xian, Guo and Tan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Chunyan Jiang, tcmjcy@126.com; Guangzhong Zhang, guangzhzh@163.com