Intestinal microbiota profiling and predicted metabolic dysregulation in psoriasis patients

Objectives The intestinal microbiota has been known to involve in obesity and host immune response. We aimed to investigate the intestinal microbiota and potential genetic function in relation to clinical presentation in psoriasis patients. Methods Faecal microbiota and predicted genetic function in...

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Published inExperimental dermatology Vol. 27; no. 12; pp. 1336 - 1343
Main Authors Chen, Yi‐Ju, Ho, Hsiu J., Tseng, Ching‐Hung, Lai, Zi‐Lun, Shieh, Jeng‐Jer, Wu, Chun‐Ying
Format Journal Article
LanguageEnglish
Published Denmark Wiley Subscription Services, Inc 01.12.2018
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Summary:Objectives The intestinal microbiota has been known to involve in obesity and host immune response. We aimed to investigate the intestinal microbiota and potential genetic function in relation to clinical presentation in psoriasis patients. Methods Faecal microbiota and predicted genetic function inferred from high‐throughput 16S ribosomal RNA sequencing were analysed between psoriasis (n = 32) and age‐, gender‐ and body mass index (BMI)‐matched non‐psoriasis subjects (n = 64), from a referral medical centre. The correlation between altered microbiota and disease activity, arthritis and systemic anti‐psoriatic drugs was also investigated. Results We observed a distinct faecal microbial community structure in psoriasis patients, with an increased abundance of phylum Firmicutes and decreased abundance of phylum Bacteroidetes, across different subgroup of subjects. Ruminococcus and Megasphaera, of the phylum Firmicutes, were the top‐two genera of discriminant abundance in psoriasis. A number of functional genes and metabolic pathways involving bacterial chemotaxis and carbohydrate transport were predicted over‐represented, whereas genes related to cobalamin and iron transport were predicted under‐represented in faecal microbiota of psoriasis patients. Conclusions The distinct faecal microbial composition in psoriasis might be associated with altered transport of carbohydrate, cobalamin and iron, as well as chemotaxis.
Bibliography:Funding information
This work was supported partly by grants MOST 104‐2314‐B‐010‐051 MY3 and TCVGH‐1046802C.
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ISSN:0906-6705
1600-0625
1600-0625
DOI:10.1111/exd.13786