Age and fecal microbial strain-specific differences in patients with spondyloarthritis

Academic Article

Abstract

  • © 2018 The Author(s). Background: Prior studies have demonstrated abnormalities in the composition of the gastrointestinal microbiota in pediatric and adult patients with spondyloarthritis (SpA). In particular, diminished fecal abundance of Faecalibacterium prausnitzii and abnormalities in both directions in the abundance of the Bacteroides genus have been identified. Methods: We obtained fecal specimens from 30 children with treatment-naïve enthesitis-related arthritis (ERA) and 19 healthy controls, as well as specimens from 11 adult patients with longstanding SpA and 10 adult healthy controls. All of the samples underwent sequencing of the 16S ribosomal DNA. A subset of the pediatric fecal samples was subjected to shotgun metagenomics sequencing. Results: ERA patients had decreased abundance of the anti-inflammatory F. prausnitzii A2-165 strain (41±28% versus 54±20% of all sequences matching F. prausnitzii, p=0.084) and an increased abundance of the control F. prausnitzii L2/6 strain (28±28% versus 15±15%, p=0.038). Similar trends were observed in adults with longstanding SpA (n=11) and controls (n=10). In contrast, the fecal abundance of Bacteroides fragilis was increased in ERA subjects (2.0±4.0% versus 0.45±0.7% of all sequences, p=0.045), yet was diminished in adult subjects (0.2±% versus 1.0±% of all sequences, p=0.106). Shotgun metagenomics sequencing of the fecal DNA in the pediatric subjects revealed diminished coverage of the butanoate pathway (abundance normalized to controls of 1±0.48 versus 0.72±0.33 in ERA, p=0.037). Conclusions: The anti-inflammatory F. prausnitzii A2-165 strain appears to be depleted in both pediatric and adult SpA. In contrast, B. fragilis may be depleted in adult disease yet abundant in pediatric SpA, suggesting developmental effects on the immune system.
  • Digital Object Identifier (doi)

    Author List

  • Stoll ML; Weiss PF; Weiss JE; Nigrovic PA; Edelheit BS; Bridges SL; Danila MI; Spencer CH; Punaro MG; Schikler K
  • Volume

  • 20
  • Issue

  • 1