J Pediatr Infect Dis 2017; 12(02): 131-135
DOI: 10.1055/s-0037-1601340
Rapid Communication
Georg Thieme Verlag KG Stuttgart · New York

Disturbance of Microbial Core Species in New-Onset Juvenile Idiopathic Arthritis

Petra Hissink Muller
1   Department of Pediatric Rheumatology, Leiden University Medical Center, Leiden, The Netherlands
,
Tim G.J. de Meij
2   Department of Pediatric Gastroenterology, VU Medical Center, Amsterdam, The Netherlands
,
Michiel Westedt
1   Department of Pediatric Rheumatology, Leiden University Medical Center, Leiden, The Netherlands
,
Evelien F.J. de Groot
2   Department of Pediatric Gastroenterology, VU Medical Center, Amsterdam, The Netherlands
,
Cornelia F. Allaart
3   Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands
,
Danielle M.C. Brinkman
1   Department of Pediatric Rheumatology, Leiden University Medical Center, Leiden, The Netherlands
,
Dieneke Schonenberg-Meinema
4   Department of Pediatric Rheumatology, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands
,
Merlijn van den Berg
4   Department of Pediatric Rheumatology, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands
,
Lisette W.A. van Suijlekom-Smit
5   Department of Pediatric Rheumatology, Sophia Children's Hospital Erasmus Medical Center, Rotterdam, The Netherlands
,
Marion van Rossum
6   Department of Pediatric Rheumatology, Amsterdam Rheumatology and immunology Center, Amsterdam, The Netherlands
,
Andries E. Budding
7   Department of Medical Microbiology, VU University Medical Center, Amsterdam, The Netherlands
,
Rebecca ten Cate
1   Department of Pediatric Rheumatology, Leiden University Medical Center, Leiden, The Netherlands
› Author Affiliations
Further Information

Publication History

29 November 2016

20 February 2017

Publication Date:
04 April 2017 (online)

Abstract

Over the past decades, the intestinal microbiota has increasingly gained attention in studies addressing the pathophysiology of (pediatric) autoimmune diseases, including inflammatory joint diseases, inflammatory bowel disease (IBD), and type 1 diabetes. In this study, we have analyzed the composition of gut microbiota of newly diagnosed juvenile idiopathic arthritis (JIA) patients, prior to initiation of disease-modifying antirheumatic drugs (DMARDs). Fecal microbiota profiles of 8 JIA patients (median age: 11.1 years, 6 girls) were compared with 22 healthy age-matched controls using IS-pro, a 16S-23S interspacer (IS) region-based, eubacterial molecular detection technique. By partial least squares discriminant analysis (PLS-DA), microbiota profiles of JIA and controls could significantly be discriminated based on a limited set of species belonging to the phylum Bacteroidetes ([Fig. 2]), but not within other phyla, with a sensitivity of 88%, specificity of 73% ([Fig. 3]), and area under the curve (AUC) 0.87 (95% CI: 0.73–0.87). These discriminative species have been considered to be part of the microbial core in healthy children.

Conclusion Our findings add to the increasing notion that the gut microbiota may be involved in the pathophysiology of JIA. Species involved in the discrimination between JIA and controls are members of the microbial core in the healthy state. Expanding knowledge on JIA-specific microbial signatures and host interactions may open avenues to explore options to develop individualized, microbiota-based preventive, and therapeutic interventions in JIA.

 
  • References

  • 1 Prakken BJ, Albani S. Using biology of disease to understand and guide therapy of JIA. Best Pract Res Clin Rheumatol 2009; 23 (5) 599-608
  • 2 Scher JU, Littman DR, Abramson SB. Microbiome in inflammatory arthritis and human rheumatic diseases. Arthritis Rheumatol 2016; 68 (1) 35-45
  • 3 Carubbi F, Ruscitti P, Pantano I , et al. Jejunoileal bypass as the main procedure in the onset of immune-related conditions: the model of BADAS. Expert Rev Clin Immunol 2013; 9 (5) 441-452
  • 4 Del Val Del Amo N, Ibanez Bosch R. Post intestinal bypass arthritis-dermatitis syndrome. Clin Exp Rheumatol 2008; 26 (2) 386
  • 5 Yeoh N, Burton JP, Suppiah P, Reid G, Stebbings S. The role of the microbiome in rheumatic diseases. Curr Rheumatol Rep 2013; 15 (3) 314
  • 6 Tejesvi MV, Arvonen M, Kangas SM , et al. Faecal microbiome in new-onset juvenile idiopathic arthritis. Eur J Clin Microbiol Infect Dis 2016; 35 (3) 363-370
  • 7 Stoll ML, Kumar R, Morrow CD , et al. Altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis. Arthritis Res Ther 2014; 16 (6) 486
  • 8 Aggarwal A, Sarangi AN, Gaur P, Shukla A, Aggarwal R. Gut microbiome in children with enthesitis-related arthritis in a developing country and the effect of probiotic administration. Clin Exp Immunol 2017; 187 (3) 480-489
  • 9 Di Paola M, Cavalieri D, Albanese D , et al. Alteration of fecal microbiota profiles in juvenile idiopathic arthritis. Associations with HLA-B27 allele and disease status. Front Microbiol 2016; 7: 1703
  • 10 Paun A, Danska JS. Modulation of type 1 and type 2 diabetes risk by the intestinal microbiome. Pediatr Diabetes 2016; 17 (7) 469-477
  • 11 Maukonen J, Kolho KL, Paasela M , et al. Altered fecal microbiota in paediatric inflammatory bowel disease. J Crohn's Colitis 2015; 9 (12) 1088-1095
  • 12 Hissink Muller P. A comparison of three treatment strategies in recent onset DMARD naïve juvenile idiopathic arthritis: 3-months results of the BeSt for Kids-Study. Late breaking abstracts presented at the ACR Annual Meeting 2014 [online]. 2014. http://acrabstracts.org/abstracts/a-comparison-of-three-treatment-strategies-in-recent-onset-dmard-naive-juvenile-idiopathic-arthritis-3-months-results-of-the-best-for-kids-study 2014 . Accessed November 19, 2014
  • 13 de Meij TG, Budding AE, de Groot EF , et al. Composition and stability of intestinal microbiota of healthy children within a Dutch population. FASEB J 2016; 30 (4) 1512-1522
  • 14 Budding AE, Grasman ME, Lin F , et al. IS-pro: high-throughput molecular fingerprinting of the intestinal microbiota. FASEB J 2010; 24 (11) 4556-4564
  • 15 Rajilić-Stojanović M, Biagi E, Heilig HG , et al. Global and deep molecular analysis of microbiota signatures in fecal samples from patients with irritable bowel syndrome. Gastroenterology 2011; 141 (5) 1792-1801
  • 16 Daniels L, Budding AE, de Korte N , et al. Fecal microbiome analysis as a diagnostic test for diverticulitis. Eur J Clin Microbiol Infect Dis 2014; 33 (11) 1927-1936
  • 17 Arvonen M, Berntson L, Pokka T, Karttunen TJ, Vähäsalo P, Stoll ML. Gut microbiota-host interactions and juvenile idiopathic arthritis. Pediatr Rheumatol Online J 2016; 14 (1) 44
  • 18 Rutayisire E, Huang K, Liu Y, Tao F. The mode of delivery affects the diversity and colonization pattern of the gut microbiota during the first year of infants' life: a systematic review. BMC Gastroenterol 2016; 16 (1) 86
  • 19 Voreades N, Kozil A, Weir TL. Diet and the development of the human intestinal microbiome. Front Microbiol 2014; 5: 494
  • 20 Markle JG, Frank DN, Mortin-Toth S , et al. Sex differences in the gut microbiome drive hormone-dependent regulation of autoimmunity. Science 2013; 339 (6123): 1084-1088
  • 21 Kalliomäki M, Collado MC, Salminen S, Isolauri E. Early differences in fecal microbiota composition in children may predict overweight. Am J Clin Nutr 2008; 87 (3) 534-538
  • 22 Bervoets L, Van Hoorenbeeck K, Kortleven I , et al. Differences in gut microbiota composition between obese and lean children: a cross-sectional study. Gut Pathog 2013; 5 (1) 10
  • 23 Santacruz A, Marcos A, Wärnberg J , et al; EVASYON Study Group. Interplay between weight loss and gut microbiota composition in overweight adolescents. Obesity (Silver Spring) 2009; 17 (10) 1906-1915