Impaired Innate Immune Function Associated with Fecal Supernatant from Crohn's Disease Patients: Insights into Potential Pathogenic Role of the Microbiome

Background:Although a dysbiosis of the intestinal microbiome plays a role in the pathogenesis of Crohn's disease (CD), the functional implication is unclear. We sought to determine the influence of fecal supernatant from patients with CD on innate immune function in neutrophil, macrophage, and epithelial cells. Metabolomic analysis was subsequently performed in an attempt to identify potential compounds responsible for the effects identified. Methods:In the fecal samples from 11 pediatric patients with CD and 10 healthy controls, 16S ribosomal and metabolomic analyses were performed. We evaluated the effect of preincubation with fecal supernatant on neutrophil, macrophage, epithelial cell survival, superoxide production, bacterial invasion, and/or bactericidal function using gentamicin protection assay. Ten substances identified as most elevated in CD compared with control samples by metabolomic analysis were similarly tested for effect on bactericidal function. Results:There were no statistically significant differences in microbial membership in fecal samples from patients with CD compared with healthy controls. However, bactericidal function was impaired in neutrophils and monocytes preincubated with supernatant from fecal samples from patients with CD. Although levels of many metabolites were noted to be altered in samples from patients with CD, the combination of the 10 most elevated compounds failed to demonstrate any effect on neutrophil bactericidal capacity. Conclusions:Fecal supernatant from patients with CD impairs intracellular bactericidal activity in neutrophils and macrophages. The functional consequences of the intestinal microbiome and its associated secreted products on innate immune function may be more critical than microbial membership in understanding the pathophysiology of CD.

[1]  Se Jin Song,et al.  The treatment-naive microbiome in new-onset Crohn's disease. , 2014, Cell host & microbe.

[2]  David C. Wilson,et al.  Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease , 2012, Nature.

[3]  M. Lukáš,et al.  Bile acid malabsorption in inflammatory bowel disease: Assessment by serum markers , 2011, Inflammatory bowel diseases.

[4]  V. Mootha,et al.  Metabolite profiles and the risk of developing diabetes , 2011, Nature Medicine.

[5]  N. Pace,et al.  Disease phenotype and genotype are associated with shifts in intestinal‐associated microbiota in inflammatory bowel diseases , 2011, Inflammatory bowel diseases.

[6]  Francis K C Hui,et al.  The arcsine is asinine: the analysis of proportions in ecology. , 2011, Ecology.

[7]  Anders F. Andersson,et al.  A pyrosequencing study in twins shows that gastrointestinal microbial profiles vary with inflammatory bowel disease phenotypes. , 2010, Gastroenterology.

[8]  Tariq Ahmad,et al.  Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci , 2010, Nature Genetics.

[9]  W. Strober Gut microbes : friends or fiends ? , 2010 .

[10]  S. Mazmanian,et al.  Inducible Foxp3+ regulatory T-cell development by a commensal bacterium of the intestinal microbiota , 2010, Proceedings of the National Academy of Sciences.

[11]  S. Carr,et al.  Metabolic Signatures of Exercise in Human Plasma , 2010, Science Translational Medicine.

[12]  William A. Walters,et al.  QIIME allows analysis of high-throughput community sequencing data , 2010, Nature Methods.

[13]  B. Nordestgaard,et al.  Penetrance of NOD2/CARD15 genetic variants in the general population , 2010, Canadian Medical Association Journal.

[14]  F. Avci,et al.  How bacterial carbohydrates influence the adaptive immune system. , 2010, Annual review of immunology.

[15]  R. Xavier,et al.  Crohn's disease‐associated adherent‐invasive E. coli are selectively favoured by impaired autophagy to replicate intracellularly , 2010, Cellular microbiology.

[16]  A. Sivignon,et al.  Crohn's disease adherent-invasive Escherichia coli colonize and induce strong gut inflammation in transgenic mice expressing human CEACAM , 2009, The Journal of experimental medicine.

[17]  J. Doré,et al.  Low counts of Faecalibacterium prausnitzii in colitis microbiota , 2009, Inflammatory bowel diseases.

[18]  J. Jansson,et al.  Metabolomics Reveals Metabolic Biomarkers of Crohn's Disease , 2009, PloS one.

[19]  M. Surette,et al.  Effects of mesalamine (5‐aminosalicylic acid) on bacterial gene expression , 2009, Inflammatory bowel diseases.

[20]  J. Doré,et al.  Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients , 2008, Proceedings of the National Academy of Sciences.

[21]  Judy H. Cho,et al.  Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease , 2008, Nature Genetics.

[22]  S. Mazmanian,et al.  A microbial symbiosis factor prevents intestinal inflammatory disease , 2008, Nature.

[23]  Mario Vaneechoutte,et al.  Active Crohn's disease and ulcerative colitis can be specifically diagnosed and monitored based on the biostructure of the fecal flora , 2008, Inflammatory bowel diseases.

[24]  R. Knight,et al.  The Human Microbiome Project , 2007, Nature.

[25]  R. Xavier,et al.  Unravelling the pathogenesis of inflammatory bowel disease , 2007, Nature.

[26]  I. Wilson,et al.  Rapid and noninvasive metabonomic characterization of inflammatory bowel disease. , 2007, Journal of proteome research.

[27]  P. Legendre,et al.  vegan : Community Ecology Package. R package version 1.8-5 , 2007 .

[28]  P. Rutgeerts,et al.  Increased permeability of macroscopically normal small bowel in Crohn's disease , 1994, Digestive Diseases and Sciences.

[29]  Laurent Beaugerie,et al.  High prevalence of adherent-invasive Escherichia coli associated with ileal mucosa in Crohn's disease. , 2004, Gastroenterology.

[30]  D. Podolsky,et al.  CARD15/NOD2 functions as an antibacterial factor in human intestinal epithelial cells. , 2003, Gastroenterology.

[31]  J. Korzenik,et al.  Is Crohn's disease an immunodeficiency? A hypothesis suggesting possible early events in the pathogenesis of Crohn's disease. , 2000, Digestive diseases and sciences.

[32]  K. H. Peterson,et al.  Epithelial permeability to proteins in the noninflamed ileum of Crohn's disease? , 1999, Gastroenterology.

[33]  N. Barnich,et al.  Presence of adherent Escherichia coli strains in ileal mucosa of patients with Crohn's disease. , 1998, Gastroenterology.

[34]  E. Lindberg,et al.  Intestinal permeability to polyethylene glycols in monozygotic twins with Crohn's disease. , 1995, Scandinavian journal of gastroenterology.

[35]  Y. Benjamini,et al.  Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .

[36]  L. Shapira,et al.  Neutrophil Defects as Risk Factors for Periodontal Diseases. , 1994, Journal of periodontology.

[37]  J. Paul Robinson,et al.  Chapter 25 Functional Measurements Using HL-60 Cells , 1994 .

[38]  J. Paul Robinson,et al.  Functional measurements using HL-60 cells. , 1994, Methods in cell biology.

[39]  T. J. Hurst,et al.  Inhibition of polymorphonuclear leucocyte phagocytosis by Porphyromonas gingivalis culture products in patients with adult periodontitis. , 1993, Archives of oral biology.

[40]  J T Boyle,et al.  Development and validation of a pediatric Crohn's disease activity index. , 1991, Journal of pediatric gastroenterology and nutrition.

[41]  J. Williams,et al.  Effect of sulphasalazine and its active metabolite, 5-amino-salicylic acid, on toxic oxygen metabolite production by neutrophils. , 1989, Gut.

[42]  G. Seymour,et al.  Modulation of human neutrophil adherence by periodontopathic bacteria: reversal by specific monoclonal antibodies. , 1989, International archives of allergy and applied immunology.

[43]  H. Ohta,et al.  Leukotoxic Activity in Actinobacillus (Haemophilus) actinomycetemcomitans Isolated from Periodontal Disease Patients , 1987, Microbiology and immunology.

[44]  R. Sjödahl,et al.  Postprandial serum bile acids in resected and non-resected patients with Crohn's disease. , 1982, Scandinavian journal of gastroenterology.