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Altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis

INTRODUCTION: Prior studies have established altered microbiota and immunologic reactivity to enteric commensal organisms in inflammatory bowel disease (IBD). Since intestinal inflammation is present in a subset of patients with both pediatric and adult spondyloarthritis (SpA), we hypothesized that...

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Autores principales: Stoll, Matthew L, Kumar, Ranjit, Morrow, Casey D, Lefkowitz, Elliot J, Cui, Xiangqin, Genin, Anna, Cron, Randy Q, Elson, Charles O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272554/
https://www.ncbi.nlm.nih.gov/pubmed/25434931
http://dx.doi.org/10.1186/s13075-014-0486-0
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author Stoll, Matthew L
Kumar, Ranjit
Morrow, Casey D
Lefkowitz, Elliot J
Cui, Xiangqin
Genin, Anna
Cron, Randy Q
Elson, Charles O
author_facet Stoll, Matthew L
Kumar, Ranjit
Morrow, Casey D
Lefkowitz, Elliot J
Cui, Xiangqin
Genin, Anna
Cron, Randy Q
Elson, Charles O
author_sort Stoll, Matthew L
collection PubMed
description INTRODUCTION: Prior studies have established altered microbiota and immunologic reactivity to enteric commensal organisms in inflammatory bowel disease (IBD). Since intestinal inflammation is present in a subset of patients with both pediatric and adult spondyloarthritis (SpA), we hypothesized that SpA patients may also have altered microbiota and immune responsiveness to enteric organisms. METHODS: Stool and blood specimens were collected from children with enthesitis-related arthritis (ERA) and non-inflammatory controls. DNA purified from stool was subject to PCR amplification and sequencing of the variable IV region from the 16S rDNA gene. IgA and IgG Enzyme-linked Immunosorbent Assays (ELISAs) were performed on select species of bacteria in most subjects. RESULTS: Twenty-five children with ERA and 13 controls were included. The ERA patients had less Faecalibacterium prausnitzii (3.8% versus 10%, P = 0.008) and lachnospiraceae family (12 versus 7.0%, P = 0.020), a statistically significant increase in bifidobacterium (1.8% versus 0%, P = 0.032) and a non-statistically significant increase in Bacteroides (21% versus 11%, P = 0.150). Akkermansia muciniphila was abundant (>2%) in 7/27 ERA patients but none of the controls (P = 0.072.) Cluster analysis revealed two clusters of ERA patients: Cluster one (n = 8) was characterized by high levels of Bacteroides genus, while a second (n = 15) cluster had similar levels as the controls. Seven of 17 (41%) of the ERA subjects in Cluster 2 compared to 0/8 of the subjects in Cluster 1 had abundant Akkermansia muciniphila (P = 0.057). Serum IgA and IgG antibody levels against F. prausnitzii and B. fragilis were similar between patients and controls, whereas the two groups showed divergent responses when the fecal relative abundances of F. prausnitzii and Bacteroides were compared individually against IgA antibody levels recognizing F. prausnitzii and B. fragilis, respectively. CONCLUSION: The abundance of F. prausnitzii in the stool among patients with ERA is reduced compared to controls, and Bacteroides and A. muciniphila are identified as associative agents in subsets of ERA patients. Differences in the humoral responses to these bacteria may contribute to disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-014-0486-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-42725542014-12-21 Altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis Stoll, Matthew L Kumar, Ranjit Morrow, Casey D Lefkowitz, Elliot J Cui, Xiangqin Genin, Anna Cron, Randy Q Elson, Charles O Arthritis Res Ther Research Article INTRODUCTION: Prior studies have established altered microbiota and immunologic reactivity to enteric commensal organisms in inflammatory bowel disease (IBD). Since intestinal inflammation is present in a subset of patients with both pediatric and adult spondyloarthritis (SpA), we hypothesized that SpA patients may also have altered microbiota and immune responsiveness to enteric organisms. METHODS: Stool and blood specimens were collected from children with enthesitis-related arthritis (ERA) and non-inflammatory controls. DNA purified from stool was subject to PCR amplification and sequencing of the variable IV region from the 16S rDNA gene. IgA and IgG Enzyme-linked Immunosorbent Assays (ELISAs) were performed on select species of bacteria in most subjects. RESULTS: Twenty-five children with ERA and 13 controls were included. The ERA patients had less Faecalibacterium prausnitzii (3.8% versus 10%, P = 0.008) and lachnospiraceae family (12 versus 7.0%, P = 0.020), a statistically significant increase in bifidobacterium (1.8% versus 0%, P = 0.032) and a non-statistically significant increase in Bacteroides (21% versus 11%, P = 0.150). Akkermansia muciniphila was abundant (>2%) in 7/27 ERA patients but none of the controls (P = 0.072.) Cluster analysis revealed two clusters of ERA patients: Cluster one (n = 8) was characterized by high levels of Bacteroides genus, while a second (n = 15) cluster had similar levels as the controls. Seven of 17 (41%) of the ERA subjects in Cluster 2 compared to 0/8 of the subjects in Cluster 1 had abundant Akkermansia muciniphila (P = 0.057). Serum IgA and IgG antibody levels against F. prausnitzii and B. fragilis were similar between patients and controls, whereas the two groups showed divergent responses when the fecal relative abundances of F. prausnitzii and Bacteroides were compared individually against IgA antibody levels recognizing F. prausnitzii and B. fragilis, respectively. CONCLUSION: The abundance of F. prausnitzii in the stool among patients with ERA is reduced compared to controls, and Bacteroides and A. muciniphila are identified as associative agents in subsets of ERA patients. Differences in the humoral responses to these bacteria may contribute to disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-014-0486-0) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-30 2014 /pmc/articles/PMC4272554/ /pubmed/25434931 http://dx.doi.org/10.1186/s13075-014-0486-0 Text en © Stoll et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Stoll, Matthew L
Kumar, Ranjit
Morrow, Casey D
Lefkowitz, Elliot J
Cui, Xiangqin
Genin, Anna
Cron, Randy Q
Elson, Charles O
Altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis
title Altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis
title_full Altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis
title_fullStr Altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis
title_full_unstemmed Altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis
title_short Altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis
title_sort altered microbiota associated with abnormal humoral immune responses to commensal organisms in enthesitis-related arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272554/
https://www.ncbi.nlm.nih.gov/pubmed/25434931
http://dx.doi.org/10.1186/s13075-014-0486-0
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