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A Shifted Urinary Microbiota Associated with Disease Activity and Immune Responses in Rheumatoid Arthritis

Recent evidence emphasized the role of the microbiota in the etiopathogenesis of rheumatoid arthritis (RA). Indeed, it has been demonstrated that urinary tract infections are implicated in RA pathogenesis. However, a definitive association between the urinary tract microbiota and RA remains to be in...

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Autores principales: Jin, Jiayang, Li, Jing, Hou, Meiling, Ding, Xu, Zhong, Yan, He, Jing, Sun, Xiaolin, Ye, Hua, Li, Ru, Wu, Lijun, Wang, Jun, Guo, Jianping, Li, Zhanguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269647/
https://www.ncbi.nlm.nih.gov/pubmed/37227288
http://dx.doi.org/10.1128/spectrum.03662-22
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author Jin, Jiayang
Li, Jing
Hou, Meiling
Ding, Xu
Zhong, Yan
He, Jing
Sun, Xiaolin
Ye, Hua
Li, Ru
Wu, Lijun
Wang, Jun
Guo, Jianping
Li, Zhanguo
author_facet Jin, Jiayang
Li, Jing
Hou, Meiling
Ding, Xu
Zhong, Yan
He, Jing
Sun, Xiaolin
Ye, Hua
Li, Ru
Wu, Lijun
Wang, Jun
Guo, Jianping
Li, Zhanguo
author_sort Jin, Jiayang
collection PubMed
description Recent evidence emphasized the role of the microbiota in the etiopathogenesis of rheumatoid arthritis (RA). Indeed, it has been demonstrated that urinary tract infections are implicated in RA pathogenesis. However, a definitive association between the urinary tract microbiota and RA remains to be investigated. Urine samples from 39 patients affected by RA, including treatment-naive patients, and 37 age- and sex-matched healthy individuals were collected. In RA patients, the urinary microbiota showed an increase in microbial richness and a decrease in microbial dissimilarity, especially in treatment-naive patients. A total of 48 altered genera with different absolute quantities were detected in patients with RA. The 37 enriched genera included Proteus, Faecalibacterium, and Bacteroides, while the 11 deficient genera included Gardnerella, Ruminococcus, Megasphaera, and Ureaplasma. Notably, the more abundant genera in RA patients were correlated with the disease activity score of 28 joints-erythrocyte sedimentation rates (DAS28-ESR) and an increase in plasma B cells. Furthermore, the altered urinary metabolites, such as proline, citric acid, and oxalic acid, were positively associated with RA patients, and they were closely correlated with urinary microbiota. These findings suggested a strong association between the altered urinary microbiota and metabolites with disease severity and dysregulated immune responses in RA patients. IMPORTANCE We revealed that the profile of the urinary tract microbiota in RA featured with increased microbial richness and shifted taxa, associated with immunological and metabolic changes of the disease, underlining the interplay between urinary microbiota and host autoimmunity.
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spelling pubmed-102696472023-06-16 A Shifted Urinary Microbiota Associated with Disease Activity and Immune Responses in Rheumatoid Arthritis Jin, Jiayang Li, Jing Hou, Meiling Ding, Xu Zhong, Yan He, Jing Sun, Xiaolin Ye, Hua Li, Ru Wu, Lijun Wang, Jun Guo, Jianping Li, Zhanguo Microbiol Spectr Research Article Recent evidence emphasized the role of the microbiota in the etiopathogenesis of rheumatoid arthritis (RA). Indeed, it has been demonstrated that urinary tract infections are implicated in RA pathogenesis. However, a definitive association between the urinary tract microbiota and RA remains to be investigated. Urine samples from 39 patients affected by RA, including treatment-naive patients, and 37 age- and sex-matched healthy individuals were collected. In RA patients, the urinary microbiota showed an increase in microbial richness and a decrease in microbial dissimilarity, especially in treatment-naive patients. A total of 48 altered genera with different absolute quantities were detected in patients with RA. The 37 enriched genera included Proteus, Faecalibacterium, and Bacteroides, while the 11 deficient genera included Gardnerella, Ruminococcus, Megasphaera, and Ureaplasma. Notably, the more abundant genera in RA patients were correlated with the disease activity score of 28 joints-erythrocyte sedimentation rates (DAS28-ESR) and an increase in plasma B cells. Furthermore, the altered urinary metabolites, such as proline, citric acid, and oxalic acid, were positively associated with RA patients, and they were closely correlated with urinary microbiota. These findings suggested a strong association between the altered urinary microbiota and metabolites with disease severity and dysregulated immune responses in RA patients. IMPORTANCE We revealed that the profile of the urinary tract microbiota in RA featured with increased microbial richness and shifted taxa, associated with immunological and metabolic changes of the disease, underlining the interplay between urinary microbiota and host autoimmunity. American Society for Microbiology 2023-05-25 /pmc/articles/PMC10269647/ /pubmed/37227288 http://dx.doi.org/10.1128/spectrum.03662-22 Text en Copyright © 2023 Jin et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Jin, Jiayang
Li, Jing
Hou, Meiling
Ding, Xu
Zhong, Yan
He, Jing
Sun, Xiaolin
Ye, Hua
Li, Ru
Wu, Lijun
Wang, Jun
Guo, Jianping
Li, Zhanguo
A Shifted Urinary Microbiota Associated with Disease Activity and Immune Responses in Rheumatoid Arthritis
title A Shifted Urinary Microbiota Associated with Disease Activity and Immune Responses in Rheumatoid Arthritis
title_full A Shifted Urinary Microbiota Associated with Disease Activity and Immune Responses in Rheumatoid Arthritis
title_fullStr A Shifted Urinary Microbiota Associated with Disease Activity and Immune Responses in Rheumatoid Arthritis
title_full_unstemmed A Shifted Urinary Microbiota Associated with Disease Activity and Immune Responses in Rheumatoid Arthritis
title_short A Shifted Urinary Microbiota Associated with Disease Activity and Immune Responses in Rheumatoid Arthritis
title_sort shifted urinary microbiota associated with disease activity and immune responses in rheumatoid arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269647/
https://www.ncbi.nlm.nih.gov/pubmed/37227288
http://dx.doi.org/10.1128/spectrum.03662-22
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