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Uremic Toxin-Producing Bacteroides Species Prevail in the Gut Microbiota of Taiwanese CKD Patients: An Analysis Using the New Taiwan Microbiome Baseline

RATIONALE AND OBJECTIVE: Gut microbiota have been targeted by alternative therapies for non-communicable diseases. We examined the gut microbiota of a healthy Taiwanese population, identified various bacterial drivers in different demographics, and compared them with dialysis patients to associate k...

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Autores principales: Shivani, Subhashree, Kao, Cheng-Yen, Chattopadhyay, Amrita, Chen, Jenn-Wei, Lai, Liang-Chuan, Lin, Wei-Hung, Lu, Tzu-Pin, Huang, I-Hsiu, Tsai, Mong-Hsun, Teng, Ching-Hao, Wu, Jiunn-Jong, Hsieh, Yi-Hsien, Wang, Ming-Cheng, Chuang, Eric Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086402/
https://www.ncbi.nlm.nih.gov/pubmed/35558102
http://dx.doi.org/10.3389/fcimb.2022.726256
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author Shivani, Subhashree
Kao, Cheng-Yen
Chattopadhyay, Amrita
Chen, Jenn-Wei
Lai, Liang-Chuan
Lin, Wei-Hung
Lu, Tzu-Pin
Huang, I-Hsiu
Tsai, Mong-Hsun
Teng, Ching-Hao
Wu, Jiunn-Jong
Hsieh, Yi-Hsien
Wang, Ming-Cheng
Chuang, Eric Y.
author_facet Shivani, Subhashree
Kao, Cheng-Yen
Chattopadhyay, Amrita
Chen, Jenn-Wei
Lai, Liang-Chuan
Lin, Wei-Hung
Lu, Tzu-Pin
Huang, I-Hsiu
Tsai, Mong-Hsun
Teng, Ching-Hao
Wu, Jiunn-Jong
Hsieh, Yi-Hsien
Wang, Ming-Cheng
Chuang, Eric Y.
author_sort Shivani, Subhashree
collection PubMed
description RATIONALE AND OBJECTIVE: Gut microbiota have been targeted by alternative therapies for non-communicable diseases. We examined the gut microbiota of a healthy Taiwanese population, identified various bacterial drivers in different demographics, and compared them with dialysis patients to associate kidney disease progression with changes in gut microbiota. STUDY DESIGN: This was a cross-sectional cohort study. SETTINGS AND PARTICIPANTS: Fecal samples were obtained from 119 healthy Taiwanese volunteers, and 16S rRNA sequencing was done on the V3-V4 regions to identify the bacterial enterotypes. Twenty-six samples from the above cohort were compared with fecal samples from 22 peritoneal dialysis and 16 hemodialysis patients to identify species-level bacterial biomarkers in the dysbiotic gut of chronic kidney disease (CKD) patients. RESULTS: Specific bacterial species were identified pertaining to different demographics such as gender, age, BMI, physical activity, and sleeping habits. Dialysis patients had a significant difference in gut microbiome composition compared to healthy controls. The most abundant genus identified in CKD patients was Bacteroides, and at the species level hemodialysis patients showed significant abundance in B. ovatus, B. caccae, B. uniformis, and peritoneal dialysis patients showed higher abundance in Blautia producta (p ≤ 0.05) than the control group. Pathways pertaining to the production of uremic toxins were enriched in CKD patients. The abundance of the bacterial species depended on the type of dialysis treatment. CONCLUSION: This study characterizes the healthy gut microbiome of a Taiwanese population in terms of various demographics. In a case-control examination, the results showed the alteration in gut microbiota in CKD patients corresponding to different dialysis treatments. Also, this study identified the bacterial species abundant in CKD patients and their possible role in complicating the patients’ condition.
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spelling pubmed-90864022022-05-11 Uremic Toxin-Producing Bacteroides Species Prevail in the Gut Microbiota of Taiwanese CKD Patients: An Analysis Using the New Taiwan Microbiome Baseline Shivani, Subhashree Kao, Cheng-Yen Chattopadhyay, Amrita Chen, Jenn-Wei Lai, Liang-Chuan Lin, Wei-Hung Lu, Tzu-Pin Huang, I-Hsiu Tsai, Mong-Hsun Teng, Ching-Hao Wu, Jiunn-Jong Hsieh, Yi-Hsien Wang, Ming-Cheng Chuang, Eric Y. Front Cell Infect Microbiol Cellular and Infection Microbiology RATIONALE AND OBJECTIVE: Gut microbiota have been targeted by alternative therapies for non-communicable diseases. We examined the gut microbiota of a healthy Taiwanese population, identified various bacterial drivers in different demographics, and compared them with dialysis patients to associate kidney disease progression with changes in gut microbiota. STUDY DESIGN: This was a cross-sectional cohort study. SETTINGS AND PARTICIPANTS: Fecal samples were obtained from 119 healthy Taiwanese volunteers, and 16S rRNA sequencing was done on the V3-V4 regions to identify the bacterial enterotypes. Twenty-six samples from the above cohort were compared with fecal samples from 22 peritoneal dialysis and 16 hemodialysis patients to identify species-level bacterial biomarkers in the dysbiotic gut of chronic kidney disease (CKD) patients. RESULTS: Specific bacterial species were identified pertaining to different demographics such as gender, age, BMI, physical activity, and sleeping habits. Dialysis patients had a significant difference in gut microbiome composition compared to healthy controls. The most abundant genus identified in CKD patients was Bacteroides, and at the species level hemodialysis patients showed significant abundance in B. ovatus, B. caccae, B. uniformis, and peritoneal dialysis patients showed higher abundance in Blautia producta (p ≤ 0.05) than the control group. Pathways pertaining to the production of uremic toxins were enriched in CKD patients. The abundance of the bacterial species depended on the type of dialysis treatment. CONCLUSION: This study characterizes the healthy gut microbiome of a Taiwanese population in terms of various demographics. In a case-control examination, the results showed the alteration in gut microbiota in CKD patients corresponding to different dialysis treatments. Also, this study identified the bacterial species abundant in CKD patients and their possible role in complicating the patients’ condition. Frontiers Media S.A. 2022-04-26 /pmc/articles/PMC9086402/ /pubmed/35558102 http://dx.doi.org/10.3389/fcimb.2022.726256 Text en Copyright © 2022 Shivani, Kao, Chattopadhyay, Chen, Lai, Lin, Lu, Huang, Tsai, Teng, Wu, Hsieh, Wang and Chuang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Shivani, Subhashree
Kao, Cheng-Yen
Chattopadhyay, Amrita
Chen, Jenn-Wei
Lai, Liang-Chuan
Lin, Wei-Hung
Lu, Tzu-Pin
Huang, I-Hsiu
Tsai, Mong-Hsun
Teng, Ching-Hao
Wu, Jiunn-Jong
Hsieh, Yi-Hsien
Wang, Ming-Cheng
Chuang, Eric Y.
Uremic Toxin-Producing Bacteroides Species Prevail in the Gut Microbiota of Taiwanese CKD Patients: An Analysis Using the New Taiwan Microbiome Baseline
title Uremic Toxin-Producing Bacteroides Species Prevail in the Gut Microbiota of Taiwanese CKD Patients: An Analysis Using the New Taiwan Microbiome Baseline
title_full Uremic Toxin-Producing Bacteroides Species Prevail in the Gut Microbiota of Taiwanese CKD Patients: An Analysis Using the New Taiwan Microbiome Baseline
title_fullStr Uremic Toxin-Producing Bacteroides Species Prevail in the Gut Microbiota of Taiwanese CKD Patients: An Analysis Using the New Taiwan Microbiome Baseline
title_full_unstemmed Uremic Toxin-Producing Bacteroides Species Prevail in the Gut Microbiota of Taiwanese CKD Patients: An Analysis Using the New Taiwan Microbiome Baseline
title_short Uremic Toxin-Producing Bacteroides Species Prevail in the Gut Microbiota of Taiwanese CKD Patients: An Analysis Using the New Taiwan Microbiome Baseline
title_sort uremic toxin-producing bacteroides species prevail in the gut microbiota of taiwanese ckd patients: an analysis using the new taiwan microbiome baseline
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086402/
https://www.ncbi.nlm.nih.gov/pubmed/35558102
http://dx.doi.org/10.3389/fcimb.2022.726256
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