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Profiling the Urinary Microbiota in Male Patients With Bladder Cancer in China

Mounting evidence indicates that microbiome plays an important role in the development and progression of cancer. The dogma that urine in healthy individuals must be sterile has been overturned. Dysbiosis of the urinary microbiome has been revealed responsible for various urological disorders, inclu...

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Autores principales: Wu, Peng, Zhang, Guihao, Zhao, Jie, Chen, Jiawei, Chen, Yang, Huang, Weina, Zhong, Jialei, Zeng, Jiarong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990618/
https://www.ncbi.nlm.nih.gov/pubmed/29904624
http://dx.doi.org/10.3389/fcimb.2018.00167
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author Wu, Peng
Zhang, Guihao
Zhao, Jie
Chen, Jiawei
Chen, Yang
Huang, Weina
Zhong, Jialei
Zeng, Jiarong
author_facet Wu, Peng
Zhang, Guihao
Zhao, Jie
Chen, Jiawei
Chen, Yang
Huang, Weina
Zhong, Jialei
Zeng, Jiarong
author_sort Wu, Peng
collection PubMed
description Mounting evidence indicates that microbiome plays an important role in the development and progression of cancer. The dogma that urine in healthy individuals must be sterile has been overturned. Dysbiosis of the urinary microbiome has been revealed responsible for various urological disorders, including prostate cancer. The link between chronic inflammation, microbiome and solid tumors has been established for various neoplastic diseases. However, a detailed and comprehensive analysis of urinary microenvironment of bladder cancer has not been yet reported. We performed this study to characterize the potential urinary microbial community possibly associated with bladder cancer. Mid-stream urine was collected from 31 male patients with bladder cancer and 18 non-neoplastic controls. DNA was extracted from urine pellet samples and processed for high throughput 16S rRNA amplicon sequencing of the V4 region using Illumina MiSeq. Sequencing reads were filtered using QIIME and clustered using UPARSE. We observed increased bacterial richness (Observed Species, Chao 1 and Ace indexes; cancer vs. control; 120.0 vs. 56.0; 134.5 vs. 68.3; and 139.6 vs. 72.9, respectively), enrichment of some bacterial genera (e.g., Acinetobacter, Anaerococcus, and Sphingobacterium) and decrease of some bacterial genera (e.g., Serratia, Proteus, and Roseomonas) in cancer group when compared to non-cancer group. Significant difference in beta diversity was found between cancer and non-cancer group, among different risk level, but not among different tumor grade. Enrichment of Herbaspirillum, Porphyrobacter, and Bacteroides was observed in cancer patients with high risk of recurrence and progression, which means these genera maybe potential biomarkers for risk stratification. The PICRUSt showed that various functional pathways were enriched in cancer group, including Staphylococcus aureus infection, glycerolipid metabolism and retinol metabolism. To our knowledge, we performed the most comprehensive study to date to characterize the urinary microbiome associated with bladder cancer. A better understanding of the role of microbiome in the development and progression of bladder cancer could pave a new way for exploring new therapeutic options and biomarkers.
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spelling pubmed-59906182018-06-14 Profiling the Urinary Microbiota in Male Patients With Bladder Cancer in China Wu, Peng Zhang, Guihao Zhao, Jie Chen, Jiawei Chen, Yang Huang, Weina Zhong, Jialei Zeng, Jiarong Front Cell Infect Microbiol Microbiology Mounting evidence indicates that microbiome plays an important role in the development and progression of cancer. The dogma that urine in healthy individuals must be sterile has been overturned. Dysbiosis of the urinary microbiome has been revealed responsible for various urological disorders, including prostate cancer. The link between chronic inflammation, microbiome and solid tumors has been established for various neoplastic diseases. However, a detailed and comprehensive analysis of urinary microenvironment of bladder cancer has not been yet reported. We performed this study to characterize the potential urinary microbial community possibly associated with bladder cancer. Mid-stream urine was collected from 31 male patients with bladder cancer and 18 non-neoplastic controls. DNA was extracted from urine pellet samples and processed for high throughput 16S rRNA amplicon sequencing of the V4 region using Illumina MiSeq. Sequencing reads were filtered using QIIME and clustered using UPARSE. We observed increased bacterial richness (Observed Species, Chao 1 and Ace indexes; cancer vs. control; 120.0 vs. 56.0; 134.5 vs. 68.3; and 139.6 vs. 72.9, respectively), enrichment of some bacterial genera (e.g., Acinetobacter, Anaerococcus, and Sphingobacterium) and decrease of some bacterial genera (e.g., Serratia, Proteus, and Roseomonas) in cancer group when compared to non-cancer group. Significant difference in beta diversity was found between cancer and non-cancer group, among different risk level, but not among different tumor grade. Enrichment of Herbaspirillum, Porphyrobacter, and Bacteroides was observed in cancer patients with high risk of recurrence and progression, which means these genera maybe potential biomarkers for risk stratification. The PICRUSt showed that various functional pathways were enriched in cancer group, including Staphylococcus aureus infection, glycerolipid metabolism and retinol metabolism. To our knowledge, we performed the most comprehensive study to date to characterize the urinary microbiome associated with bladder cancer. A better understanding of the role of microbiome in the development and progression of bladder cancer could pave a new way for exploring new therapeutic options and biomarkers. Frontiers Media S.A. 2018-05-31 /pmc/articles/PMC5990618/ /pubmed/29904624 http://dx.doi.org/10.3389/fcimb.2018.00167 Text en Copyright © 2018 Wu, Zhang, Zhao, Chen, Chen, Huang, Zhong and Zeng. http://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 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 Microbiology
Wu, Peng
Zhang, Guihao
Zhao, Jie
Chen, Jiawei
Chen, Yang
Huang, Weina
Zhong, Jialei
Zeng, Jiarong
Profiling the Urinary Microbiota in Male Patients With Bladder Cancer in China
title Profiling the Urinary Microbiota in Male Patients With Bladder Cancer in China
title_full Profiling the Urinary Microbiota in Male Patients With Bladder Cancer in China
title_fullStr Profiling the Urinary Microbiota in Male Patients With Bladder Cancer in China
title_full_unstemmed Profiling the Urinary Microbiota in Male Patients With Bladder Cancer in China
title_short Profiling the Urinary Microbiota in Male Patients With Bladder Cancer in China
title_sort profiling the urinary microbiota in male patients with bladder cancer in china
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990618/
https://www.ncbi.nlm.nih.gov/pubmed/29904624
http://dx.doi.org/10.3389/fcimb.2018.00167
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