Cargando…
Gut mucosal virome alterations in ulcerative colitis
OBJECTIVE: The pathogenesis of UC relates to gut microbiota dysbiosis. We postulate that alterations in the viral community populating the intestinal mucosa play an important role in UC pathogenesis. This study aims to characterise the mucosal virome and their functions in health and UC. DESIGN: Dee...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582748/ https://www.ncbi.nlm.nih.gov/pubmed/30842211 http://dx.doi.org/10.1136/gutjnl-2018-318131 |
_version_ | 1783428386997141504 |
---|---|
author | Zuo, Tao Lu, Xiao-Juan Zhang, Yu Cheung, Chun Pan Lam, Siu Zhang, Fen Tang, Whitney Ching, Jessica Y L Zhao, Risheng Chan, Paul K S Sung, Joseph J Y Yu, Jun Chan, Francis K L Cao, Qian Sheng, Jian-Qiu Ng, Siew C |
author_facet | Zuo, Tao Lu, Xiao-Juan Zhang, Yu Cheung, Chun Pan Lam, Siu Zhang, Fen Tang, Whitney Ching, Jessica Y L Zhao, Risheng Chan, Paul K S Sung, Joseph J Y Yu, Jun Chan, Francis K L Cao, Qian Sheng, Jian-Qiu Ng, Siew C |
author_sort | Zuo, Tao |
collection | PubMed |
description | OBJECTIVE: The pathogenesis of UC relates to gut microbiota dysbiosis. We postulate that alterations in the viral community populating the intestinal mucosa play an important role in UC pathogenesis. This study aims to characterise the mucosal virome and their functions in health and UC. DESIGN: Deep metagenomics sequencing of virus-like particle preparations and bacterial 16S rRNA sequencing were performed on the rectal mucosa of 167 subjects from three different geographical regions in China (UC=91; healthy controls=76). Virome and bacteriome alterations in UC mucosa were assessed and correlated with patient metadata. We applied partition around medoids clustering algorithm and classified mucosa viral communities into two clusters, referred to as mucosal virome metacommunities 1 and 2. RESULTS: In UC, there was an expansion of mucosa viruses, particularly Caudovirales bacteriophages, and a decrease in mucosa Caudovirales diversity, richness and evenness compared with healthy controls. Altered mucosal virome correlated with intestinal inflammation. Interindividual dissimilarity between mucosal viromes was higher in UC than controls. Escherichia phage and Enterobacteria phage were more abundant in the mucosa of UC than controls. Compared with metacommunity 1, metacommunity 2 was predominated by UC subjects and displayed a significant loss of various viral species. Patients with UC showed substantial abrogation of diverse viral functions, whereas multiple viral functions, particularly functions of bacteriophages associated with host bacteria fitness and pathogenicity, were markedly enriched in UC mucosa. Intensive transkingdom correlations between mucosa viruses and bacteria were significantly depleted in UC. CONCLUSION: We demonstrated for the first time that UC is characterised by substantial alterations of the mucosa virobiota with functional distortion. Enrichment of Caudovirales bacteriophages, increased phage/bacteria virulence functions and loss of viral-bacterial correlations in the UC mucosa highlight that mucosal virome may play an important role in UC pathogenesis. |
format | Online Article Text |
id | pubmed-6582748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-65827482019-07-05 Gut mucosal virome alterations in ulcerative colitis Zuo, Tao Lu, Xiao-Juan Zhang, Yu Cheung, Chun Pan Lam, Siu Zhang, Fen Tang, Whitney Ching, Jessica Y L Zhao, Risheng Chan, Paul K S Sung, Joseph J Y Yu, Jun Chan, Francis K L Cao, Qian Sheng, Jian-Qiu Ng, Siew C Gut Gut Microbiota OBJECTIVE: The pathogenesis of UC relates to gut microbiota dysbiosis. We postulate that alterations in the viral community populating the intestinal mucosa play an important role in UC pathogenesis. This study aims to characterise the mucosal virome and their functions in health and UC. DESIGN: Deep metagenomics sequencing of virus-like particle preparations and bacterial 16S rRNA sequencing were performed on the rectal mucosa of 167 subjects from three different geographical regions in China (UC=91; healthy controls=76). Virome and bacteriome alterations in UC mucosa were assessed and correlated with patient metadata. We applied partition around medoids clustering algorithm and classified mucosa viral communities into two clusters, referred to as mucosal virome metacommunities 1 and 2. RESULTS: In UC, there was an expansion of mucosa viruses, particularly Caudovirales bacteriophages, and a decrease in mucosa Caudovirales diversity, richness and evenness compared with healthy controls. Altered mucosal virome correlated with intestinal inflammation. Interindividual dissimilarity between mucosal viromes was higher in UC than controls. Escherichia phage and Enterobacteria phage were more abundant in the mucosa of UC than controls. Compared with metacommunity 1, metacommunity 2 was predominated by UC subjects and displayed a significant loss of various viral species. Patients with UC showed substantial abrogation of diverse viral functions, whereas multiple viral functions, particularly functions of bacteriophages associated with host bacteria fitness and pathogenicity, were markedly enriched in UC mucosa. Intensive transkingdom correlations between mucosa viruses and bacteria were significantly depleted in UC. CONCLUSION: We demonstrated for the first time that UC is characterised by substantial alterations of the mucosa virobiota with functional distortion. Enrichment of Caudovirales bacteriophages, increased phage/bacteria virulence functions and loss of viral-bacterial correlations in the UC mucosa highlight that mucosal virome may play an important role in UC pathogenesis. BMJ Publishing Group 2019-07 2019-03-06 /pmc/articles/PMC6582748/ /pubmed/30842211 http://dx.doi.org/10.1136/gutjnl-2018-318131 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Gut Microbiota Zuo, Tao Lu, Xiao-Juan Zhang, Yu Cheung, Chun Pan Lam, Siu Zhang, Fen Tang, Whitney Ching, Jessica Y L Zhao, Risheng Chan, Paul K S Sung, Joseph J Y Yu, Jun Chan, Francis K L Cao, Qian Sheng, Jian-Qiu Ng, Siew C Gut mucosal virome alterations in ulcerative colitis |
title | Gut mucosal virome alterations in ulcerative colitis |
title_full | Gut mucosal virome alterations in ulcerative colitis |
title_fullStr | Gut mucosal virome alterations in ulcerative colitis |
title_full_unstemmed | Gut mucosal virome alterations in ulcerative colitis |
title_short | Gut mucosal virome alterations in ulcerative colitis |
title_sort | gut mucosal virome alterations in ulcerative colitis |
topic | Gut Microbiota |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582748/ https://www.ncbi.nlm.nih.gov/pubmed/30842211 http://dx.doi.org/10.1136/gutjnl-2018-318131 |
work_keys_str_mv | AT zuotao gutmucosalviromealterationsinulcerativecolitis AT luxiaojuan gutmucosalviromealterationsinulcerativecolitis AT zhangyu gutmucosalviromealterationsinulcerativecolitis AT cheungchunpan gutmucosalviromealterationsinulcerativecolitis AT lamsiu gutmucosalviromealterationsinulcerativecolitis AT zhangfen gutmucosalviromealterationsinulcerativecolitis AT tangwhitney gutmucosalviromealterationsinulcerativecolitis AT chingjessicayl gutmucosalviromealterationsinulcerativecolitis AT zhaorisheng gutmucosalviromealterationsinulcerativecolitis AT chanpaulks gutmucosalviromealterationsinulcerativecolitis AT sungjosephjy gutmucosalviromealterationsinulcerativecolitis AT yujun gutmucosalviromealterationsinulcerativecolitis AT chanfranciskl gutmucosalviromealterationsinulcerativecolitis AT caoqian gutmucosalviromealterationsinulcerativecolitis AT shengjianqiu gutmucosalviromealterationsinulcerativecolitis AT ngsiewc gutmucosalviromealterationsinulcerativecolitis |