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Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome

OBJECTIVE: Faecal microbiota transplantation (FMT) is effective for the treatment of recurrent Clostridium difficile infection (CDI). Studies have shown bacterial colonisation after FMT, but data on viral alterations in CDI are scarce. We investigated enteric virome alterations in CDI and the associ...

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Autores principales: Zuo, Tao, Wong, Sunny H, Lam, Kelvin, Lui, Rashid, Cheung, Kitty, Tang, Whitney, Ching, Jessica Y L, Chan, Paul K S, Chan, Martin C W, Wu, Justin C Y, Chan, Francis K L, Yu, Jun, Sung, Joseph J Y, Ng, Siew C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868238/
https://www.ncbi.nlm.nih.gov/pubmed/28539351
http://dx.doi.org/10.1136/gutjnl-2017-313952
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author Zuo, Tao
Wong, Sunny H
Lam, Kelvin
Lui, Rashid
Cheung, Kitty
Tang, Whitney
Ching, Jessica Y L
Chan, Paul K S
Chan, Martin C W
Wu, Justin C Y
Chan, Francis K L
Yu, Jun
Sung, Joseph J Y
Ng, Siew C
author_facet Zuo, Tao
Wong, Sunny H
Lam, Kelvin
Lui, Rashid
Cheung, Kitty
Tang, Whitney
Ching, Jessica Y L
Chan, Paul K S
Chan, Martin C W
Wu, Justin C Y
Chan, Francis K L
Yu, Jun
Sung, Joseph J Y
Ng, Siew C
author_sort Zuo, Tao
collection PubMed
description OBJECTIVE: Faecal microbiota transplantation (FMT) is effective for the treatment of recurrent Clostridium difficile infection (CDI). Studies have shown bacterial colonisation after FMT, but data on viral alterations in CDI are scarce. We investigated enteric virome alterations in CDI and the association between viral transfer and clinical outcome in patients with CDI. DESIGN: Ultra-deep metagenomic sequencing of virus-like particle preparations and bacterial 16S rRNA sequencing were performed on stool samples from 24 subjects with CDI and 20 healthy controls. We longitudinally assessed the virome and bacterial microbiome changes in nine CDI subjects treated with FMT and five treated with vancomycin. Enteric virome alterations were assessed in association with treatment response. RESULTS: Subjects with CDI demonstrated a significantly higher abundance of bacteriophage Caudovirales and a lower Caudovirales diversity, richness and evenness compared with healthy household controls. Significant correlations were observed between bacterial families Proteobacteria, Actinobacteria and Caudovirales taxa in CDI. FMT treatment resulted in a significant decrease in the abundance of Caudovirales in CDI. Cure after FMT was observed when donor-derived Caudovirales contigs occupied a larger fraction of the enteric virome in the recipients (p=0.024). In treatment responders, FMT was associated with alterations in the virome and the bacterial microbiome, while vancomycin treatment led to alterations in the bacterial community alone. CONCLUSIONS: In a preliminary study, CDI is characterised by enteric virome dysbiosis. Treatment response in FMT was associated with a high colonisation level of donor-derived Caudovirales taxa in the recipient. Caudovirales bacteriophages may play a role in the efficacy of FMT in CDI. TRIAL REGISTRATION NUMBER: NCT02570477
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spelling pubmed-58682382018-03-27 Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome Zuo, Tao Wong, Sunny H Lam, Kelvin Lui, Rashid Cheung, Kitty Tang, Whitney Ching, Jessica Y L Chan, Paul K S Chan, Martin C W Wu, Justin C Y Chan, Francis K L Yu, Jun Sung, Joseph J Y Ng, Siew C Gut Gut Microbiota OBJECTIVE: Faecal microbiota transplantation (FMT) is effective for the treatment of recurrent Clostridium difficile infection (CDI). Studies have shown bacterial colonisation after FMT, but data on viral alterations in CDI are scarce. We investigated enteric virome alterations in CDI and the association between viral transfer and clinical outcome in patients with CDI. DESIGN: Ultra-deep metagenomic sequencing of virus-like particle preparations and bacterial 16S rRNA sequencing were performed on stool samples from 24 subjects with CDI and 20 healthy controls. We longitudinally assessed the virome and bacterial microbiome changes in nine CDI subjects treated with FMT and five treated with vancomycin. Enteric virome alterations were assessed in association with treatment response. RESULTS: Subjects with CDI demonstrated a significantly higher abundance of bacteriophage Caudovirales and a lower Caudovirales diversity, richness and evenness compared with healthy household controls. Significant correlations were observed between bacterial families Proteobacteria, Actinobacteria and Caudovirales taxa in CDI. FMT treatment resulted in a significant decrease in the abundance of Caudovirales in CDI. Cure after FMT was observed when donor-derived Caudovirales contigs occupied a larger fraction of the enteric virome in the recipients (p=0.024). In treatment responders, FMT was associated with alterations in the virome and the bacterial microbiome, while vancomycin treatment led to alterations in the bacterial community alone. CONCLUSIONS: In a preliminary study, CDI is characterised by enteric virome dysbiosis. Treatment response in FMT was associated with a high colonisation level of donor-derived Caudovirales taxa in the recipient. Caudovirales bacteriophages may play a role in the efficacy of FMT in CDI. TRIAL REGISTRATION NUMBER: NCT02570477 BMJ Publishing Group 2018-04 2017-05-24 /pmc/articles/PMC5868238/ /pubmed/28539351 http://dx.doi.org/10.1136/gutjnl-2017-313952 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Gut Microbiota
Zuo, Tao
Wong, Sunny H
Lam, Kelvin
Lui, Rashid
Cheung, Kitty
Tang, Whitney
Ching, Jessica Y L
Chan, Paul K S
Chan, Martin C W
Wu, Justin C Y
Chan, Francis K L
Yu, Jun
Sung, Joseph J Y
Ng, Siew C
Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome
title Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome
title_full Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome
title_fullStr Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome
title_full_unstemmed Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome
title_short Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome
title_sort bacteriophage transfer during faecal microbiota transplantation in clostridium difficile infection is associated with treatment outcome
topic Gut Microbiota
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868238/
https://www.ncbi.nlm.nih.gov/pubmed/28539351
http://dx.doi.org/10.1136/gutjnl-2017-313952
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