Gut-derived Enterococcus faecium from ulcerative colitis patients promotes colitis in a genetically susceptible mouse host

Abstract Background Recent metagenomic analyses have revealed dysbiosis of the gut microbiota of ulcerative colitis (UC) patients. However, the impacts of this dysbiosis are not fully understood, particularly at the strain level. Results We perform whole-genome shotgun sequencing of fecal DNA extrac...

Full description

Bibliographic Details
Main Authors: Jun Seishima, Noriho Iida, Kazuya Kitamura, Masahiro Yutani, Ziyu Wang, Akihiro Seki, Taro Yamashita, Yoshio Sakai, Masao Honda, Tatsuya Yamashita, Takashi Kagaya, Yukihiro Shirota, Yukako Fujinaga, Eishiro Mizukoshi, Shuichi Kaneko
Format: Article
Language:English
Published: BMC 2019-11-01
Series:Genome Biology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13059-019-1879-9
id doaj-68b91770df714adca4a5a119a9ef7e1f
record_format Article
spelling doaj-68b91770df714adca4a5a119a9ef7e1f2020-11-25T02:51:31ZengBMCGenome Biology1474-760X2019-11-0120111810.1186/s13059-019-1879-9Gut-derived Enterococcus faecium from ulcerative colitis patients promotes colitis in a genetically susceptible mouse hostJun Seishima0Noriho Iida1Kazuya Kitamura2Masahiro Yutani3Ziyu Wang4Akihiro Seki5Taro Yamashita6Yoshio Sakai7Masao Honda8Tatsuya Yamashita9Takashi Kagaya10Yukihiro Shirota11Yukako Fujinaga12Eishiro Mizukoshi13Shuichi Kaneko14Department of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Bacteriology, Graduate School of Medicinal Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Advanced Medical Technology, Graduate School of Health Medicine, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Bacteriology, Graduate School of Medicinal Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityDepartment of Gastroenterology, Graduate School of Medical Sciences, Kanazawa UniversityAbstract Background Recent metagenomic analyses have revealed dysbiosis of the gut microbiota of ulcerative colitis (UC) patients. However, the impacts of this dysbiosis are not fully understood, particularly at the strain level. Results We perform whole-genome shotgun sequencing of fecal DNA extracts from 13 healthy donors and 16 UC and 8 Crohn’s disease (CD) patients. The microbiota of UC and CD patients is taxonomically and functionally divergent from that of healthy donors, with E. faecium being the most differentially abundant species between the two microbial communities. Transplantation of feces from UC or CD patients into Il10 −/− mice promotes pathological inflammation and cytokine expression in the mouse colon, although distinct cytokine expression profiles are observed between UC and CD. Unlike isolates derived from healthy donors, E. faecium isolates from the feces of UC patients, along with E. faecium strain ATCC 19434, promotes colitis and colonic cytokine expression. Inflammatory E. faecium strains, including ATCC 19434 and a UC-derived strain, cluster separately from commercially available probiotic strains based on whole-genome shotgun sequencing analysis. The presence of E. faecium in fecal samples is associated with large disease extent and the need for multiple medications in UC patients. Conclusions E. faecium strains derived from UC patients display an inflammatory genotype that causes colitis.http://link.springer.com/article/10.1186/s13059-019-1879-9Inflammatory bowel diseaseCrohn’s diseaseMicrobiotaMetagenome
collection DOAJ
language English
format Article
sources DOAJ
author Jun Seishima
Noriho Iida
Kazuya Kitamura
Masahiro Yutani
Ziyu Wang
Akihiro Seki
Taro Yamashita
Yoshio Sakai
Masao Honda
Tatsuya Yamashita
Takashi Kagaya
Yukihiro Shirota
Yukako Fujinaga
Eishiro Mizukoshi
Shuichi Kaneko
spellingShingle Jun Seishima
Noriho Iida
Kazuya Kitamura
Masahiro Yutani
Ziyu Wang
Akihiro Seki
Taro Yamashita
Yoshio Sakai
Masao Honda
Tatsuya Yamashita
Takashi Kagaya
Yukihiro Shirota
Yukako Fujinaga
Eishiro Mizukoshi
Shuichi Kaneko
Gut-derived Enterococcus faecium from ulcerative colitis patients promotes colitis in a genetically susceptible mouse host
Genome Biology
Inflammatory bowel disease
Crohn’s disease
Microbiota
Metagenome
author_facet Jun Seishima
Noriho Iida
Kazuya Kitamura
Masahiro Yutani
Ziyu Wang
Akihiro Seki
Taro Yamashita
Yoshio Sakai
Masao Honda
Tatsuya Yamashita
Takashi Kagaya
Yukihiro Shirota
Yukako Fujinaga
Eishiro Mizukoshi
Shuichi Kaneko
author_sort Jun Seishima
title Gut-derived Enterococcus faecium from ulcerative colitis patients promotes colitis in a genetically susceptible mouse host
title_short Gut-derived Enterococcus faecium from ulcerative colitis patients promotes colitis in a genetically susceptible mouse host
title_full Gut-derived Enterococcus faecium from ulcerative colitis patients promotes colitis in a genetically susceptible mouse host
title_fullStr Gut-derived Enterococcus faecium from ulcerative colitis patients promotes colitis in a genetically susceptible mouse host
title_full_unstemmed Gut-derived Enterococcus faecium from ulcerative colitis patients promotes colitis in a genetically susceptible mouse host
title_sort gut-derived enterococcus faecium from ulcerative colitis patients promotes colitis in a genetically susceptible mouse host
publisher BMC
series Genome Biology
issn 1474-760X
publishDate 2019-11-01
description Abstract Background Recent metagenomic analyses have revealed dysbiosis of the gut microbiota of ulcerative colitis (UC) patients. However, the impacts of this dysbiosis are not fully understood, particularly at the strain level. Results We perform whole-genome shotgun sequencing of fecal DNA extracts from 13 healthy donors and 16 UC and 8 Crohn’s disease (CD) patients. The microbiota of UC and CD patients is taxonomically and functionally divergent from that of healthy donors, with E. faecium being the most differentially abundant species between the two microbial communities. Transplantation of feces from UC or CD patients into Il10 −/− mice promotes pathological inflammation and cytokine expression in the mouse colon, although distinct cytokine expression profiles are observed between UC and CD. Unlike isolates derived from healthy donors, E. faecium isolates from the feces of UC patients, along with E. faecium strain ATCC 19434, promotes colitis and colonic cytokine expression. Inflammatory E. faecium strains, including ATCC 19434 and a UC-derived strain, cluster separately from commercially available probiotic strains based on whole-genome shotgun sequencing analysis. The presence of E. faecium in fecal samples is associated with large disease extent and the need for multiple medications in UC patients. Conclusions E. faecium strains derived from UC patients display an inflammatory genotype that causes colitis.
topic Inflammatory bowel disease
Crohn’s disease
Microbiota
Metagenome
url http://link.springer.com/article/10.1186/s13059-019-1879-9
work_keys_str_mv AT junseishima gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT norihoiida gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT kazuyakitamura gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT masahiroyutani gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT ziyuwang gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT akihiroseki gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT taroyamashita gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT yoshiosakai gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT masaohonda gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT tatsuyayamashita gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT takashikagaya gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT yukihiroshirota gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT yukakofujinaga gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT eishiromizukoshi gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
AT shuichikaneko gutderivedenterococcusfaeciumfromulcerativecolitispatientspromotescolitisinageneticallysusceptiblemousehost
_version_ 1724734082841051136