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...
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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 |
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