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Pooping out miracles: scientists reveal mechanism behind fecal microbiota transplantation
-Osaka City University and IMSUT demonstrate fecal microbiota transplantation (FMT) success by revealing the coordinated effort of bacteriophages (phages) and their host bacteria in restoring human intestinal flora-

February 10, 2021

In a study published in Gastroenterology – Researchers at Osaka City University and The Institute for Medical Science, The University of Tokyo(IMSUT), in collaboration with Brigham and Women's Hospital in Boston, report the intestinal bacterial and viral metagenome information from the fecal samples of patients with recurrent Clostridioides difficile infection (rCDI). This comprehensive analysis reveals the bacteria and phages involved in pathogenesis in rCDI, and their remarkable pathways important for the recovery of intestinal flora function.

Clostridioides difficile infection (rCDI) occurs in the gut and is caused by the Gram-positive, spore-forming anaerobic bacterium, C. difficile when its spores attach to fecal matter and are transferred from hand to mouth by health care workers. Patients undergoing antibiotic treatment are especially susceptible as the microorganisms that maintain a healthy gut are greatly damaged by the antibiotics.

Treatment of rCDI involves withdrawing the causative antibiotics and initiating antibiotic therapy, although this can be very challenging. Fecal microbiota transplantation (FMT) is considered an effective alternative therapy as it addresses the issue from the ground up by replacing the damaged microflora with a healthy one through a stool transplant.

However, two deaths caused by antibiotic-resistant bacterial infections after FMT were reported in 2019, suggesting that a modification of FMT or alternatives are required to resolve safety concerns surrounding the treatment.

Researchers at Osaka City University and the Institute for Medical Science, University of Tokyo tackled this challenge head-on in a great study now published in Gastroenterology. 

Using their original analysis pipeline reported in 2020, the researchers obtained intestinal bacterial and viral metagenome information from the fecal samples of nine rCDI patients from Brigham and Women's Hospital in Boston who successfully had an FMT. They revealed the bacteria and phages involved in the pathogenesis of rCDI and the remarkable pathways important for the recovery of intestinal flora function. 

By revealing how the bacteriome and virome in the intestine work together as an organ, the research team was able to show how FMT can be as safe as swapping out a bad organ with a good one.

“Intestinal microbiota should definitely be treated as an ‘organ’!” says principal investigator Professor Satoshi Uematsu, “FMT drastically changed the intestinal bacteriome and virome and is sure to restore the intestinal bacterial and viral functions.”

In the post-COVID-19 world, rCDI will become one of the more pressing international diseases. There is no doubt that FMT is an important therapeutic strategy for rCDI. "In addition to a variety of clinical surveys, comprehensive metagenomic analysis is very important in considering the safety of FMT.," say Dr. Kosuke Fujimoto and Prof. Seiya Imoto.

 


 

About the research

Kosuke Fujimoto1,2,3, Yasumasa Kimura4, Jessica R Allegretti5, Mako Yamamoto6, Yao-zhong Zhang6, Kotoe Katayama6, Georg Tremmel7, Yunosuke Kawaguchi1, Masaki Shimohigoshi1, Tetsuya Hayashi1, Miho Uematsu1, Kiyoshi Yamaguchi8, Yoichi Furukawa8, Yutaka Akiyama9, Rui Yamaguchi7, Sheila E. Crowe10, Peter B. Ernst11,12,13, Satoru Miyano7, Hiroshi Kiyono11,12,14,15, Seiya Imoto6,16* and Satoshi Uematsu1,2,3,16*
(*Corresponding-author), February 9, 2021, "Functional Restoration of Bacteriomes and Viromes by Fecal Microbiota Transplantation"Gastroenterology (IF=17.373). 

1Department of Immunology and Genomics, Osaka City University Graduate School of Medicine 
2Division of Metagenome Medicine, Human Genome Center, The Institute of Medical Science, The University of Tokyo
3Division of Innate Immune Regulation, International Research and Development Center for Mucosal Vaccines, The Institute of Medical Science, The University of Tokyo
4Division of Systems Immunology, The Institute of Medical Science, The University of Tokyo
5Division of Gastroenterology, Hepatology, and Endoscopy, Department of Medicine, Brigham and Women’s Hospital
6Division of Health Medical Intelligence, Human Genome Center, The Institute of Medical Science, The University of Tokyo
7Laboratory of DNA Information Analysis, Human Genome Center, The Institute of Medical Science, The University of Tokyo
8Division of Clinical Genome Research, The Institute of Medical Science, The University of Tokyo
9Department of Computer Science, Tokyo Institute of Technology
10Department of Medicine, University of California, San Diego
11Division of Gastroenterology, Department of Medicine, CU-UCSD Center for Mucosal Immunology, Allergy and Vaccines, University of California San Diego
12Division of Comparative Pathology and Medicine, Department of Pathology, University of California San Diego
13Center for Veterinary Sciences and Comparative Medicine, University of California, San Diego
14Department of Mucosal Immunology, IMSUT Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo
15International Research and Development Center for Mucosal Vaccines, The Institute of Medical Science, The University of Tokyo
16Collaborative Research Institute for Innovative Microbiology, The University of Tokyo

DOI:10.1053/j.gastro.2021.02.013
URL:https://www.gastrojournal.org/article/S0016-5085(21)00400-5/fulltext
 

Fundings

This research was sponsored by the Takeda Science Foundation, the Canon Foundation and strategic programs for innovative research field 1 from Ministry of Education, Culture, Sports, Science and Technology of Japan, the Center of Innovation Program from Japan Science and Technology Agency
 

Related Faculty Members

Utokyo People Satoshi UEMATSU Open a new window

Utokyo People Kosuke FUJIMOTO Open a new window

Utokyo People Seiya IMOTO Open a new window

Division of Metagenome Medicine(IMSUT) Open a new window

Division of Innate Immune Regulation(IMSUT) Open a new window