Title |
Dynamic changes in short- and long-term bacterial composition following fecal microbiota transplantation for recurrent Clostridium difficile infection
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Published in |
Microbiome, March 2015
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DOI | 10.1186/s40168-015-0070-0 |
Pubmed ID | |
Authors |
Alexa Weingarden, Antonio González, Yoshiki Vázquez-Baeza, Sophie Weiss, Gregory Humphry, Donna Berg-Lyons, Dan Knights, Tatsuya Unno, Aleh Bobr, Johnthomas Kang, Alexander Khoruts, Rob Knight, Michael J Sadowsky |
Abstract |
Fecal microbiota transplantation (FMT) is an effective treatment for recurrent Clostridium difficile infection (CDI) that often fails standard antibiotic therapy. Despite its widespread recent use, however, little is known about the stability of the fecal microbiota following FMT. Here we report on short- and long-term changes and provide kinetic visualization of fecal microbiota composition in patients with multiply recurrent CDI that were refractory to antibiotic therapy and treated using FMT. Fecal samples were collected from four patients before and up to 151 days after FMT, with daily collections until 28 days and weekly collections until 84 days post-FMT. The composition of fecal bacteria was characterized using high throughput 16S rRNA gene sequence analysis, compared to microbiota across body sites in the Human Microbiome Project (HMP) database, and visualized in a movie-like, kinetic format. FMT resulted in rapid normalization of bacterial fecal sample composition from a markedly dysbiotic state to one representative of normal fecal microbiota. While the microbiome appeared most similar to the donor implant material 1 day post-FMT, the composition diverged variably at later time points. The donor microbiota composition also varied over time. However, both post-FMT and donor samples remained within the larger cloud of fecal microbiota characterized as healthy by the HMP. Dynamic behavior is an intrinsic property of normal fecal microbiota and should be accounted for in comparing microbial communities among normal individuals and those with disease states. This also suggests that more frequent sample analyses are needed in order to properly assess success of FMT procedures. |
X Demographics
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 24 | 41% |
United Kingdom | 7 | 12% |
Spain | 3 | 5% |
France | 1 | 2% |
Switzerland | 1 | 2% |
Venezuela, Bolivarian Republic of | 1 | 2% |
Myanmar | 1 | 2% |
Australia | 1 | 2% |
Austria | 1 | 2% |
Other | 1 | 2% |
Unknown | 18 | 31% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 39 | 66% |
Scientists | 15 | 25% |
Practitioners (doctors, other healthcare professionals) | 5 | 8% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 11 | 3% |
Denmark | 2 | <1% |
South Africa | 1 | <1% |
France | 1 | <1% |
Brazil | 1 | <1% |
New Zealand | 1 | <1% |
Unknown | 323 | 95% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 73 | 21% |
Researcher | 69 | 20% |
Student > Bachelor | 42 | 12% |
Student > Master | 37 | 11% |
Professor > Associate Professor | 15 | 4% |
Other | 50 | 15% |
Unknown | 54 | 16% |
Readers by discipline | Count | As % |
---|---|---|
Agricultural and Biological Sciences | 89 | 26% |
Medicine and Dentistry | 55 | 16% |
Biochemistry, Genetics and Molecular Biology | 47 | 14% |
Immunology and Microbiology | 29 | 9% |
Engineering | 9 | 3% |
Other | 45 | 13% |
Unknown | 66 | 19% |