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Long-term taxonomic and functional divergence from donor bacterial strains following fecal microbiota transplantation in immunocompromised patients
Immunocompromised individuals are at high risk of developing Clostridium difficile-associated disease (CDAD). Fecal microbiota transplantation (FMT) is a highly effective therapy for refractory or recurrent CDAD and, despite safety concerns, has recently been offered to immunocompromised patients. W...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5565110/ https://www.ncbi.nlm.nih.gov/pubmed/28827811 http://dx.doi.org/10.1371/journal.pone.0182585 |
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author | Moss, Eli L. Falconer, Shannon B. Tkachenko, Ekaterina Wang, Mingjie Systrom, Hannah Mahabamunuge, Jasmin Relman, David A. Hohmann, Elizabeth L. Bhatt, Ami S. |
author_facet | Moss, Eli L. Falconer, Shannon B. Tkachenko, Ekaterina Wang, Mingjie Systrom, Hannah Mahabamunuge, Jasmin Relman, David A. Hohmann, Elizabeth L. Bhatt, Ami S. |
author_sort | Moss, Eli L. |
collection | PubMed |
description | Immunocompromised individuals are at high risk of developing Clostridium difficile-associated disease (CDAD). Fecal microbiota transplantation (FMT) is a highly effective therapy for refractory or recurrent CDAD and, despite safety concerns, has recently been offered to immunocompromised patients. We investigated the genomics of bacterial composition following FMT in immunocompromised patients over a 1-year period. Metagenomic, strain and gene-level bacterial dynamics were characterized in two CDAD-affected hematopoietic stem cell (HCT) recipients following FMT. We found alterations in gene content, including loss of virulence and antibiotic resistance genes. These alterations were accompanied by long-term bacterial divergence at the species and strain levels. Our findings suggest limited durability of the specific bacterial consortium introduced with FMT and indicate that alterations of the functional potential of the microbiome are more complex than can be inferred by taxonomic information alone. Our observation that FMT alone cannot induce long-term donor-like alterations of the microbiota of HCT recipients suggests that FMT cannot indefinitely supersede environmental and/or host factors in shaping bacterial composition. |
format | Online Article Text |
id | pubmed-5565110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55651102017-08-28 Long-term taxonomic and functional divergence from donor bacterial strains following fecal microbiota transplantation in immunocompromised patients Moss, Eli L. Falconer, Shannon B. Tkachenko, Ekaterina Wang, Mingjie Systrom, Hannah Mahabamunuge, Jasmin Relman, David A. Hohmann, Elizabeth L. Bhatt, Ami S. PLoS One Research Article Immunocompromised individuals are at high risk of developing Clostridium difficile-associated disease (CDAD). Fecal microbiota transplantation (FMT) is a highly effective therapy for refractory or recurrent CDAD and, despite safety concerns, has recently been offered to immunocompromised patients. We investigated the genomics of bacterial composition following FMT in immunocompromised patients over a 1-year period. Metagenomic, strain and gene-level bacterial dynamics were characterized in two CDAD-affected hematopoietic stem cell (HCT) recipients following FMT. We found alterations in gene content, including loss of virulence and antibiotic resistance genes. These alterations were accompanied by long-term bacterial divergence at the species and strain levels. Our findings suggest limited durability of the specific bacterial consortium introduced with FMT and indicate that alterations of the functional potential of the microbiome are more complex than can be inferred by taxonomic information alone. Our observation that FMT alone cannot induce long-term donor-like alterations of the microbiota of HCT recipients suggests that FMT cannot indefinitely supersede environmental and/or host factors in shaping bacterial composition. Public Library of Science 2017-08-21 /pmc/articles/PMC5565110/ /pubmed/28827811 http://dx.doi.org/10.1371/journal.pone.0182585 Text en © 2017 Moss et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Moss, Eli L. Falconer, Shannon B. Tkachenko, Ekaterina Wang, Mingjie Systrom, Hannah Mahabamunuge, Jasmin Relman, David A. Hohmann, Elizabeth L. Bhatt, Ami S. Long-term taxonomic and functional divergence from donor bacterial strains following fecal microbiota transplantation in immunocompromised patients |
title | Long-term taxonomic and functional divergence from donor bacterial strains following fecal microbiota transplantation in immunocompromised patients |
title_full | Long-term taxonomic and functional divergence from donor bacterial strains following fecal microbiota transplantation in immunocompromised patients |
title_fullStr | Long-term taxonomic and functional divergence from donor bacterial strains following fecal microbiota transplantation in immunocompromised patients |
title_full_unstemmed | Long-term taxonomic and functional divergence from donor bacterial strains following fecal microbiota transplantation in immunocompromised patients |
title_short | Long-term taxonomic and functional divergence from donor bacterial strains following fecal microbiota transplantation in immunocompromised patients |
title_sort | long-term taxonomic and functional divergence from donor bacterial strains following fecal microbiota transplantation in immunocompromised patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5565110/ https://www.ncbi.nlm.nih.gov/pubmed/28827811 http://dx.doi.org/10.1371/journal.pone.0182585 |
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