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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...

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Autores principales: Moss, Eli L., Falconer, Shannon B., Tkachenko, Ekaterina, Wang, Mingjie, Systrom, Hannah, Mahabamunuge, Jasmin, Relman, David A., Hohmann, Elizabeth L., Bhatt, Ami S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
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.
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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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