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Dynamics of the fecal microbiome in patients with recurrent and nonrecurrent Clostridium difficile infection
BACKGROUND: Recurrent Clostridium difficile infection (CDI) remains problematic, with up to 30 % of individuals diagnosed with primary CDI experiencing at least one episode of recurrence. The success of microbial-based therapeutics, such as fecal microbiota transplantation, for the treatment of recu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847246/ https://www.ncbi.nlm.nih.gov/pubmed/27121861 http://dx.doi.org/10.1186/s13073-016-0298-8 |
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author | Seekatz, Anna Maria Rao, Krishna Santhosh, Kavitha Young, Vincent Bensan |
author_facet | Seekatz, Anna Maria Rao, Krishna Santhosh, Kavitha Young, Vincent Bensan |
author_sort | Seekatz, Anna Maria |
collection | PubMed |
description | BACKGROUND: Recurrent Clostridium difficile infection (CDI) remains problematic, with up to 30 % of individuals diagnosed with primary CDI experiencing at least one episode of recurrence. The success of microbial-based therapeutics, such as fecal microbiota transplantation, for the treatment of recurrent CDI underscores the importance of restoring the microbiota. However, few studies have looked at the microbial factors that contribute to the development of recurrent disease. Here we compare microbial changes over time in patients with or without recurrence to identify microbial signatures associated with the development of recurrence. METHODS: We used 16S rRNA-encoding gene sequence analysis to compare the fecal microbiota of 93 patients with recurrent and nonrecurrent CDI, sampled longitudinally. Cross-group and intra-individual differences in microbial community diversity and similarity were compared prior to the development of recurrent disease and over time. RESULTS: Samples from these patient groups exhibited variable community profiles, clustering into four distinct community groups. Cross-group comparison of the index sample collected from patients that did or did not develop recurrence revealed differences in diversity and community structure (analysis of molecular variance, p < 0.05). Intra-individual comparisons of the microbiota were more informative and samples from recurrent patients were less likely to recover in diversity (Chi-square test, p < 0.005), exhibiting less community similarity overall (Kruskal–Wallis test, p < 0.05). Interestingly, patients with severe disease harbored a significantly less diverse community, a trend that was observed across both nonrecurrent and recurrent patient groups (Wilcoxon test, p < 0.05). CONCLUSIONS: To date, this study represents one of the largest studies focused on the relationship between predictive signals from the gut microbiota and the development of recurrent CDI. Our data demonstrate that specific microbiota-derived characteristics associate with disease severity and recurrence and that future studies could incorporate these characteristics into predictive models. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13073-016-0298-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4847246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48472462016-04-28 Dynamics of the fecal microbiome in patients with recurrent and nonrecurrent Clostridium difficile infection Seekatz, Anna Maria Rao, Krishna Santhosh, Kavitha Young, Vincent Bensan Genome Med Research BACKGROUND: Recurrent Clostridium difficile infection (CDI) remains problematic, with up to 30 % of individuals diagnosed with primary CDI experiencing at least one episode of recurrence. The success of microbial-based therapeutics, such as fecal microbiota transplantation, for the treatment of recurrent CDI underscores the importance of restoring the microbiota. However, few studies have looked at the microbial factors that contribute to the development of recurrent disease. Here we compare microbial changes over time in patients with or without recurrence to identify microbial signatures associated with the development of recurrence. METHODS: We used 16S rRNA-encoding gene sequence analysis to compare the fecal microbiota of 93 patients with recurrent and nonrecurrent CDI, sampled longitudinally. Cross-group and intra-individual differences in microbial community diversity and similarity were compared prior to the development of recurrent disease and over time. RESULTS: Samples from these patient groups exhibited variable community profiles, clustering into four distinct community groups. Cross-group comparison of the index sample collected from patients that did or did not develop recurrence revealed differences in diversity and community structure (analysis of molecular variance, p < 0.05). Intra-individual comparisons of the microbiota were more informative and samples from recurrent patients were less likely to recover in diversity (Chi-square test, p < 0.005), exhibiting less community similarity overall (Kruskal–Wallis test, p < 0.05). Interestingly, patients with severe disease harbored a significantly less diverse community, a trend that was observed across both nonrecurrent and recurrent patient groups (Wilcoxon test, p < 0.05). CONCLUSIONS: To date, this study represents one of the largest studies focused on the relationship between predictive signals from the gut microbiota and the development of recurrent CDI. Our data demonstrate that specific microbiota-derived characteristics associate with disease severity and recurrence and that future studies could incorporate these characteristics into predictive models. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13073-016-0298-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-27 /pmc/articles/PMC4847246/ /pubmed/27121861 http://dx.doi.org/10.1186/s13073-016-0298-8 Text en © Seekatz et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Seekatz, Anna Maria Rao, Krishna Santhosh, Kavitha Young, Vincent Bensan Dynamics of the fecal microbiome in patients with recurrent and nonrecurrent Clostridium difficile infection |
title | Dynamics of the fecal microbiome in patients with recurrent and nonrecurrent Clostridium difficile infection |
title_full | Dynamics of the fecal microbiome in patients with recurrent and nonrecurrent Clostridium difficile infection |
title_fullStr | Dynamics of the fecal microbiome in patients with recurrent and nonrecurrent Clostridium difficile infection |
title_full_unstemmed | Dynamics of the fecal microbiome in patients with recurrent and nonrecurrent Clostridium difficile infection |
title_short | Dynamics of the fecal microbiome in patients with recurrent and nonrecurrent Clostridium difficile infection |
title_sort | dynamics of the fecal microbiome in patients with recurrent and nonrecurrent clostridium difficile infection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847246/ https://www.ncbi.nlm.nih.gov/pubmed/27121861 http://dx.doi.org/10.1186/s13073-016-0298-8 |
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