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1775. Microbiome-Based Classifiers Accurately Differentiate Infectious Diarrhea From Functional Gastrointestinal Disorders and Provide Population-Scale Confidence Measures of Fecal Microbiota Restoration in Recurrent C. DifficileInfection
BACKGROUND: Fecal microbiota therapy is being actively pursued as treatment for recurrent C. difficile infection (rCDI), as well as for other GI disease indications associated with dysbiosis, for example, irritable bowel syndrome (IBS). RBX2660 is a microbiota-based drug designed to restore a health...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252580/ http://dx.doi.org/10.1093/ofid/ofy209.160 |
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author | Wu, Qinglong Ross, Cana Jones, Courtney Blount, Ken Savidge, Tor |
author_facet | Wu, Qinglong Ross, Cana Jones, Courtney Blount, Ken Savidge, Tor |
author_sort | Wu, Qinglong |
collection | PubMed |
description | BACKGROUND: Fecal microbiota therapy is being actively pursued as treatment for recurrent C. difficile infection (rCDI), as well as for other GI disease indications associated with dysbiosis, for example, irritable bowel syndrome (IBS). RBX2660 is a microbiota-based drug designed to restore a healthier microbiome and has demonstrated clinical efficacy for preventing rCDI. Despite this and other treatment successes, our understanding of functional microbiota reconstitution at the population scale is still evolving, as is the ability to distinguish IBS from CDI recurrence. Herein we describe development of a Random Forest classifier for CDI diagnosis, and we evaluate microbiome restoration in participants of the Phase 2 trial of RBX2660. METHODS: Fecal 16S rDNA sequences from 2,129 subjects enrolled in diverse multi-center cohorts were analyzed (1,235 adults and 447 children with CDI, AAD, IBS, or controls). Technical variations due to different DNA extraction, primer region coverage, and sequencing platforms were addressed using closed-reference OTU picking with UCLUST. The RDP classifier and SILVA database assigned taxonomy for each OTU sequence. Stratified random sampling with 50 repeated tests of microbiota training sets was performed for supervised learning. Microbiota signatures of patients in the RBX2660 PUNCH CD2 trial were then assessed using classifiers built to predict CDI treatment outcomes and IBS misdiagnosis. RESULTS: Random Forest built the best classifiers accurately predicting 97.7% of CDI cases, and confidently distinguished CDI from IBS patients based on their microbiome signatures (figure). RBX2660 treatment significantly restored microbiota community composition in rCDI cases compared with placebo controls. CONCLUSION: Random Forest classifiers built on a population-scale study of microbiota composition in patients with GI disease provide a highly accurate predictor of CDI cases versus potential IBS misdiagnosis in adults and children. RBX2660 significantly reduced disease classification scores in rCDI patients with a healthy-like microbiota reconstitution markedly accelerating after 30 days of treatment. This study was funded by 1UO1 AI24290-01 and Rebiotix, Inc. [Image: see text] DISCLOSURES: C. Jones, Rebiotix, Inc.: Employee, Salary. K. Blount, Rebiotix, Inc.: Employee, Salary. T. Savidge, Rebiotix: Grant Investigator, Research grant. |
format | Online Article Text |
id | pubmed-6252580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62525802018-11-28 1775. Microbiome-Based Classifiers Accurately Differentiate Infectious Diarrhea From Functional Gastrointestinal Disorders and Provide Population-Scale Confidence Measures of Fecal Microbiota Restoration in Recurrent C. DifficileInfection Wu, Qinglong Ross, Cana Jones, Courtney Blount, Ken Savidge, Tor Open Forum Infect Dis Abstracts BACKGROUND: Fecal microbiota therapy is being actively pursued as treatment for recurrent C. difficile infection (rCDI), as well as for other GI disease indications associated with dysbiosis, for example, irritable bowel syndrome (IBS). RBX2660 is a microbiota-based drug designed to restore a healthier microbiome and has demonstrated clinical efficacy for preventing rCDI. Despite this and other treatment successes, our understanding of functional microbiota reconstitution at the population scale is still evolving, as is the ability to distinguish IBS from CDI recurrence. Herein we describe development of a Random Forest classifier for CDI diagnosis, and we evaluate microbiome restoration in participants of the Phase 2 trial of RBX2660. METHODS: Fecal 16S rDNA sequences from 2,129 subjects enrolled in diverse multi-center cohorts were analyzed (1,235 adults and 447 children with CDI, AAD, IBS, or controls). Technical variations due to different DNA extraction, primer region coverage, and sequencing platforms were addressed using closed-reference OTU picking with UCLUST. The RDP classifier and SILVA database assigned taxonomy for each OTU sequence. Stratified random sampling with 50 repeated tests of microbiota training sets was performed for supervised learning. Microbiota signatures of patients in the RBX2660 PUNCH CD2 trial were then assessed using classifiers built to predict CDI treatment outcomes and IBS misdiagnosis. RESULTS: Random Forest built the best classifiers accurately predicting 97.7% of CDI cases, and confidently distinguished CDI from IBS patients based on their microbiome signatures (figure). RBX2660 treatment significantly restored microbiota community composition in rCDI cases compared with placebo controls. CONCLUSION: Random Forest classifiers built on a population-scale study of microbiota composition in patients with GI disease provide a highly accurate predictor of CDI cases versus potential IBS misdiagnosis in adults and children. RBX2660 significantly reduced disease classification scores in rCDI patients with a healthy-like microbiota reconstitution markedly accelerating after 30 days of treatment. This study was funded by 1UO1 AI24290-01 and Rebiotix, Inc. [Image: see text] DISCLOSURES: C. Jones, Rebiotix, Inc.: Employee, Salary. K. Blount, Rebiotix, Inc.: Employee, Salary. T. Savidge, Rebiotix: Grant Investigator, Research grant. Oxford University Press 2018-11-26 /pmc/articles/PMC6252580/ http://dx.doi.org/10.1093/ofid/ofy209.160 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Wu, Qinglong Ross, Cana Jones, Courtney Blount, Ken Savidge, Tor 1775. Microbiome-Based Classifiers Accurately Differentiate Infectious Diarrhea From Functional Gastrointestinal Disorders and Provide Population-Scale Confidence Measures of Fecal Microbiota Restoration in Recurrent C. DifficileInfection |
title | 1775. Microbiome-Based Classifiers Accurately Differentiate Infectious Diarrhea From Functional Gastrointestinal Disorders and Provide Population-Scale Confidence Measures of Fecal Microbiota Restoration in Recurrent C. DifficileInfection |
title_full | 1775. Microbiome-Based Classifiers Accurately Differentiate Infectious Diarrhea From Functional Gastrointestinal Disorders and Provide Population-Scale Confidence Measures of Fecal Microbiota Restoration in Recurrent C. DifficileInfection |
title_fullStr | 1775. Microbiome-Based Classifiers Accurately Differentiate Infectious Diarrhea From Functional Gastrointestinal Disorders and Provide Population-Scale Confidence Measures of Fecal Microbiota Restoration in Recurrent C. DifficileInfection |
title_full_unstemmed | 1775. Microbiome-Based Classifiers Accurately Differentiate Infectious Diarrhea From Functional Gastrointestinal Disorders and Provide Population-Scale Confidence Measures of Fecal Microbiota Restoration in Recurrent C. DifficileInfection |
title_short | 1775. Microbiome-Based Classifiers Accurately Differentiate Infectious Diarrhea From Functional Gastrointestinal Disorders and Provide Population-Scale Confidence Measures of Fecal Microbiota Restoration in Recurrent C. DifficileInfection |
title_sort | 1775. microbiome-based classifiers accurately differentiate infectious diarrhea from functional gastrointestinal disorders and provide population-scale confidence measures of fecal microbiota restoration in recurrent c. difficileinfection |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252580/ http://dx.doi.org/10.1093/ofid/ofy209.160 |
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