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Predictive Metagenomic Analysis of Autoimmune Disease Identifies Robust Autoimmunity and Disease Specific Microbial Signatures

Angelina Volkova, Kelly V. Ruggles
doi: https://doi.org/10.1101/779967
Angelina Volkova
1Institute for Systems Genetics, New York University Grossman School of Medicine, New York, NY, USA
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Kelly V. Ruggles
1Institute for Systems Genetics, New York University Grossman School of Medicine, New York, NY, USA
2Division of Translational Medicine, Department of Medicine, New York University Grossman School of Medicine, New York, NY, USA
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  • For correspondence: Kelly.Ruggles@nyulangone.org
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ABSTRACT

Within the last decade, numerous studies have demonstrated changes in the gut microbiome associated with specific autoimmune diseases. Due to differences in study design, data quality control, analysis and statistical methods, many results of these studies are inconsistent and incomparable. To better understand the relationship between the intestinal microbiome and autoimmunity, we have completed a comprehensive re-analysis of 42 studies focusing on the gut microbiome in twelve autoimmune diseases to identify a microbial signature predictive of multiple sclerosis (MS), inflammatory bowel disease (IBD), rheumatoid arthritis (RA) and general autoimmune disease using both 16S rRNA sequencing data and shotgun metagenomics data. To do this, we used four machine learning algorithms, random forest, eXtreme Gradient Boosting (XGBoost), ridge regression and support vector machine with radial kernel and recursive feature elimination to rank disease predictive taxa comparing disease vs. healthy participants and pairwise comparisons of each disease. Comparing the performance of these models, we found XGBoost and random forest, tree-based methods capable of handling sparse multidimensional data, to consistently produce the best results. Through this modeling, we identified a number of taxa consistently identified as dysregulated in a general autoimmune disease model including Odoribacter, Lachnospiraceae Clostridium and Mogibacteriaceae implicating all as potential factors connecting the gut microbiome and to autoimmune response. Further, we computed pairwise comparison models to identify disease specific taxa signatures highlighting a role for Peptostreptococcaceae and Ruminococcaceae Gemmiger in IBD and Akkermansia, Butyricicoccus and Mogibacteriaceae in MS. We then connected a subset of these taxa with potential metabolic alterations based on metagenomic/metabolomic correlation analysis, identifying 250 metabolites associated with autoimmunity-predictive taxa.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • Additional studies have been reprocessed and added to the analysis.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted October 26, 2020.
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Predictive Metagenomic Analysis of Autoimmune Disease Identifies Robust Autoimmunity and Disease Specific Microbial Signatures
Angelina Volkova, Kelly V. Ruggles
bioRxiv 779967; doi: https://doi.org/10.1101/779967
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Predictive Metagenomic Analysis of Autoimmune Disease Identifies Robust Autoimmunity and Disease Specific Microbial Signatures
Angelina Volkova, Kelly V. Ruggles
bioRxiv 779967; doi: https://doi.org/10.1101/779967

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