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dc.contributor.authorLee, Sonny T. M.  Concept link
dc.contributor.authorKahn, Stacy A.  Concept link
dc.contributor.authorDelmont, Tom O.  Concept link
dc.contributor.authorShaiber, Alon  Concept link
dc.contributor.authorEsen, Ozcan C.  Concept link
dc.contributor.authorHubert, Nathaniel A.  Concept link
dc.contributor.authorMorrison, Hilary G.  Concept link
dc.contributor.authorAntonopoulos, Dionysios A.  Concept link
dc.contributor.authorRubin, David T.  Concept link
dc.contributor.authorEren, A. Murat  Concept link
dc.date.accessioned2017-05-16T18:40:15Z
dc.date.available2017-05-16T18:40:15Z
dc.date.issued2017-05-04
dc.identifier.citationMicrobiome 5 (2017): 50en_US
dc.identifier.urihttps://hdl.handle.net/1912/8983
dc.description© The Author(s), 2017. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Microbiome 5 (2017): 50, doi:10.1186/s40168-017-0270-x.en_US
dc.description.abstractFecal microbiota transplantation (FMT) is an effective treatment for recurrent Clostridium difficile infection and shows promise for treating other medical conditions associated with intestinal dysbioses. However, we lack a sufficient understanding of which microbial populations successfully colonize the recipient gut, and the widely used approaches to study the microbial ecology of FMT experiments fail to provide enough resolution to identify populations that are likely responsible for FMT-derived benefits. We used shotgun metagenomics together with assembly and binning strategies to reconstruct metagenome-assembled genomes (MAGs) from fecal samples of a single FMT donor. We then used metagenomic mapping to track the occurrence and distribution patterns of donor MAGs in two FMT recipients. Our analyses revealed that 22% of the 92 highly complete bacterial MAGs that we identified from the donor successfully colonized and remained abundant in two recipients for at least 8 weeks. Most MAGs with a high colonization rate belonged to the order Bacteroidales. The vast majority of those that lacked evidence of colonization belonged to the order Clostridiales, and colonization success was negatively correlated with the number of genes related to sporulation. Our analysis of 151 publicly available gut metagenomes showed that the donor MAGs that colonized both recipients were prevalent, and the ones that colonized neither were rare across the participants of the Human Microbiome Project. Although our dataset showed a link between taxonomy and the colonization ability of a given MAG, we also identified MAGs that belong to the same taxon with different colonization properties, highlighting the importance of an appropriate level of resolution to explore the functional basis of colonization and to identify targets for cultivation, hypothesis generation, and testing in model systems. The analytical strategy adopted in our study can provide genomic insights into bacterial populations that may be critical to the efficacy of FMT due to their success in gut colonization and metabolic properties, and guide cultivation efforts to investigate mechanistic underpinnings of this procedure beyond associations.en_US
dc.description.sponsorshipAME was supported by the Frank R. Lillie Research Innovation Award and startup funds from the University of Chicago. This project was supported by the Mutchnik Family Charitable Fund and the University of Chicago Gastro-Intestinal Research Foundation.en_US
dc.language.isoen_USen_US
dc.publisherBioMed Centralen_US
dc.relation.urihttps://doi.org/10.1186/s40168-017-0270-x
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectFecal microbiota transplantationen_US
dc.subjectColonizationen_US
dc.subjectMetagenomicsen_US
dc.subjectMetagenome-assembled genomesen_US
dc.titleTracking microbial colonization in fecal microbiota transplantation experiments via genome-resolved metagenomicsen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/s40168-017-0270-x


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Attribution 4.0 International
Except where otherwise noted, this item's license is described as Attribution 4.0 International