2026-09-19T22:55:57Zhttps://dspace.mit.edu/server/oai/request

oai:dspace.mit.edu:1721.1/1032732026-06-16T18:52:26Zcom_1721.1_7582com_1721.1_7581col_1721.1_131022

Eric Alm. Smillie, Christopher Scott Massachusetts Institute of Technology. Computational and Systems Biology Program. Massachusetts Institute of Technology. Computational and Systems Biology Program 2016-06-22T17:54:52Z 2016-06-22T17:54:52Z 2015 2016 http://hdl.handle.net/1721.1/103273 951809332 Thesis: Ph. D., Massachusetts Institute of Technology, Computational and Systems Biology Program, February 2016. Cataloged from PDF version of thesis. Includes bibliographical references (pages 99-110). The vast community of microbes that inhabit the human body, the human microbiota, is important to human health and disease. These microbes contribute to human metabolism, the development of the immune system and pathogen resistance, while imbalances among them have been associated with several diseases. In this work, I develop computational methods to gain key insights into the ecological principles that shape these communities. In the first chapter, I develop an evolutionary rate heuristic that leads to the discovery of a massive network of recently exchanged genes, connecting diverse bacteria throughout the human microbiota. Using this network, I examine the roles of phylogenetic distance, geographic proximity and ecological overlap in shaping rates of horizontal gene transfer. Of these factors, ecological similarity is the principal force shaping gene exchange. In the second chapter, I focus on the microbial communities within a person, identifying the factors that affect the stability of the human microbiota. Alpha-diversity is strongly correlated with stability, but the direction of this correlation changes depending on the body site or subject being examined. In contrast, beta-diversity is consistently negatively correlated to stability. I show that a simple equilibrium model explains these results and accurately predicts the correlation between diversity and stability in every body site, thus reconciling these seemingly contradictory relationships into a single model. In the final chapter, I explore the use of fecal microbiota transplantation (FMT) to treat recurrent Clostridium difficile infection. I develop a new method to infer the genotypes and frequencies of bacterial strains in metagenomics samples. I apply this method to a dataset covering twenty patients before and after FMT, uncovering key ecological rules that govern the colonization and growth of bacteria in human subjects after FMT. by Christopher Scott Smillie. Ph.D. 110 pages eng Massachusetts Institute of Technology M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 Computational and Systems Biology Program. Computational insights into the ecology of the human microbiota Thesis application/pdf false Publication unknown unknown <Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="10a698aa-eaa7-4e64-80d6-ab6503dc8a1b"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>Computational insights into the ecology of the human microbiota</Title> <PublishedIn> <Publication> </Publication> </PublishedIn> <PublicationDate>2016</PublicationDate> <Authors> <Author> <DisplayName>Smillie, Christopher Scott</DisplayName> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Massachusetts Institute of Technology</DisplayName> <OrgUnit /> </Publisher> </Publishers> <License>http://dspace.mit.edu/handle/1721.1/7582</License> <Keyword>Computational and Systems Biology Program.</Keyword> <Abstract>The vast community of microbes that inhabit the human body, the human microbiota, is important to human health and disease. These microbes contribute to human metabolism, the development of the immune system and pathogen resistance, while imbalances among them have been associated with several diseases. In this work, I develop computational methods to gain key insights into the ecological principles that shape these communities. In the first chapter, I develop an evolutionary rate heuristic that leads to the discovery of a massive network of recently exchanged genes, connecting diverse bacteria throughout the human microbiota. Using this network, I examine the roles of phylogenetic distance, geographic proximity and ecological overlap in shaping rates of horizontal gene transfer. Of these factors, ecological similarity is the principal force shaping gene exchange. In the second chapter, I focus on the microbial communities within a person, identifying the factors that affect the stability of the human microbiota. Alpha-diversity is strongly correlated with stability, but the direction of this correlation changes depending on the body site or subject being examined. In contrast, beta-diversity is consistently negatively correlated to stability. I show that a simple equilibrium model explains these results and accurately predicts the correlation between diversity and stability in every body site, thus reconciling these seemingly contradictory relationships into a single model. In the final chapter, I explore the use of fecal microbiota transplantation (FMT) to treat recurrent Clostridium difficile infection. I develop a new method to infer the genotypes and frequencies of bacterial strains in metagenomics samples. I apply this method to a dataset covering twenty patients before and after FMT, uncovering key ecological rules that govern the colonization and growth of bacteria in human subjects after FMT.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication>