Genetic Manipulation of Bacteroides for Transient Colonization of Germ-free Mice

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dc.contributor.advisorGeuking, Markus
dc.contributor.authorDong, Sharon
dc.contributor.committeememberHarrison, Joe
dc.contributor.committeememberHirota, Simon
dc.contributor.committeememberBuret, Andre
dc.date2022-06
dc.date.accessioned2022-05-04T16:45:40Z
dc.date.available2022-05-04T16:45:40Z
dc.date.issued2022-04
dc.description.abstractHuman and murine hosts have a dynamic relationship with the microbes that colonize their bodily surfaces. Shifts in composition of the community of microbes, or their function, are implicated in many chronic and/or inflammatory conditions. There are currently gaps in understanding whether these shifts cause disease phenotypes or are artefacts of changed host conditions due to disease. The ability to tease apart these dynamics by generating bacterial tools that limited bacterial exposure of germ-free mice to a certain time-period was explored in this thesis. I target genes in synthesis pathways of two uniquely-bacterial amino acids, meso-diaminopimelic acid (mDAP) and D-Alanine (D-Ala) in a species of interest, Bacteroides thetaiotaomicron. These amino acids are incorporated into the peptidoglycan, or cell wall, of most bacteria, like B. thetaiotaomicron. This study builds on concepts from a previously developed E. coli strain called HA107, where disruption of these two synthesis pathways generated an auxotrophic mutant that grew if supplemented with said amino acids, however, did not proliferate and persist in germ-free murine gastrointestinal tracts. I designed deletion alleles that would exchange with the functional allele of target genes, and transferred the allelic exchange vector, pExchange, containing the deletion allele into B. thetaiotaomicron through conjugation. The double and triple gene deletion mutants failed to grow when not supplemented with mDAP and D-Ala. This mutation strategy may be adapted to genetically manipulate other notable Bacteroides species. The generated auxotrophic mutants from this study will be useful tools in answering questions regarding how timing or dosage of bacterial exposure affect health or disease outcomes in germ-free mice.en_US
dc.identifier.citationDong, S. (2022). Genetic manipulation of Bacteroides for transient colonization of germ-free mice (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca.en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/39728
dc.identifier.urihttp://hdl.handle.net/1880/114608
dc.language.isoengen_US
dc.publisher.facultyCumming School of Medicineen_US
dc.publisher.institutionUniversity of Calgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.en_US
dc.subjectbacterial geneticsen_US
dc.subjectgerm freeen_US
dc.subjecttransient colonizationen_US
dc.subject.classificationGeneticsen_US
dc.subject.classificationMicrobiologyen_US
dc.titleGenetic Manipulation of Bacteroides for Transient Colonization of Germ-free Miceen_US
dc.typemaster thesisen_US
thesis.degree.disciplineMedicine – Microbiology & Infectious Diseasesen_US
thesis.degree.grantorUniversity of Calgaryen_US
thesis.degree.nameMaster of Science (MSc)en_US
ucalgary.item.requestcopytrueen_US
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