{"id":{"repo_id":"calgary","oai_identifier":"oai:ucalgary.scholaris.ca:1880/109358"},"canonical_url":"https://search.dev.ndltd.org/etd/calgary/oai:ucalgary.scholaris.ca:1880/109358","repository":{"repo_id":"calgary","name":"University of Calgary","base_url":"https://ucalgary.scholaris.ca/server/oai/request"},"display":{"title":"Characterizing the Role of the Type VI Secretion System in Interbacterial Species Interactions and Pathogenesis","abstract":"Bacteria require molecular mechanisms to properly sense and respond to their environment. This allows them to compete for specific niches, persist in polymicrobial communities, and contribute to virulence and pathogenesis. One mechanism Gram-negative bacteria have adapted is the use of type VI secretion systems (T6SS). The T6SS is a large needle complex that spans across the entire bacterial cell wall and functions through a contraction mechanism that results in the delivery of toxic effector proteins into neighbouring cells. Virulence is achieved through the targeting of essential components found in either eukaryotic or prokaryotic organisms, including cell wall, membrane lipids, and DNA. Despite the importance of the T6SS as an interbacterial weapon, there still exists an incomplete understanding of how T6SS expressing species can co-exist and the implications of antagonistic responses in shaping polymicrobial communities. Further, these species are often subject to a changing environment and yet, the role of environmental signals and their influence on interspecies interactions and the expression of the T6SS, remain largely unknown. Here, I examined the role of the T6SS in the context of multispecies communities. Using a mix of two antagonistic T6SS strains, Vibrio cholerae V52 and Aeromonas hydrophila SSU, both species co-existed despite active bacterial killing. Fluorescence microscopy analyses revealed survival was possible through the formation of sister-cell clusters. Cluster formation was dependent on T6SS effector delivery, highlighting a unique mechanism where destructive responses can mediate protection within a community. I also examined the environmental signals that activate the T6SS using Pseudomonas aeruginosa PAO1, a strain with a tightly regulated T6SS, as a model system. Results reveal that extracellular DNA, prevalent in cystic fibrosis sputum, activates the H1-T6SS cluster of P. aeruginosa. The addition of excess magnesium ions in the media negates the effect of eDNA on T6SS activation, suggesting eDNA may be a chelator of membrane ions and T6SS activation is a consequence of a perturbed membrane. Overall, I provide new insight into how bacterial communities are shaped, and the type of adaptations bacteria undergo to better survive and compete in the environment.","abstract_html":"Bacteria require molecular mechanisms to properly sense and respond to their environment. This allows them to compete for specific niches, persist in polymicrobial communities, and contribute to virulence and pathogenesis. One mechanism Gram-negative bacteria have adapted is the use of type VI secretion systems (T6SS). The T6SS is a large needle complex that spans across the entire bacterial cell wall and functions through a contraction mechanism that results in the delivery of toxic effector proteins into neighbouring cells. Virulence is achieved through the targeting of essential components found in either eukaryotic or prokaryotic organisms, including cell wall, membrane lipids, and DNA. Despite the importance of the T6SS as an interbacterial weapon, there still exists an incomplete understanding of how T6SS expressing species can co-exist and the implications of antagonistic responses in shaping polymicrobial communities. Further, these species are often subject to a changing environment and yet, the role of environmental signals and their influence on interspecies interactions and the expression of the T6SS, remain largely unknown. Here, I examined the role of the T6SS in the context of multispecies communities. Using a mix of two antagonistic T6SS strains, Vibrio cholerae V52 and Aeromonas hydrophila SSU, both species co-existed despite active bacterial killing. Fluorescence microscopy analyses revealed survival was possible through the formation of sister-cell clusters. Cluster formation was dependent on T6SS effector delivery, highlighting a unique mechanism where destructive responses can mediate protection within a community. I also examined the environmental signals that activate the T6SS using Pseudomonas aeruginosa PAO1, a strain with a tightly regulated T6SS, as a model system. Results reveal that extracellular DNA, prevalent in cystic fibrosis sputum, activates the H1-T6SS cluster of P. aeruginosa. The addition of excess magnesium ions in the media negates the effect of eDNA on T6SS activation, suggesting eDNA may be a chelator of membrane ions and T6SS activation is a consequence of a perturbed membrane. Overall, I provide new insight into how bacterial communities are shaped, and the type of adaptations bacteria undergo to better survive and compete in the environment.","abstract_has_math":false,"creators":["Wong, Megan Jee Quin"],"institution":"Cumming School of Medicine","degree_name":"Master of Science (MSc)","degree_level":null,"degree_discipline":"Medicine – Biochemistry and Molecular Biology","degree_department":null,"school":null,"contributors":[],"advisors":["Dong, Tao G."],"committee_chairs":[],"committee_members":["Devinney, Rebekah","Schriemer, David C."],"year":2018,"date_issued":"2018-12-14","date_published":"2018-12-14","updated_at":"2026-07-24T01:30:33Z","subjects":["Vibrio cholerae","Aeromonas hydrophila","Pseudomonas aeruginosa","T6SS","type VI secretion system","bacterial competition","microbial communities","T6SS signaling"],"languages":["en"],"rights":["University 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."],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier.doi","label":"DOI","values":["http://dx.doi.org/10.11575/PRISM/34978"],"render_values":[{"text":"http://dx.doi.org/10.11575/PRISM/34978","href":"http://dx.doi.org/10.11575/PRISM/34978","code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/1880/109358","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Dong, Tao G."]},{"key":"dc:contributor.committeemember","label":"Committee Member","values":["Devinney, Rebekah","Schriemer, David C."]},{"key":"dc:creator","label":"Author","values":["Wong, Megan Jee Quin"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2019-06"]},{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2018-12-17T17:21:43Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2018-12-17T17:21:43Z"]},{"key":"dc:date.issued","label":"Date","values":["2018-12-14"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["University of Calgary"]},{"key":"dc:type","label":"Dc Type","values":["master thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Medicine – Biochemistry and Molecular Biology"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science (MSc)"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Calgary"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Vibrio cholerae","Aeromonas hydrophila","Pseudomonas aeruginosa","T6SS","type VI secretion system","bacterial competition","microbial communities","T6SS signaling"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["University of Calgary graduate students retain copyright ownership and moral rights for their thesis. 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The T6SS is a large needle complex that spans across the entire bacterial cell wall and functions through a contraction mechanism that results in the delivery of toxic effector proteins into neighbouring cells. Virulence is achieved through the targeting of essential components found in either eukaryotic or prokaryotic organisms, including cell wall, membrane lipids, and DNA. Despite the importance of the T6SS as an interbacterial weapon, there still exists an incomplete understanding of how T6SS expressing species can co-exist and the implications of antagonistic responses in shaping polymicrobial communities. Further, these species are often subject to a changing environment and yet, the role of environmental signals and their influence on interspecies interactions and the expression of the T6SS, remain largely unknown. Here, I examined the role of the T6SS in the context of multispecies communities. Using a mix of two antagonistic T6SS strains, Vibrio cholerae V52 and Aeromonas hydrophila SSU, both species co-existed despite active bacterial killing. Fluorescence microscopy analyses revealed survival was possible through the formation of sister-cell clusters. Cluster formation was dependent on T6SS effector delivery, highlighting a unique mechanism where destructive responses can mediate protection within a community. I also examined the environmental signals that activate the T6SS using Pseudomonas aeruginosa PAO1, a strain with a tightly regulated T6SS, as a model system. Results reveal that extracellular DNA, prevalent in cystic fibrosis sputum, activates the H1-T6SS cluster of P. aeruginosa. The addition of excess magnesium ions in the media negates the effect of eDNA on T6SS activation, suggesting eDNA may be a chelator of membrane ions and T6SS activation is a consequence of a perturbed membrane. Overall, I provide new insight into how bacterial communities are shaped, and the type of adaptations bacteria undergo to better survive and compete in the environment."]},{"key":"dc:title","label":"Title","values":["Characterizing the Role of the Type VI Secretion System in Interbacterial Species Interactions and Pathogenesis"]}]}],"canonical_facts":{"dc:contributor.advisor":["Dong, Tao G."],"dc:contributor.committeemember":["Devinney, Rebekah","Schriemer, David C."],"dc:creator":["Wong, Megan Jee Quin"],"dc:date":["2019-06"],"dc:date.accessioned":["2018-12-17T17:21:43Z"],"dc:date.available":["2018-12-17T17:21:43Z"],"dc:date.issued":["2018-12-14"],"dc:description.abstract":["Bacteria require molecular mechanisms to properly sense and respond to their environment. This allows them to compete for specific niches, persist in polymicrobial communities, and contribute to virulence and pathogenesis. 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Here, I examined the role of the T6SS in the context of multispecies communities. Using a mix of two antagonistic T6SS strains, Vibrio cholerae V52 and Aeromonas hydrophila SSU, both species co-existed despite active bacterial killing. Fluorescence microscopy analyses revealed survival was possible through the formation of sister-cell clusters. Cluster formation was dependent on T6SS effector delivery, highlighting a unique mechanism where destructive responses can mediate protection within a community. I also examined the environmental signals that activate the T6SS using Pseudomonas aeruginosa PAO1, a strain with a tightly regulated T6SS, as a model system. Results reveal that extracellular DNA, prevalent in cystic fibrosis sputum, activates the H1-T6SS cluster of P. aeruginosa. The addition of excess magnesium ions in the media negates the effect of eDNA on T6SS activation, suggesting eDNA may be a chelator of membrane ions and T6SS activation is a consequence of a perturbed membrane. Overall, I provide new insight into how bacterial communities are shaped, and the type of adaptations bacteria undergo to better survive and compete in the environment."],"dc:identifier.doi":["http://dx.doi.org/10.11575/PRISM/34978"],"dc:identifier.uri":["http://hdl.handle.net/1880/109358"],"dc:language.iso":["en"],"dc:publisher.institution":["University of Calgary"],"dc:rights":["University 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."],"dc:subject":["Vibrio cholerae","Aeromonas hydrophila","Pseudomonas aeruginosa","T6SS","type VI secretion system","bacterial competition","microbial communities","T6SS signaling"],"dc:title":["Characterizing the Role of the Type VI Secretion System in Interbacterial Species Interactions and Pathogenesis"],"dc:type":["master thesis"],"thesis:degree_discipline":["Medicine – Biochemistry and Molecular Biology"],"thesis:degree_name":["Master of Science (MSc)"],"thesis:institution_name":["University of Calgary"]},"updated_at":"2026-07-24T01:30:33Z"}