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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/32297
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dc.contributor.advisorPoinar, Hendrik-
dc.contributor.authorSidhu, Ravneet Kaur-
dc.date.accessioned2025-09-12T19:16:56Z-
dc.date.available2025-09-12T19:16:56Z-
dc.date.issued2025-
dc.identifier.urihttp://hdl.handle.net/11375/32297-
dc.descriptionPh.D. Thesisen_US
dc.description.abstractYersinia pestis, the causative agent of the Black Death (1346-1353), has caused three historical and ongoing pandemics. The first Plague pandemic (541-740 CE), for which the Plague of Justinian was its herald (541-549 CE), the second Plague pandemic (1346-1840 CE), beginning with the Black Death (1346-1353 CE), and the third Plague pandemic (1850 CE-present), which resulted in the dissemination of global reservoirs, and continues to cause outbreaks today. Within the past fifteen years, hundreds of ancient genomes have been sequenced from historical and pre-historical outbreaks of the disease to address questions related to the bacterium’s virulence, global spread, and long-term, persistent outbreaks. In this dissertation, I present 15 new ancient Y. pestis genomes from Denmark (n = 13) and Turkey (n = 2), dated to the second Plague pandemic. Using these ancient samples and several modern isolates from collections at the Institut Pasteur, I perform phylogenetic, genomic, and functional analyses to study the persistence of the bacterium during the second Plague pandemic with respect to its spread and virulence. Specifically, I describe recurrent epidemic waves of the Plague throughout Denmark over a three-hundred-year period and assess the relationship between ancient strains from Denmark and other European countries. I de novo assemble the PCP1 plasmids in ancient and modern strains, revealing for the first time the sequence of the PCP1∆pla plasmid, and hypothesize the genomic and molecular characteristics of pla-reduced Y. pestis strains. Using modern pla-reduced isolates from Vietnam, I show the decreased virulence and increased time-to-death in these later-dated, pla-reduced strains, found in varying extents in all three pandemics. Furthermore, I predict that pla-reduced strains arise following rounds of high-mortality outbreaks of Plague, as a way for the bacterium to persist in its scarcely populated rodent hosts. Finally, I turn my attention towards modern-day Turkey, situated near the Caucasus Mountains, a region long hypothesized to host Plague reservoirs which caused the re-emergent epidemic waves of the second Plague pandemic. Here, I show the first genomic evidence of Plague in the Ottoman Empire, provide an updated second pandemic phylogeny, and I discuss current limitations in synthesizing genomic and historical data.en_US
dc.language.isoenen_US
dc.subjectAncient DNAen_US
dc.subjectYersinia pestisen_US
dc.subjectVirulence evolutionen_US
dc.subjectSecond Plague Pandemicen_US
dc.subjectPlagueen_US
dc.subjectTurkeyen_US
dc.subjectDenmarken_US
dc.subjectPlasminogen activatoren_US
dc.titleExploring the Evolutionary History of Yersinia pestis: A Persistent Pandemic Pathogenen_US
dc.typeThesisen_US
dc.contributor.departmentBiologyen_US
dc.description.degreetypeDissertationen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
dc.description.layabstractThe Plague, a disease caused by the bacterium Yersinia pestis, has caused three historical and ongoing pandemics. In recent years, there has been a rise in research involving the recovery of ancient Plague DNA from victims of the disease. In this dissertation, I utilize ancient Plague DNA to expand our understanding of the second Plague pandemic (~1346-1840), which spread throughout Afro-Eurasia, causing repeated outbreaks, over the course of four centuries. With data collected from three independent research projects, I explore the persistence of the bacterium. The first research project analyzes the relationships between ancient Plague strains from Medieval and Early Modern Denmark over a three-hundred-year period. Here, we focus on the introduction, spread, and extinction of the Plague in a single country. The second research project utilizes both ancient and modern strains of Y. pestis to characterize the causes and impacts of reduced copies of the Plasminogen Activator (pla) gene, which is vital for invasive infection. In the final project, I search for Plague in human and animal remains from modern-day Turkey, hypothesized to have been the home of long-term, second pandemic reservoirs. Through the recovery of ancient genomes, I describe phylogenetic and genomic patterns of persistence in Y. pestis and emphasize current limitations associated within ancient Plague research.en_US
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