{"id":{"repo_id":"nmu","oai_identifier":"oai:commons.nmu.edu:theses-1945"},"canonical_url":"https://search.dev.ndltd.org/etd/nmu/oai:commons.nmu.edu:theses-1945","repository":{"repo_id":"nmu","name":"Northern Michigan University","base_url":"https://commons.nmu.edu/do/oai/"},"display":{"title":"Bartonella in Small Mammals from Montana and Idaho","abstract":"<p><em>Bartonella</em> bacteria are widespread zoonotic pathogens that infect a diverse range of small mammals, yet their prevalence and distribution remain understudied in many host species. In this study, <em>Bartonella</em> infection was assessed across multiple small mammal species, revealing an overall prevalence of approximately 37% based on droplet digital PCR (ddPCR) screening. Following ddPCR screening, individuals that yielded positive results were selected for further analysis including genetic sequencing of the RNA polymerase b-subunit (<em>rpoB</em>) gene. While 116 individuals of 313 tested positive, only 63 samples were successfully sequenced, likely due to low infection loads. BLAST analysis suggested the presence of several <em>Bartonella</em> species among the infected samples, with <em>B. grahamii</em> and <em>B. washoensis</em> being the most frequently detected. Phylogenetic analyses using both Bayesian inference (MrBayes) and maximum likelihood (IQ-TREE) approaches demonstrated strong host-associated clustering of known <em>Bartonella </em>species. These findings provide important insights into <em>Bartonella</em> prevalence, distribution, diversity, and host specificity.</p>","abstract_html":"&lt;p&gt;&lt;em&gt;Bartonella&lt;/em&gt; bacteria are widespread zoonotic pathogens that infect a diverse range of small mammals, yet their prevalence and distribution remain understudied in many host species. In this study, &lt;em&gt;Bartonella&lt;/em&gt; infection was assessed across multiple small mammal species, revealing an overall prevalence of approximately 37% based on droplet digital PCR (ddPCR) screening. Following ddPCR screening, individuals that yielded positive results were selected for further analysis including genetic sequencing of the RNA polymerase b-subunit (&lt;em&gt;rpoB&lt;/em&gt;) gene. While 116 individuals of 313 tested positive, only 63 samples were successfully sequenced, likely due to low infection loads. BLAST analysis suggested the presence of several &lt;em&gt;Bartonella&lt;/em&gt; species among the infected samples, with &lt;em&gt;B. grahamii&lt;/em&gt; and &lt;em&gt;B. washoensis&lt;/em&gt; being the most frequently detected. Phylogenetic analyses using both Bayesian inference (MrBayes) and maximum likelihood (IQ-TREE) approaches demonstrated strong host-associated clustering of known &lt;em&gt;Bartonella &lt;/em&gt;species. These findings provide important insights into &lt;em&gt;Bartonella&lt;/em&gt; prevalence, distribution, diversity, and host specificity.&lt;/p&gt;","abstract_has_math":false,"creators":["Greenman, Emily"],"institution":null,"degree_name":"Master of Science","degree_level":"Thesis","degree_discipline":"Biology","degree_department":null,"school":null,"contributors":["Josh Sharp"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2025,"date_issued":"2025-05-01T07:00:00Z","date_published":"2025-05-01T07:00:00Z","updated_at":"2026-07-24T03:24:36Z","subjects":[],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://commons.nmu.edu/theses/872","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Josh Sharp"]},{"key":"dc:creator","label":"Author","values":["Greenman, Emily"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2030-03-31T07:00:00Z"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biology"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://commons.nmu.edu/theses/872"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["<p><em>Bartonella</em> bacteria are widespread zoonotic pathogens that infect a diverse range of small mammals, yet their prevalence and distribution remain understudied in many host species. In this study, <em>Bartonella</em> infection was assessed across multiple small mammal species, revealing an overall prevalence of approximately 37% based on droplet digital PCR (ddPCR) screening. Following ddPCR screening, individuals that yielded positive results were selected for further analysis including genetic sequencing of the RNA polymerase b-subunit (<em>rpoB</em>) gene. While 116 individuals of 313 tested positive, only 63 samples were successfully sequenced, likely due to low infection loads. BLAST analysis suggested the presence of several <em>Bartonella</em> species among the infected samples, with <em>B. grahamii</em> and <em>B. washoensis</em> being the most frequently detected. Phylogenetic analyses using both Bayesian inference (MrBayes) and maximum likelihood (IQ-TREE) approaches demonstrated strong host-associated clustering of known <em>Bartonella </em>species. These findings provide important insights into <em>Bartonella</em> prevalence, distribution, diversity, and host specificity.</p>"]},{"key":"dc:title","label":"Title","values":["Bartonella in Small Mammals from Montana and Idaho"]}]}],"canonical_facts":{"dc:contributor":["Josh Sharp"],"dc:creator":["Greenman, Emily"],"dc:date.available":["2030-03-31T07:00:00Z"],"dc:description.abstract":["<p><em>Bartonella</em> bacteria are widespread zoonotic pathogens that infect a diverse range of small mammals, yet their prevalence and distribution remain understudied in many host species. In this study, <em>Bartonella</em> infection was assessed across multiple small mammal species, revealing an overall prevalence of approximately 37% based on droplet digital PCR (ddPCR) screening. Following ddPCR screening, individuals that yielded positive results were selected for further analysis including genetic sequencing of the RNA polymerase b-subunit (<em>rpoB</em>) gene. While 116 individuals of 313 tested positive, only 63 samples were successfully sequenced, likely due to low infection loads. BLAST analysis suggested the presence of several <em>Bartonella</em> species among the infected samples, with <em>B. grahamii</em> and <em>B. washoensis</em> being the most frequently detected. Phylogenetic analyses using both Bayesian inference (MrBayes) and maximum likelihood (IQ-TREE) approaches demonstrated strong host-associated clustering of known <em>Bartonella </em>species. These findings provide important insights into <em>Bartonella</em> prevalence, distribution, diversity, and host specificity.</p>"],"dc:identifier":["https://commons.nmu.edu/theses/872"],"dc:title":["Bartonella in Small Mammals from Montana and Idaho"],"thesis:degree_discipline":["Biology"],"thesis:degree_level":["Thesis"],"thesis:degree_name":["Master of Science"]},"updated_at":"2026-07-24T03:24:36Z"}