<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Eneku W</submitter><funding>Makerere University</funding><funding>Armed Forces Health Surveillance Branch</funding><funding>US Department of Defense Threat Reduction Agency</funding><pagination>2473159</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11878166</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>&lt;b>Background:&lt;/b> Fleas transmit a variety of zoonotic agents whose epidemiology and public health risk remains poorly understood in sub-Saharan Africa, including Uganda particularly outside plague-endemic areas. Common flea-borne zoonotic agents include &lt;i>Rickettsia felis&lt;/i> and &lt;i>Yersinia pestis.&lt;/i>. &lt;b>Objectives:&lt;/b> The study aimed at detecting and characterising flea-borne pathogens in peridomestic environments in Uganda. &lt;b>Methods:&lt;/b> We collected fleas from domestic animals, chickens, rodents, and homestead environments; pooled them by species, collection time, and host species. A total of 172 pools were analyzed for &lt;i>Y. pestis Pla&lt;/i> gene. Further, 62 pools were tested for &lt;i>Rickettsia&lt;/i> species &lt;i>gltA, ompA&lt;/i>, and &lt;i>htrA&lt;/i> genes by PCR and Sanger sequencing. &lt;b</pubmed_abstract><journal>Infection ecology &amp; epidemiology</journal><pubmed_title>Molecular detection and characterization of &amp;lt;i&amp;gt;Rickettsia felis&amp;lt;/i&amp;gt;, &amp;lt;i&amp;gt;R. asembonensis&amp;lt;/i&amp;gt;, and &amp;lt;i&amp;gt;Yersinia pestis&amp;lt;/i&amp;gt; from peri-domestic fleas in Uganda.</pubmed_title><pmcid>PMC11878166</pmcid><funding_grant_id>HDTRA1-15-1-0043</funding_grant_id><pubmed_authors>Atim G</pubmed_authors><pubmed_authors>Erima B</pubmed_authors><pubmed_authors>Byarugaba Karuhize D</pubmed_authors><pubmed_authors>Mworozi E</pubmed_authors><pubmed_authors>Wabwire-Mangen F</pubmed_authors><pubmed_authors>Douglas C</pubmed_authors><pubmed_authors>Cleary Gillian N</pubmed_authors><pubmed_authors>Koehler William J</pubmed_authors><pubmed_authors>von Fricken Emery M</pubmed_authors><pubmed_authors>Tweyongyere R</pubmed_authors><pubmed_authors>Ukuli Aquino Q</pubmed_authors><pubmed_authors>Kibuuka H</pubmed_authors><pubmed_authors>Eneku W</pubmed_authors><pubmed_authors>Tugume T</pubmed_authors><pubmed_authors>Byaruhanga Maranda A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular detection and characterization of &amp;lt;i&amp;gt;Rickettsia felis&amp;lt;/i&amp;gt;, &amp;lt;i&amp;gt;R. asembonensis&amp;lt;/i&amp;gt;, and &amp;lt;i&amp;gt;Yersinia pestis&amp;lt;/i&amp;gt; from peri-domestic fleas in Uganda.</name><description>&lt;b>Background:&lt;/b> Fleas transmit a variety of zoonotic agents whose epidemiology and public health risk remains poorly understood in sub-Saharan Africa, including Uganda particularly outside plague-endemic areas. Common flea-borne zoonotic agents include &lt;i>Rickettsia felis&lt;/i> and &lt;i>Yersinia pestis.&lt;/i>. &lt;b>Objectives:&lt;/b> The study aimed at detecting and characterising flea-borne pathogens in peridomestic environments in Uganda. &lt;b>Methods:&lt;/b> We collected fleas from domestic animals, chickens, rodents, and homestead environments; pooled them by species, collection time, and host species. A total of 172 pools were analyzed for &lt;i>Y. pestis Pla&lt;/i> gene. Further, 62 pools were tested for &lt;i>Rickettsia&lt;/i> species &lt;i>gltA, ompA&lt;/i>, and &lt;i>htrA&lt;/i> genes by PCR and Sanger sequencing. &lt;b</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-06-01T21:11:07.004Z</modification><creation>2025-04-04T02:47:53.787Z</creation></dates><accession>S-EPMC11878166</accession><cross_references><pubmed>40041476</pubmed><doi>10.1080/20008686.2025.2473159</doi></cross_references></HashMap>