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        <identifier>oai:figshare.com:article/34049449</identifier>
        <datestamp>2026-10-01T17:46:46Z</datestamp>
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        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>&lt;p&gt;Ordinary Least Squares model and ANOVA results.&lt;/p&gt;</dc:title>
          <dc:creator>Egie E. Enabuele (25158001)</dc:creator>
          <dc:creator>Roy N. Platt II (13783184)</dc:creator>
          <dc:creator>Ehizogie E. Adeyemi (25158004)</dc:creator>
          <dc:creator>Martins S. O. Aisien (25158007)</dc:creator>
          <dc:creator>Oluwaremilekun G. Ajakaye (4243018)</dc:creator>
          <dc:creator>Mahmud U. Ali (25158010)</dc:creator>
          <dc:creator>Ebube C. Amaechi (25158013)</dc:creator>
          <dc:creator>Tolulope E. Atalabi (25158016)</dc:creator>
          <dc:creator>Timothy Auta (25158019)</dc:creator>
          <dc:creator>Oluwaseun B. Awosolu (25158022)</dc:creator>
          <dc:creator>Adamu G. Dagona (25158025)</dc:creator>
          <dc:creator>Omoyemwen Edo-Taiwo (25158028)</dc:creator>
          <dc:creator>Chika P. Ejikeugwu (25158031)</dc:creator>
          <dc:creator>Christopher Igbeneghu (25158034)</dc:creator>
          <dc:creator>Victor S. Njom (10928747)</dc:creator>
          <dc:creator>Marian Onwude-Agbugui (25158037)</dc:creator>
          <dc:creator>Mary-Kate N. Orji (25158040)</dc:creator>
          <dc:creator>Funso O. P. Oyinloye (25158043)</dc:creator>
          <dc:creator>Esther Oyemade (25158046)</dc:creator>
          <dc:creator>Habibat J. Ozemoka (25158049)</dc:creator>
          <dc:creator>Christopher R. Pam (25158052)</dc:creator>
          <dc:creator>Uchenna I. Ugah (25158055)</dc:creator>
          <dc:creator>Jenna M. Hulke (25158058)</dc:creator>
          <dc:creator>Grace A. Arya (25158061)</dc:creator>
          <dc:creator>Timothy J. C. Anderson (7548590)</dc:creator>
          <dc:subject>Physical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>tight cluster regardless</dc:subject>
          <dc:subject>internal transcribed spacer</dc:subject>
          <dc:subject>genome sequencing revealed</dc:subject>
          <dc:subject>approach requires reinterpretation</dc:subject>
          <dc:subject>also genome sequenced</dc:subject>
          <dc:subject>14 nigerian locations</dc:subject>
          <dc:subject>schistosomes containing 50</dc:subject>
          <dc:subject>early generation hybrids</dc:subject>
          <dc:subject>documenting zoonotic infection</dc:subject>
          <dc:subject>detecting zoonotic infection</dc:subject>
          <dc:subject>div &gt;&lt; p</dc:subject>
          <dc:subject>suggesting zoonotic infection</dc:subject>
          <dc:subject>132 parasites isolated</dc:subject>
          <dc:subject>schistosoma haematobium &lt;/</dc:subject>
          <dc:subject>livestock schistosome markers</dc:subject>
          <dc:subject>bovis cox1 &lt;/</dc:subject>
          <dc:subject>zoonotic infection</dc:subject>
          <dc:subject>livestock schistosomes</dc:subject>
          <dc:subject>schistosoma &lt;/</dc:subject>
          <dc:subject>zoonotic infections</dc:subject>
          <dc:subject>schistosome epidemiology</dc:subject>
          <dc:subject>recent hybrids</dc:subject>
          <dc:subject>bovis &lt;/</dc:subject>
          <dc:subject>haematobium &lt;/</dc:subject>
          <dc:subject>cox1 &lt;/</dc:subject>
          <dc:subject>livestock parasites</dc:subject>
          <dc:subject>livestock counterparts</dc:subject>
          <dc:subject>curassoni &lt;/</dc:subject>
          <dc:subject>cox &lt;/</dc:subject>
          <dc:subject>wide ancestry</dc:subject>
          <dc:subject>well differentiated</dc:subject>
          <dc:subject>used approaches</dc:subject>
          <dc:subject>typically inferred</dc:subject>
          <dc:subject>southern nigeria</dc:subject>
          <dc:subject>results demonstrate</dc:subject>
          <dc:subject>northern nigeria</dc:subject>
          <dc:subject>modest levels</dc:subject>
          <dc:subject>misleading inference</dc:subject>
          <dc:subject>low levels</dc:subject>
          <dc:subject>human urine</dc:subject>
          <dc:description>&lt;div&gt;&lt;p&gt;The nuclear, internal transcribed spacer (ITS) and mitochondrial &lt;i&gt;cox1&lt;/i&gt; markers are widely used to differentiate &lt;i&gt;Schistosoma haematobium&lt;/i&gt; from its livestock counterparts, &lt;i&gt;S. bovis&lt;/i&gt; and &lt;i&gt;S. curassoni&lt;/i&gt;. &lt;i&gt;Schistosoma&lt;/i&gt; isolated from humans with ITS and &lt;i&gt;cox&lt;/i&gt;1 alleles from livestock parasites are typically inferred to be zoonotic infections and those with heterozygous ITS alleles (suggesting mixed species ancestry) are classified as recent hybrids. These classifications assume that the ITS and cox1 markers accurately reflect genome-wide ancestry. Here, we evaluated the reliability of this classification scheme by genotyping ITS and &lt;i&gt;cox1&lt;/i&gt; from 132 parasites isolated from human urine, and from 37 adult schistosomes collected from cattle at 14 Nigerian locations. We also genome sequenced each sample to empirically determine livestock schistosome ancestry. ITS/&lt;i&gt;cox1&lt;/i&gt; genotyping suggested extensive recent hybridization and zoonotic infection. Among parasites from humans, 10.1% carried both &lt;i&gt;S. curassoni&lt;/i&gt; and &lt;i&gt;S. haematobium&lt;/i&gt; ITS, consistent with F1 or early generation hybrids, 21% had livestock schistosome markers at both &lt;i&gt;cox1&lt;/i&gt; and ITS suggesting zoonotic infection, while 13.7% carried &lt;i&gt;S. bovis cox1&lt;/i&gt; alongside mixed &lt;i&gt;S. curassoni&lt;/i&gt; and &lt;i&gt;S. haematobium&lt;/i&gt; ITS, suggesting more complex ancestry. Genome sequencing revealed a very different picture. All parasites from humans formed a tight cluster regardless of ITS or &lt;i&gt;cox1&lt;/i&gt; genotype, while all worms from cattle were well differentiated. We found no schistosomes containing 50% livestock parasite ancestry consistent with F1s. Instead, we observed regionally varying levels of &lt;i&gt;S. bovis&lt;/i&gt; introgression, with modest levels in southern Nigeria (mean = 4.9%) and low levels in northern Nigeria (mean = 0.06%). These results demonstrate that: (i) two-locus genotyping is uninformative for detecting zoonotic infection or recent hybridization between &lt;i&gt;S. haematobium&lt;/i&gt; and livestock schistosomes and (ii) previous data generated using this approach requires reinterpretation. These findings reveal the limitations of widely-used approaches for documenting zoonotic infection and hybridization between &lt;i&gt;S. haematobium&lt;/i&gt; and livestock schistosome species.&lt;/p&gt;&lt;/div&gt;</dc:description>
          <dc:date>2026-10-01T17:46:27Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1371/journal.ppat.1014625.t002</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/_p_Ordinary_Least_Squares_model_and_ANOVA_results_p_/34049449</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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