<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Ndlovu IS</submitter><funding>Neurosurgical Research Foundation</funding><pubmed_abstract>&lt;i>Trichinella&lt;/i> infections have been documented globally and have been detected in wild and/or domestic animals except Antarctica. There is paucity of information in the metabolic responses of hosts during &lt;i>Trichinella&lt;/i> infections and biomarkers for infection that can be used in the diagnosis of the disease. The current study aimed to apply a non-targeted metabolomic approach to identify &lt;i>Trichinella zimbabwensis&lt;/i> biomarkers including metabolic response from sera of infected Sprague-Dawley rats. Fifty-four male Sprague-Dawley rats were randomly assigned into &lt;i>T. zimbabwensis&lt;/i> infected group (&lt;i>n&lt;/i> = 36) and the non-infected control (&lt;i>n&lt;/i> = 18). Results from the study showed that the metabolic signature of &lt;i>T. zimbabwensis&lt;/i> infection consists of enriched methyl</pubmed_abstract><journal>Frontiers in molecular biosciences</journal><pagination>1128542</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9983363</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Preliminary insights on the metabolomics of &lt;i>Trichinella zimbabwensis&lt;/i> infection in Sprague Dawley rats using GCxGC-TOF-MS (untargeted approach).</pubmed_title><pmcid>PMC9983363</pmcid><pubmed_authors>Mukaratirwa S</pubmed_authors><pubmed_authors>Chaisi M</pubmed_authors><pubmed_authors>Ndlovu IS</pubmed_authors><pubmed_authors>Silas E</pubmed_authors><pubmed_authors>Tshilwane SI</pubmed_authors><pubmed_authors>Vosloo A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preliminary insights on the metabolomics of &lt;i>Trichinella zimbabwensis&lt;/i> infection in Sprague Dawley rats using GCxGC-TOF-MS (untargeted approach).</name><description>&lt;i>Trichinella&lt;/i> infections have been documented globally and have been detected in wild and/or domestic animals except Antarctica. There is paucity of information in the metabolic responses of hosts during &lt;i>Trichinella&lt;/i> infections and biomarkers for infection that can be used in the diagnosis of the disease. The current study aimed to apply a non-targeted metabolomic approach to identify &lt;i>Trichinella zimbabwensis&lt;/i> biomarkers including metabolic response from sera of infected Sprague-Dawley rats. Fifty-four male Sprague-Dawley rats were randomly assigned into &lt;i>T. zimbabwensis&lt;/i> infected group (&lt;i>n&lt;/i> = 36) and the non-infected control (&lt;i>n&lt;/i> = 18). Results from the study showed that the metabolic signature of &lt;i>T. zimbabwensis&lt;/i> infection consists of enriched methyl</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-08-15T03:05:41.875Z</modification><creation>2025-05-29T16:30:31.952Z</creation></dates><accession>S-EPMC9983363</accession><cross_references><pubmed>36876045</pubmed><doi>10.3389/fmolb.2023.1128542</doi></cross_references></HashMap>