<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>20(2)</volume><submitter>Phuklia W</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Murine typhus is a flea-borne disease caused by Rickettsia typhi that typically presents as an acute febrile illness. The diagnosis is often missed, leading to delays in appropriate treatment. A qPCR targeting a single gene (ompB) for R. typhi is widely used for diagnosis; however, it has low sensitivity for detecting bacterial DNA in patients' blood. We aimed to increase sensitivity of detection of R. typhi using qPCR by targeting a gene containing repetitive sequences, sca2 (surface cell antigen 2).&lt;h4>Methodology&lt;/h4>We compared diagnostic accuracy with the standard assay targeting single sequence ompB (outer membrane protein B). Specificity, sensitivity, and bacterial load measurement of both assays were compared using stored EDTA-anticoagulated buffy coat samples fr</pubmed_abstract><journal>PLoS neglected tropical diseases</journal><pagination>e0014004</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12919770</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Targeting surface cell antigen 2 increases sensitivity of Rickettsia typhi detection.</pubmed_title><pmcid>PMC12919770</pmcid><pubmed_authors>Phuklia W</pubmed_authors><pubmed_authors>Mayxay M</pubmed_authors><pubmed_authors>Ashley EA</pubmed_authors><pubmed_authors>Vongphachanh S</pubmed_authors><pubmed_authors>Padith K</pubmed_authors><pubmed_authors>Phommasone K</pubmed_authors><pubmed_authors>Chansamouth V</pubmed_authors><pubmed_authors>Newton PN</pubmed_authors><pubmed_authors>Robinson MT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting surface cell antigen 2 increases sensitivity of Rickettsia typhi detection.</name><description>&lt;h4>Background&lt;/h4>Murine typhus is a flea-borne disease caused by Rickettsia typhi that typically presents as an acute febrile illness. The diagnosis is often missed, leading to delays in appropriate treatment. A qPCR targeting a single gene (ompB) for R. typhi is widely used for diagnosis; however, it has low sensitivity for detecting bacterial DNA in patients' blood. We aimed to increase sensitivity of detection of R. typhi using qPCR by targeting a gene containing repetitive sequences, sca2 (surface cell antigen 2).&lt;h4>Methodology&lt;/h4>We compared diagnostic accuracy with the standard assay targeting single sequence ompB (outer membrane protein B). Specificity, sensitivity, and bacterial load measurement of both assays were compared using stored EDTA-anticoagulated buffy coat samples fr</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-16T10:06:00.488Z</modification><creation>2026-07-09T10:48:53.016Z</creation></dates><accession>S-EPMC12919770</accession><cross_references><pubmed>41712622</pubmed><doi>10.1371/journal.pntd.0014004</doi></cross_references></HashMap>