<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(7)</volume><submitter>Deng Z</submitter><pubmed_abstract>Tuberculosis remains a major global health threat, with existing detection methods often limited by efficiency and resource demands. Our previous PAM-dependent dsDNA Target-activated Cas12f1 &lt;i>Trans&lt;/i> Reporter (PDTCTR) fluorescence sensing platform, while effective for PAM-dependent pathogen detection, was constrained by its reliance on specialized fluorescence equipment and lack of visual output, limiting its use in resource-limited settings. To overcome these limitations, we introduce an innovative RPA/CRISPR-Cas12f1_ge4.1 dual-mode system for rapid &lt;i>Mycobacterium tuberculosis&lt;/i> detection. This system combines engineered Cas12f_ge4.1 with recombinase polymerase amplification (RPA), offering both fluorescent and lateral flow detection. It achieves high sensitivity with detection li</pubmed_abstract><journal>Microbiology spectrum</journal><pagination>e0265224</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12211024</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Rapid and sensitive detection of &amp;lt;i&amp;gt;Mycobacterium tuberculosis&amp;lt;/i&amp;gt; using the RPA/Cas12f1_ge4.1 system with fluorescence and lateral flow readouts.</pubmed_title><pmcid>PMC12211024</pmcid><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Weng X</pubmed_authors><pubmed_authors>Deng Z</pubmed_authors><pubmed_authors>Luo G</pubmed_authors><pubmed_authors>Wen P</pubmed_authors><pubmed_authors>Zou T</pubmed_authors><pubmed_authors>Zhou X</pubmed_authors><pubmed_authors>Gan T</pubmed_authors><pubmed_authors>Tang H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rapid and sensitive detection of &amp;lt;i&amp;gt;Mycobacterium tuberculosis&amp;lt;/i&amp;gt; using the RPA/Cas12f1_ge4.1 system with fluorescence and lateral flow readouts.</name><description>Tuberculosis remains a major global health threat, with existing detection methods often limited by efficiency and resource demands. Our previous PAM-dependent dsDNA Target-activated Cas12f1 &lt;i>Trans&lt;/i> Reporter (PDTCTR) fluorescence sensing platform, while effective for PAM-dependent pathogen detection, was constrained by its reliance on specialized fluorescence equipment and lack of visual output, limiting its use in resource-limited settings. To overcome these limitations, we introduce an innovative RPA/CRISPR-Cas12f1_ge4.1 dual-mode system for rapid &lt;i>Mycobacterium tuberculosis&lt;/i> detection. This system combines engineered Cas12f_ge4.1 with recombinase polymerase amplification (RPA), offering both fluorescent and lateral flow detection. It achieves high sensitivity with detection li</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-06-01T15:40:35.563Z</modification><creation>2026-04-08T13:44:10.867Z</creation></dates><accession>S-EPMC12211024</accession><cross_references><pubmed>40488470</pubmed><doi>10.1128/spectrum.02652-24</doi></cross_references></HashMap>