<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Chen X</submitter><pubmed_abstract>Anisakidosis is a food-borne parasitic disease (FBPD) caused by the third-stage larvae of the family Anisakidae. Therefore, it is important to develop a simple, rapid and equipment-free detection method for anisakids in fish samples or seafood since current methods are time-consuming and require complex instruments. In this study, a recombinase polymerase amplification (RPA)-based method was established for the first time to detect anisakids by targeting the internal transcribed spacer (ITS) regions. The detection results were visualized by including SYBR Green I (SG) in the method. The sensitivity of RPA-SG assay was 10&lt;sup>2&lt;/sup> copies per reaction of recombinant plasmid (within 20 min at 37°C), similar to quantitative real-time PCR (qPCR). The assay had high specificity for detecting </pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>1026129</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9756439</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Rapid visual detection of anisakid nematodes using recombinase polymerase amplification and SYBR Green I.</pubmed_title><pmcid>PMC9756439</pmcid><pubmed_authors>Qiu Y</pubmed_authors><pubmed_authors>Zhao L</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Dong Z</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Bai X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rapid visual detection of anisakid nematodes using recombinase polymerase amplification and SYBR Green I.</name><description>Anisakidosis is a food-borne parasitic disease (FBPD) caused by the third-stage larvae of the family Anisakidae. Therefore, it is important to develop a simple, rapid and equipment-free detection method for anisakids in fish samples or seafood since current methods are time-consuming and require complex instruments. In this study, a recombinase polymerase amplification (RPA)-based method was established for the first time to detect anisakids by targeting the internal transcribed spacer (ITS) regions. The detection results were visualized by including SYBR Green I (SG) in the method. The sensitivity of RPA-SG assay was 10&lt;sup>2&lt;/sup> copies per reaction of recombinant plasmid (within 20 min at 37°C), similar to quantitative real-time PCR (qPCR). The assay had high specificity for detecting </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T12:01:48.469Z</modification><creation>2025-02-19T03:00:11.917Z</creation></dates><accession>S-EPMC9756439</accession><cross_references><pubmed>36532447</pubmed><doi>10.3389/fmicb.2022.1026129</doi></cross_references></HashMap>