Hong Lin, Song Zhao, Yuying Ye, Lei Shao, Nizhen Jiang, Kun Yang
{"title":"荧光重组酶辅助扩增法检测微小巴贝斯虫。","authors":"Hong Lin, Song Zhao, Yuying Ye, Lei Shao, Nizhen Jiang, Kun Yang","doi":"10.3347/kjp.2022.60.3.201","DOIUrl":null,"url":null,"abstract":"<p><p>Babesia microti is one of the most common causative agents of babesiosis. A sensitive and rapid detection is necessary for screening potentially infected individuals. In this study, B. microti cytochrome c oxidase subunit I (cox1) was selected as the target gene, multiple primers were designed, and optimized by a recombinase-aided amplification (RAA) assay. The optimal primers and probe were labeled with fluorescein. The sensitivity of fluorescent RAA (fRAA) was evaluated using gradient diluents of the cox1 recombinant plasmid and genomic DNA extracted from whole blood of B. microti infected mice. The specificity of fRAA was assessed by other transfusion transmitted parasites. The analytical sensitivity of the fRAA assay was 10 copies of recombinant plasmid per reaction and 10 fg/µl B. microti genomic DNA. No cross-reaction with any other blood-transmitted parasites was observed. Our results demonstrated that the fRAA assay would be rapid, sensitive, and specific for the detection of B. microti.</p>","PeriodicalId":49938,"journal":{"name":"Korean Journal of Parasitology","volume":"60 3","pages":"201-205"},"PeriodicalIF":1.4000,"publicationDate":"2022-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/80/d9/kjp-60-3-201.PMC9256288.pdf","citationCount":"2","resultStr":"{\"title\":\"A Fluorescent Recombinase Aided Amplification Assay for Detection of Babesia microti.\",\"authors\":\"Hong Lin, Song Zhao, Yuying Ye, Lei Shao, Nizhen Jiang, Kun Yang\",\"doi\":\"10.3347/kjp.2022.60.3.201\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Babesia microti is one of the most common causative agents of babesiosis. A sensitive and rapid detection is necessary for screening potentially infected individuals. In this study, B. microti cytochrome c oxidase subunit I (cox1) was selected as the target gene, multiple primers were designed, and optimized by a recombinase-aided amplification (RAA) assay. The optimal primers and probe were labeled with fluorescein. The sensitivity of fluorescent RAA (fRAA) was evaluated using gradient diluents of the cox1 recombinant plasmid and genomic DNA extracted from whole blood of B. microti infected mice. The specificity of fRAA was assessed by other transfusion transmitted parasites. The analytical sensitivity of the fRAA assay was 10 copies of recombinant plasmid per reaction and 10 fg/µl B. microti genomic DNA. No cross-reaction with any other blood-transmitted parasites was observed. Our results demonstrated that the fRAA assay would be rapid, sensitive, and specific for the detection of B. microti.</p>\",\"PeriodicalId\":49938,\"journal\":{\"name\":\"Korean Journal of Parasitology\",\"volume\":\"60 3\",\"pages\":\"201-205\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2022-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/80/d9/kjp-60-3-201.PMC9256288.pdf\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Korean Journal of Parasitology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3347/kjp.2022.60.3.201\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/6/30 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"PARASITOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Korean Journal of Parasitology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3347/kjp.2022.60.3.201","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/6/30 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"PARASITOLOGY","Score":null,"Total":0}
引用次数: 2
摘要
微巴贝斯虫是巴贝斯虫病最常见的病原体之一。灵敏而快速的检测对于筛查潜在的感染者是必要的。本研究以微孢子虫细胞色素c氧化酶亚基I (cox1)为靶基因,设计了多个引物,并通过重组酶辅助扩增(RAA)实验对引物进行了优化。用荧光素标记最佳引物和探针。采用梯度稀释法对感染微螺旋体小鼠全血中提取的cox1重组质粒和基因组DNA进行荧光RAA (fRAA)敏感性评价。通过其他输血传播寄生虫来评估fRAA的特异性。fRAA检测的分析灵敏度为每个反应10拷贝重组质粒和10 fg/µl B. microti基因组DNA。未见与其他血源性寄生虫发生交叉反应。结果表明,该方法具有快速、灵敏、特异性强的特点。
A Fluorescent Recombinase Aided Amplification Assay for Detection of Babesia microti.
Babesia microti is one of the most common causative agents of babesiosis. A sensitive and rapid detection is necessary for screening potentially infected individuals. In this study, B. microti cytochrome c oxidase subunit I (cox1) was selected as the target gene, multiple primers were designed, and optimized by a recombinase-aided amplification (RAA) assay. The optimal primers and probe were labeled with fluorescein. The sensitivity of fluorescent RAA (fRAA) was evaluated using gradient diluents of the cox1 recombinant plasmid and genomic DNA extracted from whole blood of B. microti infected mice. The specificity of fRAA was assessed by other transfusion transmitted parasites. The analytical sensitivity of the fRAA assay was 10 copies of recombinant plasmid per reaction and 10 fg/µl B. microti genomic DNA. No cross-reaction with any other blood-transmitted parasites was observed. Our results demonstrated that the fRAA assay would be rapid, sensitive, and specific for the detection of B. microti.
期刊介绍:
The Korean Journal of Parasitology is the official journal paperless, on-line publication after Vol. 53, 2015 of The Korean Society for Parasitology and Tropical Medicine. Abbreviated title is ‘Korean J Parasitol’. It was launched in 1963. It contains original articles, case reports, brief communications, reviews or mini-reviews, book reviews, and letters to the editor on parasites of humans and animals, vectors, host-parasite relationships, zoonoses, and tropical medicine. It is published bimonthly in February, April, June, August, October, and December each year. Supplement numbers are at times published. All of the manuscripts are peer-reviewed.