杜氏利什曼原虫
脱氧核酶
生物
清脆的
检出限
分子生物学
DNA
病毒学
微生物学
化学
利什曼病
基因
内脏利什曼病
免疫学
生物化学
色谱法
作者
Hua Gao,Miaomiao Feng,Feng Li,Kaixiang Zhang,Ting Zhang,Zifang Zhang,Cheng-Yun Yang,Ruijie Deng,Junrong Zhang,Peng Jiang
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2022-10-07
卷期号:7 (10): 2968-2977
被引量:15
标识
DOI:10.1021/acssensors.2c01104
摘要
Early diagnosis of parasitic diseases can dramatically alleviate medical, economic, and social burdens. Herein, we report a sensitive and label-free assay for diagnosing single-celled parasitic infections using G-quadruplex (G4) DNAzyme as a reporter for CRISPR/Cas12. The substitution of a fluorescent DNA reporter with G4 DNAzyme increased the sensitivity for detecting Leishmania donovani (L. donovani) by 5 times and obviated the need for using chemically labeled DNA probes. The G4 DNAzyme-substrated CRISPR/Cas12 (GsubCas12) assay yielded a limit of detection of 3.1 parasites in the detection of cultured L. donovani and was further applied to analyze L. donovani in infected mice. The results showed that the GsubCas12 assay could positively detect L. donovani in spleen samples from infected mice about 2 weeks after low-dose inoculation, nearly 2 weeks earlier than that of parasitological analysis. GsubCas12 assay is promising as a diagnostic tool for parasitic infection in resource-limited regions.
科研通智能强力驱动
Strongly Powered by AbleSci AI