重组酶聚合酶扩增
清脆的
反式激活crRNA
计算生物学
生物
重组酶
放大器
聚合酶链反应
Cas9
遗传学
基因
重组
作者
Pei Wang,Bo Guo,Xue Zhang,Yue Wang,Guang Yang,Hui Shen,Song Gao,Lihui Zhang
标识
DOI:10.1021/acs.jafc.2c08689
摘要
Acute hepatopancreatic necrosis disease (AHPND) is one of the most devastating diseases in aquaculture, causing significant economic losses in seafood supplies worldwide. Early detection is critical for its prevention, which requires reliable and fast-responding diagnosis tools with point-of-care testing (POCT) capacity. Recombinase polymerase amplification (RPA) has been combined with CRISPR/Cas12a for AHPND diagnosis with a two-step procedure, but the operation is inconvenient and has the risk of carryover contamination. Here, we develop an RPA-CRISPR one-pot assay that integrates RPA and CRISPR/Cas12a cleavage into simultaneous reactions. Using the special design of crRNA, which is based on suboptimal protospacer adjacent motifs (PAM), RPA and Cas12a are made compatible in one pot. The assay is highly specific with a good sensitivity of 102 copies/reaction. This study provides a new choice for AHPND diagnosis with a POCT facility and sets a good example for developing RPA-CRISPR one-pot molecular diagnosis assays.
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