Naked-eye on-site detection platform for Pasteurella multocida based on the CRISPR-Cas12a system coupled with recombinase polymerase amplification

被引:17
|
作者
Hao, Jie [1 ,2 ,3 ]
Xie, Longfei [1 ,2 ,3 ]
Yang, Tianmu [1 ,2 ,3 ]
Huo, Zhipeng [1 ,2 ,3 ]
Liu, Guifang [1 ,2 ,3 ]
Liu, Yahong [1 ,2 ,3 ,4 ]
Xiong, Wenguang [1 ,2 ,3 ,4 ]
Zeng, Zhenling [1 ,2 ,3 ,4 ]
机构
[1] South China Agr Univ, Guangdong Prov Key Lab Vet Pharmaceut Dev & Safety, Guangzhou 510642, Peoples R China
[2] South China Agr Univ, Coll Vet Med, Natl Risk Assessment Lab Antimicrobial Resistance, Guangzhou 510642, Peoples R China
[3] South China Agr Univ, Natl Lab Safety Evaluat Environm Assessment Vet Dr, Guangzhou 510642, Peoples R China
[4] South China Agr Univ, Natl Reference Lab Vet Drug Residues, Guangzhou 510642, Peoples R China
基金
中国国家自然科学基金;
关键词
Pasteurella multocida; CRISPR; Cas12a; Recombinase polymerase amplification (RPA); Cas12a-NEye; Naked-eye readout; On-site detection; NUCLEIC-ACID DETECTION; ASSAY;
D O I
10.1016/j.talanta.2022.124220
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Pasteurella multocida (P. multocida) is an important pathogenic bacterium that poses a serious threat to the development of the livestock economy and human health. Currently, the existing methods for P. multocida detection are time-consuming and require complex professional operations, limiting the application of field detection. In the study, we presented a single-pot naked-eye CRISPR-Cas12a platform (Cas12a-NEye) for the detection of P. multocida. The round tube cover allowed more Cas12a detection solution to be temporarily stored than the flat cap, enabling single-pot assays and avoiding aerosol contamination. The positive samples generated obvious red using naked eye using no excitation light and the negative samples generated blue. The limit of detection (LOD) was a single copy, without cross-reactivity with other closely related bacteria. Furthermore, we validated this platform using 16 P. multocida clinical lung samples and obtained consistent results with the realtime quantitative polymerase chain reaction (qPCR) method. The entire experimental process included rapid DNA extraction (<1 h) and Cas12a-NEye assay (25 min), which was accomplished within 1.5 h. Thus, this "sample-to-answer" platform has significant potential for P. multocida detection.
引用
收藏
页数:8
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