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Rapid and Visual Detection of Heterodera schachtii Using Recombinase Polymerase Amplification Combined with Cas12a-Mediated Technology

文献类型： 外文期刊

作者： Yao, Ke 1 ; Peng, Deliang 2 ; Jiang, Chen 2 ; Zhao, Wei 2 ; Li, Guangkuo 1 ; Huang, Wenkun 2 ; Kong, Lingan 2 ; Gao, Haif 1 ;

作者机构： 1.Zhejiang Univ, Inst Biotechnol, Coll Agr & Biotechnol, Hangzhou 310058, Peoples R China

2.Chinese Acad Agr Sci, Inst Plant Protect, State Key Lab Biol Plant Dis & Insect Pests, Beijing 100089, Peoples R China

3.Xinjiang Acad Agr Sci, Sci Observing & Expt Stn Korla, Key Lab Integrated Pest Management Crop Northwest, Minist Agr,Inst Plant Protect, Urumqi 830091, Peoples R China

关键词： recombinase polymerase amplification (RPA); sugar beet cyst nematode; Heterodera schachtii; lateral flow dipstick (LFD); Cas12a

期刊名称：INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES （ 影响因子：5.924； 五年影响因子：6.132 ）

ISSN：

年卷期： 2021 年 22 卷 22 期

页码：

收录情况： SCI

摘要： Heterodera schachtii is a well-known cyst nematode that causes serious economic losses in sugar beet production every year. Rapid and visual detection of H. schachtii is essential for more effective prevention and control. In this study, a species-specific recombinase polymerase amplification (RPA) primer was designed from a specific H. schachtii sequence-characterized amplified region (SCAR) marker. A band was obtained in reactions with DNA from H. schachtii, but absent from nontarget cyst nematodes. The RPA results could be observed by the naked eye, using a lateral flow dipstick (LFD). Moreover, we combined CRISPR technology with RPA to identify positive samples by fluorescence detection. Sensitivity analysis indicated that 10(-4) single cysts and single females, 4(-3) single second-stage juveniles, and a 0.001 ng genomic DNA template could be detected. The sensitivity of the RPA method for H. schachtii detection is not only higher than that of PCR and qPCR, but can also provide results in < 1 h. Consequently, the RPA assay is a practical and useful diagnostic tool for early diagnosis of plant tissues infested by H. schachtii. Sugar beet nematodes were successfully detected in seven of 15 field sugar beet root samples using the RPA assay. These results were consistent with those achieved by conventional PCR, indicating 100% accuracy of the RPA assay in field samples. The RPA assay developed in the present study has the potential for use in the direct detection of H. schachtii infestation in the field.

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