单长林,周 圆,李孝军.玉米细菌性枯萎病菌荧光重组酶介导
等温扩增检测方法的建立与应用[J].广东农业科学,2021,48(1):111-118 |
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玉米细菌性枯萎病菌荧光重组酶介导
等温扩增检测方法的建立与应用 |
Establishment and Application of Fluorescent Recombinase-aided Amplification Method for Pantoea stewartii subsp. stewarii Detection |
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DOI:10.16768/j.issn.1004-874X.2020.07.014 |
中文关键词: 玉米细菌性枯萎病菌 pstS-glmS 序列 重组酶介导等温扩增 荧光探针 快速检测 |
英文关键词: Pantoea stewartii subsp. stewarii pstS-glmS sequence recombinase-aided amplification fluorescent
probe rapid detection |
基金项目:浙江省基础公益研究项目(GN18C140001) |
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中文摘要: |
【目的】建立一种快速、灵敏、特异的玉米细菌性枯萎病菌(Pantoea stewartii subsp. stewarii)
重组酶介导等温扩增(recombinase-aided amplification,RAA)检测方法。【方法】以玉米细菌性枯萎病菌
pstS-glmS 基因序列作为靶标序列,设计、合成荧光 RAA 检测引物和探针,并进行灵敏性测定、特异性验证;使
用建立的荧光 RAA 检测方法检测玉米模拟样本和玉米真实样本,参照标准 SN/T 1375-2004 方法同步复核,评估
荧光 RAA 检测方法的可靠性。【结果】成功建立了玉米细菌性枯萎病菌荧光 RAA 检测方法。该方法反应快速,
在 39℃条件下 20 min 内即可完成检测反应,特异性好,且灵敏度为 280 fg/μL;利用该方法检测 6 份模拟样本
结果阳性,24 份真实样本结果呈阴性,与参照标准 SN/T 1375-2004 检测结果一致。【结论】成功建立了玉米细
菌性枯萎病菌快速、灵敏和特异的荧光 RAA 检测方法,可用于玉米细菌性枯萎病菌的现场检测。 |
英文摘要: |
【Objective】The study was conducted to develop a rapid, sensitive and specific assay for detection of
Pantoea stewartii subsp. stewarii based on fluorescent recombinase-aided amplification(RAA).【Method】The pstSglmS sequence of P. stewartii subsp. stewarii was used as target sequence, and the specific primers and probes were designed
and synthesized to establish a fluorescent RAA assay for rapid detection of P. stewartii subsp. stewarii. The sensitivity and
specificity of the fluorescent method was detected. Simulated samples and actual samples were used to evaluate the reliability
of fluorescent RAA, with the SN/T 1375-2004 as standard for verification.【Result】A fluorescent RAA for detection of P.
stewartii subsp. stewarii was established, which could detect P. stewartii subsp. stewarii specifically at 39℃ within 20 min.
The sensitivity of the fluorescent RAA was 280 fg/μL. With the established method, 6 simulated samples were positive and
24 real samples were negative with the same results as SN/T 1375-2004.【Conclusion】The fluorescent RAA method for
detection of P. stewartii subsp. stewarii is rapid, sensitive and specific, which is proved to be a great choice for site monitoring
of P. stewartii subsp. stewarii. |
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