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首页> 外文期刊>Journal of applied microbiology >Detection of Clavibacter michiganensis subsp. sepedonicus by AmpliDet RNA, a new technology based on real time monitoring of NASBA amplicons with a molecular beacon
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Detection of Clavibacter michiganensis subsp. sepedonicus by AmpliDet RNA, a new technology based on real time monitoring of NASBA amplicons with a molecular beacon

机译:密歇根州细枝杆菌亚种的检测由AmpliDet RNA分离的败血症,这是一种基于分子信标实时监控NASBA扩增子的新技术

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Aims: To develop a procedure for direct detection of viable cells of Clavibacter michiganensis subsp. sepedonicus (Cms), the causal organism of bacterial ring rot in potato, based on AmpliDet RNA~TM, in which amplicons generated by nucleic acid sequence based amplification (NASBA) are monitored in real time with a molecular beacon. Methods and Results: Five methods were evaluated and fine-tuned for extraction of RNA from Cms. The most efficient non-commercial RNA extraction method included an enzymatic breakdown of the cell wall followed by a phenol extraction. AmpliDet RNA enabled detection of 10 000 molecules of purified rRNA per reaction and 100 cfu of Cms per reaction in more complex samples. Two primer pairs were tested with DNA and RNA purified from Cms. One primer pair was able to distinguish live from dead cells. Conclusions: An AmpliDet RNA was developed which enabled fast and specific detection of viable cells of Cms in complex substrates at a detection limit of 100 cfu per reaction. Significance and Impact of the Study: This novel AmpliDet RNA is carried out in sealed tubes, thus reducing the risk of carry-over contamination. The method will be particularly suitable for studies on the epidemiology of Cms in which viable cells should be exclusively detected.
机译:目的:建立一种直接检测密歇根氏杆菌亚种活细胞的程序。以AmpliDet RNATM为基础的马铃薯细菌性环腐病的病原体sepedonicus(Cms),其中通过分子信标实时监测基于核酸序列的扩增(NASBA)产生的扩增子。方法和结果:评估并微调了5种方法从Cms中提取RNA。最有效的非商业性RNA提取方法包括酶解细胞壁,然后进行苯酚提取。 AmpliDet RNA能够在更复杂的样品中检测每个反应1万个分子的纯化rRNA和每个反应100 cfu Cms。用从Cms纯化的DNA和RNA测试了两个引物对。一对引物能够区分活细胞和死细胞。结论:开发了一种AmpliDet RNA,能够快速,特异性地检测复杂底物中Cms的活细胞,每个反应的检测限为100 cfu。研究的意义和影响:这种新型AmpliDet RNA在密封管中进行,从而降低了残留污染的风险。该方法将特别适合于Cms的流行病学研究,在这些研究中应专门检测活细胞。

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