首页> 外文期刊>Journal of Applied Entomology >A rapid detection of the pinewood nematode, Bursaphelenchus xylophilus in stored Monochamus alternatus by rDNA amplification.
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A rapid detection of the pinewood nematode, Bursaphelenchus xylophilus in stored Monochamus alternatus by rDNA amplification.

机译:通过rDNA扩增快速检测储存的 Monochamus alternatus 中的松木线虫 Bursaphelenchus xylophilus

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摘要

Pine wilt disease (PWD) caused by pinewood nematode (PWN) Bursaphelenchus xylophilus has originated serious loss to pine forestry around the world. Monochamus alternatus is the most important vector of B. xylophilus in Japan and China. It is necessary to develop an efficient method to store M. alternatus for subsequent PCR detection of B. xylophilus. In the present study, beetle samples carrying nematodes were stored in 75% alcohol. A simple procedure was firstly developed for isolating B. xylophilus DNA in 2 mg stored beetle tissue carrying nematodes for subsequent nematode detection by PCR amplification. The B. xylophilus - specific amplicon of 403 bp (DQ855275) was generated by PCR assay from the stored beetle tissue. To our knowledge, this is the first report of a rapid detection of the pine wood nematode - B. xylophilus in stored M. alternatus by rDNA amplification established without a separate nematode extraction. This result will provide a useful method to detect B. xylophilus in stored M. alternatus.
机译:由松材线虫(PWN)引起的松枯病(PWD) Bursaphelenchus xylophilus 已使全世界的松树林遭受了严重损失。 Monochamus alternatus 是 B最重要的媒介。日本和中国的xylophilus 。有必要开发一种有效的方法来存储M。 Alternatus 用于随后的 B PCR检测。木糖。在本研究中,携带线虫的甲虫样品存储在75%的酒精中。首先开发了一种简单的方法来分离B。 2 mg储存的带有线虫的甲虫组织中的木杆菌DNA,用于随后通过PCR扩增检测线虫。 B。通过PCR测定从储存的甲虫组织中产生了403bp的木糖杆菌特异性扩增子(DQ855275)。据我们所知,这是快速检测松木线虫-B的第一份报告。木糖储存在 M中。无需分离线虫提取物即可通过rDNA扩增建立交替链霉菌。该结果将提供检测B的有用方法。木糖储存在 M中。交替

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