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首页> 外文期刊>Nematology >Variability of the ITS rDNA and identification of Nacobbus aberrans (Thorne, 1935) Thorne & Allen, 1944 (Nematoda: Pratylenchidae) by rDNA amplification.
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Variability of the ITS rDNA and identification of Nacobbus aberrans (Thorne, 1935) Thorne & Allen, 1944 (Nematoda: Pratylenchidae) by rDNA amplification.

机译:ITS rDNA的变异性以及通过rDNA扩增鉴定Nacobbus aberrans(Thorne,1935)Thorne&Allen,1944(Nematoda:Pratylenchidae)。

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摘要

In order to identify the false root-knot nematode, Nacobbus aberrans, a nematode of quarantine importance, investigations were undertaken at the molecular level. Study of the ITS rDNA region among six South American populations showed an extremely high polymorphism. This polymorphism is due to point mutation insertions-deletions, the importance of which is increased by the presence of a degenerate microsatellite in this region. The usefulness of the ITS rDNA is therefore questionable when designing a species-specific identification tool. A study based on partial sequences of the 18S gene was carried out. A conserved part of the 18S gene, with a low level of variation when compared to Pratylenchus spp. and Meloidogyne spp., was found in all the N. aberrans populations tested. The primer set designed for this part of the 18S gene allows the amplification of a 295 bp fragment in all the N. aberrans populations tested. No amplification was obtained with other species belonging to Pratylenchidae, Heteroderidae or Hoplolaimidae. This PCR-based identification tool is effective on all N. aberrans migratory stages. From this study it is concluded that this N. aberrans specific primer set may provide a very useful tool for the identification of South American N. aberrans populations and thereby assist diagnosticians in implementing N. aberrans quarantine regulations..
机译:为了鉴定假的根结线虫,Nacobbus aberrans,一种具有重要检疫性的线虫,在分子水平上进行了研究。对六个南美人口中ITS rDNA区域的研究显示出极高的多态性。这种多态性是由于点突变插入-缺失引起的,该区域的简并微卫星的存在增加了其重要性。因此,在设计物种特异性识别工具时,ITS rDNA的有用性值得怀疑。基于18S基因的部分序列进行了研究。 18S基因的保守部分,与Pratylenchus spp相比,变异程度低。和Meloidogyne spp。,被发现在所有测试的北非猪笼草种群中。为18S基因这一部分设计的引物组可在所有测试的美国猪笼草种群中扩增295 bp片段。没有其他属于Pra科,杂种科或霍普莱德科的物种的扩增。这种基于PCR的鉴定工具在所有N. aberrans迁徙阶段均有效。从这项研究中得出的结论是,该N. aberrans特异性引物组可能为鉴定南美N. aberrans种群提供非常有用的工具,从而协助诊断人员实施N. aberrans检疫法规。

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