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利用特异性引物检测外生菌根中的夏季块菌(Tuber aestivum Vittad.)及其土壤中的分布。

Detection of summer truffle (Tuber aestivum Vittad.) in ectomycorrhizae and in soil using specific primers.

机构信息

Institute of Microbiology, ASCR, Prague, Czech Republic.

出版信息

FEMS Microbiol Lett. 2011 May;318(1):84-91. doi: 10.1111/j.1574-6968.2011.02243.x. Epub 2011 Mar 8.

DOI:10.1111/j.1574-6968.2011.02243.x
PMID:21385201
Abstract

Tuber aestivum is becoming an important commodity of great economical value in some European countries. At the same time, it is a highly protected organism in other countries, where it needs careful treatment. A reliable method of detection in roots and soil is thus needed for assessment of geographic distribution, ecological studies and inoculation efficiency testing in man-made experiments. A PCR-based method of detection of T. aestivum using specific primers was therefore developed. A pair of PCR primers Tu1sekvF/Tu2sekvR selective for T. aestivum and some genotypes of Tuber mesentericum was designed on the basis of the known internal transcribed spacer T. aestivum sequences. TaiI restriction cleavage was then used to distinguish the two species. The selectivity of the designed primer pair was evaluated using DNA extracted from specimens of a further 13 Tuber spp. Subsequently, the selectivity and robustness to false-positive results with nontarget DNA of the designed primers was compared with two other primer pairs (UncI/UncII and BTAE-F/BTAEMB-R). The occurrence of T. aestivum in soil and ectomycorrhizae collected in its native habitat has been successfully detected using the designed primers and nested PCR. The method is reliable and thus suitable for detection of T. aestivum in the field.

摘要

块菌在一些欧洲国家已成为具有重要经济价值的重要商品。与此同时,在其他国家,块菌是一种受到高度保护的生物,需要谨慎处理。因此,需要一种可靠的方法来检测根和土壤中的块菌,以便评估其地理分布、生态研究和人为实验中的接种效率测试。因此,开发了一种基于 PCR 的检测 T. aestivum 的方法,使用特定的引物。基于已知的 T. aestivum 内部转录间隔区序列,设计了一对针对 T. aestivum 和一些 Tuber mesentericum 基因型的 PCR 引物 Tu1sekvF/Tu2sekvR。然后使用 TaiI 限制性内切酶切割来区分这两个物种。使用从另外 13 种 Tuber spp. 提取的 DNA 评估了设计引物的选择性。随后,将设计引物的选择性和对非目标 DNA 的假阳性结果的稳健性与另外两对引物(UncI/UncII 和 BTAE-F/BTAEMB-R)进行了比较。使用设计的引物和嵌套 PCR 成功检测到了在其原生栖息地采集的土壤和外生菌根中的 T. aestivum。该方法可靠,因此适合在野外检测 T. aestivum。

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