Misawa Hiroki, Tateishi Yu, Horimai Yuka, Mizuno Aira, Hida Fuuma, Furukawa Hitoshi, Kobayashi Hisayasu, Kawai Masataka, Yamanaka Takashi, Fukuda Masaki, Yamada Akiyoshi
Graduate School of Science and Technology, Shinshu University.
Faculty of Agriculture, Shinshu University.
Mycoscience. 2024 Jun 5;65(4):191-198. doi: 10.47371/mycosci.2024.05.001. eCollection 2024.
is an edible ectomycorrhizal mushroom that forms a symbiotic association with Pinaceae trees by constructing a large extraradical mycelial area (called a shiro) in the soil. The detection of this fungal mycelium in the soil is crucial for estimating the success of outplanted mycorrhizal seedlings inoculated with under experimental conditions. Although several -specific DNA markers have been reported for efficient detection in the field, no comparative study has been conducted to assess their effectiveness. In the present study, we targeted the nuclear ribosomal DNA intergenic spacer 2 (IGS2) region for the detection of . The newly designed TmSP-I-2F/TmSP-I-2R primer pair, which targets a partial IGS2 sequence (543 bp), effectively detected from pine root and soil samples via PCR assay, outperforming other -specific primers. In combination with a PCR system targeting LTR DNA markers that were previously developed, a PCR system with the TmSP-I-2F/TmSP-I-2R primer pair set can expedite investigations of the dynamics of genets in mycorrhizas and shiro.
是一种可食用的外生菌根真菌,通过在土壤中构建一个大型的根外菌丝区域(称为菌索)与松科树木形成共生关系。在实验条件下,检测土壤中的这种真菌菌丝体对于评估接种了该真菌的外植菌根幼苗的成功情况至关重要。尽管已经报道了几种用于田间高效检测的该真菌特异性DNA标记,但尚未进行比较研究来评估它们的有效性。在本研究中,我们针对核糖体DNA基因间隔区2(IGS2)区域进行该真菌的检测。新设计的TmSP-I-2F/TmSP-I-2R引物对靶向部分IGS2序列(543 bp),通过PCR检测有效地从松树根和土壤样本中检测到了该真菌,其性能优于其他该真菌特异性引物。与先前开发的靶向LTR DNA标记的PCR系统相结合,具有TmSP-I-2F/TmSP-I-2R引物对的PCR系统可以加快对菌根和菌索中该真菌基因动态的研究。