Department of Agriculture, Graduate School of Science and Technology, Shinshu University, Nagano, Minami-minowa, 8304399-4598, Japan.
Department of Bioscience and Biotechnology, Faculty of Agriculture, Shinshu University, Nagano, Minami-minowa, 8304399-4598, Japan.
Mycorrhiza. 2021 May;31(3):335-347. doi: 10.1007/s00572-021-01028-3. Epub 2021 Mar 24.
In vitro ectomycorrhizal synthesis of Tricholoma matsutake with host plants has been widely conducted to elucidate fungal symbiotic properties for future cultivation practices. Here, we report on the importance of basidiospore inocula for this fungus to provide ectomycorrhizal seedlings in vitro. Ectomycorrhizal pine seedlings synthesized in vitro with cultured mycelium of T. matsutake (isolate #45 or #84) in a 250-mL culture vessel (soil volume) were transplanted to a large 1-L culture vessel. Fresh basidiospores of this fungus were aseptically inoculated on the ectomycorrhizal root system. The ectomycorrhizal seedlings in the 1-L vessel were grown for 9 months, and some plants were further grown for 6 more months under non-aseptic conditions in 4.1-L jars. The ectomycorrhizal seedlings previously inoculated with isolate #84 in the 1-L vessel showed significant ectomycorrhizal biomass (mycorrhizal root length) after spore inoculation. The ectomycorrhizal seedlings in the 4.1-L vessel showed large shiro structures (> 10 cm in diameter). PCR amplification of intergenic spacer 1 of the rRNA gene and long terminal repeat retroelement of T. matsutake in ectomycorrhizal root tips in both the 1-L vessels and 4.1-L jars revealed the presence of amplicons of the previously inoculated culture isolate of T. matsutake and the new genet(s) that established via germination of the inoculated basidiospores. This is the first report that inoculated basidiospores of T. matsutake germinated and colonized the host root to generate ectomycorrhizae in vitro.
在体外进行香菇与宿主植物的外生菌根合成已广泛用于阐明真菌共生特性,以促进未来的栽培实践。在这里,我们报告了担子孢子接种物对该真菌的重要性,以提供体外外生菌根苗。用香菇(分离株 #45 或 #84)的培养菌丝在 250 毫升培养瓶(土壤体积)中体外合成的外生菌根松苗被移植到一个大的 1 升培养瓶中。该真菌的新鲜担子孢子在无菌条件下接种到外生菌根根系上。在 1 升瓶中生长 9 个月的外生菌根苗,在非无菌条件下进一步在 4.1 升罐中生长 6 个月。先前在 1 升瓶中用分离株 #84 接种的外生菌根苗在孢子接种后显示出显著的外生菌根生物量(菌根根长)。在 4.1 升罐中的外生菌根苗显示出较大的白色结构(直径大于 10 厘米)。聚合酶链反应扩增 rRNA 基因的基因间 spacer 1 和香菇的长末端重复反转元件在外生菌根根尖中,无论是在 1 升瓶还是 4.1 升罐中,都显示出先前接种的香菇培养分离株和通过接种的担子孢子萌发建立的新基因(s)的扩增子。这是第一个报道香菇接种的担子孢子萌发并定植宿主根,在体外生成外生菌根的报告。