de la Bastide P Y, Kropp B R, Piché Y
Département des Sciences Forestières, Université Laval, Cité universitaire, Québec, Canada.
Appl Environ Microbiol. 1995 Oct;61(10):3609-16. doi: 10.1128/aem.61.10.3609-3616.1995.
An in vitro study investigated mechanisms for the development of genetically variable mycorrhizal mycelia for Laccaria bicolor. Seedlings of jack pine (Pinus banksiana) grown nonaseptically in an autoclaved soil substrate were given different L. bicolor inoculum treatments. These included (i) a dikaryotic mycelium genotype (D); (ii) D and basidiospores collected from one group of five sporophores (T1); (iii) D and basidiospores collected from 10 sporophores, two from each of five different groups (T5); (iv) T1 alone; (v) T5 alone; and (vi) a noninoculated control. Dikaryotic mycelial inoculum was provided at the time of sowing, while basidiospore inoculum was added at 10 weeks after seed germination. Sporophore formation was induced after 20 weeks of growth, and dikaryotic cultures were isolated from their tissue. Seedlings were harvested, and growth and mycorrhization were assessed. Levels of both were generally lower for T1-treated seedlings, compared with seedlings receiving D, while levels for T5-treated seedlings were intermediate. Sporophore genotype variability was assessed for inoculum treatments by using the isoenzymatic marker leucine aminopeptidase. The greatest genetic variability was seen with the basidiospore treatments T1 and T5, with up to four leucine aminopeptidase patterns per seedling. The mixed treatments D plus T1 and D plus T5 produced most frequently, but not exclusively, the inoculated dikaryon genotype. After isoenzyme results were assessed, variable sporophore isolates of mixed treatments were analyzed with randomly amplified polymorphic DNA and PCR mitochondrial DNA markers to determine if they were formed by dikaryon-monokaryon crosses between the inoculated dikaryon and monosporous mycelia.(ABSTRACT TRUNCATED AT 250 WORDS)
一项体外研究调查了双色蜡蘑遗传可变菌根菌丝体发育的机制。在经过高压灭菌的土壤基质中无菌培养的短叶松(Pinus banksiana)幼苗接受了不同的双色蜡蘑接种处理。这些处理包括:(i)双核菌丝体基因型(D);(ii)D以及从一组五个子实体收集的担孢子(T1);(iii)D以及从10个子实体收集的担孢子,这10个子实体来自五个不同组中的每组两个(T5);(iv)仅T1;(v)仅T5;以及(vi)未接种的对照。播种时提供双核菌丝体接种物,而担孢子接种物在种子萌发后10周添加。生长20周后诱导子实体形成,并从其组织中分离出双核培养物。收获幼苗并评估其生长和菌根形成情况。与接受D处理的幼苗相比,T1处理的幼苗的这两个指标水平通常较低,而T5处理的幼苗的水平处于中间。通过使用同工酶标记亮氨酸氨肽酶对接种处理的子实体基因型变异性进行评估。在担孢子处理T1和T5中观察到最大的遗传变异性,每个幼苗最多有四种亮氨酸氨肽酶模式。混合处理D加T1和D加T5最常产生,但并非仅产生接种的双核基因型。在评估同工酶结果后,使用随机扩增多态性DNA和PCR线粒体DNA标记对混合处理的可变子实体分离物进行分析,以确定它们是否由接种的双核体和单核菌丝体之间的双核体 - 单核体杂交形成。(摘要截短于250字)