Norway spruce (Picea abies (L.) Karst.) seedlings were inoculated with the ectomycorrhizal fungus Laccaria bicolor ((Marie) Orton), strain S238 N, in axenic conditions. The presence of the fungus slowed tap–root elongation by 26% during the first 15 d after inoculation and then stimulated it by 136%. In addition, it multiplied in vitro lateral root formation by 4.3, the epicotyl growth of the seedlings by 8.4 and the number of needles by 2. These effects were maintained when the fungus was separated from the roots by a cellophane membrane preventing symbiosis establishment, thus suggesting that the fungus acted by non-nutritional effects. We tested the hypothesis that IAA produced by L. bicolor S238 N would be responsible for the stimulation of fungal induced rhizogenesis. We showed in previous work that L. bicolor S238 N can synthesize IAA in pure culture. Exogenous IAA supplies (100 and 500 μm) reproduced the stimulating effect of the fungus on root branching but inhibited root elongation. The presence of 2,3,5-triiodobenzoic acid (TIBA) in the culture medium significantly depressed lateral root formation of inoculated seedlings. As TIBA had no significant effect on IAA released in the medium by L. bicolor S238 N, but counteracted the stimulation of lateral rhizogenesis induced by an exogenous supply of IAA, we suggest that TIBA inhibited the transport of fungal IAA in the root. Furthermore TIBA blocked the colonization of the main root cortex by L. bicolor S238 N and the formation of the Hartig net. These results specified the role of fungal IAA in the stimulation of lateral rhizogenesis and in ectomycorrhizal symbiosis establishment.

Basidiocarps of Pisolithus associated with indigenous (Afzelia quanzensis Welw.) and introduced (Pinus caribaea Mor. and Eucalyptus camaldulensis Dehnh.) hosts in the lowland forests of the Coast Province of Kenya are morphologically distinct. Genetic variability among 52 Pisolithus basidiocarps, collected beneath the various host plants, was examined based on sequence polymorphism within the internal transcribed spacer (ITS) and intergenic spacer (IGS1) of ribosomal DNA genes. Variability in ITS and IGS1 sequences indicated that the three host-associated morphotypes were genetically different. Consensus trees generated by bootstrap analysis of sequence data of Pisolithus isolates from Australia and Kenya are polyphyletic and strongly suggest that the three different morphotypes/genotypes present in Kenya represent separate biological species. In addition, our data indicate that little genetic exchange occurs in silva between these species.

IAA production by the ectomycorrhizal fungus Paxillus involutus grown in pure culture was investigated by testing IAA accumulation or IAA-synthesizing activity. All the Paxillus involutus strains studied released indole compounds either when incubated with 0·5 mm tryptophan or in its absence. HPLC analyses of indole compounds all yielded two main peaks identified by reference to controls as being IAA and indole-3-carboxylic acid and a small peak of indole-3-aldehyde. Mass spectrometry unequivocally confirmed IAA production in the culture filtrates and in the incubation solution used to study in vitro IAA-synthesizing activity. The IAA-synthesizing activity was found to vary widely, from 7·6 to 137·4 nmol IAA h−1 g−1 f. wt, between strains. The mycorrhizal activity of these strains with seedlings of Pinus sylvestris cultured under aseptic conditions was tested. Fungal strains that were characterized in pure culture conditions by high IAA-synthesizing activity induced more fine roots and significantly higher numbers of mycorrhizas than strains which showed a low activity of IAA synthesizing enzymes. The increased ectomycorrhiza formation was generally accompanied by an increased growth of seedlings.