• Fungal strains of the ‘Hymenoscyphus ericae aggregate’ (Helotiales, Ascomycota) were tested for their ability to form ecto-(ECM) and ericoid (ERM) mycorrhizas.
• Twelve fungal test isolates were inoculated in vitro onto sterile ectomycorrhizal and ericoid host plants.
• Five isolates of ectomycorrhizal origin formed ECM, three isolates of ericoid origin formed ERM, but none of the tested isolates was able to form both ECM and ERM. Confirmed ectomycorrhizal strains formed the characteristic black-and-hyaline mantles of the Piceirhiza bicolorata morphotype. This morphology represented an intermediate stage, where mantle-colour changed from light brown to black. The progressive darkening appeared to result from a gradual acropetal melanization of the outer mantle layer.
• The synthesis results confirm that the ability to form both ecto- and ericoid mycorrhizal symbioses has evolved within the H. ericae aggregate. In addition, a phylogeny based on ITS1–5.8S–ITS2 rDNA sequences showed that the aggregate includes the ect(endo)mycorrhizal dark septate fungus Phialophora finlandia, grouping with four of the ECM-forming strains. The H. ericae aggregate therefore contains a number of closely related taxa with wide ecological attributes.
More than 95% of fine roots of boreal forest trees are ectomycorrhizal (Taylor et al., 2000). The fungal species that form ectomycorrhizas have traditionally been associated with a number of basidiomycetes forming conspicuous epigeic or hypogeic sporocarps (Molina et al., 1992; Smith & Read, 1997). However, several corticoid basidiomycetes and teleomorphic, anamorphic and sterile ascomycetes have been shown to form ectomycorrhizal relationships (Mikola, 1965; Danielson, 1984; Yang & Wilcox, 1984; Wilcox & Wang, 1987a,b; Ursic & Peterson, 1997; Vrålstad et al., 1998, 2000; Bergero et al., 2000; Grogan et al., 2000; Kõljalg et al., 2000). In a recent study, Vrålstad et al. (2000) demonstrated that fungal strains derived from the ectomycorrhizal morphotype Piceirhiza bicolorata (Brand et al., 1992) constituted an assemblage of very close relatives of the ericoid mycorrhizal fungus H. ericae. An inferred ITS1-phylogeny gave a 100% supported evolutionary clade of 15 closely related P. bicolorata ITS1-genotypes that embraced the ITS-genotypes of the H. ericae and S. vaccinii ex-types. This clade, consisting of five subclades, was collectively referred to as the H. ericae aggregate. The hypothesis was put forward that ericoid and ectomycorrhizal plants might share mycobionts of this species complex. However, the lack of resynthesis studies, using both ericoid and ectomycorrhizal hosts, prevented a test of this hypothesis.
Support for this hypothesis was presented by Bergero et al. (2000), who collected ecto- and ericoid mycorrhizal samples from neighbouring plants of Quercus ilex and Erica arborea in a Mediterranean forest habitat. They demonstrated that ectomycorrhizal root tips of Q. ilex harboured fungi (Oidiodendron spp. and unidentified sterile mycelia) that, in vitro, formed ericoid mycorrhizas with E. arborea. No fully developed ectomycorrhizas were observed when Q. ilex seedlings were re-inoculated with these fungal isolates, but sections of swollen root tips revealed a poorly developed mantle and/or coils inside the epidermal cells. A rudimentary Hartig net was also observed. Their results indicate that ericoid mycorrhizal fungi may coexist in ericaceous and ectomycorrhizal plants. Further support comes from the study of the mitotic fungus Phialophora finlandia, commonly referred to as Mycelium radicis atrovirens (MRA) or dark septate endophytes (DSE) (Jumpponen & Trappe, 1998), that forms ectomycorrhizas and/or ectendomycorrhizas with hardwoods and conifers, respectively (Wilcox & Wang, 1987a,b). Monreal et al. (1999) found that the ectomycorrhizal strain of P. finlandia (FAG15 = UAMH7454) formed typical ericoid mycorrhizas with the shrub Gaultheria shallon (Ericales). Thus, reports of ectomycorrhizal, ectendomycorrhizal and ericoid mycorrhizal behaviour for this particular strain of P. finlandia are available (Wilcox & Wang, 1987a,b; Monreal et al., 1999). Monreal et al. (1999) also showed that P. finlandia clustered in the H. ericae group based on sequence similarity analysis of the internal transcribed spacer 2 (ITS2).
In the present study, 12 fungal strains (12 ITS1-genotypes) of the H. ericae aggregate were inoculated in vitro onto sterile ectomycorrhizal and ericoid mycorrhizal hosts. The syntheses were conducted in order to determine: if putative ectomycorrhizal strains of the H. ericae aggregate were capable of reforming the black-and-hyaline mantles characteristic of the Piceirhiza bicolorata morphotype, from which they were originally isolated; and if single strains could form a mycorrhizal association with both ericoid and ectomycorrhizal hosts. We also provide complete ITS1-5.8S-ITS2 rDNA sequences of the 12 test isolates, and report on their phylogenetic relatedness to Phialophora finlandia.
Materials and Methods
Table 1 lists the source and origin of the fungal test isolates along with their reported ITS1-genotypes (cf. Vrålstad et al., 2000) and EMBL/GenBank/DDBJ accession numbers of the ITS1-5.8S-ITS2 sequences used in the present study. Seeds of Norway spruce (Picea abies[L.] Karst.), Scots pine (Pinus sylvestris L.) and birch (Betula pubescens Ehrh.) were soaked overnight in sterile de-ionized H2O, then surface sterilized in 30% (100 volumes) hydrogen peroxide for 20 min, rinsed in sterile de-ionized water and germinated on water agar. After 4 wk, sterile seedlings were transferred to 300 ml conical flasks containing 150 ml of sterile peat/vermiculite (1 : 7 by volume) moistened with 110 ml of modified Melin–Norkrans (MMN) medium (Marx, 1969). The medium contained only 1 g l−1 glucose in order to reduce possible adverse effects on mycorrhizal formation caused by high levels of exogenous carbon. Agar plugs with mycelia from 4-wk-old-colonies of each test isolate were used to inoculate the flasks. Two replicate flasks for each isolate-host combination and two replicate flasks of noninoculated control plants were maintained in a greenhouse under natural light conditions. The maximum temperature was set to 18°C. Flasks were harvested after 3 months and the root systems examined for mycorrhizal formation under a dissection microscope. Pine seedlings were also harvested after 7 months, as no mycorrhizal root tips were found after 3 months on any of the isolate/host combinations.
Table 1. Fungal test isolates of the Hymenoscyphus ericae aggregate
Source: ARON, Ascomycete research group of Oslo, Norway (University of Oslo, Department of Biology, Division of Botany and Plant Physiology); UAMH, University of Alberta Mold Herbarium and Culture Collection, Edmonton, Atlanta, Canada.
*Culture derived from type specimen. **Shares 99% ITS-sequence identity with UAMH6735.
Synthesis plates (9 cm Petri dishes) for ericoid mycorrhizal synthesis experiments were prepared using sterile MMN medium with N and P concentrations reduced to 1/10 of the standard concentration. Sterile carbon filter papers (Macherey & Nagel Co., Düren, Germany) were placed over the medium, and agar plugs from actively growing colonies of the test isolates (Table 1) were transferred directly onto the carbon papers at the centre of the Petri dishes. Three replicate Petri dishes per isolate were allowed to grow for 1 month at 25°C. Seeds from fresh fruits of Vaccinium vitis-idaea were removed from the fruit, rinsed in sterile de-ionized water, surface sterilized in 30% hydrogen peroxide for 20 min, rinsed in sterile de-ionized water, and plated onto sterile 1/10 MMN agar plates. The seeds were allowed to germinate and grow for 2–3 wk in the glasshouse under conditions as described above. Two or three sterile V. vitis-idaea seedlings were transferred to each synthesis Petri dish containing the test fungi growing on the carbon filters, with seedling radicles placed near the growing mycelium. Three seedlings were kept as noninoculated controls. The dishes, including the control seedlings, were placed in the glasshouse with small disks (2 cm diameter) of black paper placed on the lids in order to shade the mycelium and roots from direct sunlight. The plates were harvested after 4 wk, during which time most of the seedlings showed considerable growth.
Synthesized ectomycorrhizal (ECM) roots were excised and fixed in 3% glutaraldehyde in phosphate buffer (pH 6.8) and stored at 4°C. The ECM roots were rinsed three times in the phosphate buffer, and dehydrated in an increasing ethanol series culminating with two changes (3 h each) of 100% ethanol. The ECM roots were then embedded in LR-White Resin (London Resin Company Ltd, London, UK) containing UV-accelerator using an increasing series of ethanol: LR-White (3 : 1, 12 h; 1 : 1, 12 h and 1 : 3, 12 h), and finally two changes (12 h each) of pure LR-White. Individual ECM roots were embedded in fluid LR-White in gelatine capsules by polymerization under UV-illumination for 18–24 h. Longitudinal sections (3–7 µm) of LR-White embedded ECM roots (2–4 of each isolate-host combination) were cut with glass knives on a MT5000 Sorvall® ultratome (Du Pont Company, Biomedical Products Division, Wilmington, DE, USA). Sections were transferred to glass microscope slides onto a drop of 10% acetone solution, and gently heat fixed (3 min on a 80°C heat block). Sections were stained with Fast Green F.C.F. (1% in gdH20; Johansen, 1940) for 1 min at 80°C, and rinsed in a 10% acetone solution. Sections were then counter-stained in a weak dilution (1/1000 of the standard concentration) of Alsop staining solution (basic fuchsin and toluidine blue in PEG 200; Alsop, 1971) for 15–30 s at room temperature, and finally rinsed in 10% acetone. This procedure stained hyaline fungal and plant cell walls purple to blue (Alsop) while the fungal cytoplasm was coloured bright turquoise by the Fast-Green F. C. F. solution. The sections were heat dried, mounted in Eukitt (Kebo lab, Oslo, Norway; O. Kindler GmbH & Co., Frieburg, Germany), examined for the presence of mantle and Hartig net using a Zeiss compound microscope, and finally, photographed using a Zeiss MC80 microscope camera (Carl Zeiss Jena GmbH, Jena, Germany).
The entire seedling root systems of the inoculated V. vitis-idaea were gently removed from the carbon filter and stained in 1% safranin (Johansen, 1940) for 20 min and rinsed in distilled H2O. Portions of the root systems were then mounted in water and examined at 400× for the presence of root-associated hyphae and intracellular infection using a Zeiss Axioplan compound microscope fitted with a MC100 camera.
The complete ITS1-5.8S-ITS2 rDNA was sequenced from the 12 test isolates (Table 1) as described by Vrålstad (2001), and sequences of P. finlandia (AF011327), Hyaloscypha aureliella (Nyl.) Huhtinen (U57495) and Botrytis cinerea (Z99664) were retrieved from the EMBL/GenBank/DDBJ sequence databases. The sequences were manually aligned in BioEdit (version 220.127.116.11; Hall, 1999). Maximum parsimony analyses were conducted in a beta version of PAUP* (version 4.04; Swofford, 1999) with the branch and bound search algorithm and legal character states being A, C, G, T and – (gap). Hyaloscypha aureliella and B. cinerea were used as outgroups. To assess the support for individual clades, a bootstrap analysis using the branch and bound option was performed with 2000 replicates where only clades with bootstrap support > 70% were retained in the bootstrap consensus tree.
The outcome of the inoculation trials is shown in Table 2. The H. ericae isolates of ericoid origin (UAMH5828, UAMH6735, ARON2888.S) all formed numerous intracellular infections within the cortical cells of the hair roots of V. vitis-idaea (Fig. 1a). None of these three isolates formed any ecto- or endomycorrhizal associations with the ectomycorrhizal hosts. However, in some instances, superficial hyphal associations with the roots were observed (Table 2). Three out of nine H. ericae-like isolates of ectomycorrhizal origin (ARON2810.S, ARON2893.S, ARON2917.S) formed ectomycorrhizas with all three ectomycorrhizal host plant species (Table 2). In the P. sylvestris inoculations, none of the isolate-host combinations developed visible ectomycorrhizal tips after three months, but after an additional 4 months, brown to black ectomycorrhizal morphotypes were observed. Another isolate of ectomycorrhizal origin, ARON2906.S, formed typical P. bicolorata mycorrhizas with spruce and birch, but failed to produce any mycorrhizas with pine. The ARON2948.S isolate of ectomycorrhizal origin failed to produce ECM with spruce and pine, but two mycorrhizal tips were found on one birch plant. This isolate also formed a superficial hyphal association with roots of V. vitis-idaea. None of the ECM-forming isolates produced any structures that resembled ericoid mycorrhizal infections when inoculated onto V. vitis-idaea. However, three of the isolates (ARON2810.S, ARON2906.S, ARON2917.S) penetrated the cortical cells of the older parts of the root systems, with no obvious reaction by the root cells to the hyphal penetration. In addition, the hyphae of these isolates that were associated with the root surface changed from a purely linear growth form to a more cellular, monilioid growth pattern. Three isolates of ectomycorrhizal origin (ARON2879.S, ARON2894.S, ARON2903.S) did not associate with the roots of any of the four host plant species, while another isolate of ectomycorrhizal origin (ARON2916.S) formed a superficial hyphal association with roots of B. pubescens and V. vitis-idaea. All control plants remained non-mycorrhizal.
Table 2. Results of inoculation trials between isolates of the Hymenoscyphus ericae aggregate and potential ectomycorrhizal and ericoid hosts
Number of replicates, 2 for ectomycorrhizal host plants and 3 for the ericoid mycorrhizal host plant. +, confirmed ectomycorrhizal (P. abies, P. sylvestris, B. pubescens) or ericoid mycorrhizal (V. vitis-idaea) formation. −, lacking mycorrhizal formation.
i Intracellular hyphal penetrations in older roots.
s Hyphae found in association with the root surface, but with no obvious interaction between the potential symbionts.
While the five ECM-forming isolates of this study (ARON2810.S, ARON2893.S, ARON2906.S, ARON2917.S, ARON2948.S) had been isolated from field collected ectomycorrhizas of the distinctive black-and-hyaline Piceirhiza bicolorata morphotype (Fig. 1b), the isolates formed in vitro a series of morphotypes ranging in colour from light brown to charcoal black. For presentation purposes, this series has been divided roughly into three major groups: (I) light brown to brown morphotypes (outer mantle hyphae hyaline, subhyaline to brown; Fig. 1c–e); (II) dark brown to black morphotypes with hyaline tips =P. bicolorata (outer mantle hyphae melanized except where enclosing the root apex; Fig. 1f); and (III) charcoal black, Cenococcum-like morphotypes (outer mantle hyphae melanized continuously around the root apex; Fig. 1g,h). In the ARON2948.S-birch combination, only two brown ectomycorrhizal roots were observed. After 3 months, the isolates ARON2810.S, ARON2893.S and ARON2906.S had formed ECM that fit into all morphotype categories (Fig. 1c–h and 2a,b,h), while at this stage, isolate ARON2917.S had only formed morphotypes of group I (Fig. 2c). After 7 months, the latter isolate had developed fully melanized mycorrhizal tips with pine. In general, ectomycorrhizal tips were 1–3 mm in length (cf. Fig. 1h), and possessed sparse to extensive amounts of narrow (1.8–2.4 µm) and regularly septate extramatrical hyphae (Fig. 1c–g). Extramatrical hyphae were initially hyaline and smooth, later darkly pigmented, smooth to finely verrucose. Fig. 2 details a number of longitudinal sections of LR-white resin embedded ECM roots of isolate-host combinations representing the three morphotype groups. In all cases, the sections showed dense, continuous mantles (5–70 µm in thickness) and narrow, well developed uniseriate Hartig nets (Fig. 2). No intracellular penetrations were observed in the ECM roots in any of the isolate-host combinations. Fungal cytoplasm within active hyphae of mantles and Hartig nets was coloured bright turquoise by the Fast-Green F.C.F.-solution, and appeared as bright turquoise ‘granulae’ within hyphal cross sections (Fig. 2d–g,i). In the partial and completely melanized morphotypes, the mantles were consistently two-layered, with an outer melanized mantle layer (D1) and an inner hyaline layer (D2) from where the hyaline Hartig net extended between the root cells (Fig. 2a,d,i). In ECM roots of birch, the Hartig net was restricted to the epidermis, which consisted of a single layer of radially elongated cells (cf. Fig. 2a,c,d,f). In ECM roots of spruce and pine, the Hartig net always extended to the first layer of epidermal cells, and one to three cell layers further into the cortex (cf. Fig. 2b,e,h–i). Hyphae were never observed in the endodermis. The epidermal cells were often filled with tannins (Fig. 2e,i), and cortical cells were sometimes internally delineated with discrete, brown droplets (Fig. 2e) previously ascribed to polyphenolic deposits (Pichéet al., 1983). In all sections of apparently vital, intact ECM roots, the hyphae of the D2 mantle layer and Hartig net were consistently hyaline. In some sections of moribund ECM roots of pine, the plant cells had started to disintegrate while the still intact Hartig net was darkly pigmented. A darkly pigmented Hartig net was occasionally observed in the cortex of some long roots.
ITS-phylogeny of ericoid, ecto- and nonmycorrhizal strains of the H. ericae aggregate
Parsimony analyses of the included ITS1-5.8S-ITS2 rDNA sequences yielded 16 most parsimonious trees (MPTs). Fig. 3 shows the bootstrap consensus tree with clades that yielded > 70% bootstrap support. The bootstrap consensus tree retained one 100% supported main clade of the ingroup (the H. ericae aggregate), which was subdivided into five major subclades. Subclade 1 (100% supported) includes strictly ericoid mycorrhizal isolates of ‘true’H. ericae. Subclade 2 (99% supported) includes P. finlandia and four of the confirmed ectomycorrhizal test isolates. Subclade 3 (100% supported) includes the three isolates that did not associate with roots of any of the host plant species. Subclade 4 includes one single ectomycorrhizal isolate, and subclade 5 includes the isolate that only formed a superficial hyphal association with some of the host roots (Fig. 3, Table 2).
Sequence similarity analysis of the internal transcribed spacer 2 (ITS2) has previously shown a link between the ectomycorrhizal fungus P. finlandia and H. ericae (Monreal et al., 1999), and the parsimony analysis of the complete ITS-region in the present study showed that P. finlandia grouped within subclade 2 of the H. ericae aggregate (Fig. 3). Hence, the isolates of subclade 2 are closer related to P. finlandia than to H. ericae. In the present study, only ‘true’H. ericae isolates of ericoid mycorrhizal origin (i.e. subclade 1, Fig. 3) formed classic ericoid mycorrhizal associations, while ectomycorrhizal formation was restricted to P. finlandia-like strains of ectomycorrhizal origin (subclade 2) as well as the single isolate of subclade 4. These results suggest that both ericoid and ectomycorrhizal symbioses have evolved within the H. ericae aggregate (Fig. 3), but do not support the hypothesis that single isolates have the ability to form both kinds of mycorrhizal symbioses. Hence, the H. ericae aggregate seems to contain a number of closely related taxa with wide ecological attributes.
We found that four of the five confirmed ectomycorrhizal strains of the H. ericae aggregate formed black-and-hyaline morphotypes that shared anatomical features with the original description of P. bicolorata (Brand et al., 1992) from which they originated. This morphotype appeared to represent an intermediate developmental stage in a sequence from light brown, dark brown, black-and-hyaline to completely black morphotypes, caused by a gradual acropetal melanization of the outer (D1) mantle layer. P. finlandia has been reported to produce ectomycorrhizal morphotypes ranging from light amber, brown, bicoloured to black (Wilcox & Wang, 1987a; Ursic & Peterson, 1997), which correspond to the observed morphotypes of our study. A progressive blackening of mycorrhizas formed by the ectomycorrhizal basidiomycete Tricholoma matsutake, from light brown, bicoloured to black morphotypes, was recently reported (Gill et al., 2000). The blackening was due to increased deposition of plant polyphenols and subsequent necrosis, with the totally black morphotypes being devoid of an intact mantle (Gill et al., 2000). By contrast, the darkening of the morphotypes in the present study did not appear to affect ectomycorrhizal structures of the ECM roots.
The anamorph genus Phialophora Medlar represents a poorly defined assemblage of darkly pigmented and little differentiated hyphomycetes, which have their teleomorphs in a broad range of ascomycete orders (e.g. Helotiales, Caliciales, Sordariales and Diaporthales), and represent soil, wood and plant saprobes, specialized plant and human pathogens as well as mutualists (Gams, 2000). P. finlandia has been reported to be beneficial, promoting the growth and survival of their ectomycorrhizal hosts both in highly acidic environments (Wilcox & Wang, 1987b) and iron contaminated soils (Lobuglio & Wilcox, 1988). Wilcox & Wang (1987a) conducted a long-term study on the ectomycorrhizal development of P. finlandia on red pine (Pinus resinosa), red spruce (Picea rubens) and yellow birch (Betula alleghaiensis) and found that the mantle developed before and after the Hartig net in ECM roots of birch and conifers, respectively. P. finlandia occupied long roots through a continuum of root sizes forming a Hartig net in virtually all roots (Wilcox & Wang, 1987a), as was occasionally observed in our study. Such a Hartig net, running through cortex of the long roots, may serve as an internal source of inoculum for ectomycorrhizal infection of emerging short roots.
The isolates of subclade 2 melanized more quickly than the single isolate of subclade 4, corroborating observed axenic culture features (cf. Vrålstad et al., 2000). Axenic culture isolates from subclade 2 regularly turned charcoal black within a week of subculturing, while the isolate from subclade 4 remained hyaline up to 4 wk before melanization occurred (Vrålstad et al., 2000). The black colonies possessed whitish margins of hyaline, actively growing hyphae (Vrålstad et al., 2000), a ‘bicoloured’ morphological feature also expressed in the ectomycorrhizal structures.
The ecto- and ericoid mycorrhizal potentials of the isolates of subclade 3 and subclade 5 (Fig. 3) remain uncertain. These isolates were originally derived from P. bicolorata ectomycorrhizas, but it is possible that they represented nonmycorrhizal mantle-associated or root-endophytic fungi. The isolates of subclade 3 remained hyaline in axenic culture (Vrålstad et al., 2000), suggesting that these isolates were unlikely to be responsible for the black-and-hyaline ECM morphotype from which they originated. Sequences of the complete ITS-region show that these isolates are more divergent from H. ericae (Fig. 3) than previously suggested based on partial ITS1-data (cf. Figure 2 in Vrålstad et al., 2000).
The black morphotypes produced by ectomycorrhizal members of the H. ericae aggregate (group III, cf. Fig. 1g–h and 2h) resemble the ECM morphotype produced by Cenococcum geophilum (Agerer & Gronbach, 1988). Wilcox & Wang (1987a,b) concluded that microscopic examination was required in order to distinguish between C. geophilum, P. finlandia and Chloridium paucisporum ectomycorrhizas. It is highly probable that the prevalence of C. geophilum has been largely overestimated in ectomycorrhizal studies at the expense of H. ericae- and P. finlandia-like representatives.
Melanized cell walls are not common among ectomycorrhizal fungi, except in tomentelloid basidiomycetes (Kõljalg et al., 2000) and the ascomycetes C. geophilum, Chloridium paucisporum, P. finlandia (Wilcox & Wang, 1987a,b) as well as the ectomycorrhizal strains of the H. ericae aggregate. Fungal melanins may act as a boundary between fungal cells and their environments, and protect against physical, chemical and biological stresses (Pigott, 1982; Wheeler & Bell, 1988; Gadd, 1993; Butler et al., 2001). The P. bicolorata morphotype has been observed to dominate root systems of hardwood and conifer seedlings colonizing heavy metal contaminated Cu-mine spoils in central Norway (Vrålstad et al., 2000; Vrålstad, 2001). It was suggested that a high tolerance to certain heavy metals by the fungi of the H. ericae aggregate forming the P. bicolorata morphotype, was responsible for the high prevalence of these fungi. Furthermore, it was observed that the P. bicolorata morphotype was much more abundant in postfire habitats than in undisturbed forest habitats (Vrålstad et al., 2000; Vrålstad, 2001). Microscopic examinations of the partially and fully melanized morphotypes formed by the H. ericae-like relatives revealed an inner mantle layer and Hartig net that remained hyaline. The melanized hyphae of the outer mantle layer and extramatrical mycelium may function as protective barriers between the external environment and the active fungus-plant symbiosis inside the root. This could be a key-factor to their apparent successful colonization of burnt and metal polluted habitats.
This work was financially supported by the University of Oslo (UiO), Norway, the Swedish University of Agricultural Sciences, Uppsala (SLU) Sweden, a scholarship from the Research Council of Norway (NFR) and grants from the Nansen foundation and the Sønnerland foundation to T. Vrålstad. Resynthesis experiments were conducted at the Swedish Agricultural University at the department of Forest Mycology and Pathology, and the anatomical studies were prepared at the Electron Microscopy Laboratory, UiO. We are most grateful to Torill Rolfsen, Tove Bakar, Anne Vegusdal Synnstad and Trygve Krekling for technical advise and support, and to Arne Holst-Jensen for critical reading and comments on the manuscript. This study partially fulfils the requirements for T. Vrålstad’s Ph.D. degree on ‘Molecular ecology of root-associated mycorrhizal and non-mycorrhizal ascomycetes’, and is part of T. Schumacher’s project on ‘molecular ecology of mycorrhizal and non-mycorrhizal ascomycetes’ supported by the NFR (Grant 115538/410).