Impact Factor 4.259 | CiteScore 4.30
More on impact ›

Original Research ARTICLE

Front. Microbiol., 20 February 2019 | https://doi.org/10.3389/fmicb.2019.00307

The Ectomycorrhizospheric Habitat of Norway Spruce and Tricholoma vaccinum: Promotion of Plant Growth and Fitness by a Rich Microorganismic Community

Katharina Wagner1†‡, Katrin Krause1*‡, Ramses Gallegos-Monterrosa2, Dominik Sammer1†, Ákos T. Kovács2† and Erika Kothe1
  • 1Microbial Communication, Institute of Microbiology, Friedrich Schiller University Jena, Jena, Germany
  • 2Terrestrial Biofilms Group, Institute of Microbiology, Friedrich Schiller University Jena, Jena, Germany

The contribution of the mycorrhizospheric microbes in a stand of ectomycorrhizal Norway spruce (Picea abies) featuring mycorrhiza with the basidiomycete Tricholoma vaccinum was addressed by microbiome analysis and in vitro reconstruction of microbial as well as plant-microbe interactions. The protective role of the mycorrhizal fungus with respect to pathogen attack could be validated against Botrytis cinerea and Heterobasidion annosum in co-cultures revealing reduced pathogen growth, higher survival rate of the spruce trees and reduced symptoms on needles upon symbiosis with T. vaccinum. The community structure was shown to yield a high diversity in ECM forming basidiomycetes of Thelephorales and Agaricales associated with a rich bacterial diversity dominated by Rhizobiales with the most abundant Nitrobacter winogradski (3.9%). Isolated bacteria were then used to address plant growth promoting abilities, which included production of the phytohormone indole-3-acetic acid (performed by 74% of the bacterial isolates), siderophores (22%), and phosphate mobilization (23%). Among the isolates, mycorrhiza helper bacteria (MHB) were identified, with Bacillus cereus MRZ-1 inducing hyperbranching in T. vaccinum, supporting tree germination, shoot elongation, and root formation as well as higher mycorrhization rates. Thus, a huge pool of potential MHB and fungal community with widely distributed auxin-production potential extended the ability of T. vaccinum to form ectomycorrhiza. The forest community profited from the mycorrhizal fungus T. vaccinum, with spruce survival enhanced by 33% in microcosms using soil from the native habitat. A higher fungal abundance and diversity in cases where the tree had died during the experiment, showing that decomposition of plant litter from a dead tree supported a different community. T. vaccinum thus actively structured the community of microorganisms in its habitat.

Introduction

Forest ecosystems are stabilized by the mutual symbiosis between tree roots and mainly basidiomycete fungi forming the ectomycorrhizal symbiosis with nutrient and water supply to the roots in exchange for photosynthesis products from the tree. In the specific mutualistic symbiosis between mainly basidiomycete fungi and trees, the ectomycorrhiza (ECM), the fungal partner forms a mantle around the short roots of its host, which has been suggested to protect the tree from pathogen attack (Smith and Read, 1987). In addition, hyphae grow between the rhizosphere cells forming the Hartig’ net which is the interface for nutrient and signal exchange (for review, see Raudaskoski and Kothe, 2015). Since mycorrhiza is known to increase tree fitness, the late stage basidiomycete Tricholoma vaccinum was chosen for investigation. It forms host specific spruce ectomycorrhiza (Asiimwe et al., 2012). T. vaccinum produces the auxin phytohormone indole-3-acetic acid (IAA), which promotes higher branching and increases hyphal lengths of the mycelium, combined with an increased Hartig’ net formation during symbiosis (Krause et al., 2015).

However, additional functions may be supplied by the rich microbiota present in the surrounding soil. To address interactions in the ectomycorrhizosphere, the microbiome of this habitat needs to be addressed with specific regard to the ectomycorrhiza. Here, Tricholoma vaccinum and Norway spruce (Picea abies) were investigated and the community assessed in a natural stand of spruce/T. vaccinum.

Spruce is the most common tree in Europe, making up over 30% of German and Switzerland forests, and 10% of the total land area are covered by P. abies owing to forestry management (Klimo et al., 2000). Spruce pathogens include Botrytis cinerea leading to blight especially in seedlings, and Heterobasidion annosum leading to root and butt rot. The gray mold B. cinerea is a virulent and common plant pathogen. It shows low host selectivity and mainly infects the needles of conifers (Williamson et al., 2007). Counter-acting induction of systemic acquired resistance involves up-regulation of salicylic acid, shown to be produced by, e.g., the fungus T. vaccinum in pure culture (Wagner, 2016). Therefore, an effect of mycorrhiza on protecting young seedlings in a systemic manner can be tested. On contrast, H. annosum is a typical forest root pathogen (Lundén et al., 2015). Two types, one more prevalent on pine (P type on Pinus species) and one on fir or spruce (S/F on species of Abies/Picea; see Asiegbu et al., 2005) have been assigned. The second type thus can be used to study root pathogenic fungi for a protective effect of mycorrhiza. The different strategies employed by these two pathogens lend themselves for investigation of beneficial interactions protecting the tree.

In addition, other saprophytic and parasitic fungi, as well as bacteria, archaea, protists, nematodes or viruses are present in forest soil (Bais et al., 2004). This microbial community structure and diversity is considered an important factor in responding to anthropogenic or other ecosystem disturbances (Baldrian et al., 2012). In coniferous forest soils, fungi are dominant in plant litter decomposition in the upper horizon (Buee et al., 2009), and competition within the diverse fungal community would affect fungal pathogens (Alabouvette, 1990). Bacteria more often are involved in the biogeochemical cycles in lower horizons (Bååth and Anderson, 2003). The habitat around the mycorrhized roots with its microbiota is defined as mycorrhizosphere (Johansson et al., 2004). The chemical communication in the mycorrhizosphere represents a complex process and includes diverse phytohormones, pheromones and various allelochemicals with different structures, e.g., steroids and proteins (Raudaskoski and Kothe, 2015, and citations therein).

Mycorrhiza helper bacteria (MHB) can enhance mycorrhiza establishment or increase mycorrhization strength on an individual plant (Deveau et al., 2012; Wu et al., 2012). MHBs can impact phosphate and iron nutrition (Ahmad et al., 2008), and they can mediate plant defense by signals supporting mycorrhiza formation (Wang et al., 1993). Other plant growth promoting bacteria are also present in the rhizosphere and can supply traits like nitrogen fixation, phosphate mobilization, antifungal or antibacterial properties, as well as cyanide, phytohormone, or siderophore synthesis (Saharan and Nehra, 2011). The phytohormone indole-3-acetic acid (IAA) is required for cell growth and differentiation in the plant and stimulates Hartig’ net development (Gea et al., 1994). Therefore, microorganisms that are able to produce IAA (or IAA inhibiting compounds) are able to modulate ectomycorrhization (Tsavkelova et al., 2006; Hause and Schaarschmidt, 2009).

Here, we aimed to characterize the natural mycorrhizosphere community of soil below T. vaccinum fruiting bodies found with their host P. abies. The influence of the community was investigated in microcosm experiments, and the response of the community to tree death from an ectomycorrhizosphere to a forest soil community was evaluated. Isolated community members were checked for their influence on either symbiotic partner in vitro, and plant growth promoting as well as specific mycorrhiza helper functions were verified. In co-cultivation, the protection of spruce against two known pathogens was shown for inoculation with T. vaccinum. With this combined approach, we could show the impact of T. vaccinum on the community structure, identify potential functions of the mycorrhizosphere community and link both to spruce health.

Materials and Methods

Soil Sampling and Characterization

Soil was sampled in the rhizosphere of two spruce trees in a forest dominated by spruce and pine trees near Jena, Germany at a marked point with the coordinates 50°55′10.8”N 11°31′30.4”E at different time points over 3 years to validate the general mycorrhizosphere community stability and response to seasonal changes. The samples were taken, where T. vaccinum fruiting bodies had been found and morphotyping had validated occurrence of T. vaccinum (Supplementary Figure S1). Sampling dates for sequential extraction were in October 2012, for the investigation of fungal community in March 2014 and for the investigation of bacterial community at six time points in October 2012, April 2013, October 2013, April 2014, October 2014, and April 2015. Soil was taken from the organic horizon (O) with litter and humus rich zones (L and H horizon) in 1–10 cm depth. The soil was transferred immediately to the laboratory at 4°C and sieved with a 3–4 mm mesh to eliminate bigger plant material.

The pH was measured as described by Minasny et al. (2011). For sequential extraction, soil was air-dried and sieved to <2 mm. Extraction was performed in triplicates for the mobile (F1) and specifically absorbed (F2) fraction for the biomobile and bioavailable element contents (Supplementary Table S1, Schütze et al., 2014). Sequential extraction and analysis of the carbon (C), sulfur (S), and nitrogen (N) contents in the soil samples were performed as described earlier (Schütze et al., 2013).

DNA Extraction, Pyrosequencing, and Bioinformatics Community Evaluation

Total DNA of the microbial community was isolated using the MoBio Soil DNA Extraction Kit (MoBio Laboratories, Carlsbad, CA, United States) with four extractions of 0.3 g soil each to gain a representative result. DNA was stored at -20°C, and samples sent to GATC Biotech (Konstanz, Germany) for pyrosequencing after amplification of bacterial 16S rRNA (using primers 27F: AGA GTT TGA TCC TGG CTC AG and 534R: ATT ACC GCG GCT GCT GG) or fungal ITS1 (primers ITS1F: CTT GGT CAT TTA GAG GAA GTA A and ITS2: GCT GCG TTC TTC ATC GAT GC; Gardes and Bruns, 1993). The reason for using ITS2 was to show broader coverage of fungal lineages as compared to using the ITS4 primer (Ihrmark et al., 2012). FLX titanium and paired-end Illumina sequencing was used. Non-chimeric unique clusters (see Supplementary Table S2 for read statistics and OTU assignment) were used for BLASTn analysis with an E-value cutoff of 1e-06 by non-redundant ITS references from UNITE database (updated on February, 2014) for fungi and 16S rDNA sequences from Ribosomal Database Project (RDP release 11, updated on March 2014; Cole et al., 2009). Sequences were deposited at GenBank MG255224-MG255268 (fungal ITS) and at GenBank MG282098-MG282149 (bacterial16S rRNA). Sequences for all representative species were retrieved from the mentioned databases and aligned using MAFFT online (version 7)1. The alignment was corrected manually, a neighbor-joining tree constructed and data bootstrapped using MrBayes (Bayesian Inference of Phylogeny, version 3.2)2 with 6 Mio generations for bacteria and 1 Mio generations for fungi. Rarefaction was controlled (see Supplementary Figure S2).

Isolation of Bacteria and Identification

A dilution series in 0.9% NaCl was plated on Standard I medium (StdI; Merck, Darmstadt, Germany). After incubation at 28°C for 2 days, colony forming units (CFU/g soil) were determined. Morphologically different isolates were selected as operational taxonomic units (OTUs) for further analyses. From the total OTUs, 94 were randomly selected for further identification. Fast DNA isolation was achieved by boiling a loop of biomass in 50 μl distillated water for 5 min. DNA was isolated using CTAB preparation (Ausubel et al., 1992). 16S rDNA sequence was amplified with the primers A1 (GAG TTT GAT CAT GGC TCA) and B6 (TTG CGG GAC TTA ACC CAA CAT) using PCR (program: 95°C for 3 min, 35 cycles of 95°C 30 sec, annealing at 52°C for 45 s, elongation at 72°C for 1 min 30 s, and final extension at 72°C for 10 min). Fragments were eluted from agarose gel and directly used for sequencing at GATC (Konstanz, Germany) or cloned into pGEM-TEasyTM vector (Promega, Madison, United States) followed by transformation into competent Escherichia coli DH5α cells. Plasmids were isolated using the GeneJetTM Plasmid Miniprep Kit after manufacturers’ instructions (Fermentas, Heidelberg, Germany). BlastN search was used to identify the isolates on genus level at www.ncbi.nlm.nih.gov.

Screening of Bacteria for Plant Growth Promotion Abilities

Selected bacteria were incubated for 2–3 days in liquid StdI at room temperature. Optical densities (OD600) of the cultures were measured and their supernatant used for Salkowski assay to determine IAA concentrations (Gordon and Weber, 1951). The ability to produce siderophores or mobilize phosphate were assessed on CAS (Schwyn and Neilands, 1987) or Pikovskaya agar medium (Mehta and Nautiyal, 2001) after 1 week of incubation at room temperature. The production of antibiotics was tested using the gram negative bacterium Escherichia coli and the gram positive Micrococcus luteus. They were grown by shaking in 30 ml liquid StdI medium for 12 h. Hundred microliter of both liquid cultures were transferred in 7 ml StdI with 7% agar, and transferred on plates with bacterial cultures to check their ability to produce antibiotics. All experiments were performed in triplicates and controls with non-inoculated plates were used. We additionally selected four bacteria (MRZ-1 through MRZ-4) based on their characteristics and investigated growth on nitrogen-free medium (5 g glucose, 5 g mannitol, 0.1 g CaCl2 × 2H2O, 5 mg Na2MoO4 × 2H2O, 0.9 g K2HPO4, 0.1 g KH2PO4, 0.01 g FeSO4 × H2O) for potential nitrogen fixation. These isolates (Bacillus cereus MRZ-1 (JMRC:ST:036355), Lysinibacillus sp. MRZ-2 (JMRC:ST:036356), Bacillus pumilus MRZ-3 (JMRC:ST:036358), and Bacillus zhangzhouensis MRZ-4 (JMRC:ST:036357) were deposited at Jena Microbial Resource Collection (JMRC), Jena, Germany.

Effect of Selected Bacterial Isolates on T. vaccinum and/or P. abies

To evaluate the effects of isolated bacteria on T. vaccinum GK6514 (JMRC:FSU:4731, JMRC, Jena, Germany), 100 μl supernatant of bacterial overnight cultures (isolates MRZ-1 through MRZ-4, and pure StdI medium for control) grown in StdI (Merck, Darmstadt, Germany) were obtained and plated on modified Melin Norkrans b (MMNb) medium (Kottke et al., 1987), followed by T. vaccinum inoculation and cultivation over 4 weeks. The mycelial diameter and hyphal branching were recorded counting 100 hyphal tips selected randomly for branching within 500 μm distance from the tip. The influence of volatiles was examined using divided plates, where one half was inoculated with bacteria (four isolates: MRZ-1 through MRZ-4, and without inoculation for control) on StdI medium, while the other half contained 2 weeks old colonies of T. vaccinum on MMNb medium. After 20 days the evaluation of growth properties was performed using the software Spot version 4.6 (Diagnostic Instruments, Munich, Germany). Every treatment was performed in triplicates. The impact of the bacteria on germination of Picea abies seedlings (Landesforst Mecklenburg-Vorpommern, Germany) was investigated on germination medium (Krause and Kothe, 2006) using bacterial overnight cultures (set to OD600 = 0.1 after washing in 0.9% NaCl) and surface sterilized seeds, mixed for 1 min, and transferred to germination medium (ten seeds per plate). For control, treatment without bacteria was performed. All experiments were performed in triplicates. Data were recorded after 20 days.

For the investigation of the mycorrhization rate with selected bacteria, P. abies and T. vaccinum were cultivated in hydroponic cultures (Henke et al., 2015a) after axenic P. abies pre-cultivation on germination medium over 4 weeks and in the hydroponic system over 3 weeks before T. vaccinum was inoculated. After 3 more weeks, 100 μl of the selected bacteria with an OD600 of 0.1 washed in 0.9% NaCl were inoculated. After 3 months, the hydroponic cultures were evaluated for spruce vitality, root and shoot biomass, root architecture, fungal biomass and the mycorrhization rate of the root system in percentage of total roots with obvious mantle formation or mycorrhiza-typical thickened and coiled short root morphology.

Isolation of Fungi With Selective Media

A soil dilution series (1 g soil 1:10 w/v in 0.9% NaCl) was plated on MMNb, well suited for ectomycorrhizal basidiomycetes, or supplemented minimal medium (SUP), optimal for the growth of mucoromycetes (Wöstemeyer, 1985). Spectinomycin or cycloheximide were added to prevent bacterial growth or inhibit most fungi to provide access to some resistant but less competitive genera like Absidia. Incubation at 22 or 28°C for 3–4 days or 4 weeks to select slow growing fungi was followed by selection of different OTUs and the total number of fungal colony forming units (cfu) was calculated. DNA was isolated from all OTUs with three freeze/thaw cycles of the mycelium in liquid nitrogen followed by heating for 1 min at 50°C followed by ITS PCR (primers ITS1: TCC GTA GGT GAA CCT GCG G and ITS 4: TCC TCC GCT TAT TGA TAT GC; see Innis et al., 1990) and identification was performed through sequencing (GATC Biotech, Germany).

Microcosm Experiments

Microcosm tubes of 50 ml contained 20 ml sieved (<2 mm) soil with its natural microbial community. After treatment with 30% hydrogen peroxide for 1.5 h and rinsing with sterilized water P. abies seeds were placed on germination medium (Kottke et al., 1987). A 2 months sterily pre-grown P. abies seedling was planted using a sterile spatula and watered with sterile tap water. The microcosms were inoculated with T. vaccinum GK6514 and/or plus and minus mating types of the ubiquitous soil fungus Mucor mucedo (SF:JMRC:000620 or SF:JMRC:000621, JMRC, Jena, Germany). Strains of Mucor were chosen, because they may affect phytohormone signaling of fungi and trees and modulate their morphology (Wagner et al., 2016). Using a sterile stamp 7 mm diameter inocula of T. vaccinum were transferred from MMNb cultivation plates and for M. mucedo the same procedure was performed from SUP cultivation plates. The microcosms were incubated in a climate chamber (12 h light/23°C; 12 h dark/17°C; 80% humidity) and watered with 1 ml sterile tap water weekly (n = 12). After 8 weeks, vitality of trees (living or dead), microorganisms plated on SUP and MMNb for OTUs, and fungal CFU were checked.

Effect of T. vaccinum on Spruce Pathogens

To analyze the role of T. vaccinum to protect the tree from pathogen attack Botrytis cinerea (SF:JMRC:001099) and Heterobasidion annosum S/F type (SF:JMRC:008560; both JRMC, Jena, Germany) were used. Well-overgrown agar blocks (5 mm × 5 mm) of both fungi were inoculated on MMNb plates with pre-grown (2 weeks) T. vaccinum, (see Supplementary Figure S3). After 2 weeks, pathogen growth was evaluated in comparison with pure cultures of the fungi using Image J 1.463. The effect of volatiles of T. vaccinum on the phytopathogens was scored using divided plates with pure and co-cultures (see Supplementary Figure S3B). The disease symptoms of pathogens were checked with plate cultures (see Supplementary Figure S3C), where an axenic 8 weeks old spruce seedling was placed between two sterile cellophane membranes with fungal inocula on MMN agar media with 2% glucose and without malt extract (modified after Kottke et al., 1987). For quantitative data on pathogen protection, hydroponic cultures (Henke et al., 2015a) were used with the more aggressive and faster pathogen, B. cinerea (see Supplementary Figure S3D). Three 8 weeks old spruce seedlings were inoculated with two well-overgrown agar blocks of T. vaccinum. After 3 weeks B. cinerea was added (n = 4). Cultures containing either T. vaccinum or the pathogen were used as control. After 1 month, living trees were counted, root and shoot dried and biomass examined.

In silico Analyses

The genome of T. vaccinum GK6514 was screened for genes involved in the biosynthesis of the pigment melanin, extending both to DHN melanin (Tsai et al., 1999) and L-DOPA melanin (Eisenman and Casadevall, 2012). The genome is available on request via JGI IMG4 under the submission ID59348. BLASTN search was performed with software sequenceserver5 and with NCBI database6.

Statistical Analyses

Every treatment was performed in triplicates if not mentioned otherwise. The statistical analyses for comparison of two treatments was performed with unpaired Student’s t-test, and for more than two treatments with one-way analysis of variance (ANOVA) after Levene’s test. Tukey test was used for post hoc analyses. Significance levels are indicated with small letters and were set to P < 0.05. Data are shown as average values ± standard deviation.

Results

The Mycorrhizosphere Habitat

In order to establish potential interactions of fungi or bacteria present in the mycorrhizosphere surrounding T. vaccinum ectomycorrhiza, soil from the natural habitat was characterized. The soil samples were slightly acidic at pH 6.5 and featured high concentrations of bioavailable lanthanides, Pb and Mn (see Supplementary Table S1). A high C (26.92% ± 0.012) to N (0.84% ± 0.008) ratio of 32:1 and raised S contents (0.11% ± 0.009) were observed.

In soil from O, L, and H horizon of this forest habitat, the fungal community composition was determined (Figure 1). For fungi it revealed 53 OTUs consisting mainly of Basidiomycota (99.95%), with almost 95% of the basidiomycetes being ectomycorrhizal members of Thelephorales and 3.5% Agaricales (Table 1). Among the most abundant genera, 16 basidiomycetes, 12 with an ectomycorrhizal lifestyle, were identified. At species level, the dominant species clearly was Tomentella lateritia.

FIGURE 1
www.frontiersin.org

Figure 1. Ectomycorrhizosphere community assessment by ITS and 16S rDNA sequencing. Composition of fungi, bacteria and archaea by most abundant reads (%) are shown.

TABLE 1
www.frontiersin.org

Table 1. Identified OTUs by pyrosequencing (90% sequence similarity level) and their different lifestyles.

The bacterial community showed a high diversity with 1517 different bacterial OTUs detected (Supplementary Table S3). The five most abundant genera were Rhodoplanes (19.5%), Pedomicrobium (8.16%), Afipia (6.93%), Methylibium (5.02%), and Dongia (4.67%), the three dominant ones being Rhizobiales (compare Figure 1). On species level, the mycorrhizosphere was dominated by the Rhizobiales member Nitrobacter winogradskyi with 3.9% of reads, with another 0.5% being other Rhizobiales with potential function in nitrogen cycling (Figure 2).

FIGURE 2
www.frontiersin.org

Figure 2. Phylogenetic tree of the 16S rDNA fragments of the most abundant species (over 0.5% composition reads) on 93% sequence similarity level. Relevance in nitrogen cycling is indicated for nitrogen fixation (green), nitrification (blue), and denitrification (red).

Of the detected OTUs, 505 represented less than 0.01% of the total community (<18 reads), containing mainly Gram-positives with high species heterogeneity (44% Actinobacteria). Among the archaea, low abundance and low diversity, again hinting at nitrogen cycling, was detected.

Physiological Traits of Isolated Fungi and Bacteria

To assess the physiological potential of strains present in the mycorrhizosphere, fungal and bacterial isolates were obtained. On complex media the conidiospore forming genus Penicillium dominated. At lower temperature and with increased incubation time, fungi with different life styles were isolated (Table 2). Using antibiotics, different taxa were enriched with cycloheximide selecting for Absidia mucoromycetes and ascomycetous Hypocreales, namely Lecanicillum, Acremonium, Beauveria, and Penicillium (see Table 2), while spectinomycin led to Penicillium and Beauveria isolation, with the Hypocreales fungus Pochonia and the Mucoromycota Mortierella and Umbelopsis being enriched. Of all fungal isolates, only 6.3% produced IAA without tryptophan addition, and 7.4% with the addition of 0.5 mM tryptophan to the medium.

TABLE 2
www.frontiersin.org

Table 2. Isolated fungi and their different life styles.

To detect seasonal changes in the mycorrhizosphere community and the related changes in ecological functions relating to the formation of mycorrhiza and tree growth, bacteria were isolated in three different years from the same site during spring and autumn (Figure 3). The average bacterial abundance was found to be around 107 with 111 isolated strains belonging to Bacillus (n = 29), Pseudomonas (n = 27), Micrococcus (n = 11), Streptomyces (n = 6), Bacteroides and α- and ß-proteobacteria including Burkholderia (n = 2). The selected isolates could be shown to provide a range of plant growth promoting abilities with changes visible specifically for siderophore production between different time points and seasons (Supplementary Figure S4). Around 23% of the isolates produced siderophores, 22% mobilized phosphate, and around 74% excreted the phytohormone IAA. Streptomycetes, Micrococcus and Pseudomonas showed the highest potential to mobilize phosphate, and all of the dominant phyla produced IAA (Supplementary Table S3).

FIGURE 3
www.frontiersin.org

Figure 3. Composition of the isolated bacteria (%) at different sampling times.

T. vaccinum Alters the Fungal Community Structure in Microcosms

To see the influence of T. vaccinum on fungal community and spruce health, we used microcosms with soil obtained from the habitat. After 8 weeks of cultivation, the transplanted spruce seedlings showed a high mortality. A tendency to a higher vitality with T. vaccinum (58% alive compared to 25% in control) was visible. Inoculation with the non-wood degrading mucoromycete M. mucedo slightly increased spruce health (42% alive). No significant difference of shoot, primary and lateral root growth, or needle development was obtained at the seedling stage (data not shown).

An effect of T. vaccinum on the mycorrhizosphere was obtained in the microcosms containing dead trees. There, T. vaccinum significantly increased the number of fungal colonies and OTUs indicating a higher prevalence of plant decomposers, if T. vaccinum was present (Figure 4).

FIGURE 4
www.frontiersin.org

Figure 4. Fungal CFU (A) and OTUs (B) compared between microcosms non-inoculated (black), inoculated with M. mucedo (light gray) or T. vaccinum (dark gray) of living or dead spruce trees. Significance level, p < 0.05, error bars indicate standard deviation; n = 12.

To show the ability of T. vaccinum to degrade plant material, it was grown on MMNb where the only C source was replaced by cellulose, the main component of plant cell walls, which supported growth (Supplementary Figure S5).

Mycorrhiza Helper Bacteria

Four isolates were selected based on their ability to produce IAA, siderophores, or to grow on nitrogen-free medium suggesting nitrogen fixation (Supplementary Tables S3, S4). Bacillus cereus MRZ-1, Lysinibacillus sp. MRZ-2, Bacillus pumilus MRZ-3 and Bacillus zhangzhouensis MRZ-4 all synthesized IAA, but did not solubilize phosphate; B. cereus MRZ-1 produced IAA only in the presence of an additional tryptophan source. All, with the exception of Lysinibacillus sp. MRZ-2, grew on nitrogen-free medium. These were tested for their effect on Tricholoma and mycorrhiza.

Volatile compounds produced by bacteria B. cereus MRZ-1, Lysinibacillus sp. MRZ-2, and B. zhangzhouensis MRZ-4 affected fungal growth and significantly reduced the colony diameter of axenically grown T. vaccinum (Figure 5), when co-cultivated on divided plates that allow for volatile transmission, but not for diffusion of compounds. Volatiles, especially of B. cereus MRZ-1, strongly induced the formation of a brownish pigment by T. vaccinum which was not observed using bacterial supernatant (Supplementary Figure S6). To see whether this pigment might be melanin, the genome of T. vaccinum was checked for genes involved in melanin biosynthesis. Genes alb1 (ID: g2107.t1), arp1 (g3608.t1), arp2 (g10130.t1), abr1 (g4688.t1), and abr2 (g3608.t1), known to be involved in the biosynthesis of DHN melanin, as well as the laccase lac1 (g4688.t1) of L-DOPA melanin biosynthesis could be identified.

FIGURE 5
www.frontiersin.org

Figure 5. Influence of bacterial volatiles in divided plates on the diameter of the colony of T. vaccinum, significance level p < 0.05, n = 3.

In addition to volatiles, supernatants were checked for morphological effects. B. cereus MRZ-1 sterile culture filtrate increased primary and secondary hyphal branching of T. vaccinum (number of 1st order branches increased from 1.76 to 2.95 and 2nd order branches from 1.01 to 2.83), which was not the case with the other bacteria tested.

As for an impact on tree development, germination rate of spruce seedlings inoculated with the bacterial suspension showed a slight increase (Figure 6). A significantly higher number of germinated seeds had an elongated germination tube after 20 days (not shown). Moreover, the length of the germination tubes that sometimes already developed into a shoot was significantly enhanced when treated with B. cereus MRZ-1, B. pumilus MRZ-3, and B. zhangzhouensis MRZ-4 (see Figure 6B).

FIGURE 6
www.frontiersin.org

Figure 6. Effect of suspension of the selected bacterial isolates on P. abies (A) germination and (B) germination tube or shoot length, significance level p < 0.05. Effect of bacterial suspension on mycorrhized trees after 3 months of incubation with total number of lateral branches per root system (C) or percentage of total mycorrhized roots (D), error bars indicate standard deviations, n = 3.

Suspension of the two isolates with best effects were then screened for their impact on mycorrhization. After 3 months, mycorrhiza formation was slightly improved by B. cereus MRZ-1 with increased number of lateral branches in the root system (see Figure 6C) and mycorrhization rates (see Figure 6D).

T. vaccinum Reduced Pathogen Growth

The protection of mycorrhiza against pathogen attack was shown using T. vaccinum, which significantly reduced the growth of both pathogens tested in vitro (Supplementary Figure S7).

The reduced growth of the root pathogen H. annosum already allows for some protection of the host tree. In this case, volatiles emitted by T. vaccinum had no effect on H. annosum in divided plates.

For the more severe and faster growing needle pathogen B. cinerea, a slight effect of volatiles was seen in addition to growth reduction in co-culture indicating the potential to work at a distance (see Supplementary Figure S7).

In hydroponic mycorrhizal co-cultures, T. vaccinum redirected the growth of B. cinerea to the medium-air interface, away from the T. vaccinum inoculant. From 12 incubated spruces, all survived when inoculated with T. vaccinum or in the co-inoculation of T. vaccinum and B. cinerea. All spruces of both treatments appeared healthy, whereas only 9 of 12 spruces that were incubated with the pathogen alone were alive. The pathogen stayed at the root and caused typical disease symptoms like needle discoloration, needle death or black points at needles (Figure 7).

FIGURE 7
www.frontiersin.org

Figure 7. Spruce seedlings inoculated with T. vaccinum (A,D), with B. cinerea displaying typical symptoms in needle development (B,E), co-inoculated, healthy seedlings (F), and without fungal inoculation (C).

Discussion

Here, we analyzed the composition of the microbial community in a spruce mycorrhizosphere and the effect of the ectomycorrhizal fungus T. vaccinum on community structure in a microcosm experiment. Pyrosequencing revealed a high diversity in Basidiomycota, whereas Ascomycota were underrepresented, and other phyla did not appear. Ten most abundant OTUs featured an ECM lifestyle, and clearly reflected the fact that forest trees are colonized by different ECM fungi simultaneously (Smith and Read, 1987). We also could show a much higher diversity at the sampling site than had been reported earlier for the ECM community of Norway spruce with 34 different taxa, which is known to change between tree species, geographical as well as climatic conditions, soil composition and seasons (Dighton et al., 2005; Korkama et al., 2006). Thus, a saturated diversity sampling seems to be highly important, which was checked in this study by rarefaction analysis (compare Supplementary Figure S2). Remarkably, the 10 most abundant OTUs from this work were not represented in the P. abies ECM study performed by Korkama et al. (2006) indicating the high variability between habitats.

We isolated common soil colonizing and fast growing fungi, which might have outcompeted in culture other slower growing fungi detected in amplicon sequencing. The isolates belong to the genera Umbelopsis, Penicillium, Mortierella, Absidia (Warcup, 1951), insect or nematode parasites Beauveria (Meyling and Eilenberg, 2006) and Pochonia (Atkins et al., 2003). Umbelopsis ramanniana, different Penicillium species, Beauveria bassiana and Pochonia bulbillosa were frequently found in free soil, the rhizosphere, mycorrhizosphere and hyphosphere of spruce trees (Voronina, 2011). Additionally, Penicillium and Umbelopsis species have been described as endophytes in spruce roots (Kernaghan and Patriquin, 2011). Species of Lecanicillium (Goettel et al., 2008) and Acremonium (Latch, 1994) can colonize grasses as endophytes, but were also found in the rhizosphere of healthy black spruce trees (Vujanovic et al., 2007) and Lecanicillium sp. in the hyphosphere (Voronina, 2011).

Voronina (2011) showed increased mycomycete diversity in T. fulvum mycorrhizosphere compared to the hyphosphere alone, which was not the case for most of the other studied ECM fungi. These experiments fit well with the microcosm studies, where a higher abundance and diversity of fungi was observed with dead spruce trees that might provide a saprotrophic food source. Since T. vaccinum is able to use cellulose as sole C source, its degradative capacity could possibly have supported the growth of other fungi through decomposition of dead spruce trees. The ability of ECM fungi to live as saprotrophs which can decompose plant litter is intensively discussed (Baldrian, 2009). The sequenced genome of T. vaccinum covers multiple gene copies coding for cellulolytic enzymes and laccases – more than the ECM average (Wagner et al., 2015). Interestingly, its activity decreased in the presence of spruce root exudates, functioning as early signaling molecules (Wagner et al., 2015). For other ECM fungi, decomposition of proteins, cellulose, hemicellulose and other organic carbons was shown, as well as the colonization of soil organic matter patches (Haselwandter et al., 1990; Bending and Read, 1995).

The high C:N ratio detected at the test site suggests that the studied mycorrhizosphere is a nitrogen limited habitat with a potentially reduced microbial activity (Paul, 2014). Research pointed out that nitrogen fixation is essential in mycorrhizal interactions and raised the question if the symbiotic fungal partners can perform this task, or if this function is delegated to MHB (Mikola, 1986). This hypothesis was strengthened by detection of nitrogen fixing Bradyrhizobium japonicum on non-legumes, as is seen with the present study (Lian et al., 2002). Further, three of four proposed MHB showed growth on nitrogen-free medium suggesting nitrogen fixation (compare Supplementary Table S4).

ECM microbial communities are diverse, but share structural similarities not present with the surrounding bulk soil. Uroz et al. (2012) identified Proteobacteria with 56%; the 10 dominant genera were Acidobacteria (19%), Burkholderia (6%; with a function in mineral weathering), Rhodoplanes (5%), Chitinophage (4%), and Bradyrhizobium (4%) in the mycorrhizosphere of oak with Scleroderma citrinum and Xerocomus pruinatus. Here Alphaproteobacteria dominated the mycorrhizophere, including two Bradyrhizobium species (together 2.27%) and Rhodoplanes (together 4.24%).

A largely dissimilar microbial diversity was observed by analysis of cultivated microbial isolates, showing the bias of cultivation versus different recovery rates during DNA isolation, amplification and sequencing. Our isolation supported fast growers and omitted obligate symbionts and other bacteria with special growth requirements (compare Bakken, 1997). We isolated mostly streptomycetes, pseudomonads, and Bacillus or Micrococcus species, indicating the higher abundance of Gram-positives and pseudomonads compared to the pyrosequencing result. Sixty Pseudomonas fluorescens strains had been isolated from a mycorrhizosphere including 81% inorganic phosphate mobilizers, 80% IAA and 74% siderophore producers (Frey-Klett et al., 2005). These values are higher compared to our results, which might be attributed to our broader selection for all bacterial phyla with, e.g., actinobacteria that have been shown to impact the symbiosis positively, like the positive effect reported for Streptomyces orientalis on spore germination of Glomus mosseae (Mugnier and Mosse, 1987).

The majority of the isolated bacteria showed plant growth promoting abilities; especially auxin biosynthesis was found with most strains. IAA is able to increase branching of T. vaccinum and increases mycorrhization with P. abies (Krause et al., 2015). Thus, hyperbranching in the presence of B. cereus MRZ-1 might be related to IAA produced only when tryptophan from root exudates induces IAA synthesis (Frey-Klett et al., 2005). Changes in the IAA flux, induced by morphogenic compounds in the mycorrhizosphere like the fungal intermediate D’orenone, also may alter the physiology of the symbiotic partners and ECM formation (Wagner et al., 2015). Moreover, all four MHB produced IAA and stimulated the germination and shoot growth in P. abies. Siderophores produced by three of the selected bacteria (B. cereus MRZ-1, B. pumilus MRZ-3, B. zhangzhouensis MRZ-4) may be involved in shoot elongation seen with MHB through enhanced iron bioavailability in addition to siderophores from ECM and AM fungi reported to increase iron uptake in host plants (Haselwandter, 1995). The siderophore production and phosphate mobilization ability varied between our samples, possibly caused by a seasonal effect, abiotic factors like water availability, or heterogeneity in the sampling microhabitat.

B. cereus MRZ-1 showed the highest potential as MHB because it positively affected spruce germination and shoot growth, enhanced lateral branching and the rate of mycorrhization and spruce health. Moreover, volatiles changed T. vaccinum morphology by increasing its pigment production and reducing the mycelia diameter. We interpret this feature of a somewhat decreased extraradical growth not detrimental to advancing mycorrhization, since an earlier and more pronounced formation of intraradical symbiotic structures might be the result of this interaction. This warrants further research into signaling via volatile compounds. The pigment production might be linked to melanin, reported to mediate fungal stress resistance toward radiation, drought or reactive oxygen species, as well as being a virulence factor for plant and human pathogens (Pagano and Dhar, 2015). The initiation of pigment production in T. vaccinum thus could be a stress response induced through bacterial volatiles, and subsequently increase fungal vitality and thus mycorrhization.

T. vaccinum enhanced the survival rate of spruce trees during 8 weeks of incubation, which is impressive because mycorrhization evolves over several months. The positive effect on the plant partner in early mycorrhization has been discussed to involve stimulation of defense mechanisms with phytohormone signaling, because T. vaccinum is able to produce jasmonic acid, ethylene and salicylic acid (Wagner, 2016), with jasmonic and salicylic acids known to increase spruce defense against the stem and butt rot causing fungus H. parviporum (Arnerup et al., 2013). While the related H. annosum that infects spruce via the root (Stenlid and Johansson, 1987) did not respond to volatiles produced by T. vaccinum, the pathogen B. cinerea was impaired in growth. The induction of systemic acquired resistance through salicylic acid production by T. vaccinum can confer protection even against a needle pathogen such as B. cinerea. In addition, volatiles of T. vaccinum included potential antimicrobial compounds, like the typical fungal volatiles octen3-ol and 3-octanone, the terpenoid plant metabolites limonene and β- barbatene, as well as geosmin (Wagner, 2016). The mycorrhization with T. vaccinum, at the same time, changed the VOC pattern of spruce. Increased limonene production with antimicrobial activity (Henke et al., 2015b) may also have contributed to resistance against B. cinerea root infection. Thus, further research on the precise identification of the chemical components of the volatiles involved in the specific interaction is needed.

With the holistic approach on the entire mycorrhizosphere, we could show complex interactions involving more than two partners. T. vaccinum, as ectomycorrhizal fungus, enhances survival of its host, spruce. At the same time, T. vaccinum can suppress pathogen attack likely by induction of plant defense and antimicrobial activity of T. vaccinum compounds. A third function of T. vaccinum is correlated with its saprotrophic growth, where it decomposed dead host material and, thus, changed the fungal community present in the mycorrhizosphere. Bacteria isolated from mycorrhizspheric soil were shown to act as MHB through the production of phytohormones and volatiles, which might be true as well for other, non-cultivable members of the bacterial community.

Author Contributions

KW designed and conducted experiments, analyzed, and wrote the first draft of the manuscript. DS, RG-M, and KK conducted experiments, analyzed, and contributed to the manuscript preparation. AK, KK, and EK designed experiments, interpreted results, and contributed to the manuscript preparation.

Funding

This research was funded and supported by the Max Planck Society, Germany via the International Max Planck Research School, by the Excellence Graduate School GSC 214, by the Friedrich Schiller University Jena and the Research Training Group GRK 1257 funded by the German Science foundation. RG-M was supported by Consejo Nacional de Ciencia y Tecnología-German Academic Exchange Service (CONACyT-DAAD).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We would like to thank David Heil for the characterization and identification of fungal strains, Johannes Gmeiner for the characterization of bacterial strains and plant pathogen experiments, and the numerous practical course students between 2013 and 2015 for their contribution in isolating bacterial strains. Further, we thank Dirk Merten for sequential extraction and we acknowledge Ines Hilke from the Max Planck Institute of Biogeochemistry in Jena for CNS analyzes, Matthias Gube for T. vaccinum fruiting bodies and Jennifer Stoiber-Lipp for support in rarefaction analysis.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2019.00307/full#supplementary-material

Footnotes

  1. ^http://mafft.cbrc.jp/alignment/server/
  2. ^http://mrbayes.sourceforge.net/
  3. ^http://rsb.info.nih.gov/ij/download.html
  4. ^http://img.jgi.doe.gov/
  5. ^http://www.sequenceserver.com
  6. ^http://blast.ncbi.nlm.nih.gov

References

Ahmad, F., Ahmad, I., and Khan, M. (2008). Screening of free-living rhizospheric bacteria for their multiple plant growth promoting activities. Microbiol. Res. 163, 173–181. doi: 10.1016/j.micres.2006.04.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Alabouvette, C. (1990). “Biological control of Fusarium wilt pathogens in suppressive soils” in Biological Control of Soil-Borne Plant Pathogens, ed. D. Hornby (Wallingford, CAB International), 27–43.

Google Scholar

Arnerup, J., Nemesio-Gorriz, M., Lunden, K., Asiegbu, F. O., Stenlid, J., and Elfstrand, M. (2013). The primary module in norway spruce defence signalling against H. annosum s.l. seems to be jasmonate-mediated signalling without antagonism of salicylate-mediated signalling. Planta 237, 1037–1045. doi: 10.1007/s00425-012-1822-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Asiegbu, F. O., Adomas, A., and Stenlid, J. (2005). Conifer root and butt rot caused by Heterobasidion annosum (Fr.) Bref. s.l. Mol. Plant Pathol. 6, 395–409. doi: 10.1111/j.1364-3703.2005.00295.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Asiimwe, T., Krause, K., Schlunk, I., and Kothe, E. (2012). Modulation of ethanol stress tolerance by aldehyde dehydrogenase in the mycorrhizal fungus Tricholoma vaccinum. Mycorrhiza 22, 471–484. doi: 10.1007/s00572-011-0424-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Atkins, S. D., Hidalgo-Diaz, L., Clark, I. M., Morton, C. O., Montes de Oca, N., Gray, P. A., et al. (2003). Approaches for monitoring the release of Pochonia chlamydosporia var. catenulata, a biocontrol agent of root-knot nematodes. Mycol. Res. 107, 206–212. doi: 10.1017/S095375620300724X

PubMed Abstract | CrossRef Full Text | Google Scholar

Ausubel, F. M., Brent, R., Kingston, R. E., Moore, D. D., Seidman, J., Smith, J. A., et al. (1992). Short Protocols in Molecular Biology. New York, NY: John Wiley and Sons.

Google Scholar

Bååth, E., and Anderson, T.-H. (2003). Comparison of soil fungal/bacterial ratios in a pH gradient using physiological and PLFA-based techniques. Soil Biol. Biochem. 35, 955–963. doi: 10.1016/S0038-0717(03)00154-8

CrossRef Full Text | Google Scholar

Bais, H. P., Park, S.-W., Weir, T. L., Callaway, R. M., and Vivanco, J. M. (2004). How plants communicate using the underground information superhighway. Trends Plant Sci. 9, 26–32. doi: 10.1016/j.tplants.2003.11.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Bakken, L. R. (1997). “Culturable and nonculturable bacteria in soil”, in Modern Soil Microbiology, eds J. D. van Elsas, J. T. Trevors and E. M. H. Wellington (New York, NY: Marcel Dekker Inc), 47–61.

Google Scholar

Baldrian, P. (2009). Ectomycorrhizal fungi and their enzymes in soils: is there enough evidence for their role as facultative soil saprotrophs? Oecologia 161, 657–660.

PubMed Abstract | Google Scholar

Baldrian, P., Kolařík, M., Štursová, M., Kopecký, J., Valášková, V., Větrovský, T. et al. (2012). Active and total microbial communities in forest soil are largely different and highly stratified during decomposition. ISME J. 6, 248–258. doi: 10.1038/ismej.2011.95

PubMed Abstract | CrossRef Full Text | Google Scholar

Bending, G. D., and Read, D. J. (1995). The structure and function of the vegetative mycelium of ectomycorrhizal plants. VI. Activities of nutrient mobilizing enzymes in birch litter colonized by Paxillus involutus (Fr.) Fr. New Phytol. 130, 411–417. doi: 10.1111/j.1469-8137.1995.tb01835.x

CrossRef Full Text | Google Scholar

Buee, M., Reich, M., Murat, C., Morin, E., Nilsson, R. H., Uroz, S., et al. (2009). 454 Pyrosequencing analyses of forest soils reveal an unexpectedly high fungal diversity. New Phytol. 184, 449–456. doi: 10.1111/j.1469-8137.2009.03003.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Cole, J. R., Wang, Q., Cardenas, E., Fish, J., Chai, B., Farris, R. J., et al. (2009). The Ribosomal Database Project: improved alignments and new tools for rRNA analysis. Nucleic Acids Res. 37, D141–D145. doi: 10.1093/nar/gkn879

PubMed Abstract | CrossRef Full Text | Google Scholar

Deveau, A., Plett, J. M., Legué, V., Frey-Klett, P., and Martin, F. (2012). “Communication between plant, ectomycorrhizal fungi and helper bacteria”, in Biocommunication of Fungi, ed. G. Witzany (Haarlem: Springer), 229–247.

Google Scholar

Dighton, J., White, J. F. Jr., White, J., and Oudemans, P. (2005). The Fungal Community: Its Organization and Role in the Ecosystem. Boca Raton, FL: CRC Press. doi: 10.1201/9781420027891

CrossRef Full Text | Google Scholar

Eisenman, H. C., and Casadevall, A. (2012). Synthesis and assembly of fungal melanin. Appl. Microbiol. Biotechnol. 93, 931–940. doi: 10.1007/s00253-011-3777-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Frey-Klett, P., Chavatte, M., Clausse, M. L., Courrier, S., Le Roux, C., Raaijmakers, J., et al. (2005). Ectomycorrhizal symbiosis affects functional diversity of rhizosphere fluorescent pseudomonads. New Phytol. 165, 317–328. doi: 10.1111/j.1469-8137.2004.01212.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Gardes, M., and Bruns, T. D. (1993). ITS primers with enhanced specificity for basidiomycetes-application to the identification of mycorrhizae and rusts. Mol. Ecol. 2, 113–118. doi: 10.1111/j.1365-294X.1993.tb00005.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Gea, L., Normand, L., Vian, B., and Gay, G. (1994). Structural aspects of ectomycorrhiza of Pinus pinaster (Ait.) Sol. formed by an IAA-overproducer mutant of Hebeloma cylindrosporum romagnési. New Phytol. 128, 659–670. doi: 10.1111/j.1469-8137.1994.tb04030.x

CrossRef Full Text | Google Scholar

Goettel, M. S., Koike, M., Kim, J. J., Aiuchi, D., Shinya, R., and Brodeur, J. (2008). Potential of Lecanicillium spp. for management of insects, nematodes and plant diseases. J. Invertebr. Pathol. 98, 256–261. doi: 10.1016/j.jip.2008.01.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Gordon, S. A., and Weber, R. P. (1951). Colorimetric estimation of indoleacetic acid. Plant Physiol. 26, 192–195. doi: 10.1104/pp.26.1.192

PubMed Abstract | CrossRef Full Text | Google Scholar

Haselwandter, K. (1995). Mycorrhizal fungi: siderophore production. Crit. Rev. Biotechnol. 15, 287–291. doi: 10.3109/07388559509147414

CrossRef Full Text | Google Scholar

Haselwandter, K., Bobleter, O., and Read, D. (1990). Degradation of 14C-labelled lignin and dehydropolymer of coniferyl alcohol by ericoid and ectomycorrhizal fungi. Arch. Microbiol. 153, 352–354. doi: 10.1007/BF00249004

CrossRef Full Text | Google Scholar

Hause, B., and Schaarschmidt, S. (2009). The role of jasmonates in mutualistic symbioses between plants and soil-born microorganisms. Phytochemistry 70, 1589–1599. doi: 10.1016/j.phytochem.2009.07.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Henke, C., Jung, E.-M., and Kothe, E. (2015a). Hartig’net formation of Tricholoma vaccinum-spruce ectomycorrhiza in hydroponic cultures. Environ. Sci. Pollut. Res. 22, 19394–19399. doi: 10.1007/s11356-015-4354-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Henke, C., Kunert, M., Veit, D., Kunert, G., Krause, K., Kothe, E., et al. (2015b). Analysis of volatiles from Picea abies triggered by below-ground interactions. Environ. Exp. Bot. 110, 56–61.

Google Scholar

Ihrmark, K., Bödeker, I. T., Cruz-Martinez, K., Friberg, H., Kubartova, A., Schenck, J., et al. (2012). New primers to amplify the fungal ITS2 region–evaluation by 454-sequencing of artificial and natural communities. FEMS Microbiol. Ecol. 82, 666–677. doi: 10.1111/j.1574-6941.2012.01437.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Innis, M., Gelfand, D., Sninsky, J., and White, T. (1990). PCR Protocols: A Guide to Methods and Applications. San Diego, CA: Academic Press.

Google Scholar

Johansson, J. F., Paul, L. R., and Finlay, R. D. (2004). Microbial interactions in the mycorrhizosphere and their significance for sustainable agriculture. FEMS Microbiol. Ecol. 48, 1–13. doi: 10.1016/j.femsec.2003.11.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Kernaghan, G., and Patriquin, G. (2011). Host associations between fungal root endophytes and boreal trees. Microb. Ecol. 62, 460–473. doi: 10.1007/s00248-011-9851-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Klimo, E., Hager, H., and Kulhavý, J. (2000). Spruce monocultures in central Europe: problems and prospects. Eur. Forest Inst. Portal 33, 1–208.

Google Scholar

Korkama, T., Pakkanen, A., and Pennanen, T. (2006). Ectomycorrhizal community structure varies among Norway spruce (Picea abies) clones. New Phytol. 171, 815–824. doi: 10.1111/j.1469-8137.2006.01786.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Kottke, I., Guttenberger, M., Hampp, R., and Oberwinkler, F. (1987). An in vitro method for establishing mycorrhizae on coniferous tree seedlings. Trees 1, 191–194. doi: 10.1007/BF00193562

CrossRef Full Text | Google Scholar

Krause, K., Henke, C., Asiimwe, T., Ulbricht, A., Klemmer, S., Schachtschabel, D., et al. (2015). Indole-3-acetic acid biosynthesis, secretion, and its morphological effects on Tricholoma vaccinum-spruce ectomycorrhiza. Appl. Environ. Microbiol. 81, 7003–7011. doi: 10.1128/AEM.01991-15

PubMed Abstract | CrossRef Full Text

Krause, K., and Kothe, E. (2006). Use of RNA fingerprinting to identify fungal genes specifically expressed during ectomycorrhizal interaction. J. Basic Microbiol. 46, 387–399. doi: 10.1002/jobm.200610153

PubMed Abstract | CrossRef Full Text | Google Scholar

Latch, G. (1994.) Influence of Acremonium endophytes on perennial grass improvement. N. Z. J. Agric. Res. 37, 311–318. doi: 10.1080/00288233.1994.9513069

CrossRef Full Text

Lian, B., Souleimanov, A., Zhou, X., Smith, D. L. (2002). In vitro induction of lipo-chitooligosaccharide production in Bradyrhizobium japonicum cultures by root extracts from non-leguminous plants. Microbiol. Res. 157, 157–160. doi: 10.1078/0944-5013-00145

PubMed Abstract | CrossRef Full Text | Google Scholar

Lundén, K., Danielsson, M., Durling, M. B., Ihrmark, K., Nemesio Gorriz, M., Stenlid, J., et al. (2015). Transcriptional responses associated with virulence and defence in the interaction between Heterobasidion annosum s.s. and Norway spruce. PLoS One 10:e0131182. doi: 10.1371/journal.pone.0131182

PubMed Abstract | CrossRef Full Text | Google Scholar

Mehta, S., and Nautiyal, C. S. (2001). An efficient method for qualitative screening of phosphate-solubilizing bacteria. Curr. Microbiol. 43, 51–56. doi: 10.1007/s002840010259

PubMed Abstract | CrossRef Full Text | Google Scholar

Meyling, N. V., and Eilenberg, J. (2006). Occurrence and distribution of soil borne entomopathogenic fungi within a single organic agroecosystem. Agric. Ecosyst. Environ. 113, 336–341. doi: 10.1016/j.agee.2005.10.011

CrossRef Full Text | Google Scholar

Mikola, P. U. (1986). Relationship between nitrogen fixation and mycorrhiza. MIRCEN J. Appl. Microbiol. Biotechnol. 2, 275–282. doi: 10.1007/BF00933493

CrossRef Full Text | Google Scholar

Minasny, B., McBratney, A. B., Brough, D. M., and Jacquier, D. (2011). Models relating soil pH measurements in water and calcium chloride that incorporate electrolyte concentration. Eur. J. Soil Sci. 62, 728–732. doi: 10.1111/j.1365-2389.2011.01386.x

CrossRef Full Text | Google Scholar

Mugnier, J., and Mosse, B. (1987). Spore germination and viability of a vesicular arbuscular mycorrhizal fungus, Glomus mosseae. Transact. Br. Mycol. Soc. 88, 411–413. doi: 10.1016/S0007-1536(87)80018-9

CrossRef Full Text | Google Scholar

Pagano, M. C., and Dhar, P. P. (2015). “Fungal pigments: an overview,” in Fungal Biomolecules: Sources, Applications and Recent Developments. eds V. K. Gupta, R. L. Mach, and S. Sreenivasaprasad (Oxford: Wiley-Blackwell), 173.

Google Scholar

Paul, E. A. (2014). Soil Microbiology, Ecology and Biochemistry. Amsterdam: Academic press.

Google Scholar

Raudaskoski, M., and Kothe, E. (2015). Novel findings on the role of signal exchange in arbuscular and ectomycorrhizal symbioses. Mycorrhiza 25, 243–252. doi: 10.1007/s00572-014-0607-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Saharan, B., and Nehra, V. (2011). Plant growth promoting rhizobacteria: a critical review. LSMR 21, 1–30.

Google Scholar

Schütze, E.,Merten, D., Nietzsche, S., Senftleben, D., Roth, M., et al. (2014). Growth of streptomycetes in soil and their impact on bioremediation. J. Hazard. Mater. 267, 128–135. doi: 10.1016/j.jhazmat.2013.12.055

PubMed Abstract | CrossRef Full Text | Google Scholar

Schütze, E., Weist, A., Klose, M., Wach, T., Schumann, M., Nietzsche, S., et al. (2013). Taking nature into lab: biomineralization by heavy metal-resistant streptomycetes in soil. Biogeosciences 10, 3605–3614. doi: 10.5194/bg-10-3605-2013

CrossRef Full Text | Google Scholar

Schwyn, B., and Neilands, J. B. (1987). Universal chemical assay for the detection and determination of siderophores. Anal. Biochem. 160, 47–56. doi: 10.1016/0003-2697(87)90612-9

CrossRef Full Text | Google Scholar

Smith, S. E., and Read, D. J. (1987). Mycorrhizal Symbiosis, 2nd Edn. San Diego, CA: Academic press.

Google Scholar

Stenlid, J., and Johansson, M. (1987). Infection of roots of Norway spruce (Picea abies) by Heterobasidion annosum. Eur. J. For. Pathol. 17, 217–226. doi: 10.1111/j.1439-0329.1987.tb01019.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Tsai, H. F., Wheeler, M. H., Chang, Y. C., and Kwon-Chung, K. J. (1999). A developmentally regulated gene cluster involved in conidial pigment biosynthesis in Aspergillus fumigatus. J. Bacteriol. 181, 6469–6477.

PubMed Abstract | Google Scholar

Tsavkelova, E. A., Klimova, S. Y., Cherdyntseva, T. A., and Netrusov, A. I. (2006). Hormones and hormone-like substances of microorganisms: a review. Appl. Biochem. Microbiol. 42, 229–235. doi: 10.1134/S000368380603001X

PubMed Abstract | CrossRef Full Text | Google Scholar

Uroz, S., Oger, P., Morin, E., and Frey-Klett, P. (2012). Distinct ectomycorrhizospheres share similar bacterial communities as revealed by pyrosequencing-based analysis of 16S rRNA genes. Appl. Environ. Microbiol. 78, 3020–3024. doi: 10.1128/AEM.06742-11

PubMed Abstract | CrossRef Full Text | Google Scholar

Voronina, E. Y. (2011). Effect of the mycorrhizosphere on soil micromycete biodiversity and community structure and its relation to the rhizosphere and hyphosphere effects. Microbiology 80, 584–590. doi: 10.1134/S0026261711040217

CrossRef Full Text | Google Scholar

Vujanovic, V., Hamelin, R., Bernier, L., Vujanovic, G., and St-Arnaud, M. (2007). Fungal diversity, dominance, and community structure in the rhizosphere of clonal Picea mariana plants throughout nursery production chronosequences. Microb. Ecol. 54, 672–684. doi: 10.1007/s00248-007-9226-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Wagner, K. (2016). Chemical Communication Between Soil Microorganisms, Basidiomycetes and Their Tree Host. Dissertation, University of Jena, Jena.

Wagner, K., Krause, K., David, A., Kai, M., Jung, E.-M., Sammer, D. et al. (2016). Influence of zygomycete-derived D’orenone on IAA signaling in Tricholoma-spruce ectomycorrhiza. Environ. Microbiol. 18, 2470–2480. doi: 10.1111/1462-2920.13160

PubMed Abstract | CrossRef Full Text | Google Scholar

Wagner, K., Linde, J., Krause, K., Gube, M., Koestler, T., Sammer, D. et al. (2015). Tricholoma vaccinum host communication during ectomycorrhiza formation. FEMS Microbiol. Ecol. 91:fiv120. doi: 10.1093/femsec/fiv120

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Y., Brown, H., Crowley, D., and Szaniszlo, P. (1993). Evidence for direct utilization of a siderophore, ferrioxamine B, in axenically grown cucumber. Plant Cell Environ. 16, 579–585. doi: 10.1111/j.1365-3040.1993.tb00906.x

CrossRef Full Text | Google Scholar

Warcup, J. (1951). The ecology of soil fungi. Trans. Br. Mycol. Soc. 34, 376–399. doi: 10.1016/S0007-1536(51)80065-2

CrossRef Full Text | Google Scholar

Williamson, B., Tudzynski, B., Tudzynski, P., and van Kan, J. A. L. (2007). Botrytis cinerea: the cause of grey mould disease. Mol. Plant Pathol. 8, 561–580. doi: 10.1111/j.1364-3703.2007.00417.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Wöstemeyer, J. (1985). Strain-dependent variation in ribosomal DNA arrangement in Absidia glauca. Eur. J. Biochem. 146, 443–448. doi: 10.1111/j.1432-1033.1985.tb08671.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, X.-Q., Hou, L.-L., Sheng, J.-M., Ren, J.-H., Zheng, L., Chen, D., et al. (2012). Effects of ectomycorrhizal fungus Boletus edulis and mycorrhiza helper Bacillus cereus on the growth and nutrient uptake by Pinus thunbergii. Biol. Fertil. Soils 48, 385–391. doi: 10.1007/s00374-011-0638-1

CrossRef Full Text | Google Scholar

Keywords: ectomycorrhiza, community, microcosm, indole-3-acetic acid, Tricholoma, plant growth promoting bacteria

Citation: Wagner K, Krause K, Gallegos-Monterrosa R, Sammer D, Kovács ÁT and Kothe E (2019) The Ectomycorrhizospheric Habitat of Norway Spruce and Tricholoma vaccinum: Promotion of Plant Growth and Fitness by a Rich Microorganismic Community. Front. Microbiol. 10:307. doi: 10.3389/fmicb.2019.00307

Received: 27 September 2018; Accepted: 05 February 2019;
Published: 20 February 2019.

Edited by:

Jonathan Michael Plett, Western Sydney University, Australia

Reviewed by:

Jessie Karen Uehling, University of California, Berkeley, United States
François Noêl Le Tacon, INRA Université de Lorraine and INRA, France
Sabine Dagmar Zimmermann, Centre National de la Recherche Scientifique (CNRS), France

Copyright © 2019 Wagner, Krause, Gallegos-Monterrosa, Sammer, Kovács and Kothe. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Katrin Krause, Katrin.Krause@uni-jena.de

Present address: Katharina Wagner, Food GmbH Jena, Analytik & Consulting, Jena, Germany; Dominik Sammer, Wacker Biotech GmbH, Jena, Germany; Ákos T. Kovács, Technical University of Denmark, Department of Biotechnology and Biomedicine, Lyngby, Denmark

These authors have contributed equally to this work