The Piriformospora indica effector PIIN_08944 promotes the mutualistic Sebacinalean symbiosis

Pathogenic and mutualistic microbes actively suppress plant defense by secreting effector proteins to manipulate the host responses for their own benefit. Current knowledge about fungal effectors has been mainly derived from biotrophic and hemibiotrophic plant pathogenic fungi and oomycetes with restricted host range. We studied colonization strategies of the root endophytic basidiomycete Piriformospora indica that colonizes a wide range of plant species thereby establishing long-term mutualistic relationships. The release of P. indica’s genome helped to identify hundreds of genes coding for candidate effectors and provides an opportunity to investigate the role of those proteins in a mutualistic symbiosis. We demonstrate that the candidate effector PIIN_08944 plays a crucial role during fungal colonization of Arabidopsis thaliana roots. PIIN_08944 expression was detected during chlamydospore germination, and fungal deletion mutants (Pi_Δ08944) showed delayed root colonization. Constitutive over-expression of PIIN_08944 in Arabidopsis rescued the delayed colonization phenotype of the deletion mutant. PIIN_08944-expressing Arabidopsis showed a reduced expression of flg22-induced marker genes of pattern-triggered immunity (PTI) and the salicylic acid (SA) defense pathway, and expression of PIIN_08944 in barley reduced the burst of reactive oxygen species (ROS) triggered by flg22 and chitin. These data suggest that PIIN_08944 contributes to root colonization by P. indica by interfering with SA-mediated basal immune responses of the host plant. Consistent with this, PIIN_08944-expressing Arabidopsis also supported the growth of the biotrophic oomycete Hyaloperonospora arabidopsidis while growth of the necrotrophic fungi Botrytis cinerea on Arabidopsis and Fusarium graminearum on barley was not affected.

Introduction

During their lifecycle, plant roots are constantly exposed to a multitude of microorganisms in the rhizosphere. These interactions which can either be parasitic or mutualistic have a great impact on agriculture and forest life (Harrison, 1999; Sanders, 2011). Mycorrhizal symbioses, an association between plant roots and soil fungi, and the symbiosis of plants with rhizobia have been the main focus of studies on beneficial plant–microbe interactions. Whereas mycorrhizal symbioses are very abundant in nature and are formed by more than 90% of plant species with diverse soil fungi, rhizobial interactions have a narrow host range. Nevertheless, both interactions are beneficial to their hosts, resulting in an increase in phosphorus and/or nitrogen uptake (Parniske, 2008; Sanders, 2011).

Piriformospora indica, a basidiomycete fungus with an endophytic life style, colonizes the roots of a wide variety of monocotyledonous and dicotyledonous plants, including the model plants Arabidopsis and barley and establishes a Sebacinalean symbiosis (Varma et al., 1999; Peškan-Berghöfer et al., 2004; Lee et al., 2011; Qiang et al., 2012a; Glaeser et al., 2015). P. indica was initially discovered in the Indian Thar desert in northwest Rajasthan and has been extensively investigated for its beneficial effects during interaction with plants. Previous reports have shown that infestation by P. indica spores and/or culture filtrates leads to growth promotion, enhanced resistance to biotic and abiotic stresses, increase grain yield, and enhanced phosphate and nitrate uptake (Peškan-Berghöfer et al., 2004; Sherameti et al., 2005; Waller et al., 2005; Deshmukh and Kogel, 2007; Achatz et al., 2010; Yadav et al., 2010). The successful interaction between P. indica with its hosts is achieved through an active suppression of part of the host defense responses (Jacobs et al., 2011). The fungus has evolved a dual colonization strategy whereby it initially colonizes living root cortex cells biotrophically (3 dpi) and later switches to a cell death-associated colonization stage (7 and 14 dpi), where it grows mostly on dead plant material (Jacobs et al., 2011; Qiang et al., 2012b; Lahrmann et al., 2013). As a consequence, the level of fungal colonization was influenced by the cell death inhibitor protein BAX INHIBITOR 1, at least during the first 3 weeks after colonization of barley roots (Deshmukh et al., 2006). Furthermore, several phytohormones affect plant colonization by P. indica. For example, ethylene signaling supports the colonization of barley and Arabidopsis roots by P. indica. In addition, genes involved in the biosynthesis and signaling of ethylene, auxin, abscisic acid (ABA) and gibberellic acid (GA) were found to be differentially regulated during colonization of barley roots by P. indica (Schäfer et al., 2009; Khatabi et al., 2012). While, it has been reported that P. indica is indeed capable of producing the auxin indole acetic acid (IAA) in culture medium and also regulate auxin-induced genes in roots, this auxin was not required for growth promotion, but rather supported the biotrophic colonization of barley (Vadassery et al., 2008; Lee et al., 2011; Hilbert et al., 2012).

Similarly to plant pathogenic fungi, mutualistic fungi have also evolved the ability to deliver molecules, called effectors, inside the cells to manipulate the host metabolism, and enhance microbial infection (de Jonge et al., 2010; Kloppholz et al., 2011; Plett et al., 2011; Rafiqi et al., 2012). Effectors, which can exert their actions either in the host cytoplasm or apoplast, often lack conserved domains and are usually under high selective pressure from the host (Dodds et al., 2009; de Jonge et al., 2010; Rafiqi et al., 2010). While effectors from pathogenic fungi have been extensively studied, little is known about effectors secreted by mutualistic symbionts. Two independent studies, reported the involvement of mutualistic fungal effector proteins in the establishment and maintenance of symbiosis in endo- and ectomycorrhiza, allowing the fungus to manipulate the plant defense response in both cases (Kloppholz et al., 2011; Plett et al., 2011, 2014). The release of the P. indica genome (Zuccaro et al., 2011) allowed the identification of hundreds of genes coding for small secreted proteins (SSPs < 300 aa). These proteins are considered candidate effectors. Twenty five of P. indica’s effector candidates contain a highly conserved pattern of seven amino acid “RSIDELD” at the C-terminus collectively known as the DELD effectors. Although it is speculated that the DELD motif could function in effector translocation in a similar way as the RXLR and LFLAK motifs found in oomycete effectors (Whisson et al., 2007; Schornack et al., 2010) and/or in signaling, the exact function of the DELD motifs is still unknown. While several P. indica effector candidates, including some of the DELD effectors, are induced exclusively either in Arabidopsis or barley and thus behave host specifically, a small group were expressed in both Arabidopsis and barley (i.e., host unspecific; Lahrmann et al., 2013). Despite the fact that several P. indica effector candidates including some of the DELD effectors were up-regulated in planta (Zuccaro et al., 2011) their virulence functions during the interaction between P. indica with plants are largely unknown, opening new avenues to investigate their role in the Sebacinalean symbiosis.

In this study, we investigate the function of the P. indica effector candidate PIIN_08944, a non DELD effector, during the interaction of plants with P. indica. We show that the candidate effector contributes to plant colonization by the mutualistic fungus by suppressing the salicylate (SA)-mediated basal resistance response. Moreover, we found that PIIN_08944 also supports growth of the biotrophic oomycete Hyaloperonospora arabidopsidis, while growth of the necrotrophic fungi Botrytis cinerea and Fusarium graminearum were unaffected.

Materials And Methods

Fungal and Plant Materials and Root Inoculation

Piriformospora indica (Verma et al., 1998) cultures (DSM11827, Deutsche Sammlung für Mikroorganismen und Zellkulturen, DSMZ, Braunschweig, Germany) were propagated at 28°C in liquid complete medium (CM; Pham et al., 2004) supplemented with 2% glucose on a shaker at 140 rpm. For solid medium, 1.5% agar was added to the CM medium. Hygromycin B (100 μg/ml) was supplemented for growth of P. indica transformants.

Barley seeds (Hordeum vulgare cv. Golden Promise) were surface sterilized with 70% ethanol for 2 min, 12% sodium hypochlorite for 1.5 h, and washed with sterile distilled water for 3 h. Sterilized seeds were kept in the dark for 3 days on sterile wet filter paper at room temperature. For colonization studies, 3-day-old barley seedlings were transferred into sterile jars containing 1/10 PNM medium (Basiewicz et al., 2012) supplemented with 0.4% (w/v) GELRITE (Duchefa) and inoculated with P. indica chlamydospore suspension (500,000 chlamydospore mL^-1 in 0.002% TWEEN20). Inoculated plants were transferred to a growth chamber and grown under a dark/light cycle of 16 h light (110 μmol m^-2 s^-1) at 24°C and 8 h dark at 18°C. Control plants were treated with water containing 0.002% (v/v) TWEEN20. Root samples were collected at the indicated time points and immediately frozen in liquid nitrogen.

Arabidopsis thaliana seeds (ecotype Columbia-0, col-0) were surface sterilized with 70% ethanol for 1 min, for 10 min with 6% sodium hypochlorite, and washed six times for 5 min in sterile water. Seeds were placed on A. thaliana medium + sucrose (ATS) medium (5 mM KNO₃, 2.5 mM KH₂PO₄ 2 mM MgSO₄, 2 mM Ca(NO₃)₂, 50 μM Fe-EDTA 70 μM H ₃BO₃, 14 μM MnCI₂, 0.5 μM CuSO₄, 1 μM ZnSO₄, 0.2 μM NaMoO₄, 10 μM NaCl, 0.01 μM CoCl₂; Estelle and Somerville, 1987) containing 0.4% (w/v) GELRITE (Duchefa) and grown vertically in square petri dishes under a dark/light cycle of 16 h light (110 μmol m^-2 s^-1) at 23°C and 8 h dark at 18°C. For inoculation, Arabidopsis roots of 7-day-old seedlings were inoculated with 1 ml of 500,000 chlamydospores mL^-1. Root material was harvested and immediately frozen in liquid nitrogen at 3, 7, 14, and 21 days post inoculation (dpi). For each time point, roots from 80 to 100 plants were harvested. For all root inoculation experiments, chlamydospores were collected from 3 to 4-week-old P. indica cultures grown on solid CM medium using water containing 0.002% (v/v) TWEEN20.

Plasmid Construction and Generation of Transgenic Arabidopsis and Barley Plants

PIIN_08944 lacking the predicted signal peptide was amplified from cDNA by PCR using primers GS-08944dSP-F and SmaI-08944-R (Supplementary Table S1). For cDNA synthesis, total RNA from P. indica was extracted using TRIzol (Invitrogen); cDNA was synthesized using the qScript cDNA synthesis kit (Quanta Biosciences) following the manufacturer’s instructions. For the generation of GFP-PIIN_08944 fusion construct, GFP (Green Fluorescence Protein) was amplified using primers SmaI-GFP-F and ATG-GSGFP-R (Supplementary Table S1) and the PCR products of PIIN_08944 and GFP were fused by overlap extension PCR. The fusion construct was ligated at the SmaI site in the pUBI-AB vector¹ (DNA Cloning Service, Hamburg, Germany) and the entire cassette was inserted at the SfII restriction site into the binary vector pLH6000² (DNA Cloning Service, Hamburg, Germany) under the control of the maize ubiquitin promoter or the SmaI restriction site in the expression vector pICH (Weber et al., 2011) under the control of the constitutive CaMV35S promoter. The resulting plasmids pLH6000 UBI::GFP-8944 and pICH CaMV35S::8944 were confirmed by sequencing (Sequence Laboratories Göttingen, Germany) before plant transformation. For Arabidopsis transformation, the plasmid pICH CaMV35S::8944 was introduced into Agrobacterium tumefaciens strain GV3101 by electroporation and selected on LB medium containing kanamycin (25 μg/ml), gentamycin (20 μg/ml), and rifampicin (15 μg/ml) antibiotics. Transformation and regeneration of Arabidopsis was performed by floral dip (Clough and Bent, 1998) and transformants were selected on MS (Murashige and Skoog) medium containing kanamycin (25 μg/ml). For barley transformation, the pLH6000 UBI::GFP-8944 plasmid was used. Transgenic barley plants were generated as described (Imani et al., 2011).

DNA, RNA Extraction and Quantitative Real-time PCR

For genomic DNA and total RNA extraction, plant and fungal materials were powdered under liquid nitrogen using a mortar and pestle. Genomic DNA was isolated following the method of Doyle and Doyle (Doyle, 1987). For gene expression studies, seedlings were grown on solid half strength MS medium for 2 weeks and then transferred in six-well-plates containing liquid half-strength MS medium. After a recovery phase of 3 days, flg22 (Davids Biotechnology, Germany) was pipetted to each well containing MS medium with seedlings in a final concentration of 100 nM flg22 and harvested after 0, 2, 6, and 12 h. For all experiments, total RNA was extracted from plant or fungal materials using TRIzol (Invitrogen), and aliquots were used for cDNA synthesis with the qScript cDNA synthesis kit (Quanta Biosciences). Forty nanograms of genomic DNA or cDNA were used as template for quantitative real-time PCR (qPCR) analysis, using the SYBR Green JumpStart Taq ReadyMix (Sigma–Aldrich) and the 7500 FAST Real-Time PCR System under standard conditions (Applied Biosystems). For the detection of fungal and plant DNA, the primers ITS_F/ITS_R and UBQ4_F/UBQ4_R were used (Supplementary Table S1). The relative fungal genomic DNA or relative gene expression were calculated using the 2^-ΔCT method (Livak and Schmittgen, 2001).

Construction of Knockout Vector, P. indica Transformation

In order to generate a genomic deletion of the PIIN_08944 gene, a hygromycin B resistance cassette was introduced by homologous recombination at the PIIN_08944 locus. A 180 bp fragment (5′ UTR region), upstream and a 1000 bp fragment (3′ UTR region), downstream of PIIN_08944 was amplified by PCR using the primers KpnI_US_8944F/KpnI_US_8944R and StuI_DS_8944F/SacI_DS_8944R, respectively. The fragments were cloned into the flanking KpnI and StuI/SacI restriction sites of the hygromycin B resistance cassette into the pHSP70 vector derived from the pbshhn-Tef vector (Kamper, 2004) by replacing the TEF promoter with the Hsp70 promoter. The constructed plasmid was confirmed by sequencing (Sequence Laboratories Göttingen, Germany) and used to transform P. indica following the PEG mediated transformation protocol (Hilbert et al., 2012).

Southern Blot

To verify integration of the hygromycin resistance cassette into the nuclear genome of P. indica, Southern blot analysis was performed. Genomic DNA from 7-day-old cultures grown on CM medium was extracted; 10–20 μg of extracted DNA was digested overnight with SacI (NEB). The digested DNA was separated on 0.9% TAE agarose gel for 5 h at 80 V and blotted onto a nylon membrane (AmershamBiosciences Hybond-N+, GE Healthcare) over night. The DNA was UV cross-linked to the membrane in a GS GENE LINKER UV chamber (BIO-RAD) using an auto cross-linking program (C2, 50 mμ Joule). The labeling of the Hygromycin B probe was performed using the Prime-a-Gene^® Labeling System according to the manufacturer’s instructions (Promega). Hybridization and washing steps were performed at 65°C. The membrane was exposed on phosphorimaging screens (Bio-Rad) and signals were detected using a molecular imager and the Quantity One software (Bio-Rad).

PIIN_8944 Transcript Analysis

To assess the disruption of the PIIN_08944 gene in P. indica, mRNA expression analysis was performed using reverse transcriptase-PCR (RT-PCR). RNA was extracted from 7-day-old P. indica cultures grown on CM medium/plates or from Arabidopsis roots inoculated with the P. indica deletion mutant, harvested at 3, 7, 14, and 21 dpi. cDNA was synthesized from total RNA and 40 ng served as template for RT-PCR in a final volume of 25 μl, and a thermal cycling period of 30 cycles. The P. indica ubiquitin gene PIIN_01523 served as a reference.

Plant Infection Assays

For Arabidopsis leaf inoculation, B. cinerea strain B05.10 (Rui and Hahn, 2007) was cultured on HA agar as described (Doehlemann et al., 2006); conidia concentration was adjusted to 2 × 10⁵ conidia per mL^-1 in potato dextrose broth (PDB). Fifteen rosette leaves were detached from 10 different 4-week-old plants and transferred into square petri plates containing 1% agar. Five μl droplets of the conidial suspension was pipetted onto each side of the middle vein and incubated during a 12 h photoperiod at 22°C. Disease symptom progression was analyzed by measuring the lesion size (in centimeter) at 5 dpi from the digital images using the Image J free software program³ by calculating the percentage of leaf area showing disease symptoms relative to the non-inoculated area. Two week old Arabidopsis seedlings were sprayed with the H. arabidopsidis isolate Noks1 (Holub and Beynon, 1997) at a spore concentration of 30,000 spores mL^-1. Infection development was scored 4 days after infection by counting sporangiophores on true leaves (Tome et al., 2014).

For barley leaf inoculation, F. graminearum, Fg-IFA65 (Jansen et al., 2005) was cultured on SNA agar as described (Koch et al., 2013) and conidia concentration was adjusted to 5 × 10⁵ mL^-1 in 0.02% Tween 20. Leaves of 3-week-old barley of each transgenic line (T2 generation) and empty vector (EV) control plants were detached and transferred into square petri plates containing 1% agar. Each leaf was inoculated with 20 μl and plates were incubated at 22°C with a 16 h photoperiod for up to 6 days. Disease symptoms were analyzed by measuring the lesion size/area using the Image J free software program³ and the relative amount of fungal biomass determined by qPCR after DNA extraction using the β-tubulin gene (FGSG_09530) as normalization control.

For barley root infection, roots of 3-day-old seedlings were dip-inoculated in a F. graminearum conidial suspension for 30 min, then transferred into pots containing a 2:1 mixture of expanded clay (Seramis, Masterfoods, Verden, Germany) and Oil-Dri (Damolin, Mettmann, Germany) and allowed to grow in a growth chamber under long day conditions (dark/light cycle of 16 h light (110 μmol m^-2 s^-1) at 24°C and 8 h dark at 18°C) for up to 2 weeks. Plants were carefully collected, roots washed with H₂O and the root length (in cm) and root fresh weight (in mg) were determined.

Measurement of ROS

Leaf disks from 3-week-old barley plants (HvPIIN_08944 or EV control) or 4-week-old Arabidopsis plants (AtPIIN_08944 or WT control) were cut and pre-incubated overnight in sterile distil water in 96 well micro-titer plate. Water is carefully discarded and the leaf disks are treated with luminol (Sigma, A8511-5 g) 40 μl luminol buffer [15 mg/ml], 400 μl horseradish peroxidase [1 mg/ml] and elicitor [100 nM flg22, 200 mg/ml crab shell chitin (sigma–aldrich) or water control]. Immediately after treatment, luminescence was measured in a TECAN infinite^® F200 micro plate reader (TECAN, Switzerland). The relative light units over time as a result of the production of oxygen radicals were measured for 50 min.

Statistical Analysis

All experiments were repeated at least two to three times in each case as indicated in the figure legends. A student’s two-tailed t test was used to determine the significance of the data reported in this study. Differences were considered to be significant at P ≤ 0.05.

Results

In silico Analysis of the P. indica Effector Candidate PIIN_08944

The genome of P. indica revealed the existence of 543 small secreted proteins (Zuccaro et al., 2011; Rafiqi et al., 2013). PIIN_08944 is a small secreted protein containing 120 amino acids (aa; GenBank:CCA74964.1) that lacks cysteine residues. The presence of an N-terminal signal peptide has been a main criterion for selecting fungal genes coding for putative effectors. Using SignalP 4.0 (Petersen et al., 2011), PIIN_08944 was predicted to contain a 23 aa signal peptide located at the N-terminal (aa 1–23); the TMHMM software (Krogh et al., 2001) failed to detect a transmembrane domain. Search for other conserved domains using the conserved domain database at NCBI⁴ and pfam version 27.0 (EMBL-EBI⁵) did not reveal any conserved domains. Moreover the protein did not show a significant sequence similarity to proteins with known functions of other organisms.

PIIN_08944 is Expressed During Colonization of Arabidopsis Roots

To confirm previous results and to benchmark our colonization assay, we investigated the increase in fungal biomass during P. indica colonization of Arabidopsis and barley roots by using qPCR. Similar colonization pattern were observed for both plant species over a time period of 21 days. The relative amount of fungal DNA increased in roots from 3 to 21 dpi, with a more than 20-fold increase in barley (Figure 1A) and 300-fold increase in Arabidopsis (Figure 1B) relative to plant DNA. This is in agreement with published results (Pedrotti et al., 2013).

FIGURE 1

FIGURE 1. Colonization of plant roots by Piriformospora indica increases over time. (A) Roots of 3-day-old barley grown on 1/10 PNM agar in sterile glass jars, were inoculated with chlamydospores of P. indica. Colonization levels were determined at 3, 7, 14, and 21 dpi as the relative amount of fungal DNA by qPCR using barley (HvUBQ-60-Deg) and fungal (ITS) specific primers. Values represent the mean ± SE of two independent experiments. (B) Seven-day-old Arabidopsis seedlings were inoculated with chlamydospores of P. indica. Colonization levels were determined at 3, 7, 14, and 21 dpi as the relative amount of fungal DNA by qPCR using Arabidopsis (AtUBQ4) and fungal (ITS) specific primers. Data represents the Ct thresholds of ITS relative to the Ct thresholds of AtUBQ-4 (±SE obtain from three technical replicates of one biological experiment). Experiments were repeated twice with similar results. Asterisks indicate significance between time points at ^∗P < 0.05, ^∗∗P < 0.01, ^∗∗∗P < 0.001 analyzed by student’s t-test. (C) Analysis of PIIN_08944 expression by semi-quantitative RT-PCR. Transcripts of PIIN_08944 were detected in in vitro germinated P. indica chlamydospores (CS) grown in CM liquid medium for 7 days and in planta during colonization of Arabidopsis roots by P. indica by RT-PCR. Transcript abundance increased over time from 3 to 21 dpi. The P. indica ubiquitin (UBQ) gene served as reference.

Based on microarray expression datasets, several of P. indica’s effector candidates, including the DELDs are strongly expressed during symbiosis (Zuccaro et al., 2011). To determine the expression pattern of PIIN_08944, we reviewed the literature and a public available dataset from ArrayExpress⁶(E-GEOD-47775) for PIIN_08944 and compared it to P. indica’s effector candidates that contain the DELD motif (DELD effectors; Zuccaro et al., 2011). PIIN_08944 showed very high levels of expression (log₂ of 11.4) compared to DELD genes and therefore ranked on the fourth position after candidate effectors PIIN_09226, PIIN_00561, PIIN_05098, and PIIN_09643. PIIN_08944 is found in the top 20% of all expressed genes of P. indica grown under minimal PNM medium (Lahrmann et al., 2013). Since the published time-course experiment did not reveal any significant differential expression at 3 and 14 dpi (Zuccaro et al., 2011; Lahrmann et al., 2013, Lahrmann, 2014), we expanded our analysis to 21 dpi and examined the expression profile of PIIN_08944 by RT-PCR (Figure 1C). PIIN_08944 transcripts were detected in RNA from in vitro germinated P. indica chlamydospores as well as colonized Arabidopsis roots. The increase in transcript abundance from 3 to 21 days is correlated with the increase in fungal biomass as the ubiquitin reference gene (PIIN_01523) also increased in abundance over the time course. This result is in agreement with our analysis of the public available microarray data where PIIN_08944 did not show differential regulation.

P. indica Deletion Mutants (Pi_Δ08944) Show Reduced Colonization of Arabidopsis Roots

To investigate the impact of PIIN_08944 on root colonization, deletion mutants of P. indica lacking PIIN_08944 (Pi_Δ08944) were generated using homologous gene replacement. After transformation of P. indica protoplasts and selection on hygromycin containing CM medium, five transformants were recovered. RT-PCR on RNA extracted from cultures grown on CM medium confirmed deletion of PIIN_08944 as evident by the absence of transcripts (Supplementary Figure S4A). To further confirm that PIIN_08944 expression was not induced in the mutants during root colonization, Arabidopsis roots were inoculated with all five P. indica deletion mutants and RT-PCR analysis was performed after roots were harvested at 3, 7, 14, and 21 dpi. In two Pi_Δ08944 mutants (strains PiT1 and PiT2), transcripts could not be detected at all analyzed time points (Figure 2A). To elucidate the number of insertion of the hygromycin resistance cassette in the genome of P. indica we performed southern blot analysis. PiT1 contained two copies and PiT2 contained one copy of T-DNA (Supplementary Figure S4B).

FIGURE 2

FIGURE 2. Characterization of P. indica Knockout Strains Pi_Δ08944 (PiT1-PiT5). (A) Roots of 7-day-old Arabidopsis seedlings were inoculated with chlamydospores of Pi_Δ08944 strains PiT1 or PiT2, respectively. The roots were harvested at 3, 7, 14, and 21 dpi and PIIN_08944 transcript levels were determined from extracted RNA by RT-PCR using PIIN_08944 specific primer. PIIN_08944 transcripts from Pi_Δ08944 strains were not detected in planta. The P. indica ubiquitin UBQ gene served as reference. (B) Deletion of PIIN_08944 delays colonization of Arabidopsis roots. Roots of 7-day-old Arabidopsis seedlings were inoculated with Pi_Δ08944 (PiT1) and wt, respectively. (C) Colonization of PIIN_08944-expressing Arabidopsis with Pi_Δ08944 (PiT1) mutant. Roots of 7-day-old AtPIIN_08944OE seedlings or wt were inoculated with Pi_Δ08944. Fungal biomass was determined at 3, 7, 14, and 21 dpi as relative amount of fungal DNA by qPCR using fungal (ITS) and plant (AtUBQ4) specific primers. Data displays the Ct thresholds of ITS relative to the Ct thresholds of AtUBQ- 4 (±SE obtain from three technical replicates of one biological experiment). Experiments were repeated twice with similar results. Asterisks indicate significance at ^∗P < 0.05, ^∗∗P < 0.01 analyzed by Student’s t-test.

To assess whether the deletion of PIIN_08944 has any effect on the growth rate of P. indica, we monitored the progression of growth of PiT1 and PiT2 on CM plates over a period of 21 days and compared it to the wild type (wt). The deletion of PIIN_08944 did not affect the colony morphology (Supplementary Figure S1) and the growth rate of P. indica (data not shown). However, when Arabidopsis roots were inoculated with Pi_Δ08944 (PiT1), colonization was significantly delayed compared to roots inoculated with the wt strain over the analyzed period of 21 days (Figure 2B), demonstrating that PIIN_08944 likely plays a crucial role in the colonization process of roots by P. indica.

In Planta Expression of PIIN_08944 Rescues the Delayed Growth Phenotype of Pi_Δ08944

To investigate whether PIIN_08944 is able to rescue the delayed colonization phenotype of Pi_Δ08944, we generated Arabidopsis plants expressing PIIN_08944 under the control of the constitutive 35 s CaMV promoter (AtPIIN_08944OE plants). The integration of the PIIN_08944 transgene was confirmed by PCR analysis. Several independent AtPIIN_08944OE (T1 generation) plants were selected and self-pollinated to produce T2 generation lines. RT-PCR analysis confirmed that PIIN_08944 was highly expressed in independent T2 transgenic plants (Supplementary Figure S4C). No difference in plant growth was observed between AtPIIN_08944OE vs. the corresponding wt plants (data not shown). To further expand this finding, transgenic barley plants expressing a fusion between PIIN_08944 and GFP under the constitutive maize ubiquitin promoter were generated (HvPIIN_08944OE plants). Genomic insertion of a construct coding for a GFP:PIIN_08944 fusion protein was confirmed by PCR analysis and accumulation of GFP:PIIN_08944 in transgenic barley lines (T2 generation) was confirmed using western blot analysis. The analysis showed that GFP:PIIN_08944 was correctly expressed and no truncated versions were produced except for line 19 (Supplementary Figure S2). Consistent with the above finding, no difference in plant growth was observed between HvPIIN_08944OE vs. the corresponding wt (data not shown). Together these data show that the expression of PIIN_08944 does not affect development of barley and Arabidopsis. When roots of AtPIIN_08944OE plants were inoculated with Pi_Δ08944, colonization rate was similar in AtPIIN_08944OE vs. wt plants at 3 and 7 dpi. At 14 and 21 dpi colonization was higher in AtPIIN_08944OE plants vs. wt (Figure 2C). Additionally, HvPIIN_08944OE plants showed enhanced root colonization compared to wt barley, when inoculated by P. indica (Supplementary Figure S3). These data suggest that PIIN_08944 supports P. indica’s colonization during interaction with plants.

PIIN_08944 Interferes with Basal Defense Response in Arabidopsis and Barley

Previous reports showed that jasmonic acid (JA) supports colonization of Arabidopsis roots by P. indica (Jacobs et al., 2011). The same report showed that P. indica inhibits plant defense in roots, as evidenced by the strong suppression of the pattern-triggered immunity (PTI) marker WRKY22 (Colcombet and Hirt, 2008) and the SA marker CBP60g (Wang et al., 2009). However, whether P. indica deploys effectors to manipulate host hormone signaling has not been reported. Since the in planta expression of PIIN_08944 leads to enhanced colonization by P. indica, we speculated that PIIN_08944 might suppress the host immune response to support fungal growth. To address this question, AtPIIN_08944OE and wt seedlings were treated with the peptide flg22, a PAMP (pathogen-associated molecular pattern) derived from bacterial flagellin. After harvesting at 0, 2, 6, and 12 h post treatment (hpt), transcript abundance of WRKY22 and CBP60g were assessed by qPCR. In agreement with previous results (Colcombet and Hirt, 2008; Wang et al., 2009; Jacobs et al., 2011), genes were induced at 2, 6, and/or 12 hpt in the wt plants (control). In contrast, the flg22-induced expression of CBP60g and WRKY22 was suppressed in AtPIIN_08944OE plants (Figure 3A).

FIGURE 3

FIGURE 3. Assessment of the immune status of AtPIIN_08944OE plants. (A) Two-week-old AtPIIN_08944OE and the respective wt plants were treated with 100 nM flg22 in six well plates. RNA was extracted at 0 (untreated control), 2, 6, and 12 hpt and qPCR was performed. Suppression of flg22-induced transcription was observed for AtWRKY22 and CBP60g. Arabidopsis UBQ-4 was used for normalization. Values are means ± SE of two independent experiments. (B) Detached leaves of four to 6-week-old AtPIIN_08944OE (lines #L6, #L10) and the respective wt plants were inoculated with conidia of Botrytis cinerea. Photographs were taken 5 dpi. (C) Average lesion size of AtPIIN_08944OE (lines #L6 and #L10) and the wt plants after inoculation with B. cinerea. Averages were calculated from 10 to 15 leaves per line. Values are means ± SE of three independent experiments. (D) Two-week-old AtPIIN_08944OE seedlings (lines #4 #L6 #L10) and wt plants were sprayed with spores of Hyaloperonospora arabidopsidis and sporangiophores development on true leaves determined 4 dpi. For each line at least 100 plants were analyzed. Values are means ± SE of two independent experiments. Asterisks indicate significant differences at ^∗P < 0.05, ^∗∗P < 0.01, ^∗∗∗P < 0.001 as analyzed by student’s t-test.

We further analyzed the ability of PIIN_08944 to suppress PTI in barley by analyzing reactive oxygen species (ROS) production after flg22 and chitin treatment. In HvPIIN_08944OE plants, flg22-induced ROS accumulation was reduced to about 50%, while chitin-induced ROS production was almost completely suppressed (Figures 4A,B). Notably, however, overexpression of PIIN_08944 did not suppress flg22-induced ROS production in Arabidopsis (Figure 4C).

FIGURE 4

FIGURE 4. Assessment of flg22 and chitin-induced reactive oxygen species (ROS) accumulation in barley and Arabidopsis tissue. Leaf disks of 3-week-old barley HvPIIN_08944-OE or EV control plants were treated with (A) 100 nM flg22, and (B) 200 mg/ml crab shell chitin. (C) Leaf disks of 4-week-old AtPIIN_08944-OE or wt Arabidopsis plants were treated with 100 nM flg22. ROS was determined by measuring the relative light unit over time with a luminol-chemiluminescence assay using a Tecan reader. Error bars represent the mean ± SE of three independent experiments. (RLU, relative light units; EV, empty vector).

PIIN_08944-enhanced root colonization by P. indica and at suppression of PTI responses raised the possibility that plant infection by fungal pathogens could also be affected. To address this question, we tested PIIN_08944-overexpressing plants with the necrotrophic ascomycete fungi B. cinerea (Bc) and F. graminearum (Fg) as well as the obligate biotrophic oomycete pathogen H. arabidopsidis (Hpa). When leaves of 4-week-old transgenic plants were inoculated with B. cinerea, no difference in lesion size or infection rate was observed in AtPIIN_08944OE vs. wt plants at 5 dpi (Figures 3B,C). Similarly, when HvPIIN_08944OE plants were inoculated with F. graminearum, the lesion size and the relative amount of fungal DNA was similar in transgenic vs. wt plants. Consistent with this finding, root lengths and root fresh weights were similar between transgenic and wt plants (Figure 5). However, in clear contrast, AtPIIN_08944OE plants showed enhanced susceptibility to Hpa compared to wt plants as observed by a higher number of sporangiophores on the true leaves of AtPIIN_08944OE vs. wt plants (Figure 3D). These findings support the hypothesis that PIIN_08944 plays a critical role in the Sebacinalean symbiosis by interfering with the plant’s SA-mediated basal resistance response.

FIGURE 5

FIGURE 5. Characterization of barley HvPIIN_08944OE plants inoculated with macroconidia of Fusarium graminearum. Root length (A) and root fresh weight (B) of six plants per line inoculated with F. graminearum. Values represent the mean with ± SE of three independent experiments. (C) Detached leaves of 3-week-old HvPIIN_08944OE plants (#4 #8 #14) and EV control were inoculated with F. graminearum. Photographs were taken 6 dpi. The experiment was repeated three times with similar outcome (D) Relative fungal biomass on detached HvPIIN_08944OE (#4 #8 #14) and EV control leaves by qPCR. Values represent the mean with ±SE of three independent experiments.

Discussion

In the present work, we have corroborated and extended previous reports showing that mutualistic fungi, like pathogens, use effectors to suppress or circumvent host defense. MiSSP7, an effector of the ectomycorrhizal fungus Laccaria bicolor, and SP7, an effector of the arbuscular mycorrhizal fungus Glomus intraradices, suppresses host immunity to promote root symbiosis. SP7 targets the pathogenesis-related transcription factor ERF19 in the nucleus, while MiSSP7 targets the repressor proteins JAZ5 and JAZ6 in the nucleus and therefore inhibits the expression of JA-induced genes thereby promotes root colonization by the mycorrhizal fungus (Kloppholz et al., 2011; Plett et al., 2011; Plett et al., 2014).

The genome of P. indica contains hundreds of putative effector genes coding for SSPs (Zuccaro et al., 2011). About 123 out of 216 SSPs were responsive to colonization either on Arabidopsis or barley (Lahrmann et al., 2013), which also may indicate that colonization on different hosts needs a specialized set of effectors. Interestingly, 21 SSPs were expressed at similar symbiotic stages both in Arabidopsis and barley, suggesting that these effector candidates might target similar cellular processes. Our results show that PIIN_08944 is a host unspecific effector which is exploited by P. indica to target conserved molecular processes in different plants and therefore act as a general determinant of compatibility during plant root colonization.

The accumulation of PIIN_08944 transcripts in in vitro germinated chlamydospores shows that PIIN_08944 is induced before direct contact with a host, which also suggests that the induction is not dependent on a plant signal. Moreover, PIIN_08944 was not differentially expressed in the course of P. indica’s colonization of Arabidopsis roots, which is consistent with our analysis of public available microarray data (Lahrmann et al., 2013). However, based on the available microarray data, PIIN_08944 is among the top 20% of highly expressed P. indica genes. In support of our finding, the effector AvrM of the rust fungus Melampsora lini also was not differentially regulated during colonization of flax, and its expression was independent of a host-derived signal (Catanzariti et al., 2006). One reason for the accumulation of PIIN_08944 in germinating spores could be that this effector is important to counteract the pre-invasive host defenses and thereby might prepare the host cell for subsequent hyphal colonization. Therefore it is not surprising that the expression of effectors can be induced even before host contact has been established.

The observation that deletion of PIIN_08944 impaired the ability of P. indica to colonize Arabidopsis roots suggests that the effector contributes to fungal colonization during the interaction of P. indica with its host plant. The loss of virulence was rescued by the in planta expression of PIIN_08944. This finding also raises the possibility that PIIN_08944 is secreted and operates inside host cells. Furthermore, barley plants expressing PIIN_08944, showed enhanced colonization when inoculated with the P. indica wt strain, indicating that the protein also contributes to colonization on barley root (Supplementary Figure S3).

The ability of PIIN_08944 to suppress flg22-induced defense responses, which was observed by the dampened expression of the marker gene WRKY22, suggests that the effector interferes with early PTI signaling. Suppression of the SA marker CBP60g is most likely an indirect result of early PTI suppression (Tsuda et al., 2013). This hypothesis is further supported in that AtPIIN_08944OE and HvPIIN_08944OE plants did not resist the necrotrophic fungal pathogens F. graminearum and B. cinerea as these fungi are highly sensitive to JA-mediated defense responses (Gottwald et al., 2012; Aubert et al., 2015). The phytohormone SA is widely accepted to be involved in resistance against biotrophic pathogens (Glazebrook, 2005). The suppression of the SA marker gene CBP60g, might also explain the enhanced susceptibility observed for AtPIIN_08944 plants to Hpa. Earlier reports suggested that P. indica recruits JA signaling to counter SA associated defense as showed by the up-regulation of VEGETATIVE STORAGE PROTEIN 2 (VSP2), a marker gene for JA on P. indica colonized plants (Jacobs et al., 2011). We speculate that PIIN_08944 is unlikely to affect the JA response as necrotrophic Bc infection on Arabidopsis AtPIIN_08944OE plants and Fg infection on barley HvPIIN_08944OE plants were similar to wt.

Interestingly, flg22- and chitin-mediated ROS production was reduced on HvPIIN_08944OE plants but not in transgenic Arabidopsis. This finding might indicate that P. indica can exploit PIIN_08944 to suppress early PTI responses triggered by chitin perception during fungal colonization of roots. At present it remains unclear whether there are differences in early PTI signaling events in barley vs. Arabidopsis. The differential ROS response mediated by PIIN_08944 in barley vs. Arabidopsis may hint to such difference. However, whether PIIN_08944 is able to suppress chitin-induced ROS burst in Arabidopsis still needs further investigation.

Taken together, our results show that P. indica has evolved effectors such as PIIN_08944 as important determinants that contribute to the establishment and/or maintenance of a mutualistic relationship during interaction with plants. Moreover, the suppressive activity of PIIN_08944 in a dicot (Arabidopsis) and a monocot (barley) might give a first hint on our understanding at the molecular level, how P. indica can colonize a broad spectrum of different plant species. It is plausible that several other effector candidates may contribute in shaping the colonization process of P. indica. Therefore it would be important to investigate the role played by other P. indica effector candidates during root colonization.

Author Contributions

FA and K-HK designed the research. FA and DB performed the experiments. FA, JS, and K-HK analyzed data. FA, JS and K-HK wrote the manuscript.

Acknowledgment

This work was supported by the German Research Council (DFG) to K-HK.

Supplementary Material

The Supplementary Material for this article can be found online at: http://journal.frontiersin.org/article/10.3389/fpls.2015.00906

FIGURE S1 | Phenotypic analysis of Piriformospora indica Pi_Δ08944 mutants (PiT1 and PiT2) and wt. Fungal growth rates and morphology was similar between Pi_Δ08944 mutants (PiT1 and PiT2) and the wt fungus.

FIGURE S2 | Analysis of HvPIIN_08944OE in barley plants. Western blot analysis of transgenic barley expressing GFP: PIIN_08944 fusion protein using anti GFP antibody. No band was observed in wt plants (c), a lower GFP band (∼27 kDa) was observed in the GFP control, and a 39 KDa band corresponding to GFP: PIIN_08944 was observed in HvPIIN_08944OE plants.

FIGURE S3 | Enhanced colonization by P. indica of barley expressing PIIN_08944. Roots of 3-day-old transgenic barley seedlings or the EV control were inoculated with P. indica chlamydospore. Root material was harvested at 3, 7, 14, and 21 dpi; genomic DNA was extracted and the relative amount of fungal biomass was determined by qPCR using plant and fungal specific primers. Data represent the mean with ±SD of two independent experiments. Asterisks indicate significance at ^∗P < 0.05 analyzed using student’s t-test.

FIGURE S4 | Analysis of P. indica transgenic mutants and transgenic Arabidopsis. (A) Relative expression of PIIN_08944 in in vitro germinated spores of the five Pi_Δ08944 strains vs. wt by RT-PCR. PIIN_08944 transcripts accumulated only in wt. The P. indica ubiquitin UBQ gene served as reference. (B) Determination of T-DNA copy numbers in Pi_Δ08944 transformants by Southern blot analysis. Genomic DNA from transformants and wt was digested with SacI, separated on 0.9% TAE agarose gel, transferred to a nylon membrane, and hybridized with a ³²P radio-labeled ³²P-dCTP 600 bp fragment of hygromycin B (hph). Three out of the five transformants have one copy of T-DNA inserted in the genome, while two have two copies. Lanes 1–5: PiT1 to PiT5. (C) Expression analysis of Arabidopsis expressing PIIN_08944 (upper panel) and ubiquitin UBQ (lower panel) by RT-PCR. #1–#17: independent AtPIIN_08944OE, C: Wt.

TABLE S1 | List of primers used.

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.

Footnotes

1. ^http://dna-cloning.com/skripte/puc/puc.html
2. ^http://dna-cloning.com/skripte/binaries/bin.html
3. ^http://imagej.nih.gov/ij/
4. ^http://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi
5. ^http://pfam.xfam.org/
6. ^http://www.ebi.ac.uk/arrayexpress

References

Achatz, B., Kogel, K. H., Franken, P., and Waller, F. (2010). Piriformospora indica mycorrhization increases grain yield by accelerating early development of barley plants. Plant Signal. Behav. 5, 1685–1687. doi: 10.4161/psb.5.12.14112

PubMed Abstract | CrossRef Full Text | Google Scholar

Aubert, Y., Widemann, E., Miesch, L., Pinot, F., and Heitz, T. (2015). CYP94-mediated jasmonoyl-isoleucine hormone oxidation shapes jasmonate profiles and attenuates defence responses to Botrytis cinerea infection. J. Exp. Bot. 66, 3879–3892. doi: 10.1093/jxb/erv190

PubMed Abstract | CrossRef Full Text | Google Scholar

Basiewicz, M., Weiss, M., Kogel, K. H., Langen, G., Zorn, H., and Zuccaro, A. (2012). Molecular and phenotypic characterization of Sebacina uermifera strains associated with orchids, and the description of Piriformospora williamsii sp nov. Fungal Biol. 116, 204–213. doi: 10.1016/j.funbio.2011.11.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Catanzariti, A. M., Dodds, P. N., Lawrence, G. J., Ayliffe, M. A., and Ellis, J. G. (2006). Haustorially expressed secreted proteins from flax rust are highly enriched for avirulence elicitors. Plant Cell 18, 243–256. doi: 10.1105/tpc.105.035980

PubMed Abstract | CrossRef Full Text | Google Scholar

Clough, S. J., and Bent, A. F. (1998). Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. 16, 735–743. doi: 10.1046/j.1365-313x.1998.00343.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Colcombet, J., and Hirt, H. (2008). Arabidopsis MAPKs: a complex signalling network involved in multiple biological processes. Biochem. J. 413, 217–226. doi: 10.1042/BJ20080625

PubMed Abstract | CrossRef Full Text | Google Scholar

de Jonge R., van Esse H. P., Kombrink, A., Shinya, T., Desaki, Y., Bours, R., et al. (2010). Conserved fungal LysM effector Ecp6 prevents chitin-triggered immunity in plants. Science 329, 953–955. doi: 10.1126/science.1190859

PubMed Abstract | CrossRef Full Text | Google Scholar

Deshmukh, S., Hückelhoven, R., Schäfer, P., Imani, J., Sharma, M., Weiss, M., et al. (2006). The root endophytic fungus Piriformospora indica requires host cell death for proliferation during mutualistic symbiosis with barley. Proc. Natl. Acad. Sci. U.S.A. 103, 18450–18457. doi: 10.1073/pnas.0605697103

PubMed Abstract | CrossRef Full Text | Google Scholar

Deshmukh, S. D., and Kogel, K. H. (2007). Piriformospora indica protects barley from root rot caused by Fusarium graminearum. J. Plant Dis. Prot. 114, 263–268.

Google Scholar

Dodds, P. N., Rafiqi, M., Gan, P. H., Hardham, A. R., Jones, D. A., and Ellis, J. G. (2009). Effectors of biotrophic fungi and oomycetes: pathogenicity factors and triggers of host resistance. N. Phytol. 183, 993–1000. doi: 10.1111/j.1469-8137.2009.02922.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Doehlemann, G., Berndt, P., and Hahn, M. (2006). Different signalling pathways involving a Galpha protein, cAMP and a MAP kinase control germination of Botrytis cinerea conidia. Mol. Microbiol. 59, 821–835. doi: 10.1111/j.1365-2958.2005.04991.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Doyle, J. J. (1987). A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem. Bull. 19, 11–15.

Google Scholar

Estelle, M. A., and Somerville, C. (1987). Auxin-resistant mutants of Arabidopsis-thaliana with an altered morphology. Mol. Gen. Genet. 206, 200–206. doi: 10.1007/BF00333575

CrossRef Full Text | Google Scholar

Glaeser, S., Imani, J., Alabid, I., Guo, H., and Kumar, N. (2015). Non-pathogenic Rhizobium radiobacter F4 deploys plant beneficial activity independent of its host Piriformospora indica. ISME J. in press.

Glazebrook, J. (2005). Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annu. Rev. Phytopathol. 43, 205–227. doi: 10.1146/annurev.phyto.43.040204.135923

PubMed Abstract | CrossRef Full Text | Google Scholar

Gottwald, S., Samans, B., Luck, S., and Friedt, W. (2012). Jasmonate and ethylene dependent defence gene expression and suppression of fungal virulence factors: two essential mechanisms of Fusarium head blight resistance in wheat? Bmc Genomics 13:369. doi: 10.1186/1471-2164-13-369

PubMed Abstract | CrossRef Full Text | Google Scholar

Harrison, M. J. (1999). Molecular and cellular aspects of the arbuscular mycorrhizal symbiosis. Annu. Rev. Plant Physiol. Plant Mol. Biol. 50, 361–389. doi: 10.1146/annurev.arplant.50.1.361

PubMed Abstract | CrossRef Full Text | Google Scholar

Hilbert, M., Voll, L. M., Ding, Y., Hofmann, J., Sharma, M., and Zuccaro, A. (2012). Indole derivative production by the root endophyte Piriformospora indica is not required for growth promotion but for biotrophic colonization of barley roots. N. Phytol. 196, 520–534. doi: 10.1111/j.1469-8137.2012.04275.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Holub, E., and Beynon, J. (1997). Symbiology of mouse-ear cress (Arabidopsis thaliana) and oomycetes. Adv. Bot. Res. 24, 227–273. doi: 10.1016/S0065-2296(08)60075-0

CrossRef Full Text | Google Scholar

Imani, J., Li, L., Schaefer, P., and Kogel, K. H. (2011). STARTS–A stable root transformation system for rapid functional analyses of proteins of the monocot model plant barley. Plant J. 67, 726–735. doi: 10.1111/j.1365-313X.2011.04620.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Jacobs, S., Zechmann, B., Molitor, A., Trujillo, M., Petutschnig, E., Lipka, V., et al. (2011). Broad-spectrum suppression of innate immunity is required for colonization of Arabidopsis roots by the fungus Piriformospora indica. Plant Physiol. 156, 726–740. doi: 10.1104/pp.111.176446

PubMed Abstract | CrossRef Full Text | Google Scholar

Jansen, C., Von Wettstein, D., Schäfer, W., Kogel, K.-H., Felk, A., and Maier, F. J. (2005). Infection patterns in barley and wheat spikes inoculated with wild-type and trichodiene synthase gene disrupted Fusarium graminearum. Proc. Natl. Acad. Sci. U.S.A. 102, 16892–16897. doi: 10.1073/pnas.0508467102

PubMed Abstract | CrossRef Full Text | Google Scholar

Kamper, J. (2004). A PCR-based system for highly efficient generation of gene replacement mutants in Ustilago maydis. Mol. Genet. Genomics 271, 103–110. doi: 10.1007/s00438-003-0962-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Khatabi, B., Molitor, A., Lindermayr, C., Pfiffi, S., Durner, J., von Wettstein, D., et al. (2012). Ethylene supports colonization of plant roots by the mutualistic fungus Piriformospora indica. PLoS ONE 7:e35502. doi: 10.1371/journal.pone.0035502

PubMed Abstract | CrossRef Full Text | Google Scholar

Kloppholz, S., Kuhn, H., and Requena, N. (2011). A secreted fungal effector of Glomus intraradices promotes symbiotic biotrophy. Curr. Biol. 21, 1204–1209. doi: 10.1016/j.cub.2011.06.044

PubMed Abstract | CrossRef Full Text | Google Scholar

Koch, A., Kumar, N., Weber, L., Keller, H., Imani, J., and Kogel, K. H. (2013). Host-induced gene silencing of cytochrome P450 lanosterol C14 alpha-demethylase-encoding genes confers strong resistance to Fusarium species. Proc. Natl. Acad. Sci. U.S.A. 110, 19324–19329. doi: 10.1073/pnas.1306373110

PubMed Abstract | CrossRef Full Text | Google Scholar

Krogh, A., Larsson, B., Von Heijne, G., and Sonnhammer, E. L. L. (2001). Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J. Mol. Biol. 305, 567–580. doi: 10.1006/jmbi.2000.4315

PubMed Abstract | CrossRef Full Text | Google Scholar

Lahrmann, U. (2014). Genomics and Transcriptomics of the Sebacinoid Fungi Piriformospora indica and Sebacina vermifera. Marburg: Philipps-Universitaẗ Marburg.

Google Scholar

Lahrmann, U., Ding, Y., Banhara, A., Rath, M., Hajirezaei, M. R., Döhlemann, S., et al. (2013). Host-related metabolic cues affect colonization strategies of a root endophyte. Proc. Natl. Acad. Sci. U.S.A. 110, 13965–13970. doi: 10.1073/pnas.1301653110

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, Y. C., Johnson, J. M., Chien, C. T., Sun, C., Cai, D., Lou, B., et al. (2011). Growth promotion of Chinese cabbage and Arabidopsis by Piriformospora indica is not stimulated by mycelium-synthesized auxin. Mol. Plant Microbe Interact. 24, 421–431. doi: 10.1094/MPMI-05-10-0110

PubMed Abstract | CrossRef Full Text | Google Scholar

Livak, K. J., and Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2(T)(-Delta Delta C) method. Methods 25, 402–408. doi: 10.1006/meth.2001.1262

PubMed Abstract | CrossRef Full Text | Google Scholar

Parniske, M. (2008). Arbuscular mycorrhiza: the mother of plant root endosymbioses. Nat. Rev. Microbiol. 6, 763–775. doi: 10.1038/nrmicro1987

PubMed Abstract | CrossRef Full Text | Google Scholar

Pedrotti, L., Mueller, M. J., and Waller, F. (2013). Piriformospora indica root colonization triggers local and systemic root responses and inhibits secondary colonization of distal roots. PLoS ONE 8:e69352. doi: 10.1371/journal.pone.0069352

PubMed Abstract | CrossRef Full Text | Google Scholar

Peškan-Berghöfer, T., Shahollari, B., Giong, P. H., Hehl, S., Markert, C., Blanke, V., et al. (2004). Association of Piriformospora indica with Arabidopsis thaliana roots represents a novel system to study beneficial plant–microbe interactions and involves early plant protein modifications in the endoplasmic reticulum and at the plasma membrane. Physiol. Plant. 122, 465–477. doi: 10.1111/j.1399-3054.2004.00424.x

CrossRef Full Text | Google Scholar

Petersen, T. N., Brunak, S., Von Heijne, G., and Nielsen, H. (2011). SignalP 4.0: discriminating signal peptides from transmembrane regions. Nat. Methods 8, 785–786. doi: 10.1038/nmeth.1701

PubMed Abstract | CrossRef Full Text | Google Scholar

Pham, G. H., Kumari, R., Singh, A., Malla, R., Prasad, R., Sachdev, M., et al. (2004). “Axenic culture of symbiotic fungus Piriformospora indica,” in Plant Surface Microbiology, eds A. Varma, L. Abbott, D. Werner, and R. Hampp (Berlin: Springer), 593–613.

PubMed Abstract | Google Scholar

Plett, J. M., Daguerre, Y., Wittulsky, S., Vayssières, A., Deveau, A., Melton, S. J., et al. (2014). Effector MiSSP7 of the mutualistic fungus Laccaria bicolor stabilizes the populus JAZ6 protein and represses jasmonic acid (JA) responsive genes. Proc. Natl. Acad. Sci. U.S.A. 111, 8299–8304. doi: 10.1073/pnas.1322671111

PubMed Abstract | CrossRef Full Text | Google Scholar

Plett, J. M., Kemppainen, M., Kale, S. D., Kohler, A., Legué, V., Brun, A., et al. (2011). A secreted effector protein of Laccaria bicolor is required for symbiosis development. Curr. Biol. 21, 1197–1203. doi: 10.1016/j.cub.2011.05.033

PubMed Abstract | CrossRef Full Text | Google Scholar

Qiang, X., Weiss, M., Kogel, K. H., and Schäfer, P. (2012a). Piriformospora indica—a mutualistic basidiomycete with an exceptionally large plant host range. Mol. Plant Pathol. 13, 508–518. doi: 10.1111/j.1364-3703.2011.00764.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Qiang, X., Zechmann, B., Reitz, M. U., Kogel, K.-H., and Schäfer, P. (2012b). The mutualistic fungus Piriformospora indica colonizes Arabidopsis roots by inducing an endoplasmic reticulum stress–triggered caspase-dependent cell death. Plant Cell 24, 794–809. doi: 10.1105/tpc.111.093260

PubMed Abstract | CrossRef Full Text | Google Scholar

Rafiqi, M., Ellis, J. G., Ludowici, V. A., Hardham, A. R., and Dodds, P. N. (2012). Challenges and progress towards understanding the role of effectors in plant-fungal interactions. Curr. Opin. Plant Biol. 15, 477–482. doi: 10.1016/j.pbi.2012.05.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Rafiqi, M., Gan, P. H., Ravensdale, M., Lawrence, G. J., Ellis, J. G., Jones, D. A., et al. (2010). Internalization of flax rust avirulence proteins into flax and tobacco cells can occur in the absence of the pathogen. Plant Cell 22, 2017–2032. doi: 10.1105/tpc.109.072983

PubMed Abstract | CrossRef Full Text | Google Scholar

Rafiqi, M., Jelonek, L., Akum, N. F., Zhang, F., and Kogel, K. H. (2013). Effector candidates in the secretome of Piriformospora indica, a ubiquitous plant-associated fungus. Front. Plant Sci. 4:228. doi: 10.3389/fpls.2013.00228

PubMed Abstract | CrossRef Full Text | Google Scholar

Rui, O., and Hahn, M. (2007). The Botrytis cinerea hexokinase, Hxk1, but not the glucokinase, Glk1, is required for normal growth and sugar metabolism, and for pathogenicity on fruits. Microbiology 153, 2791–2802.

PubMed Abstract | Google Scholar

Sanders, I. R. (2011). Mycorrhizal symbioses: how to be seen as a good fungus. Curr. Biol. 21, R550–R552. doi: 10.1016/j.cub.2011.06.022

PubMed Abstract | CrossRef Full Text | Google Scholar

Schäfer, P., Pfiffi, S., Voll, L. M., Zajic, D., Chandler, P. M., Waller, F., et al. (2009). Manipulation of plant innate immunity and gibberellin as factor of compatibility in the mutualistic association of barley roots with Piriformospora indica. Plant J. 59, 461–474. doi: 10.1111/j.1365-313X.2009.03887.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Schornack, S., van Damme, M., Bozkurt, T. O., Cano, L. M., Smoker, M., Thines, M., et al. (2010). Ancient class of translocated oomycete effectors targets the host nucleus. Proc. Natl. Acad. Sci. U.S.A. 107, 17421–17426. doi: 10.1073/pnas.1008491107

PubMed Abstract | CrossRef Full Text | Google Scholar

Sherameti, I., Shahollari, B., Venus, Y., Altschmied, L., Varma, A., and Oelmuller, R. (2005). The endophytic fungus Piriformospora indica stimulates the expression of nitrate reductase and the starch-degrading enzyme glucan-water dikinase in tobacco and Arabidopsis roots through a homeodomain transcription factor that binds to a conserved motif in their promoters. J. Biol. Chem. 280, 26241–26247.

PubMed Abstract | Google Scholar

Tome, D. F., Steinbrenner, J., and Beynon, J. L. (2014). A growth quantification assay for Hyaloperonospora arabidopsidis isolates in Arabidopsis thaliana. Methods Mol. Biol. 1127, 145–158. doi: 10.1007/978-1-62703-986-4_12

PubMed Abstract | CrossRef Full Text | Google Scholar

Tsuda, K., Mine, A., Bethke, G., Igarashi, D., Botanga, C. J., Tsuda, Y., et al. (2013). Dual regulation of gene expression mediated by extended MAPK activation and salicylic acid contributes to robust innate immunity in Arabidopsis thaliana. PLoS Genet. 9:e1004015. doi: 10.1371/journal.pgen.1004015

PubMed Abstract | CrossRef Full Text | Google Scholar

Vadassery, J., Ritter, C., Venus, Y., Camehl, I., Varma, A., Shahollari, B., et al. (2008). The role of auxins and cytokinins in the mutualistic interaction between Arabidopsis and Piriformospora indica. Mol. Plant Microbe Interact. 21, 1371–1383. doi: 10.1094/MPMI-21-10-1371

PubMed Abstract | CrossRef Full Text | Google Scholar

Varma, A., Verma, S., Sudha Sahay, N., Butehorn, B., and Franken, P. (1999). Piriformospora indica, a cultivable plant-growth-promoting root endophyte. Appl. Environ. Microbiol. 65, 2741–2744.

Google Scholar

Verma, S., Varma, A., Rexer, K.-H., Hassel, A., Kost, G., Sarbhoy, A., et al. (1998). Piriformospora indica, gen. et sp. nov., a new root-colonizing fungus. Mycologia 90, 896–903. doi: 10.2307/3761331

CrossRef Full Text | Google Scholar

Waller, F., Achatz, B., Baltruschat, H., Fodor, J., Becker, K., Fischer, M., et al. (2005). The endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield. Proc. Natl. Acad. Sci. U.S.A. 102, 13386–13391. doi: 10.1073/pnas.0504423102

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L., Tsuda, K., Sato, M., Cohen, J. D., Katagiri, F., and Glazebrook, J. (2009). Arabidopsis CaM binding protein CBP60g contributes to MAMP-induced SA accumulation and is involved in disease resistance against Pseudomonas syringae. PLoS Pathog. 5:e1000301. doi: 10.1371/journal.ppat.1000301

PubMed Abstract | CrossRef Full Text | Google Scholar

Weber, E., Engler, C., Gruetzner, R., Werner, S., and Marillonnet, S. (2011). A modular cloning system for standardized assembly of multigene constructs. PLoS ONE 6:e16765. doi: 10.1371/journal.pone.0016765

PubMed Abstract | CrossRef Full Text | Google Scholar

Whisson, S. C., Boevink, P. C., Moleleki, L., Avrova, A. O., Morales, J. G., Gilroy, E. M., et al. (2007). A translocation signal for delivery of oomycete effector proteins into host plant cells. Nature 450, 115–118. doi: 10.1038/nature06203

PubMed Abstract | CrossRef Full Text | Google Scholar

Yadav, V., Kumar, M., Deep, D. K., Kumar, H., Sharma, R., Tripathi, T., et al. (2010). A Phosphate transporter from the root endophytic fungus Piriformospora indica plays a role in phosphate transport to the host plant. J. Biol. Chem. 285, 26532–26544. doi: 10.1074/jbc.M110.111021

PubMed Abstract | CrossRef Full Text | Google Scholar

Zuccaro, A., Lahrmann, U., Güldener, U., Langen, G., Pfiffi, S., Biedenkopf, D., et al. (2011). Endophytic life strategies decoded by genome and transcriptome analyses of the mutualistic root symbiont Piriformospora indica. PLoS Pathog. 7:e1002290. doi: 10.1371/journal.ppat.1002290

PubMed Abstract | CrossRef Full Text | Google Scholar