Bioinformatics

A detailed record of the bioinformatic and statistical analyses performed in this study is provided in S1 File. Here we briefly describe each step of these analyses.

Strains and growth conditions

Escherichia coli strains were grown overnight in Lysogeny Broth (LB) or on LB agar supplemented with 100 μg/ml ampicillin or 50 μg/ml kanamycin at 37°C, as described by [50]. Agrobacterium tumefaciens strains were grown for one day in LB broth or for two days on LB agar supplemented with 50 μg/ml kanamycin at 30°C, as previously described [51]. Saccharomyces cerevisiae strains were grown at 30°C on YPDA (2% peptone, 1% yeast extract 0.01% adenine hemisulfate, 2% glucose, 2% agar; adjusted to pH 5.7). For S. cerevisiae complementation assays cells were plated on CMD tryptophan dropout medium (0.67% yeast nitrogen base, 0.064% W/L dropout supplement, 0.00033% leucine, 2% sucrose, 0.1% glucose, 2% agar, pH 5.7). To test for secretion of the SUC2 secretion signal fusion protein, fresh colonies of S. cerevisiae were streaked on CMDRAA medium (0.67% yeast nitrogen base, 0.064% W/L dropout mixture, 0.00033% leucine, 0.00033% tryptophan, 2% raffinose, 2 μg/ml antimycin A, 2% agar, pH 5.8) and compared with growth on YPDA control plates [52, 53]. E. festucae strains were grown on 2.4% Potato-Dextrose Agar (PDA) supplemented with 150 μg/ml hygromycin B or 250 μg/ml geneticin or in 2.4% Potato-Dextrose Broth (PDB) for up to seven days [54, 55]. For microscopy analyses, strains were grown on 3% water agar overlaid with 1.5% water agar [40]. All strains used in this study can be found in S2 Table.

Plant growth and endophyte inoculation

E. festucae strains were inoculated into endophyte-free seedlings of perennial ryegrass (L. perenne cv Samson) using the method previously described [56]. Inoculated plants were grown in root trainers at 22°C in a controlled growth room with a photoperiod of 16 h light (approximately 100 μE/m²/s) and 8 h dark. N. benthamiana and N. tabacum were grown at approx. 28°C in a controlled growth room with a photoperiod of 16 h light (approximately 100 μE/m²/s) and 8 h dark for 6–7 weeks. For agroinfiltration experiments (see below), plants were transferred to a greenhouse and grown at 25°C with natural lighting.

DNA isolation, PCR and sequencing

High quality genomic DNA was extracted from freeze-dried mycelium of E. festucae as previously described [57]. Plasmid DNA was extracted from E. coli using the High Pure plasmid isolation kit (Roche). DNA resolved by agarose gel electrophoresis was purified using the Wizard SV Gel and PCR Clean-Up System (Promega) or the Zymoclean Gel DNA Recovery kit (Zymo Research). PCR amplification of short DNA products was conducted with the OneTaq (NEB) polymerase according to the manufacturer’s instructions. Each reaction was set up as follows: 1× Standard OneTaq Reaction Buffer, 200 μM dNTPs, 0.2 μM for each forward and reverse primer, 0.025 units/μl OneTaq Polymerase and 20–300 ng of template DNA. If crude DNA was used as a template, 3% DMSO was added. PCRs were performed with the following Thermocycler (Eppendorf) settings: 1 min at 94°C for initial denaturation, then 30–35 cycles of 30 s at 94°C (denaturation), 30 s at 45–65°C (annealing), 1 min/kb at 68°C (extension) followed by 3–5 min at 68°C (final extension). Amplification of DNA fragments for Gibson Assembly [58] was performed with Phusion High Fidelity polymerase (ThermoFisher Scientific). Each reaction was set up as follows: 1× Phusion HF buffer, 200 μM dNTPs, 0.5 μM of each forward and reverse primer, 0.02 U/μl Phusion polymerase and 20–300 ng of template DNA. PCRs were performed with the following Thermocycler settings: 1 min at 98°C for initial denaturation, then 30–35 cycles of 30 s at 98°C (denaturation), 30 s at 59–68°C (annealing), 30 s/kb at 72°C (extension), followed by 3–5 min at 72°C (final extension). Where long primers (>30 bp) were used, a 2-step PCR was performed with the same reaction set up, but with different cycler settings: 1 min at 98°C for initial denaturation, then 5 cycles of 30 s at 98°C (denaturation), 30 s at 55°C (annealing), 30 s/kb at 72°C (extension), followed by 25 cycles of 30 s at 98°C (denaturing) and 30 s/kb at 72°C (extension). Subsequently the reaction was incubated for 3–5 min at 72°C (final extension). PCR products were purified using the Wizard SV Gel and PCR Clean-Up System (Promega). Primers were sourced from Integrated DNA Technologies. Primer sequences can be found in the S2 Table. Sequencing reactions were performed using the Big-DyeTM Terminator Version 3.1 Ready Reaction Cycle Sequencing Kit (Applied BioSystems, Carlsbad, California, USA), and separated using an ABI3730 genetic analyser (Applied Bio Systems). Sequence data was assembled and analysed using MacVector sequence assembly software, v14.5.2.

Preparation of constructs

The gpiB replacement construct, pBH1, was prepared as follows. Firstly, the 1,639 bp 5' and 1,389 bp 3' flanks of gpiB were amplified from wild type (WT) E. festucae strain Fl1 genomic DNA by PCR using BH1/BH2 and BH3/BH4 primer pairs, respectively. The 1,394 bp hygromycin resistance cassette (PtrpC-hph) sequence was then amplified from pSF15.15 DNA using the hph_F/hph_R primer pair. The 5,483 bp backbone vector, pRS426, was amplified by PCR using the pRS426_F/pRS246_R primer pair. All PCRs were performed with Phusion High-Fidelity DNA polymerase (NEB). The fragments were then assembled via Gibson Assembly [58] and the correct assembly was verified using a diagnostic restriction enzyme digest and sequencing. The replacement constructs for sspM (pBH2), sspN (pBH3) and sspO (pBH4) were generated in the same way. The 1,377 bp 5’ and 1,333 bp 3’ flanks of sspM were amplified with the BH11/BH12 and BH9/BH10 primer pairs, respectively; the 1,431 bp 5’ and 1,433 bp 3’ flanks of sspN were amplified with the BH15/BH16 and BH13/BH14 primer pairs, respectively; and the 1,443 bp 5’ and 1,318 bp 3’ flanks of sspO were amplified with the BH5/BH6 and BH7/BH8 primer pairs, respectively.

The S. cerevisiae complementation vector pSUC2T7M13ORI [52] was fully sequenced using primers BH25 to BH42 and BH61 to BH63. The nucleotide sequences encoding the secretion signals from SspN (54 bp), SspO (54 bp), SspM (54 bp) and GpiB (57 bp) were then amplified from E. festucae strain Fl1 genomic DNA with the BH21/BH22, BH70/BH71, BH68/BH69 and BH64/BH65 primer pairs, respectively, using OneTaq polymerase. In doing so, these primers added a 5’ EcoRI and 3’ XhoI restriction site to each amplified sequence. Due to difficulties in working with small fragments different cloning strategies were effective for the different fragments. The sspN fragment was cloned into the TOPO-TA vector according to the manufacturer’s instructions. Following this cloning step, pSUC2TM13ORI and the TOPO-TA vector containing the sspN secretion signal-encoding nucleotide sequence were digested with EcoRI and XhoI restriction enzymes and purified. The pSUC2TM13ORI vector backbone and secretion signal-encoding nucleotide sequence were then ligated using T4 ligase to generate pBH7. The gpiB, sspM and sspO secretion signal-encoding nucleotide sequences were directly digested with EcoRI and XhoI and purified, omitting the sub-cloning step into the TOPO-TA vector. Subsequently the nucleotide sequences were then directly ligated into EcoRI and XhoI digested pSUCTM13ORI generating pBH5 (gpiB), pBH11 (sspM) and pBH9 (sspO) respectively.

The four overexpression constructs were generated by Gibson Assembly [58] of two fragments, respectively. The 2,844 bp backbone fragment, containing a hygromycin resistance cassette, was amplified from pBH12 with the primer pair BH75/76. The nucleotide fragments encoding gpiB, sspM, sspN or sspO downstream of the Ptef promoter as well as an ampicillin resistance gene (bla) and an oriT were amplified from pBH14, pBH18, pBH21 or pBH24 respectively. For amplification, the primer pairs BH72/BH120 (3,476 bp), BH72/BH121 (3,725 bp), BH72/122 (3,525 bp) or BH72/BH123 (3,493 bp) were used, respectively. Assembly of the respective fragments generated the plasmids pBH29 (gpiB), pBH30 (sspM), pBH31 (sspN) and pBH32 (sspO).

Constructs encoding the genes of interest, C-terminally fused to an 8xHis tag, were generated via Gibson Assembly [58]. Again, each plasmid was assembled from two fragments. The 2,488 bp backbone was amplified from pBH30 using the BH176/BH75 primer pair. The forward primer, BH176, was designed in a way that it added the 8xHis tag followed by a stop codon to the fragment. The sspM-, sspN- and sspO- encoding fragments were amplified from pBH30, pBH31 and pBH32 with the primer pairs BH72/BH177 (3,728 bp), BH72/BH178 (3,528 bp) and BH72/179 (3,496 bp) respectively. The reverse primers BH177/BH178/BH179 were designed in such a way that the stop codon was removed and an overhang to the 8xHis tag was generated. The gpiB-containing fragment was generated based on a previously generated construct, pBH34. To prevent the loss of the 8xHis tag due to the addition of the GPI anchor at the omega site [59], the 8xHis tag was added 30 bp upstream of the omega site. To this end, the vector was assembled in two pieces amplified from pBH34: the 2,823 bp fragment amplified by PCR with BH181/BH75 primer pair containing the C-terminus of gpiB as well as the hygromycin resistance cassette, and the 3,377 bp fragment amplified by PCR with the BH72/BH180 primer pair encoding an ampicillin resistance gene, an OriT and the gpiB N-terminus. The primers BH180 and BH181 generated the 8xHis tag and thereby overhangs with each other. This generated the plasmids pBH56 (gpiB), pBH57 (sspM), pBH58 (sspN) and pBH59 (sspO).

For the localization constructs, the plasmid pBV579 (PN4241) encoding mCherry fused to a T-virus nuclear localization signal, was used [60]. The constructs were generated via Gibson Assembly [58] from three different fragments, generating C-terminal translational fusions between the ssp of interest and mCherry-NLS separated by a (GGGS)x2 linker to facilitate independent folding of the protein of interest and mCherry. All constructs incorporated the native ssp promoter. The 5,060 bp backbone of the vector was amplified by PCR from pBH12 with the BH76/BH78 primer pair. The 834 bp mCherry-NLS fragment was amplified by PCR from pBV579 with the BH79/BH80 primer pair, where the primer BH79 added the linker. The sspM, sspN and sspO and the corresponding promoter encoding fragments were amplified by PCR from WT genomic DNA using the primer pairs BH88/BH86 (827 bp), BH91/BH89 (977 bp) and BH93/BH94 (798 bp) respectively. Assembly of the fragments generated the plasmids pBH19, pBH22 and pBH25. All plasmids can be found in S2 Table and all primers in S3 Table.

Transformation of organisms

Chemically competent E. coli DH5α were transformed by heat-shock for 1 min at 42°C, followed by a 2 min incubation step on ice. Cells were allowed to recover for 1 h at 37°C in SOC medium and subsequently plated on LB agar containing ampicillin or kanamycin. S. cerevisiae YTK12 cells were made competent using the lithium acetate method [61], transformed by heat-shock for 30 min at 40°C [62] and plated on defined CMD tryptophan dropout medium (see above). A. tumefaciens GV3101 [63] cells were made competent and transformed by electroporation (25 mF, 2.5 kV, 200 Ω) [64]. Cells were allowed to recover in SOC medium and then plated on LB agar containing kanamycin. E. festucae Fl1 protoplasts were generated as previously described [65]. Protoplasts were transformed with up to 5 μg of the construct using the method previously described [66]. Protoplasts were allowed to regenerate overnight on regeneration agar (RG) and overlaid with RG agar containing either hygromycin B or geneticin the next day.

Protein extraction, protein purification and western blotting

For protein extraction, E. festucae strains were grown for at least 3 days in liquid PD at 22°C. Cultures were filtered through a nappy liner, washed, and snap frozen in liquid nitrogen and ground to a fine powder. Depending on the amount of mycelium, 400–800 μl of lysis buffer (50 mM NaH₂PO₄, 300 mM NaCl, 10 mM imidazole, 0.1% (v/v) IGEPAL CA360, 0.2 mM PMSF, 10 μl/ml protease inhibitory cocktail (Sigma Aldrich), 5 mM β-mercaptoethanol) was added and samples were vortexed for 10 min. Subsequently, samples were centrifuged at 14,000 g for 15 min at 4°C and the supernatant was stored at -20°C. The growth medium of each strain (50–80 ml) was collected and filtered through a 0.45 μm filter. Samples were concentrated to approx. 2 ml with Vivaspin 20 MWCO 30,000 spin columns (GE Healthcare Life Sciences) according to the manufacturer’s instructions and washed twice with 10 ml lysis buffer. Samples were stored at -20°C.

The protein purification was performed with Ni-NTA spin columns (Qiagen) according to the manufacturer’s instructions with the exception of the elution buffer (50 mM NaH₂PO₄, 300 mM NaCl, 10–500 mM imidazole, 0.1% (v/v) IGEPAL CA360), 0.2 mM PMSF, 10 μl/ml protease inhibitory cocktail (Sigma Aldrich)). Samples were loaded onto 15% (w/v) SDS polyacrylamide gels, electrophoresed at 100 V for 1.5 h then electrophoretically transferred at 30 V for 1 h to PMSF membranes (Roche). The primary antibody, rabbit α-His (Abcam, ab9108), was used in a 1:2,000 dilution and the secondary goat α-rabbit-HRP (Abcam, ab6721) in a 1:10,000 dilution. Detection was performed with the Amersham ECL western blotting detection reagent (GE Healthcare Life Sciences).

For the verification of Ssp and GpiB production in N. benthamiana, total protein was extracted from the infiltrated area. First the tissue was snap frozen, then ground to a fine powder in liquid nitrogen and subsequently resuspended in an equal volume of GTEN buffer (10% glycerol, 100 mM Tris pH 7.5, 1 mM EDTA, 150 mM NaCl, 10 mM DTT, 0.2% IGEPAL CA360, 10 μl/ml protease inhibitory cocktail (Sigma Aldrich), 1% PVP). Afterwards, samples were centrifuged at 14,000 rpm for 15 min at 4°C and the supernatant was stored at -20°C. Samples were loaded onto a 15% SDS polyacrylamide gel and transferred onto PMSF membranes (Roche) as described above. The primary antibody, a mouse α-FLAG antibody (Sigma, F6165), was used in a 1:2,000 dilution followed by the secondary goat α-mouse–HRP (Santa Cruz Biotechnology, Dallas, TX, USA) antibody in a 1:1,000 dilution.

RNA extraction and qPCR

For the determination of the gene copy number, high quality gDNA was extracted as described above and qPCR was performed with SYBR Green (Invitrogen) on a LightCycler 480 System (Roche) as per the manufacturer’s instructions. Each sample was analysed with two technical replicates. The single copy genes hepA (EfM3.043690) and pacC (EfM3.009480) were used as reference genes and the copy number was calculated relative to WT as described previously [67].

For the determination of relative expression levels, RNA was extracted from freeze-dried mycelium using TRIzol reagent (Invitrogen). Subsequently, cDNA synthesis was performed with the QuantiTect Reverse Transcriptase kit (Quiagen). The qRT-PCR was performed as described above. Each sample was analysed with two technical replicates. The genes coding for translation elongation factor 2 (EF-2, EfM3.021210) and 40S ribosomal protein S22 (S22, EfM3.016650) were chosen as reference genes as previously described [68]. The expression level was calculated relative to WT as described previously [67]. All primers used for qPCR and qRT-PCR can be found in the S3 Table.

Analysis of transmission of E. festucae mutants into L. perenne seeds

Twenty endophyte free seedlings of L. perenne cv. Samson were inoculated with three independent deletion strains of gpiB (T111, T133, T148), sspM (T52, T99, T163), sspN (T10, T30, T52) and sspO (T78, T195, T210) [56, 69]. Twenty seeds were inoculated with PD agar as mock control. Plants were grown in root trainers in the greenhouse for 7 weeks at 20°C with a photoperiod of 16 h of light and tested for presence of the endophyte by immunoblotting [70]. Five immunoblot positive plants of each strain were transferred to new pots 10 weeks post-infection and grown in the greenhouse for additional two weeks. For vernalisation, plants were transferred to a growth cabinet and cultivated for 7 weeks at 6°C with a short-day photoperiod of 8 h light and 16 h dark. Starting from four weeks until ten weeks after vernalisation, plants produced inflorescences. Ovaries were collected, stored in 95% EtOH and stained [69] when pollen was visible and ovaries mature. Stained ovaries were stored in 70% glycerol until microscopic observation. Seeds were collected, dried and stored in the fridge until further use. For microscopy and immunoblotting of seeds, the seeds were surface sterilised [56, 69], germinated on wet filter paper overnight and cross sections used for immunoblotting.

Microscopy

For microscopy of E. festucae culture growth, a small piece of a fresh colony was inoculated on the edge of a glass slide covered with a thin layer of 1.5% H₂O agar placed on an agar plate with 3% H₂O agar. Strains were incubated for 6 days before examination with an Olympus IX71 inverted fluorescence microscope using the filter sets for DIC and CFW/DAPI. For staining of the cell wall, a drop of a 3 mg/ml of Calcoflour White was added to the sample just before microscopy.

For the examination of growth and morphology of hyphae in planta, pseudostem tissue was stained with aniline blue diammonium salt (Sigma) and Wheat Germ Agglutinin conjugated to AlexaFluor488 (WGA-AF488, Molecular Probes/Invitrogen). First, infected tissue was incubated in 100% EtOH overnight at 4°C followed by an incubation in 10% KOH overnight at 4°C. Samples were washed at least 3 times with PBS (pH 7.4) before incubation in the staining solution (0.02% aniline blue, 10 ng/ml WGA-AF488, 0.02% Tween-20 (Invitrogen) in PBS (pH 7.4)) for 10 min. Samples were vacuum-infiltrated with the staining solution for 30 min and then stored at 4°C until analysis. Examination of these samples was performed with a Leica SP5 DM6000B confocal microscope (488 nm argon and 561 nm DPSS laser, 40× oil immersion objective, NA = 1.3) (Leica Microsystems). For TEM pseudostem samples were fixed with 3% glutaraldehyde and 2% formaldehyde in 0.1 M phosphate buffer, pH 7.2 for 1 h, as described previously [71]. The fixed samples were examined with a Philips CM10 TEM and the images were acquired using a SIS Morada digital camera. Sections of the resin-embedded samples were also stained with 0.05% toluidine blue in phosphate buffer and heat-fixed at approx. 100°C for 10 s. These samples were examined with a Zeiss Axiophot Microscope with Differential Interference Contrast (DIC) Optics and Colour CCD camera.

For the in planta localization of the Ssp-mCherry-NLS fusion proteins, un-fixed pseudostem samples were examined with a Leica SP5 DM6000B confocal microscope (488 nm argon and 561 nm DPSS laser, 40× oil immersion objective, NA = 1.3).

Preparation of binary vectors, agroinfiltration and suppression assay

All binary backbone vectors for transformation into Agrobacterium are listed in S2 Table. The plasmids pBH44-47 were generated via Golden Gate cloning using pICH86988 as the backbone. The nucleotide sequences of gpiB, sspM, sspN and sspO were amplified by PCR without their native secretion signal from WT E. festucae cDNA with primer pairs adding additional base pairs for the necessary overhang and a BsaI restriction site (gpiB: BH165/BH166, sspM: BH167/BH168, sspN: BH170/BH171, sspO: BH172/BH173) as described. The N. tabacum secretion signal PR1α was obtained from pUC19B (S. Marillonet, pers.comm.). The digestion and ligation were conducted either in one step or in two separate steps. The one-step reaction was performed in a total volume of 20 μl with 1 μl T4 ligase (NEB) and 1 μl BSA (NEB) and equimolar amounts of all three inserts (approx. 50 ng total). The reaction was performed in a Thermocycler (Eppendorf) with the following settings: 25 cycles of 37°C for 3 s and 16°C for 4 s, followed by 5 s inactivation at 50°C and 80°C each. For the two-step reaction, the digest was performed in a volume of 10 μl with 1 μl BSA (NEB) and equimolar amounts of each insert. The reaction was performed at 37°C for 3 h. Subsequently the reaction was inactivated by heating to 50°C. For the ligation, the volume was topped up to 20 μl per reaction including 1 μl T4 ligase (NEB). The reaction was incubated at 16°C in a Thermocycler (Eppendorf) overnight followed by an 80°C inactivation step. A diagnostic restriction digest and DNA sequencing confirmed the sequence of all vectors. Electro-competent A. tumefaciens GV3101 cells were generated and transformed as described. Cells were allowed to recover in SOC medium and subsequently plated on LB agar containing kanamycin. To perform the infiltrations, fresh strains were inoculated in 3 ml LB medium with kanamycin and incubated at 30°C overnight. The next day, cultures were spun down and resuspended in 1 ml infiltration buffer (10 mM MgCl₂, 10 mM MES-KOH, 100 μM acetosyringone). These cultures were adjusted to an OD₆₀₀ of 0.4 in the necessary amount of infiltration buffer (usually 5–10 ml) and incubated at room temperature for at least 3 h before infiltration. To confirm the expression of each of the constructs, total protein was extracted from infiltrated N. benthamiana tissue and a western blot was performed.

For HR suppression assays A. tumefaciens strains carrying plasmids encoding the potential suppression gene pBH44 (gpiB), pBH45 (sspM), pBH46 (sspN), pBH47 (sspO), pBIN-Plus-Avr3a (suppression control), pICH86966-N-3xFlag-GFP (control), pBC302-3-R3a (HR control) were infiltrated 24h before infiltration with pBC302-3-INF1 and pBIN-Plus-Avr3a (HR control).

Candidate effectors of E. festucae

The recent availability of the complete telomere-to-telomere genome sequence of E. festucae strain Fl1, which is 35 Mb in size and encodes 8,465 predicted genes on seven chromosomes [26], provided us with the opportunity to study the organization, structure and genome context of genes encoding candidate effector proteins. First, we established which of the 8,465 predicted genes likely encode secreted proteins. For this purpose, we defined a secreted protein as any protein with a predicted amino N-terminal secretion signal, as determined using the SignalP server, that targets the protein outside of the fungal plasma membrane [44]. This definition does not exclude those proteins with a predicted transmembrane domain or GPI anchor modification site. In total, 682 genes (8.1%) were predicted to encode a secreted protein. We then analysed which of the 682 predicted secreted proteins encode candidate effectors using the EffectorP server, which predicts effectors using a machine learning approach [41]. In addition, we applied a size cutoff of ≤200 amino acids, as most fungal effectors fall within this range [72]. Out of 175 predicted secreted proteins meeting this length requirement, 141 were predicted to be candidate effectors by EffectorP. For subsequent analyses the 8,465 predicted proteins were subdivided into ‘effector candidates’ (n = 141), ‘secreted’, comprising all putatively secreted proteins that are not classified as effector candidates (n = 541), and ‘non-secreted’ made up of all putatively non-secreted proteins (n = 7,783) (S4 Table).

To gain further insight into the possible functions of the 141 effector candidates, and to determine which of these predicted proteins have homologs across the Sordariomycetes, a BLASTp analysis was performed against fungal reference proteins at NCBI. Of the 141 effector candidates, 83 were found to have sequence homology to proteins present in the NCBI database (E-value cut off of ≤1e-10), but 56 of these were to uncharacterized or hypothetical proteins. Among the ‘hits’ to characterized proteins were ten cell wall-associated proteins, including hydrophobins and carbohydrate-binding proteins, two toxins and other small secreted proteins (S4 Table). The majority of ‘hits’ were to proteins from species in the Hypocreales (21 Claviceps spp., 21 Metarhizium spp., 14 Pochonia spp., 6 Moelleriella spp., 6 Ustilaginoiea spp.), with the remaining hits to proteins from other species within the Sordariomycetes. For 58 of the effector candidates, no homologs could be identified (E-value>1e-10), but analysis against a custom made Clavicipitaceae endophyte database (epichloe.massey.ac.nz)[47] found potential homologs for 20 of these proteins. The remaining 38 Ssps are apparently unique to Epichloë spp. (S4 Table).

Given many fungal effectors are cysteine-rich, a property that enables the formation of disulfide bonds and protein folding to maintain structural integrity in the protease-rich apoplast [73, 74], the frequency of cysteine residues in the effector candidates was compared with that of the secreted and non-secreted categories. As expected the candidate effectors were significantly more cysteine-rich (3.6% of residues) than either secreted (frequency = 1.7%, P = <1e-18) or non-secreted (frequency = 1.4%, P < 1e-18) (S1 File).

In smut fungi, secreted genes are predominantly arranged in clusters within the genome and are highly upregulated during tumor formation [75, 76]. We therefore tested whether the genes encoding the E. festucae effector candidates were clustered by mapping them to each of the seven chromosomes (Fig 1A). From this low-resolution analysis, it appears that the genes encoding effector candidates of E. festucae are evenly distributed throughout the genome. This conclusion was supported by an analysis comparing the within category gene distances, which concluded that genes encoding effector candidates are not clustered in the E. festucae genome (Fig 1A). Of all the genes encoding candidate effectors, only eight (four gene pairs) were found within 1 kb of each other. In fact, the mean distance between candidate effector genes was not significantly different from that expected from a random subset of the 141 genes (P = 0.236).

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Fig 1. Physical properties of genes encoding effector candidates in E. festucae.

(A) Location of genes encoding effector candidates (black circles) on the seven chromosomes of E. festucae strain Fl1. The blue line indicates AT richness in a 1,000 bp window. (B) Distance of each E. festucae gene from AT-rich regions (isochores). (C) Distance of each E. festucae gene from telomeres. (D) Distance of each E. festucae gene from MITES. Genes are divided into the categories ‘non-secreted’ (n = 7783), ‘secreted’ (n = 541) and ‘effector candidates’ (n = 141).

https://doi.org/10.1371/journal.pone.0209463.g001

E. festucae is one of several filamentous fungi that has a genome comprised of distinct gene-poor AT isochores and gene-rich GC isochores [21, 26]. Because the AT-rich regions are subject to an unusually high mutation rate [77–80] they are frequently referred to as ‘birthplaces’ for new genes such as those encoding effectors and secondary metabolites [81]. In Leptosphaeria maculans 20% of all genes in AT isochores encode small secreted proteins (SSPs, effector candidates), whereas they make up just 4.2% of all genes in GC isochores [21]. In contrast to L. maculans, there was no enrichment of genes encoding effectors in or near to AT isochores of the E. festucae genome (P = 0.369) (Fig 1B). Similarly, there was no enrichment of genes in the secreted category in AT isochores (P = 0.812) (Fig 1B). Indeed, of the 548 genes located in or within 1,000 bp of an AT isochore, only 1.5% and 4.7% encoded a protein from the candidate effector and secreted categories, respectively.

Given some fungal effector genes, such as the AVR-Pita gene from Magnaporthe oryzae [82], are found in close proximity to telomeres, we took advantage of the telomere-to-telomere E. festucae genome sequence to determine if genes encoding candidate effectors are located close to telomeres. These regions of the genome are also subject to higher mutation rates than the remainder of the genome and potential sites for the evolution of environment adaptation genes such as those encoding effectors [83, 84]. However, genes encoding effector candidates were not significantly closer to telomeres than other genes present in the E. festucae genome (P< 0.787) (Fig 1C).

Transposable elements are increasingly seen as important regulators of gene expression [85, 86], and miniature inverted-repeat transposable elements (MITES) have been postulated to play a role in the expression of E. festucae genes in planta [24, 26]. For this reason, the distance between genes encoding effector candidates and MITES was analyzed in the E. festucae genome. This analysis revealed that genes encoding effector candidates are more likely to contain a MITE within 2 kb of their transcription start site than non-secreted proteins (P = 3.56e-18, Fig 1D). Genes encoding other secreted proteins were also more likely to contain a MITE immediately upstream of their transcription start site than non-secreted proteins (P = 1.66e-7). No particular MITE family is over-represented within 2 kb of these genes.

Apart from the physical organization of effector genes within fungal genomes, the expression of these genes often follows distinct host colonization patterns and are generally more highly expressed in planta than in axenic culture [72, 87, 88]. We therefore analysed the transcript expression profiles of the three different gene categories between E. festucae grown in planta and in axenic culture (S5 Table). Genes encoding effector candidates were significantly more highly expressed in planta (mean log₂ fold difference = 1.20, P< 2e-16) (Fig 2A). Other secreted proteins were also moderately more highly expressed in planta (mean log₂ fold difference = 0.20, P = 0.004) (Fig 2A).

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Fig 2. Analysis of gene expression in WT E. festucae and symbiotic mutants of E. festucae.

(A) Log₂ fold difference in gene expression between WT E. festucae grown in planta and in culture. (B) Log₂ fold difference in gene expression between WT and a hepA deletion strain grown in culture. (C) Log₂ fold difference in gene expression between WT and ΔnoxA, ΔproA, ΔsakA and ΔhepA strains grown in planta. Number of genes in each category: ‘non-secreted’, n = 7783; ‘secreted’, n = 541; and ‘effector candidates’, n = 141.

https://doi.org/10.1371/journal.pone.0209463.g002

Given genes encoding effector candidates are preferentially silenced in axenic culture compared to in planta we examined whether this might be due to the chromatin state as shown for L. maculans where RNAi-induced silencing of DIM-5, a histone H3 lysine 9 trimethyl transferase, and heterochromatin protein 1 (HP1), led to de-repression of effector gene expression in axenic culture [89]. We therefore compared expression of E. festucae genes encoding effector candidates in a hepA (homolog of HP1) mutant versus wild type. We found candidate effector genes were moderately more highly expressed in the hepA mutant (mean log₂ fold difference = 0.310, P = 4.13e-9) (Fig 2B). For some genes, this change in gene expression was substantial. Eleven percent of candidate effectors showed log₂ fold difference in expression greater than 2, a significantly higher proportion than observed in larger secreted (1.5% of genes, P = 5e-14) or non-secreted proteins (3% of genes, P = 1e-4).

Previously we showed that disruption of the usually asymptomatic interaction between L. perenne and E. festucae by infecting the host with symbiotic mutants of E. festucae results in major changes in the fungal transcriptome [47]. We therefore tested whether effector candidate gene expression changed in the ΔsakA, ΔnoxA, ΔproA and ΔhepA symbiotic mutants using previously generated transcriptome data sets [47](Tetsuya & Scott, personal communication). Generally, genes encoding effector candidates were upregulated in each of the dysfunctional interactions (mean difference of 0.411 log2 fold units, P = 5.28 x 10–8) (Fig 2C). A closer investigation showed that ten genes encoding effector candidates SspB-SspK were consistently upregulated across all four different mutant interactions and three genes encoding effector candidates SspM-SspO were consistently down regulated [47](Tetsuya & Scott, personal communication).

In summary, the genes encoding effector candidates from E. festucae do not show a distinct distribution pattern as has been described for some other fungi, but seem to be evenly dispersed throughout the genome. These genes do not cluster, and are not preferentially located in AT-rich isochores or telomeres. However, these genes are enriched with respect to their proximity to MITES. As found for many other fungi, a significant number of genes encoding effector candidates from E. festucae are preferentially upregulated in planta. Furthermore, many of these genes are upregulated in symbiotic mutants of E. festucae that disrupt the restrictive pattern of growth observed for WT E. festucae.

Sequence analysis of downregulated effector candidates

To gain further insight into the role of E. festucae effectors in the symbiotic interaction with L. perenne, the three genes described above (sspM, EfM3.016770; sspN, EfM3.062700; and sspO, EfM3.014350) that were found to be downregulated in all four symbiotic mutant interactions, were selected for genetic analysis [47](Tetsuya & Scott, personal communication). The fact that they were among the top 100 genes upregulated in planta compared to axenic culture was an additional criterium for selecting these three genes (Fig 2A, S4 Table). A fourth gene, gpiB (EfM3.018200), encoding a putative GPI-anchored protein, was also selected for functional analysis because it had an identical expression profile to sspM, sspN and sspO [47], and because GPI-anchored proteins are known to have important roles in fungal virulence [42, 43].

cDNA sequencing confirmed that the proposed gene models for each of these four genes were correct. In the case of sspN, where two alternatively spliced forms were proposed the second of these (mRNA-2) corresponded to the cDNA sequence. The gpiB gene (EfM3.018200) is predicted to encode a protein of 126 aa with an unmodified MW of 12.61 kDa (8.7 kDa without secretion signal and C-terminus beyond the omega cleavage site), while the sspM gene (EfM3.016770) is predicted to encode a protein of 177 aa with an unmodified MW of 18.87 kDa (17.1 kDa without secretion signal). The protein encoded by sspN (EfM3.062700) is predicted to be 127 aa in length with an unmodified MW of 14.98 kDa (13.19 kDa without secretion signal), while the protein encoded by sspO (EfM3.014350) is predicted to be 104 aa in length with an unmodified MW of 11.11 kDa (9.4 kDa without secretion signal) (Fig 3).

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Fig 3. Schematic representation of the small secreted proteins SspM, SspN, SspO (effector candidates) and the GPI-anchored protein GpiB and their corresponding genes.

GpiB (EfM3.018200) is encoded by a 381 bp gene that lacks introns, and is predicted to encode a protein of 126 aa. The gene encoding the predicted 177 aa SspM (EfM3.016770) is 630 bp in size and contains one intron. SspN (EfM3.062700) is encoded by a gene of 430 bp, with one intron, and encodes a predicted protein of 127 aa. SspO (EfM3.014350) is encoded by a 398 bp gene, containing one intron, and is predicted to encode a protein of 104 aa. N-terminal secretion signals (SS) are indicated by blue boxes and post-translational modifications and structural motifs by pink bars (N-glycosylation), grey bars (GPI anchor modification site), facing arrows (protease cleavage site), hollow ovals (repeats) and small black bars (cysteine residues).

https://doi.org/10.1371/journal.pone.0209463.g003

Analysis of the selected protein sequences with InterproScan [90], SMART [91], T-Reks [92] and HHPRED [93] did not identify any conserved domains with known function, but did predict a number of different structural features and secondary modifications (Fig 3). GpiB contains a predicted N-glycosylation motif as well as a putative C-terminal GPI anchor. The SspM protein contains a possible pre-pro domain ending with a classical LxKR kexin cleavage site motif and a predicted N-glycosylation site. SspN is a repeat-containing protein, consisting of 7.5 almost perfect repeats of 15 aa. Like SspM, it also contains a putative kexin cleavage site. Analysis of the SspO sequence did not reveal any obvious structural features. Both SspM and SspO are rich in cysteines; SspO containing eight and SspM containing six downstream of the cleavage site, whereas SspN and GpiB are cysteine-free (Fig 3).

A BLASTn analysis of the four selected genes revealed a patchy distribution within the Epichloë species, with only gpiB present in all analyzed genomes available on the Kentucky Endophyte Database [94]. The observed distribution patterns did not correlate with specific hosts or the sexual phenotype of the fungus (S6 Table). Alignment of the protein sequences of interest with the corresponding homologs in other Epichloë species showed that GpiB and SspO are highly conserved (S1A and S1D Fig). Interestingly, SspM was highly conserved from the N-terminus to the proposed kexin cleavage site and less conserved beyond this site (S1B Fig). The repeat structure of SspN was also conserved, with homologs mainly differing in their number of repeats (S1C Fig). A BLASTp analysis identified homologs of Ssps and GpiB in species outside of Epichloë (S4 Table); however, none of these are functionally characterized.

GpiB, SspM, SspN and SspO are secreted

To experimentally verify secretion of the three selected candidate effectors and the GPI anchored protein, GpiB, a complementation assay was performed in S. cerevisiae. The nucleotide sequence encoding the secretion signal predicted by SignalP was ligated in frame to the N-terminus of the S. cerevisiae invertase SUC2 encoded on the pSUC2T7M13ORI vector [52]. These constructs were then transformed into the SUC2-negative yeast strain YTK12 and tested for growth on CMDRAA medium, which contains raffinose as the sole carbon source. All four test strains expressing the secretion signal-Suc2 fusion protein grew on this medium whereas the strain expressing Suc2 without a secretion signal and the untransformed YTK12 did not (Fig 4). These results indicate that the signal peptides of SspM, SspN, SspO and GpiB are sufficient to mediate secretion in S. cerevisiae.

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Fig 4. Analysis of the GpiB, SspM, SspN and SspO secretion signals in a S. cerevisiae complementation assay.

YTK12 strains transformed with pSUC2T7M13ORI encoding SUC2 transcriptionally fused to gpiB, sspM, sspN or sspO secretion signal nucleotide sequence, as well as the empty vector and YTK12-only controls. Only strains expressing the secretion signal-Suc2 fusion proteins were able to grow on defined medium with raffinose as carbon source (CMDRAA). SS, secretion signal. All strains grew on the control plates containing YPDA media.

https://doi.org/10.1371/journal.pone.0209463.g004

Analysis of secretion and processing of GpiB, SspM, SspN and SspO in E. festucae

As discussed above, many effectors are post-translationally processed (e.g. by proteolytic cleavage) or modified (e.g. by glycosylation) to their final form. To verify the secretion of these proteins in E. festucae, and to check if they are modified (Fig 3), His-tagged fusions of GpiB, SspM, SspN and SspO were purified from extracts of E. festucae mycelia (intracellular form), as well as from the liquid culture medium (extracellular form), separated by PAGE and analyzed by western blotting (Fig 5). All four proteins were present in extracts from fungal mycelia. The 13 kDa band for GpiB is larger than the predicted His-tagged size of 9.8 kDa, possibly due to the addition of the GPI anchor and/or modification by N-glycosylation. A band corresponding to SspN was detected at approx. 14 kDa, which agrees with the predicted His-tagged size of 14.31 kDa for the unprocessed protein, indicating that under the growth conditions used, this protein is not cleaved, even though it has a predicted kexin cleavage site. The signal for SspO was very faint, and slightly larger (12 kDa) than the predicted His-tagged size of 10.5 kDa for this protein. In contrast, two bands of 20 and 16 kDa were detected for SspM, with the band of higher molecular weight being very faint. SspM has a predicted His tagged size of 18.22 kDa in the unprocessed form (with its predicted pro-domain) and 12.7 in the cleaved form (without its predicted pro-domain). Taking into account a probable increase in size due to the predicted N-glycosylation, the sizes observed for SspM agrees with the predicted sizes of the kexin-unprocessed and processed forms, respectively. The presence of additional bands on the western is probably the result of non-specific binding to other proteins present in the crude extract separated on these gels.

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Fig 5. Western blot analysis of GpiB-His, SspM-His, SspN-His and SspO-His extracted from E. festucae mycelia and culture medium.

Genes of interest (gpiB, sspM, sspN and sspO) were translationally fused to an 8x His tag at the C-terminus and constructs were placed under the control of the Ptef overexpression promoter. Total protein was extracted from fungal mycelia and the corresponding growth medium, and His-tagged proteins purified on Ni-NTA spin columns eluted with increasing concentrations of imidazole. Samples were separated on a 15% SDS PAGE gel, transferred to membranes and probed with an anti-His antibody. SspM-His was extracted from E. festucae strains grown in medium buffered to pH 6.5 with 50 mM HEPES. Predicted sizes of proteins were calculated on the basis that each protein lacked the secretion signal and had the 8x His-tag.

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Analysis of the culture medium identified bands for SspO and SspM, but the latter was only detected when the culture medium was buffered to pH 6.5 with 50 mM HEPES. The bands detected for SspO and SspM were the same size as those seen in the mycelial fraction, with the latter again present as a double band. These results suggest that SspO does not contain any secondary modifications and is secreted into the culture medium, whereas SspM is processed at the predicted kexin site. The absence of bands for GpiB and SspN in the culture medium suggest that these proteins are either unstable in the culture medium or remain attached to the fungal hyphae following secretion.

Functional analysis of gpiB, sspM, sspN and sspO

To investigate whether sspM, sspN, sspO or gpiB are necessary for establishing a mutualistic symbiotic interaction, given their expression is downregulated in three different symbiotic mutants [47], each gene was individually deleted in the WT background using a gene replacement approach. Replacement constructs, pBH1–4, were prepared, and PCR-amplified linear fragments of each were transformed into WT protoplasts. Putative gene replacements were identified by PCR screening approximately. 200 independent Hyg^R transformants with primers that flank the site of hph integration. Additional PCR screening with primer sets that amplify the left and right flanks of each of the insertion sites was used to confirm the transformants selected had gene replacements. Southern blot analysis of genomic DNA extracted from these strains identified three independent deletion strains for gpiB (T111, T133, T148), sspM (T52, T99, T163) sspO (T78, T195, T210), and sspN replacement (T10, T30, T52) (S2 Fig).

To determine the phenotype of the deletion strains in culture, the whole colony morphology of each independent deletion strain was compared to that of WT, which is typically circular with white fluffy mycelium that thins and flattens towards the edges. This comparison revealed that the whole colony morphology of each deletion strain was indistinguishable from WT (Fig 6). Given this result, the hyphal morphology was more closely analysed by microscopy. E. festucae WT had smooth hyphal tips with hyphae arranged in bundles that are thicker in the more mature inner zone of the colony. Hyphae of WT had hyphal bridges, which are formed by tip-to-side fusion [40], as well as hyphal coil structures, which are thought to promote conidiophore formation [40]. When stained with Calcofluor white, which preferentially binds to chitin, the cell walls of WT hyphae uniformly fluoresced. Similar to the whole-colony comparison, each of the deletion strains had an indistinguishable phenotype to that of WT, forming hyphal bundles, with occasional hyphal fusion, and coil formation (Fig 6).

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Fig 6. Culture phenotype of WT and deletion mutant strains.

(A)-(D) Representative DIC images captured with the inverted microscope of WT and deletion mutant strains grown on 1.5% water agar for 6 days. (A) Hyphal bundle formation. (B) Hyphal fusion points. (C) Hyphal coils. (D) Hyphal tips. (E) Hyphae stained with Calcofluor white to examine cell wall composition. (F) Colony morphology of WT compared to the deletion strains grown on 2.4% PDA for 7 days. Bar: 20 μm.

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To determine the host interaction phenotype, strains were inoculated into L. perenne seedlings and the phenotype of infected plants examined eight weeks post-planting. At this time point, WT infected plants typically have 2–6 tillers that are up to 50 cm in length (Fig 7). Plants infected with the deletion mutants had the same interaction phenotype as those infected with WT, with no statistically significant difference in either the number or length of tillers (Fig 7). To analyse the cellular phenotype of the infected plants, pseudostem cross sections were fixed and embedded in resin, and slices stained with Toluidine blue. WT-infected samples typically have one to two hyphae per intercellular space and never colonize the vascular bundle tissue (Fig 8). The mutant-infected plants had the same cellular phenotype as WT plants, with one to two hyphae per intercellular space and no hyphae within the vascular bundles (Fig 8). Given these results, samples were then prepared for TEM, to give better resolution of the cellular phenotype. The cellular structure of tissue infected with E. festucae mutants was indistinguishable from WT (Fig 8). In addition, longitudinal leaf sections were infiltrated with wheat germ agglutinin, a chitin-binding lectin, conjugated to AlexaFluor 488 (WGA-AF488), as well as aniline blue, a β-glucan-binding dye, and analysed by confocal laser scanning microscopy (CLSM). Leaves infected with WT typically had one hypha (red pseudocolor, aniline blue) with regularly spaced septa (blue pseudocolor, WGA-AF488) growing between plant cells (Fig 9). These hyphae occasionally branched and where tips of branches meet, fused to establish a hyphal network throughout the leaf tissue (Fig 9). The morphology and growth pattern of the mutant hyphae were indistinguishable from WT (Fig 9).

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Fig 7. Plant phenotype of L. perenne infected with E. festucae WT and gpiB, sspM, sspN and sspO deletion mutant strains.

(A-D) Whole plant phenotype of WT and deletion mutant-infected L. perenne plants 8 weeks post-planting. (E and F) Box plots representing tiller number (E) and length (F) of ryegrass plants 8 weeks post-planting infected with E. festucae WT (n = 6) and ΔgpiB (n = 9/9/5), ΔsspM (n = 10/15/13), ΔsspN (n = 13/8/8) and ΔsspO (n = 7/8/9) mutant strains. One-way ANOVAs were used to test for differences in both plant phenotypes between wildtype and modified strains. In each case the ANOVA was fitted with R and a Bonferroni correction was applied to all p-values to account for multiple testing.

https://doi.org/10.1371/journal.pone.0209463.g007

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Fig 8. Light microscopy and transmission electron micrographs of the in planta cellular phenotype of E. festucae WT and gpiB, sspM, sspN and sspO deletion mutant strains.

(A) Light microscope analysis of fixed L. perenne pseudostem cross sections stained with Toluidine blue. The focus of the section is on the vascular bundles and surrounding regions; Bar = 10 μm. (B) TEM analysis of hyphal growth in the host apoplast; Bar = 2 μm. (C) Magnified transmission electron micrograph of one single hypha; Bar = 1 μm. Representative images from one of the independent mutants for each gene. Red arrows indicate position of hyphae and green arrows epiphyllous hyphae.

https://doi.org/10.1371/journal.pone.0209463.g008

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Fig 9. Confocal depth series images of in planta cellular phenotype of E. festucae WT and gpiB, sspM, sspN and sspO deletion mutant strains.

Infected L. perenne pseudostem samples were stained with aniline blue/WGA-AF488. Hyphae show aniline blue fluorescence of β-glucans (red pseudocolor) and chitin staining of septa with WGA-AF488 (blue pseudocolor). (A) Representative growth of WT and deletion strains in planta (z = 15 μm); Bar = 20 μm. (B) Magnification of the area boxed with white dashed lines in A, showing representative growth of the strains in more detail (z = 15 μm); Bar = 20 μm. (C) Representative hyphal branching and fusion of WT and deletion strains in planta (z = 5 μm); Bar = 10 μm.

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Next we tested whether these mutants could be vertically transmitted into the seeds of L. perenne. Plants infected with each of the individual transformants were vernalized and ovaries collected from flowers for CLSM and seed collected from mature inflorescences to test for endophyte in each of these tissues. Endophyte was shown to be present in ovaries of some of the flowers collected from plants infected with ΔgpiB, ΔsspM and ΔsspN mutants but not ΔsspO (S3 Fig; S7 Table). Seeds of ΔgpiB (2/43), ΔsspM (25/90) and ΔsspN (14/70) were immunopositive indicating that these three mutants were vertically transmitted (S7 Table). However, none of the seeds infected with ΔsspO (0/60) were found to contain endophyte suggesting this mutant was unable to be transferred to the seed.

In summary, deletion of gpiB, sspM and sspN does not result in any obvious culture or plant interaction phenotype, suggesting that the proteins encoded by these genes are not essential for any of these growth processes. Similarly, sspO appears to be dispensable for most of these growth processes but may be important for vertical transmission within the host grass.

Culture and in planta phenotype of overexpression strains

As the deletion of the four genes did not result in any obvious plant interaction phenotype, overexpression (OE) constructs were generated using the translation elongation factor (tef) promoter from Aureobasidium pullulans, which is commonly used for OE studies [37, 67]. Plasmids encoding the gpiB, sspM, sspN and sspO OE constructs (pBH29–32) were prepared and transformed into WT protoplasts and the copy number of 10 independent transformants for each construct determined (S4 Fig). A total of three strains per construct, each with a different copy number, were chosen for further analysis. In addition, the relative expression level of the gene in each of the three independent strains was determined and found to generally correlate with the copy number (S4 Fig). No difference in culture growth or morphology was observed between the OE strains and WT. To test the plant symbiotic phenotype, the OE strains were inoculated into L. perenne seedlings and infected plants examined 8 weeks post-planting. No difference in whole plant (Fig 10) or cellular phenotype (Fig 11) was observed between the OE strains and WT. In summary, these results demonstrate that overexpression of gpiB, sspM, sspN or sspO has no impact on the culture or whole plant interaction phenotype.

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Fig 10. Plant phenotype of Lolium perenne infected with E. festucae WT and gpiB, sspM, sspN and sspO OE strains.

(A-D) Whole plant phenotype of WT and OE strain-infected L. perenne plants 8 weeks post-planting. (E and F) Boxplots representing tiller number (E) and length (F) of ryegrass plants eight weeks post-planting with E. festucae WT (n = 2) and gpiB (n = 2/6/4), sspM (n = 3/2/6), sspN (n = 2/7/3) and sspO (n = 4/4) OE strains. One-way ANOVAs were used to test for differences in both plant phenotypes between wildtype and modified strains. In each case the ANOVA was fitted with R and a Bonferroni correction was applied to all p-values to account for multiple testing.

https://doi.org/10.1371/journal.pone.0209463.g010

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Fig 11. Confocal depth image series of in planta cellular phenotype of E. festucae WT and gpiB, sspM, sspN and sspO OE strains.

Infected L. perenne pseudostem samples were stained with aniline blue/WGA-AF488. Hyphae show aniline blue fluorescence of β-glucans (red pseudocolor) and chitin staining of septa with WGA-AF488 (blue pseudocolor). (A) Representative growth of WT and OE strains in planta (z = 15 μm); Bar = 20 μm. (B) Magnification of the area boxed with white dashed lines in A, showing representative growth of the strains in more detail (z = 15 nm); Bar = 20 μm. (C) Hyphal branching and fusion of WT and OE strains in planta (z = 5 nm); Bar = 20 μm.

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SspM, SspN and SspO localize extracellularly

To test whether SspM, SspN and SspO are translocated to the cytosol of the host, we generated C-terminal mCherry fusion constructs of each protein under the control of their native promoters. These constructs also contained three C-terminal tandem repeats of the simian virus large T-antigen nuclear localization signal to target the fusion proteins to the host nucleus, to enhance the signal in the cell if the proteins are translocated to the plant cytosol [60]. The constructs were transformed into protoplasts of their respective deletion strain, together with a vector encoding cytoplasmic eGFP to facilitate identification of hyphae among the plant cell background. Transformants were screened by PCR for presence of the construct and then inoculated into L. perenne seedlings. Leaf tissue was harvested from mature infected plants and examined by CSLM for mCherry localization. Although the fluorescence from the mCherry fusion proteins was generally weak in planta, a signal of sufficient intensity was detected from SspM-mCherry-NLS and SspO-mCherry-NLS in the apoplast on either side of the hyphae. For SspN-mCherry-NLS, the signal was so weak that a localization profile for this protein in endophytic hyphae was not possible. No evidence was found for localization of any of the three constructs to the plant nucleus despite examining many individual sections and fields from different plants inoculated with other transformants. By contrast, the signal for mCherry in epiphyllous hyphae on the leaf surface was relatively strong and distinctly localized along the cell walls for all three constructs, demonstrating that the proteins were secreted in planta, but appear to remain attached to the hyphal cell surface (Fig 12). These observations indicate that SspM, SspN and SspO are secreted into the apoplast and may remain attached to the hyphal cell surface post-secretion.

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Fig 12. Confocal micrographs of the localization of SspM-mCherry-NLS, SspN-mCherry-NLS and SspO-mCherry-NLS in endophytic and epiphyllous hyphae of E. festucae in mature L. perenne plants.

Besides the mCherry constructs each transformant contained eGFP to facilitate identification of the hyphae in planta; Bar = 10 μm.

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SspM, SspN, SspO and GpiB do not elicit a defense response in N. benthamiana or N. tabacum and do not suppress INF1-triggered immunity in N. benthamiana

Several fungal effector proteins have been shown to activate the plant immune system (i.e. to trigger a cell death immune response) in non-host plants upon their recognition as ‘invasion patterns’ by corresponding plant immune receptor proteins [95]. To test whether non-host plants are able to recognize GpiB or the Ssps, as invasion patterns, each was expressed in N. benthamiana and N. tabacum leaf tissue using an A. tumefaciens transient expression assay and screened for an associated cell death response. For this purpose, the cDNA sequence encoding each mature protein (i.e. lacking a native secretion signal) was fused to the nucleotide sequence encoding the N. tabacum PR1α secretion signal (for secretion to the plant apoplast) and 3xFLAG (for detection by western blot), and ligated into the pICH86988 expression vector by Golden Gate cloning. The resulting expression vectors were then transformed into A. tumefaciens strain GV3101. Strains confirmed to contain the correct construct were infiltrated into leaves of approx. five-week old N. benthamiana and N. tabacum plants, and the expression of GpiB and the three Ssps verified by western blotting using an antibody to the FLAG-Tag (S5 Fig). Plants were examined for any sign of a cell death response at one-week post-infiltration. As expected, the positive control, INF1 from Phytophthora infestans (a PAMP), triggered a strong cell death response in both N. benthamiana and N. tabacum (Fig 13A and 13B). As expected, the negative control, pICH86988 empty vector, failed to trigger cell death in these plants (Fig 13A and 13B). Unlike INF1, however, neither GpiB, nor the three Ssps, triggered cell death in N. benthamiana and N. tabacum (Fig 13A and 13B) suggesting that they are not recognized as invasion patterns by these non-host plants.

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Fig 13. A. tumefaciens transient expression assays of GpiB, SspM, SspN and SspO in the non-host plants N. benthamiana and N. tabacum.

(A) N. benthamiana and (B) N. tabacum leaf phenotypes in response to A. tumefaciens transient expression assays involving GpiB, SspM, SspN, SspO or INF1. INF1 triggers a strong cell death response, whereas the pICH86988 empty vector had no effect. (C and D) INF1-triggered cell death suppression assays in N. benthamiana with GpiB and SspM (C) and SspN and SspO (D) plus controls. GpiB or any of the three Ssps were unable to suppress INF1-triggered cell death in N. benthamiana. eGFP was used as a negative control, INF1/Avr3a as a suppression control, and Avr3a/R3a as cell death positive control. All photos were taken one-week post-infiltration.

https://doi.org/10.1371/journal.pone.0209463.g013

Many fungal effector proteins are anticipated to suppress activation of the plant immune response [1]. With this in mind, we next examined whether any of the four proteins are able to suppress the cell death response elicited by the INF1 PAMP in N. benthamiana, a model plant system for testing for this response. As before, responses were evaluated one-week post-infection. For this experiment, leaves were first infiltrated with the A. tumefaciens strain containing an expression vector for GpiB or one of the three Ssps. After 24 h, the same infiltration zone was infiltrated with the A. tumefaciens strain containing the INF1 expression vector. As the outcome of this experimental design is very sensitive to environmental influences, appropriate controls were included for each independent experiment. As expected, infiltration of an A. tumefaciens strain containing an expression vector for the P. infestans effector Avr3a 24 h after the corresponding potato resistance protein R3 resulted in a strong cell death response (Fig 13C and 13D). As expected, infiltration of an A. tumefaciens strain containing an expression vector for eGFP 24 h before INF1, gave a strong cell death response, demonstrating that eGFP is not able to suppress the cell death response caused by INF1 (Fig 13C and 13D). When Avr3 was infiltrated 24 h before INF1, the PAMP-triggered cell death response normally elicited by INF1 was strongly suppressed (Fig 13C and 13D), confirming a previous study showing that Avr3a is able to suppress INF1-triggered cell death in N. benthamiana [96]. Unlike the results shown for Avr3a, infiltration of the three Ssps or GpiB, did not result in suppression of INF1-triggered cell death (Fig 13C and 13D).

Taken together, these experiments show that neither the Ssps, nor GpiB, are recognized by the non-host plants N. tabacum and N. benthamiana, and that these proteins are unable to suppress the cell death response triggered by INF1.