- Research article
- Open Access
The beneficial fungus Piriformospora indica protects Arabidopsis from Verticillium dahliaeinfection by downregulation plant defense responses
BMC Plant Biology volume 14, Article number: 268 (2014)
Verticillium dahliae (Vd) is a soil-borne vascular pathogen which causes severe wilt symptoms in a wide range of plants. The microsclerotia produced by the pathogen survive in soil for more than 15 years.
Here we demonstrate that an exudate preparation induces cytoplasmic calcium elevation in Arabidopsis roots, and the disease development requires the ethylene-activated transcription factor EIN3. Furthermore, the beneficial endophytic fungus Piriformospora indica (Pi) significantly reduced Vd-mediated disease development in Arabidopsis. Pi inhibited the growth of Vd in a dual culture on PDA agar plates and pretreatment of Arabidopsis roots with Pi protected plants from Vd infection. The Pi-pretreated plants grew better after Vd infection and the production of Vd microsclerotia was dramatically reduced, all without activating stress hormones and defense genes in the host.
We conclude that Pi is an efficient biocontrol agent that protects Arabidopsis from Vd infection. Our data demonstrate that Vd growth is restricted in the presence of Pi and the additional signals from Pi must participate in the regulation of the immune response against Vd.
Verticillium species are wide-spread soil-borne fungi which cause vascular diseases in many plant species and are responsible for devastating diseases for plants that can thwart agricultural production. The vascular wilt fungus Verticillium dahliae (Vd), for instance, infects more than 200 plant species, among them agriculturally and horticulturally important crops and ornamental plants -. It is estimated that Vd infections are responsible for several billions of dollars of annual crop losses worldwide. Vd has a broad host range and infects plants from temperate to subtropical climates . Because of their complex life style of the Verticillium species, their control by classical pesticides or fungicides is difficult; therefore, the isolation of Verticillium-resistant cultivars is an important task for the breeders (cf. ,).
Genetic resistance against Verticillium wilt diseases has been reported for several plant species ,. The Ve gene provides resistance against race 1 isolates of Vd in tomato , and the tomato gene is also functional after expression in Arabidopsis . Many studies have used Arabidopsis for the isolation of Vd-resistant germplasm , or the identification of novel resistance traits following mutagenesis ,-. Furthermore, quite recently, a large number of proteins and metabolites from different organisms as well as phytohormones have been described to be involved in establishing partial resistance against Verticillium wilt -.
Like other Verticillium species, Vd can overwinter as mycelium in host plants or soil. The fungus can also form seed-like structures called microsclerotia, long-lived survival structures of clusters of melanized cells with thick walls, which survive in the soil without a host plant or in association with plant material for up to 20 years ,. The microsclerotia germinate in response to stimuli from root exudates . The hyphae penetrate and grow inter- and intracellularly through the root cortex toward the central cylinder of the root ,. They enter the xylem cells of the root, from where they colonize the xylem of the hypocotyl and leaves. Ultimately, the water transport is disrupted which results in the wilt phenotype -. Verticillium species are considered as hemibiotroph: a biotrophic phase within root xylem without a visible disease phenotype is followed by a necrotrophic phase in the aerial parts of the plant.
The spread of the pathogen occurs primarily by root infections from the soil. Therefore rhizosphere bacterial strains such as Pseudomonas putida B E2, Pseudomonas chlororaphis K15 or Serratia plymuthica R12  or bacterial isolates  have been shown to function as efficient biocontrol agents against Vd spread. The microbial bioagents induce antibiosis, parasitism, competition and secretion of enzymes such as glucose oxidase, chitinase and glucanase which results in the induction of disease resistance in the hosts ,.
To our knowledge, there is no report on endophytic fungi which can be used as biocontrol agent against Vd in Arabidopsis. Piriformospora indica (Pi), a cultivable basidiomycete of Sebacinales, colonizes the roots of many plant species including Arabidopsis ,. Like other members of Sebacinales, Pi is found worldwide in association with roots  and stimulates growth, biomass and seed production of the hosts ,-. The fungus promotes nitrate and phosphate uptake and metabolism ,. Pi also confers resistance against abiotic , and biotic stress .
Here, we demonstrate that Pi is an efficient biocontrol agent that protects Arabidopsis from Vd infection in vitro and in vivo by inhibiting growth of Vd in roots. Furthermore, we give evidence that a Vd-exudate compound induces cytoplasmic Ca2+ ([Ca2+]cyt) elevation and the Vd-disease development is dependent on the ethylene-activated transcription factor EIN3.
Pi inhibits growth of Vd on PDA agar plates
Pi and Vd were co-cultivated as described in Methods on a PDA agar plate for 3 weeks. Figure 1(A and B) demonstrates that Pi strongly inhibits growth of Vd hyphae. The Vd colony in the dual culture is significantly smaller than the Vd colony growing without Pi. Furthermore, the number of microsclerotia produced by Vd in the dual culture is less than the number of microsclerotia produced by Vd growing alone. No obvious inhibition zone can be detected. In contrast, growth of Pi is barely affected by the presence of Vd. This prompted us to test the role of Pi in protecting Arabidopsis plants against Vd infection.
Arabidopsis seedlings pretreated with Pi are protected against Vd infection
To investigate whether Pi can protect Arabidopsis for Vd infection, we exposed the seedlings first to Pi prior to Vd infection. Seedlings not exposed to any of the two fungi or to one of the two fungi alone served as controls (cf. Methods). The performance of the seedlings was measured after 10, 14 and 21 days, by visible inspection and measuring the fresh weights. After 10 days of co-cultivation, seedlings treated with Vd or Pi alone showed ~30% increase in the biomass compared to the untreated control seedlings. A comparable increase in the biomass was observed when the seedlings were first exposed to Pi and then to Vd or vice versa (Figure 2A). This slight increase in the biomass suggests that both fungi initially form a beneficial interaction with the seedlings, and is consistent with the idea that this phase represents a biotrophic interaction of Vd with Arabidopsis roots. On the 14th day, seedlings infected by Vd alone or first with Vd followed by Pi (1V2P) showed obviously the disease symptoms. The leaves of these seedlings became paler and the roots browner compared to the seedlings exposed to Pi or 1P2V treatments, although no significant differences in the biomass were observed for the different fungal treatments, except for Pi treatment (Figure 2A). In contrast, on the 21st day, seedlings exposed to Vd alone or exposed to Vd prior to exposure to Pi (1V2P) were severely damaged. Their fresh weights were reduced or no longer measurable. Pi treatment alone resulted in a ~30% increase in the fresh weight (Figure 2A). Interestingly, seedlings which were pretreated with Pi and then exposed to Vd (1P2V) had the same fresh weights as untreated control seedlings, although the visible inspection showed some photo-bleaching (Figure 2B). This clearly demonstrates that Pi protects Arabidopsis seedlings against Vd-induced wilt. Therefore, this experimental set-up was used to study the protective function of Pi in greater details.
The results were confirmed by calculating the Percentage Disease Index (PDI) for those seedlings treated with Vd. After 10 days of co-cultivation, the PDI for Vd and 1V2P seedlings was ~20%, and after 14 days 40-50%. After 21 days, the PDI was almost 100%. In contrast, seedlings pretreated with Pi prior to exposure to Vd (1P2V) showed a slow increase in the PDI, which reached ~30% after 21 days (Figure 2C).
Furthermore, the amount of total chlorophyll (Chl) is a sensitive marker for the fitness of a plant. On the 4th day, the shoots of Vd- and Pi- treated plants contained slightly higher Chl levels than control seedlings (Figure 3). On the 10th day, the Chl content of Vd- treated seedlings is comparable to that of control seedlings not exposed to the pathogen. Furthermore, while 1P2V seedlings had the same amount of Chl as Pi seedlings, the Chl content in 1V2P seedlings was significantly reduced (Figure 3). Comparable results were obtained for the 14th day, except that the Chl content for 1P2V seedlings was reduced compared to Pi seedlings (Figure 3). On the 21st day, Pi seedlings had the highest Chl content, 1P2V seedlings had the same amount of Chl as control seedlings not exposed to a fungus, while the Chl levels in the Vd and 1V2P plants were strongly decreased (Figure 3). This confirms the protective function of Pi against Vd infection in Arabidopsis leaves.
Pathogenesis and application of pathogen-associated molecular patterns induce stomata closure . In control plants not exposed to any fungus, between 5 and 12% of the stomata were closed. Three days after exposure of the roots to Vd, ~25% of the stomata were closed (Figure 4A), and this increased to ~30% until the 7th day. The 1V2P treatment showed ~25% stomata closure at the 7th day, and this value is comparable to that for seedlings treated with Vd alone. In contrast, exposure of the roots to Pi or first to Pi followed by Vd did not result in stomata closure and these values are comparable to those of the untreated controls (Figure 4B). This indicates that Pi prevents Vd-induced stomata closure. These results demonstrate that stomatal closure correlates nicely with the amount of total chlorophyll.
Pi represses Vd-induced genes in shoots
Vd induces defense gene expression in shoots. After 1 d, the mRNA levels for PR1 and PR2 representing SA-inducible genes and PDF1.2 for the JA/ET pathway, ERF1 and VSP2 for ET pathway were upregulated in the leaves of Vd-exposed seedlings. Except for PR2, none of the other genes responded to Pi exposure (Figure 5). After 14 d, Vd-exposed seedlings showed an even stronger upregulation of the defense genes in the leaves (Figure 5). Pretreatment of the seedlings with Pi prior to Vd infection resulted in the repression of defense gene expression compared to seedlings which were not pretreated with Pi. This provides additional evidence for the protective function of Pi against Vd infection. Furthermore, plant glutamate receptor-like (GLR) genes, GLR2.4, GLR2.5 and GLR3.3 code for putative Ca2+ transporters and are involved in defense responses -. We observed that GLR2.4 (but not GLR2.5 and GLR3.3) was upregulated in the leaves of Vd-exposed seedlings and repressed in the leaves of seedlings which were pretreated with Pi prior to Vd exposure (Figure 5 and Additional file 1: Figure S2). RabGAP22 is required for defense to V. longisporum and contributes to stomata immunity . For Vd, RabGAP11 is upregulated after exposure to Vd and significantly repressed in seedlings which were pretreated with Pi (Figure 5).
Pi strongly represses Vd-induced phytohormone accumulation in shoots
The phytohormones JA, JA-Ile, OPDA, SA, ABA and ET are crucial for the activation of defense responses. Figure 6 demonstrates that these phytohormones accumulated after Vd infection in the shoots of Arabidopsis seedlings. The phytohormone levels were also high in the 1V2P samples, while in all other cases [Control (C), Pi, 1P2V], they showed significantly lower levels. Thus, Vd-induced phytohormone accumulation is repressed if the roots are colonized by Pi prior to their exposure to Vd. Interestingly, application of Pi to roots which were already exposed to Vd did not repress the accumulation of the phytohormones in the shoots.
Pi inhibits Vd propagation and microsclerotia formation
Quantification of the amount of Vd DNA demonstrated that Vd and 1V2P seedlings contain twice as much pathogen DNA than 1P2V seedlings in both roots (Figure 7A and D) and shoots (Figure 7B and E). Interestingly, the amount of Pi DNA in the roots is identical in all Pi-treated samples and not affected by a pretreatment with Vd (Figure 7C and F). Furthermore, microscopic analysis demonstrated that the number of microsclerotia was strongly reduced in root tissue pretreated with Pi (Figure 8). This demonstrates that Pi inhibits Vd propagation and microsclerotia formation in the roots, while Vd does not affect the propagation of Pi in Arabidopsis roots.
Long-term experiments confirmed the results obtained for seedlings
In order to study long term interaction, the seedlings were grown according to the 5 regimes on Petri dishes for 10 days before transferred to sterile vermiculite for additional 14 days. All (C) seedlings and those exposed to Pi (Pi) were alive. Exposure of Pi-pretreated plants to Vd resulted in ~20% loss of the plants. However 80% of the plants, which were either exposed to Vd alone or first to Vd followed by Pi, died (Figure 9A). Furthermore, we measured the fresh weights of the seedlings which survived the treatments. Plants exposed to Pi alone showed a ~30% increase in the fresh weight. The fresh weights of 1P2V plants were comparable to those not exposed to any fungus. Vd- and 1V2P-treated seedlings showed significantly decreased fresh weights compared to all other treatments (Figure 9B). Finally, the Vd DNA amount in both shoots and roots was lower in 1P2V-treated plants compared to those treated with Vd alone or first with Vd followed by Pi (1V2P) (Figure 9C). Comparable to the results obtained with seedlings in Petri dishes (Figure 7), the Pi DNA content was the same in all Pi-treated roots (Figure 9C). This confirms that Pi inhibits Vd growth, but not vice versa.
EIN3 is required for full susceptibility of Arabidopsis to Vd
The strong upregulation of the phytohormone levels in the leaves of seedlings grown in the presence of Vd was further investigated for ET. Pantelides et al.  have shown that ET perception via ETR1 is required for Vd infection in Arabidopsis. We observed a strong requirement of EIN3 for Vd-induced disease development in Arabidopsis leaves. ein3 seedlings which were exposed to Vd alone or were first treated with Vd before application of Pi perform better than wild-type seedlings (Figure 10A, B and Additional file 1: Figure S3). Interestingly, the ET level in ein3 seedlings is much higher than in wild-type seedlings, even in the absence of Vd. Exposure of the seedlings to Vd stimulate ET accumulation even further (Figure 10C and Additional file 1: Figure S4). This suggests that ein3 seedlings try to compensate the lack of EIN3-induced genes by further stimulating ET biosynthesis, in particular after Vd infection. Taken together, these data demonstrate that EIN3-induced genes are required for pathogenicity of Vd.
Vd induces [Ca2+]cyt elevation in WT roots, but not in roots of a Ca2+ response mutant
Pathogen-associated molecular pattern-triggered immunity is often initiated by [Ca2+]cyt elevation, which can be induced by exudated compounds from pathogenic fungi [cf.  and ref. therein]. Since the putative plasma membrane-localized Ca2+-transporter gene GLR2.4 was upregulated by Vd, we tested whether exudated compounds from Vd can induce [Ca2+]cyt elevation in roots. An exudate preparation from the mycelium was applied to the roots of transgenic pMAQ2 Arabidopsis lines expressing the Ca2+-sensor apoaequorin. Under resting conditions, 21 d-old pMAQ2 lines gave [Ca2+]cyt values of 70 ± 0.6 nM (n = 16). A rapid and transient increase in the [Ca2+]cyt concentration is observed 40 sec after the application of Vd preparation (Figure 11A). Discharge at the end of the experiment demonstrates that less than 5% of the reconstituted aequorin was consumed after the stimuli, which ensures that the amount of aequorin in the sample is not limiting for the Ca2+ signal (data not shown). The [Ca2+]cyt reached a peak of ~ 400 nM after 90 to 120 sec (Figure 11A). Subsequently the Ca2+ levels steadily decreased. No [Ca2+]cyt elevation is observed with the PBS buffer treatment (Figure 11A). The magnitude of the [Ca2+]cyt response is dose-dependent (data not shown). Furthermore, an Arabidopsis cytoplasmic calcium elevation mutant1 (cycam1) which does not show [Ca2+]cyt elevation in response to exudate preparation from various pathogenic fungi  also failed to induce [Ca2+]cyt elevation in response to the Vd preparation (Figure 11B). This indicates that cycam1 is impaired in the response to exudate preparations from various pathogens. Furthermore, we crossed the apoaeqorin gene into the glr2.4, glr2.5 and glr3.3 knock-out background. Figure 11B demonstrates that the Vd exudate preparation induced [Ca2+]cyt elevation in the knock-out backgrounds, indicating that these putative plasma membrane-localized transporters do not participate in the Ca2+ uptake from the extracellular space, although the gene GLR2.4 was upregulated in Vd-infected seedlings (Figure 5).
To investigate whether [Ca2+]cyt elevation is required for disease development, cycam1 was infected with Vd and the development of the mutant seedlings was compared to that of the WT seedlings. No obvious difference of the disease symptoms in the aerial parts could be detected, which suggests that [Ca2+]cyt elevation is not essential for Vd propagation (Additional file 1: Figure S6).
Our data demonstrate that Pi is a very efficient biocontrol agent for Vd wilt in Arabidopsis. Pi restricts Vd growth both on agar plates (Figure 1) and in Arabidopsis roots, in particular when they were first colonized by Pi prior to infection with Vd (Figure 7). Molecular and biochemical analyses demonstrate that the reduced growth rate of Vd in Pi-pretreated Arabidopsis roots retards defense gene expression (Figure 5), the accumulation of defense-related phytohormones (Figure 6) and stomata closure (Figure 4). The performance of the seedlings is significantly better (Figure 2) and this also continues after shifting the seedlings to vermiculite for a longer period of time (Figure 9). Pi not only inhibits growth of Vd mycelia in Arabidopsis roots, but also prevents the spread of the pathogen to the aerial parts of the plant (Figure 7). Furthermore, microsclerotia formation is strongly reduced (Figure 8). Previously, several soil-borne bacteria have been identified as biocontrol agents for Verticillium wilt ,-. Vd can induce antimicrobial metabolites such as rutin in potato  or pathogenesis-related proteins in Arabidopsis  which participates in pathogen resistance. Prieto et al.  demonstrated that root hair colonization plays an important role in Pseudomonas spp.-mediated biocontrol activity against Verticillium wilt in olive roots. Furthermore, the Bacillus subtilis strain NCD-2 functions as a biocontrol agent against cotton Verticillium wilt, and the cotton PhoR/PhoP, two component regulatory systems, were involved in the biocontrol capability of the bacterium . Also quorum sensing is involved in the biocontrol activity of Serratia plymuthica against Vd. Moderate drought influences the effect of arbuscular mycorrhizal fungi as biocontrol agents against Verticillium-induced wilt in pepper . It appears that quite different mechanisms control the fungal spread, probably because of the complicated lifestyle of the pathogen which allows microbial interference at different levels and in different plant tissues.
An increasing number of genes were recently identified to be involved in establishing partial resistance to Verticillium wilts (cf. Background). Pathogen attack including root colonization by Vd is associated with stomata closure as one of the first line of plant defense (Figure 4). RabGAP22 is required for defense against V. longisporum and contributes to stomatal immunity . RabGAP11 gene is upregulated by Vd and repressed by Pi (Figure 5). Finally, defensins play a role in the plant defense against Vd.
Control of microsclerotia formation is crucial for preventing Verticillium spread in nature and agriculture. Our data demonstrate that Pi is quite efficient in restricting microsclerotia formation in Arabidopsis roots (Figure 8), presumable because the pathogen cannot grow fast enough in the presence of Pi. Microsclerotia formation is also suppressed by Verticillium itself, i.e. by the fungal transcription activator of adhesion Vta2, and fungi impaired in Vta2 are unable to colonize plants and induces disease symptoms . Taken together, Pi restricts Vd growth as well as hyphal and microslerotia propagation, which - in turn - causes that the plant defense processes get activated at a lower level compared to Vd treatments which might depend on Pi-plant-Vd interaction-pattern and the attack strategy of Vd. This is not only important for better performance of individual plants, but has also severe long-term consequences for the control of the Vd spread via microsclerotia in ecosystems and agricultural areas.
GRL homologs are associated with Ca2+ influx through the plasma membrane. Figure 5 demonstrates that the mRNA level for GLR2.4 is upregulated in the leaves of Vd-infected Arabidopsis seedlings and these responses are restricted by a pretreatment of the seedlings with Pi. GLR3.3 is involved in plant defense and resistance to Hyaloperonospora arabidopsidis. The protein also mediates glutathione-triggered [Ca2+]cyt transients, transcriptional changes, and innate immunity responses in Arabidopsis . GLR2.5 is upregulated in Arabidopsis cell cultures upon wounding  and GLR2.4 is induced by nematodes in Arabidopsis roots . GLR2.4, also called AUGMIN subunit 8, is a microtubule plus-end binding protein that promotes microtubule reorientation in hypocotyls ,. Microtubules and microtubule orientation are important for plant defense and immunity , and also involved in Vd-Arabidopsis interaction. Hu et al.  demonstrated that histone H2B monoubiquitination is involved in regulating the dynamics of microtubules during the defense response to Vd toxins in Arabidopsis. Yuan et al.  showed that Vd toxins disrupted microfilaments and microtubules in Arabidopsis suspension-cultured cells. Figure 11A shows that exudate compounds from Vd induces [Ca2+]cyt elevation in Arabidopsis roots. In order to test whether the [Ca2+]cyt elevation is mediated by one of the three GLRs, we generated transgenic glr3.3, glr2.5 and glr2.4 knock-out lines in the apoaequorin background and found that the [Ca2+]cyt response is not controlled by the three GLRs (Figure 11B), although the mRNA level of GLR2.4 is upregulated upon Vd infection (Figure 5). This suggests that GLRs have different functions in the Vd-Arabidopsis interaction. However, an ethylmethansulfonate-induced Arabidopsis mutant named cycam1 which is unable to induce [Ca2+]cyt elevation in response to exudate preparations from Alternaria brassicae, Rhizoctonia solani, Phytophthora parasitica var. nicotianae and Agrobacterium tumefaciens did not respond to the Vd exudate preparation (Figure 11B). This demonstrates that at least one of the Vd-induced signaling events leading the opening of Ca2+ channels or the channels themselves are identical to those responding to exudate preparations from other pathogens . However, the reduced Ca2+ response in the cycam1 mutant does not affect the disease development. It remains to be determined which is the active compound inducing the [Ca2+]cyt response in Arabidopsis roots, and what is the mutated gene in the cycam1 mutant.
Several exudated compounds have been postulated to induce pathogenicity in plants. Klosterman et al.  proposed that based on the sequence information of Verticillium species, pathogenicity may be caused by a cocktail of different compounds and elicitors with different functions in the complex pathogenicity procedure. A Verticillium crude toxin preparation has been often used, although the exact composition of this preparation and the role of the individual compounds are not clear. For instance, recently Yao et al.  have demonstrated that the Vd toxin preparation stimulates nitric oxide production in Arabidopsis which serves as a signaling intermediate downstream of H2O2 to modulate dynamic microtubule cytoskeleton. This may link the Vd toxin function again to GLR2.4, who's mRNA level is upregulated after Vd infection (Figure 5). Wang et al.  reported on the purification and characterization of a novel hypersensitive-like response-inducible protein elicitor named PevD1 from Vd that induces resistance responses in tobacco. The relationship of the bioactive compound that induces the [Ca2+]cyt response to the toxins which induce disease responses needs to be investigated.
Interestingly, we did not observe a linear relationship between the propagation of Vd in the seedlings and the accumulation of defense-related phytohormone levels. For instance, the phytohormone levels were always high when the seedlings were exposed to Vd, irrespective of whether they were exposed to Vd alone, pretreated with Pi or first with Vd followed by Pi (Figure 6), although, growth of Vd was strongly reduced by the Pi pretreatment (Figure 1). This suggests that even low infection rates of Vd are sufficient to stimulate the accumulation of the defense hormones. This might be a precaution, although propagation of Vd is inhibited when the roots were pretreated with Pi.
Various reports showed the involvement of plant hormones in the control of Verticillium growth in Arabidopsis. Stabilization of cytokinin levels enhances Arabidopsis resistance against V. longisporum. The fungus also requires JA-dependent COI1 function in roots to elicit disease symptoms in Arabidopsis shoots . Ethylene perception via the receptor ETR1 is required for Vd infection in Arabidopsis . Enhanced resistance of etr1-1 plants, but not of SA-, JA- or other ET-deficient mutants against Vd infection indicate a crucial role of ETR1 in defense against this pathogen. We observed a particularly striking resistance of the Arabidopsis ein3 mutant against Vd infection in vivo and in vitro (Additional file 1: Figure S5). This is consistent with the reports by Pantelides et al.  for etr1, although they did not observe a significant role of EIN3 in their studies. Our data demonstrate that EIN3 plays an important role in pathogenicity and will provide an important tool to identify EIN3-regulated genes which are required for Vd disease development. Furthermore, the ET level in the ein3 mutant exposed to Vd is much higher compared to Vd-exposed WT seedlings (Figure 10C). This suggests a feedback loop by which the lack of EIN3-induced defense responses in the ein3 mutant results in an additional stimulation of ET synthesis.
In summary, our data demonstrate that Pi is a very efficient biocontrol agent for Vd. This is mainly caused by the restriction of Vd growth in the presence of Pi. There appears to be additional mechanisms which prevent pathogenicity of Vd in the presence of Pi. For instance, the phytohormone levels accumulate to comparable levels in Vd and 1P2V seedlings, although Vd propagation is restricted in the presence of Pi (Figure 1). Since Pi pretreatment severely reduces defense gene expression in spite of a comparable phytohormone level in these tissues, additional signals from Pi must participate in the regulation of the immune response against Vd.
Growth conditions of seedlings and fungi
A. thaliana wild-type (ecotype Columbia-0) seeds, seeds of the glr2.4, glr2.5, glr3.3 and ein3 mutants as well as of cycam1 mutant  were surface-sterilized and placed on Petri dishes with MS media . After cold treatment at 4°C for 48 h, plates were incubated for 11 days at 22°C under long day conditions (16 h light/8 h dark; 80 μmol m-2 sec-1). Pi was grown for 3-4 weeks on KM medium as described previously . For detailed information see Section A and B in Johnson et al. . Vd (FSU-343, Jena Microbial Resource Center, Germany) was grown for 2-3 weeks on Potato Dextrose Agar (PDA) medium .
For co-cultivation assays 13 day-old A. thaliana seedlings of equal size were used. Co-cultivation of A. thaliana and the fungi Pi and/or Vd was performed under in vitro culture conditions on a nylon membrane on PNM media as described by Johnson et al. (, Section C1 - Method 1) with a few modifications. Vd was grown for 12 days and Pi for 10 days on the membrane on top of PNM medium in Petri dishes. 13-day old Arabidopsis seedlings were then transferred to the Pi or Vd plates, or mock-treated (no fungal mycelium; C). For the shifting experiments, the seedlings were transferred to plates with the other fungus after 4 days (from Vd to Pi or vice-versa). Including the (C), five different treatments were compared: (1) Arabidopsis seedlings grown without Pi or Vd (C); (2) without Pi and with Vd (Vd); (3) with Pi and without Vd (Pi); (4) with Pi for 4 days before transfer to Vd plates (1P2V) and (5) with Vd for 4 days before transfer to Pi plates (1V2P). The seedlings were harvested between 1 and 21 days after exposure to the first fungus (or mock-treatment) for further analysis. A time scheme is shown in Additional file 1: Figure S1. The light intensity (80 μmol m-2s-1) was checked weekly. Shoots and roots were harvested separately for DNA and RNA analyses.
Long term co-cultivation in sterile vermiculite
30 g vermiculite was placed into one Magenta box (Sigma-Aldrich, Germany) and autoclaved at 121°C for 30 min. After the addition of 40 ml of sterile liquid PNM medium, Arabidopsis seedlings grown in Petri dishes for 10 days were transferred to the sterile vermiculite boxes (1 plant per box). For each treatment, 16 seedlings were analyzed. After 10 days, the number of survived plants, their biomass and fungal DNA content were determined.
Gene expression analysis
RNA was isolated from shoots and reverse-transcribed for Real-time quantitative PCR analysis, using an iCycler iQ Real-time PCR detection system and iCycler software version 2.2 (Bio-Rad). Total RNA was isolated from 5 independent biological experiments of Arabidopsis shoots. cDNA was synthesized using the Omniscript cDNA synthesis kit (QIAGEN) using 1 μg RNA. For the amplification of the RT-PCR products, iQ SYBR Green Supermix (Bio-Rad) was used according to the manufacturer's protocol in a final volume of 20 μl. The iCycler was programmed to 95°C 3 min, 40 × (95°C 30 sec, 57°C 15 sec, 72°C 30 sec), 72°C 10 min, followed by a melting curve program 55°C to 95°C in increasing steps of 0.5°C. All reactions were performed in triplicate. The mRNA levels for each cDNA probe were normalized with respect to the glycerin-aldehyde-3-phosphate dehydrogenase (GAPDH) mRNA level. The primer pairs are given in Additional file 1: Table S1.
Quantification of fungal DNAs by PCR
Genomic DNA extraction was conducted with DNeasy Plant Mini Kit. 12.5 ng DNA was taken for PCR template. The reactions were performed with gene-specific primers, as given in Additional file 1: Table S1. For details see Camehl et al. .
Dual culture of Pi and Vd
Dual culture of Pi and Vd on agar plates was performed as described by Johnson et al. . A Pi plug with 5 mM diameter was placed at one end of a PDA plate and a Vd plug of the same size at the other end of the plate. The plates were incubated at 22-24°C in dark and 75% relative humidity. Photos were taken after 3 weeks of co-cultivation.
Percentage disease index (PDI) calculation
Disease index was calculated with the following formula:
n1-5 = number of affected leaves of the respective disease.
Severity grade (0-5), x1-5 = disease severity grade based on the percentage of affected leaf area. 1, 1% ≤ × ≤ 10%; 2, 10% < × ≤ 20%; 3, 20% < × ≤ 30%; 4, 30% <× ≤ 40%; 5, × > 40%; ×100: calculated in percentage scale. Disease severity was estimated on the basis of affected leaf area. 1-5 disease severity grades were described by Naik and Lakkund ,.
Quantification of jasmonic acid (JA), JA-isoleucine (JA-Ile), abscisic acid (ABA), salicylic acid (SA), oxophytodinoic acid (OPDA) and ethylene (ET)
Independent samples of 250 mg shoot material were collected from each treatment. Phytohormone extractions (JA, JA-Ile, ABA, SA and OPDA) were performed by adding 1 ml ethyl-acetate containing 60 ng of D2-JA and 40 ng of D6-ABA, D4-SA and JA-13C6-Ile (OPDA has the same internal standerd as JA) to 100 mg ground tissues. All samples were then vortexed for 10 min and centrifuged at 13,000 rpm for 20 min at 4°C. The supernatants were collected and evaporated to dryness at 30°C using a vacuum concentrator. Residues were resuspended in 500 μl MeOH:H2O (70:30, v/v) and centrifuged at 13,000 rpm for 10 min. The supernatants were collected and measured with the API 3200 LC-MS/MS system (Applied Biosystems, Framingham, USA) as previously described .
For ET measurements, 100 mg shoot material from each treatment was collected into 4 ml vials (Roth, Germany). After 4 h ET accumulation, the measurement was performed with the ETD-300 ethylene detector (Sensor Sense B.V., Nijmegen, The Netherlands).
Chlorophyll content was determined according to Yang et al.  and based on g fresh weight.
Quantification of microsclerotia
Roots of Arabidopsis seedlings from the 3 treatments with Vd were harvested after 3 weeks of co-cultivation in Petri dishes and transferred to a microscopic glass slide with 80 μl lactic acid/glycerol/H2O (1:1:1). The number of the microsclerotia formed in the roots was calculated averagely per root visually under the light microscope (magnification: x200). The experiment was performed 3 times independently and for each treatment the roots of 12 seedlings were analysed.
Cytoplasmic Ca2+ ([Ca2+]cyt) measurement
Aequorin based luminescence measurements were performed using 21-day old individual wild-type (WT) plants and mutants grown in Hoagland medium . WT aequorin (pMAQ2) plants served as control . Mutants (glr2.4, glr2.5 and glr3.3) were crossed back to wild-type expressing aequorin. After 2 generation selection based on [Ca2+]cyt responses and RT-PCR of T-DNA insertion examination, the homozygote seeds were used for the described experiments. Primers used for homozygosity tests are given in Additional file 1: Table S1. For [Ca2+]cyt measurements, approximately 70% of the roots per seedling was dissected and incubated overnight in 150 μl of 7.5 μM coelentrazine (P.J.K. GmbH, Germany) in the dark at 20°C in a 96 well plate (Thermo Fischer Scientific, Finland, cat. no. 9502887). Bioluminescence counts from roots were recorded as relative light units (RLU) with a microplate luminometer (Luminoskan Ascent, version 2.4, Thermo Electro Corporation, Finland).
Preparation of exudates from mycelia of Vd
A 5 mM Vd fungal plug was inoculated in Czapek's medium as described in Zhen et al.  and grown for 3 weeks. Then, the fungal culture was filtered through double layers of filter paper and the filtrate was centrifuged at 10,000 g for 30 min to remove the spores. The supernatant was dialyzed with a dialysis membrane (MWCO) (Spectra/Por® Float-A-lyzer®) in 10 mM phosphate buffer pH 7.0 at 4°C for 24 h. The dialyzed solution was frozen and lyophilized. The powder was dissolved in distilled water and the solution was filtered through a 0.45 μm pore size Millipore filter (Roth, Germany). The resulting filtrate was used as exudate for further experiments.
All statistical analyses were performed using Excel or SPSS 17.0 (SPSS Inc., Chicago, IL, USA) for ANOVA.
Availability of supporting data
All the supporting data are included as additional file.
- Vd :
- Pi :
- cycam1 :
Cytosolic calcium elevation mutant1
- glr Glutamate receptor :
- ein3 :
Pegg GF, Brady BL: Verticillium Wilts. CABI Publishing, Wallingford, UK; 2002.
Fradin EF, Thomma BP: Physiology and molecular aspects of Verticillium wilt diseases caused by V. dahliae and V. albo-atrum. Mol Plant Pathol. 2006, 7: 71-86. 10.1111/j.1364-3703.2006.00323.x.
Klosterman SJ, Atallah ZK, Vallad GE, Subbarao KV: Diversity, pathogenicity, and management of Verticillium species. Ann Rev Phytopathol. 2009, 47: 39-62. 10.1146/annurev-phyto-080508-081748.
Clerivet A, Deon V, Alami I, Lopez F, Geiger JP: Tyloses and gels associated with cellulose accumulation in vessels are responses of plane tree seedlings (Platanus × acerifolia) to the vascular fungus Ceratocystis fimbriata f. sp platani. Trees. 2000, 15: 25-31. 10.1007/s004680000063.
Cai Y, He X, Mo J, Sun Q, Yang J, Liu J: Molecular research and genetic engineering of resistance to Verticillium wilt in cotton: a review. Afr J Biotechnol. 2009, 8: 7363-7372.
Kawchuk LM, Hachey J, Lynch DR, Kulcsar F, van Rooijen G, Waterer DR, Robertson A, Kokko E, Byers R, Howard RJ, Fischer R, Prufer D: Tomato Ve disease resistance genes encode cell surface-like receptors. Proc Natl Acad Sci U S A. 2001, 98: 6511-6515. 10.1073/pnas.091114198.
Fradin EF, Zhang Z, Ayala JC, Castroverde CD, Nazar RN, Robb J, Liu CM, Thomma BP: Genetic dissection of Verticillium wilt resistance mediated by tomato Ve1. Plant Physiol. 2009, 150: 320-332. 10.1104/pp.109.136762.
Fradin EF, Abd-El-Haliem A, Masini L, van den Berg GC, Joosten MH: Interfamily transfer of tomato Ve1 mediates Verticillium resistance in Arabidopsis. Plant Physiol. 2011, 156: 2255-2265. 10.1104/pp.111.180067.
Schaible L, Cannon OS, Waddoups V: Inheritance of resistance to Verticillium wilt in a tomato cross. Phytopathology. 1951, 41: 986-990.
Veronese P, Narasimhan ML, Stevenson RA, Zhu JK, Weller SC: Identification of a locus controlling Verticillium disease symptom response in Arabidopsis thaliana. Plant J. 2003, 35: 574-587. 10.1046/j.1365-313X.2003.01830.x.
Pantelides IS, Tjamos SE, Paplomatas EJ: Ethylene perception via ETR1 is required in Arabidopsis infection by Verticillium dahliae. Mol Plant Pathol. 2010, 11: 191-202. 10.1111/j.1364-3703.2009.00592.x.
Tjamos SE, Flemetakis E, Paplomatas EJ, Katinakis P: Induction of resistance to Verticillium dahliae in Arabidopsis thaliana by the biocontrol agent K-165 and pathogenesis-related proteins gene expression. Mol Plant-Microbe Interact. 2005, 18: 555-561. 10.1094/MPMI-18-0555.
Ellendorff U, Fradin EF, de Jonge R, Thomma BP: RNA silencing is required for Arabidopsis defense against Verticillium wilt disease. J Exp Bot. 2009, 60: 591-602. 10.1093/jxb/ern306.
Johansson A, Staal J, Dixelius C: Early responses in the Arabidopsis-Verticillium longisporum pathosystem are dependent on NDR1, JA- and ET-associated signals via cytosolic NPR1 and RFO1. Mol Plant-Microbe Interact. 2006, 19: 958-969. 10.1094/MPMI-19-0958.
Ralhan A, Schöttle S, Thurow C, Iven T, Feussner I, Polle A, Gatz C: The vascular pathogen Verticillium longisporum requires a jasmonic acid-independent COI1 function in roots to elicit disease symptoms in Arabidopsis shoots. Plant Physiol. 2012, 159: 1192-11203. 10.1104/pp.112.198598.
Liu SY, Chen JY, Wang JL, Li L, Xiao HL, Adam SM, Dai XF: Molecular characterization and functional analysis of a specific secreted protein from highly virulent defoliating Verticillium dahliae. Gene. 2013, 529: 307-316. 10.1016/j.gene.2013.06.089.
Reusche M, Klásková J, Thole K, Truskina J, Novák O, Janz D, Strnad M, Sp°Chal L, Lipka V, Teichmann T: Stabilization of cytokinin levels enhances Arabidopsis resistance against Verticillium longisporum. Mol Plant-Microbe Interact. 2013, 26: 850-860. 10.1094/MPMI-12-12-0287-R.
Hu M, Pei BL, Zhang LF, Li Y: Histone H2B monoubiquitination is involved in regulating the dynamics of microtubules during the defense response to Verticillium dahliae toxins in Arabidopsis. Plant Physiol. 2014, 164: 1857-1865. 10.1104/pp.113.234567.
Gaspar YM, McKenna JA, McGinness BS, Hinch J, Poon S, Connelly AA, Anderson MA, Heath RL: Field resistance to Fusarium oxysporum and Verticillium dahliae in transgenic cotton expressing the plant defensin NaD1. J Exp Bot. 2014, 65: 1541-1550. 10.1093/jxb/eru021.
Roos J, Bejai S, Oide S, Dixelius C: RabGAP22 is required for defense to the vascular pathogen Verticillium longisporum and contributes to stomata immunity. PLoS One. 2014, 9: e88187-10.1371/journal.pone.0088187.
Tran VT, Braus-Stromeyer SA, Kusch H, Reusche M, Kaever A, K hn A, Valerius O, Landesfeind M, A hauer K, Tech M, Hoff K, Pena-Centeno T, Stanke M, Lipka V, Braus GH: Verticillium transcription activator of adhesion Vta2 suppresses microsclerotia formation and is required for systemic infection of plant roots. New Phytol. 2014, 202: 565-581. 10.1111/nph.12671.
Bu B, Qiu D, Zeng H, Guo L, Yuan J, Yang X: A fungal protein elicitor PevD1 induces Verticillium wilt resistance in cotton. Plant Cell Rep. 2014, 33: 461-470. 10.1007/s00299-013-1546-7.
Agrios G: Plant Pathol. 2005, Elsevier Academic Press, Burlington
Klosterman SJ, Subbarao KV, Kang S, Veronese P, Gold SE, Thomma BP, Chen Z, Henrissat B, Lee YH, Park J, Garcia-Pedrajas MD, Barbara DJ, Anchieta A, de Jonge R, Santhanam P, Maruthachalam K, Atallah Z, Amyotte SG, Paz Z, Inderbitzin P, Hayes RJ, Heiman DI, Young S, Zeng Q, Engels R, Galagan J, Cuomo CA, Dobinson KF, Ma LJ: Comparative genomics yields insights into niche adaptation of plant vascular wilt pathogens. PLoS Pathog. 2011, 7: e1002137-10.1371/journal.ppat.1002137.
Mol L, Van Riessen HW: Effect of plant roots on the germination of microsclerotia of Verticillium dahliae 1. Use of root observation boxes to assess differences among crops. Eur J Plant Pathol. 1995, 101: 673-678. 10.1007/BF01874871.
Reusche M, Thole K, Janz D, Truskina J, Rindfleisch S, Drübert C, Polle A, Lipka V, Teichmann T: Verticillium infection triggers VASCULAR-RELATED NAC DOMAIN7-dependent de novo xylem formation and enhances drought tolerance in Arabidopsis. Plant Cell. 2012, 24: 3823-3837. 10.1105/tpc.112.103374.
Zhao P, Zhao Y-L, Jin Y, Zhang T, Guo H-S: Colonization process of Arabidopsis thaliana roots by a green fluorescent protein-tagged isolate of Verticillium dahliae. Protein Cell. 2014, 5: 94-98. 10.1007/s13238-013-0009-9.
Berg G, Fritze A, Roskot N, Smalla K: Evaluation of potential biocontrol rhizobacteria from different host plants of Verticillium dahliae Kleb. J Appl Microbiol. 2001, 91: 963-971. 10.1046/j.1365-2672.2001.01462.x.
Li CH, Shi L, Han Q, Hu HL, Zhao MW, Tang CM, Li SP: Biocontrol of Verticillium wilt and colonization of cotton plants by an endophytic bacterial isolate. J Appl Microbiol. 2012, 113: 641-651. 10.1111/j.1365-2672.2012.05371.x.
Tjamos EC, Rowe RC, Heale JB, Fravel DR: Advances in Verticillium Research and Disease Management. APS Press, St. Paul, MN; 2000.
Oelmüller R, Sherameti I, Tripathi S, Varma A: Piriformospora indica, a cultivable root endophyte with multiple biotechnological applications. Symbiosis. 2009, 49: 1-17. 10.1007/s13199-009-0009-y.
Qiang X, Weiss M, Kogel KH, Schäfer P: Piriformospora indica - a mutualistic basidiomycete with an exceptionally large plant host range. Mol Plant Pathol. 2012, 13: 508-518. 10.1111/j.1364-3703.2011.00764.x.
Selosse MA, Dubois MP, Alvarez N: Do Sebacinales commonly associate with plant roots as endophytes?. Mycol Res. 2009, 113: 1062-1069. 10.1016/j.mycres.2009.07.004.
Shahollari B, Vadassery J, Varma A, Oelmüller R: A leucine-rich repeat protein is required for growth promotion and enhanced seed production mediated by the endophytic fungus Piriformospora indica in Arabidopsis thaliana. Plant J. 2007, 50: 1-13. 10.1111/j.1365-313X.2007.03028.x.
Sherameti I, Shahollari B, Venus Y, Altschmied L, Varma A, Oelmüller R: 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. 2005, 280: 26241-26247. 10.1074/jbc.M500447200.
Waller F, Achatz B, Baltruschat H, Fodor J, Becker K, Fischer M, Heier T, H°Ckelhoven R, Neumann C, von Wettstein D, Franken P, Kogel KH: The endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield. Proc Natl Acad Sci U S A. 2005, 102: 13386-13391. 10.1073/pnas.0504423102.
Yadav V, Kumar M, Deep DK, Kumar H, Sharma R, Tripathi T, Tuteja N, Saxena AK, Johri AK: A phosphate transporter from the root endophytic fungus Piriformospora indica plays a role in phosphate transport to the host plant. J Biol Chem. 2010, 285: 26532-26544. 10.1074/jbc.M110.111021.
Baltruschat H, Fodor J, Harrach BD, Niemczyk E, Barna B, Gullner G, Janeczko A, Kogel KH, Schäfer P, Schwarczinger I, Zuccaro A, Skoczowski A: Salt tolerance of barley induced by the root endophyte Piriformospora indica is associated with a strong increase in antioxidants. New Phytol. 2008, 180: 501-510. 10.1111/j.1469-8137.2008.02583.x.
Sun C, Johnson JM, Cai D, Sherameti I, Oelmüller R, Lou B: Piriformospora indica confers drought tolerance in Chinese cabbage leaves by stimulating antioxidant enzymes, the expression of drought-related genes and the plastid-localized CAS protein. J Plant Physiol. 2010, 167: 1009-1017. 10.1016/j.jplph.2010.02.013.
Stein E, Molitor A, Kogel KH, Waller F: Systemic resistance in Arabidopsis conferred by the mycorrhizal fungus Piriformospora indica requires jasmonic acid signaling and the cytoplasmic function of NPR1. Plant Cell Physiol. 2008, 49: 1747-1751. 10.1093/pcp/pcn147.
Grimmer MK, John Foulkes M, Paveley ND: Foliar pathogenesis and plant water relations: a review. J Exp Bot. 2012, 63: 4321-4431. 10.1093/jxb/ers143.
Hammes UZ, Schachtman DP, Berg RH, Nielsen E, Koch W, McIntyre LM, Taylor CG: Nematode-induced changes of transporter gene expression in Arabidopsis roots. Mol Plant-Microbe Interact. 2005, 12: 1247-1257. 10.1094/MPMI-18-1247.
Guan Y, Nothnagel EA: Binding of arabinogalactan proteins by Yariv phenylglycoside triggers wound-like responses in Arabidopsis cell cultures. Plant Physiol. 2004, 135: 1346-1366. 10.1104/pp.104.039370.
Manzoor H, Kelloniemi J, Chiltz A, Wendehenne D, Pugin A, Poinssot B, Garcia-Brugger A: Involvement of the glutamate receptor AtGLR3.3 in plant defense signaling and resistance to Hyaloperonospora arabidopsidis. Plant J. 2013, 76: 466-480. 10.1111/tpj.12311.
Johnson JM, Reichelt M, Vadassery J, Gershenzon J, Oelmüller R: An Arabidopsis mutant impaired in intracellular calcium elevation is sensitive to biotic and abiotic stress. BMC Plant Biol. 2014, 14: 162-10.1186/1471-2229-14-162.
Zhao K, Penttinen P, Chen Q, Guan T, Lindström K, Ao X, Zhang L, Zhang X: The rhizospheres of traditional medicinal plants in Panxi, China, host a diverse selection of actinobacteria with antimicrobial properties. Appl Microbiol Biotechnol. 2012, 94: 1321-1335. 10.1007/s00253-011-3862-6.
Maldonado-González MM, Bakker PA, Mercado-Blanco J: Use of Arabidopsis thaliana to study mechanisms of control of Verticillium wilt by Pseudomonas fluorescens PICF7. Commun Agric Appl Biol Sci. 2012, 77: 23-28.
Berg G, Krechel A, Ditz M, Sikora RA, Ulrich A, Hallmann J: Endophytic and ectophytic potato-associated bacterial communities differ in structure and antagonistic function against plant pathogenic fungi. FEMS Microbiol Ecol. 2005, 51: 215-229. 10.1016/j.femsec.2004.08.006.
El Hadrami A, Adam LR, Daayf F: Biocontrol treatments confer protection against Verticillium dahliae infection of potato by inducing antimicrobial metabolites. Mol Plant-Microbe Interact. 2011, 24: 328-335. 10.1094/MPMI-04-10-0098.
Prieto P, Schilirò E, Maldonado-González MM, Valderrama R, Barroso-Albarracín JB, Mercado-Blanco J: Root hairs play a key role in the endophytic colonization of olive roots by Pseudomonas spp. with biocontrol activity. Microb Ecol. 2011, 62: 435-445. 10.1007/s00248-011-9827-6.
Guo Q, Li S, Lu X, Li B, Ma P: PhoR/PhoP two component regulatory system affects biocontrol capability of Bacillus subtilis NCD-2. Genet Mol Biol. 2010, 33: 333-340. 10.1590/S1415-47572010005000032.
Müller H, Westendorf C, Leitner E, Chernin L, Riedel K, Schmidt S, Eberl L, Berg G: Quorum-sensing effects in the antagonistic rhizosphere bacterium Serratia plymuthica HRO-C48. FEMS Microbiol Ecol. 2009, 67: 468-478. 10.1111/j.1574-6941.2008.00635.x.
Garmendia I, Goicoechea N, Aguirreolea J: Moderate drought influences the effect of arbuscular mycorrhizal fungi as biocontrol agents against Verticillium-induced wilt in pepper. Mycorrhiza. 2005, 15: 345-356. 10.1007/s00572-004-0336-z.
Li F, Wang J, Ma C, Zhao Y, Wang Y, Hasi A, Qi Z: Glutamate receptor-like channel3.3 is involved in mediating glutathione-triggered cytosolic calcium transients, transcriptional changes, and innate immunity responses in Arabidopsis. Plant Physiol. 2013, 162: 1497-1509. 10.1104/pp.113.217208.
Cao L, Wang L, Zheng M, Cao H, Ding L, Zhang X, Fu Y: Arabidopsis AUGMIN subunit8 is a microtubule plus-end binding protein that promotes microtubule reorientation in hypocotyls. Plant Cell. 2013, 25: 2187-2201. 10.1105/tpc.113.113472.
Cheong MS, Kirik A, Kim JG, Frame K, Kirik V, Mudgett MB: AvrBsT acetylates Arabidopsis ACIP1, a protein that associates with microtubules and is required for immunity. PLoS Pathog. 2014, 10: e1003952-10.1371/journal.ppat.1003952.
Underwood W, Somerville SC: Perception of conserved pathogen elicitors at the plasma membrane leads to relocalization of the Arabidopsis PEN3 transporter. Proc Natl Acad Sci U S A. 2014, 110: 12492-12497. 10.1073/pnas.1218701110.
Yuan HY, Yao LL, Jia ZQ, Li Y, Li YZ: Verticillium dahliae toxin induced alterations of cytoskeletons and nucleoli in Arabidopsis thaliana suspension cells. Protoplasma. 2006, 229: 75-82. 10.1007/s00709-006-0154-6.
Yao LL, Pei BL, Zhou Q, Li YZ: NO serves as a signaling intermediate downstream of H2O2 to modulate dynamic microtubule cytoskeleton during responses to VD-toxins in Arabidopsis. Plant Signal Behav. 2012, 7: 174-177. 10.4161/psb.18768.
Wang B, Yang X, Zeng H, Liu H, Zhou T, Tan B, Yuan J, Guo L, Qiu D: The purification and characterization of a novel hypersensitive-like response-inducing elicitor from Verticillium dahliae that induces resistance responses in tobacco. Appl Microbiol Biotechnol. 2012, 93: 191-201. 10.1007/s00253-011-3405-1.
Murashige T, Skoog F: A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant. 1962, 15: 473-497. 10.1111/j.1399-3054.1962.tb08052.x.
Hill TW, Kaefer E: Improved protocols for Aspergillus minimal medium: trace element and minimal medium salt stock solutions. Fungal Genet Newsl. 2001, 48: 20-21.
Johnson JM, Sherameti I, Ludwig A, Nongbri PL, Sun C, Lou B, Varma A, Oelmüller R: Protocols for Arabidopsis thaliana and Piriformospora indica co-cultivation - A model system to study plant beneficial traits. Endocyt Cell Res. 2011, 21: 101-113.
Bains PS, Tewari JP: Purification, chemical characterization and host-specificity of the toxin produced by Alternaria brassicae. Physiol Mol Plant Pathol. 1987, 30: 259-271. 10.1016/0885-5765(87)90039-7.
Camehl I, Sherameti I, Venus Y, Bethke G, Varma A, Lee J, Oelmüller R: Ethylene signalling and ethylene-targeted transcription factors are required to balance beneficial and nonbeneficial traits in the symbiosis between the endophytic fungus Piriformospora indicaand Arabidopsis thaliana.New Phytol. 2010, 185: 1602-1673. 10.1111/j.1469-8137.2009.03149.x.
Johnson JM, Lee Y-C, Camehl I, Sun C, Yeh K-W, Oelmüller R: Piriformospora indicapromotes growth of Chinese cabbage by manipulating auxin homeostasis - role of auxin inPiriformospora indicasymbioses.Piriformospora indica: Sebacinales And Their Biotechnological Applications. Soil Biology Volume 33. Edited by: Varma A, Kost G, Oelmüller R. Springer, Berlin Heidelberg Germany; 2013:325-343. 1,
Naik ST, Lakkund LR: Diagrammatic representation of leaf area damage in tar spot of Dalbergia latifolia. Indian Forestry. 1997, 124: 1057-1058.
Wheeler BE: An Introduction to Plant Diseases. 1969, John Wiley and Sons Limited, London
Vadassery J, Reichelt M, Hause B, Gershenzon J, Boland W, Mithöfer A: CML42-mediated calcium signaling coordinates responses to Spodoptera herbivory and abiotic stresses in Arabidopsis. Plant Physiol. 2012, 159: 1159-1175. 10.1104/pp.112.198150.
Yang Y: Study on rapid determination of chlorophyll content of leaves. Chin J Spectroscopy Lab. 2002, 19: 478-481.
Vadassery J, Ranf S, Drzewiecki C, Mithöfer A, Mazars C, Scheel D, Lee J, Oelmüller R: A cell wall extract from the endophytic fungus Piriformospora indica promotes growth of Arabidopsis seedlings and induces intracellular calcium elevation in roots. Plant J. 2009, 59: 193-206. 10.1111/j.1365-313X.2009.03867.x.
Knight MR, Campbell AK, Smith SM, Trewavas AJ: Transgenic plant aequorin reports the effects of touch and cold-shock and elicitors on cytoplasmic calcium. Nature. 1991, 352: 524-526. 10.1038/352524a0.
Zhen XH, Li YZ: Ultrastructural changes and location of beta-1, 3-glucanase in resistant and susceptible cotton callus cells in response to treatment with toxin of Verticillium dahliae and salicylic acid. J Plant Physiol. 2004, 161: 1367-1377. 10.1016/j.jplph.2004.04.007.
We like to thank Sarah Mußbach and Claudia Röppischer for their excellent technical assistance. Special thanks go to Dr. Justin Lee from Leibniz Institute of Plant Biochemistry, Halle, Germany, for providing ein3 mutant seeds and to Prof. Daguang Cai from University of Kiel, Germany, for providing Vd primers. C.S. was supported by the German Science Foundation and the German Exchange Program (DAAD). R.O. and K-W.Y. are supported by a travel exchange project (DAAD).
The authors declare that they have no competing interests.
CS designed and carried out most of the experiments. YQS prepared the exudates from V. dahliae. KV helped for root microscopy and long term experiments in soil. JL and SB did the phytohormone analysis. SD, K-WY, BL and ITB contributed to the discussion. CS, IS and RO wrote the article. RO supervised the research. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Figure S1.: Co-cultivation time scheme. The seeds were first kept at 4°C in the dark for 2 days and were then transferred to a light/dark cycle at 22°C for 9 days. These seedlings were used for the experiments, by either transferring them to a plate with Vd or Pi (or no fungus, control, C) at day 0. The seedlings were harvested 10, 14 or 21 days later. In case of transfer from Vd to Pi or vice versa, the transfer occurred at day 4. Figure S2. Induction of GLR genes in shoots of Arabidopsis seedlings after 1 and 14 days. Figure S3. Phenotype of ein3-1 and WT after 21 days of co-cultivation following the 5 treatments described in Methods. Figure S4. ET content in shoots of ein3-1 seedlings after 3 weeks. Figure S5. Phenotypes of WT and ein3-1 after Vd spore inoculation in vivo and in vitro. Figure S6. Phenotype of WT and cycam1 mutant 21 days after Vd inoculation. Table S1. Primer list for RT-PCR and PCR analysis. (PDF 545 KB)
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Sun, C., Shao, Y., Vahabi, K. et al. The beneficial fungus Piriformospora indica protects Arabidopsis from Verticillium dahliaeinfection by downregulation plant defense responses. BMC Plant Biol 14, 268 (2014). https://doi.org/10.1186/s12870-014-0268-5
- Jasmonic acid
- Piriformospora indica
- Salicylic acid
- Verticillium dahliae