Shoot- and root-borne cytokinin influences arbuscular mycorrhizal symbiosis
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The arbuscular mycorrhizal (AM) symbiosis is functionally important for the nutrition and growth of most terrestrial plants. Nearly all phytohormones are employed by plants to regulate the symbiosis with AM fungi, but the regulatory role of cytokinin (CK) is not well understood. Here, we used transgenic tobacco (Nicotiana tabacum) with a root-specific or constitutive expression of CK-degrading CKX genes and the corresponding wild-type to investigate whether a lowered content of CK in roots or in both roots and shoots influences the interaction with the AM fungus Rhizophagus irregularis. Our data indicates that shoot CK has a positive impact on AM fungal development in roots and on the root transcript level of an AM-responsive phosphate transporter gene (NtPT4). A reduced CK content in roots caused shoot and root growth depression following AM colonization, while neither the uptake of phosphorus or nitrogen nor the root transcript levels of NtPT4 were significantly affected. This suggests that root CK may restrict the C availability from the roots to the fungus thus averting parasitism by AM fungi. Taken together, our study indicates that shoot- and root-borne CK have distinct roles in AM symbiosis. We propose a model illustrating how plants may employ CK to regulate nutrient exchange with the ubiquitous AM fungi.
KeywordsNicotiana tabacum Rhizophagus irregularis Symbiosis Cytokinin Carbon Phosphate transporter genes
The arbuscular mycorrhizal (AM) symbiosis, a widespread association between terrestrial plants and fungi of the phylum Glomeromycota, is regulated from the plant side by nearly all known phytohormones (Bucher et al. 2014; Gutjahr 2014; Pozo et al. 2015). Cytokinins (CK) constitute a class of phytohormones that regulates many fundamental aspects of plant development (Kieber and Schaller 2014; Werner and Schmülling 2009). Plants colonized by AM fungi generally have enhanced CK levels in both shoots and roots compared with non-AM (NAM) plants (Allen et al. 1980; Barker and Tagu 2000; Shaul-Keinan et al. 2002). Yet, the function of CK in AM symbioses is poorly understood.
The AM fungi are obligate biotrophs that obtain photosynthetically fixed carbon (C) in colonized roots via transport of sugars from root cortex cells to the intracellular arbuscules in the apoplast of the root cortex cells and to the intercellular hyphae (Helber et al. 2011; Smith and Read 2008). In exchange, the AM mycelium spreading into the soil takes up mineral nutrients particularly phosphorus (P), along with nitrogen (N) and other minerals, transports them through their hyphae towards the root, and delivers them via the arbuscules into the surrounding plant cells (Marschner 1995; Nouri et al. 2014). The mycorrhizal delivery of P is regulated by the root through particular phosphate (Pi) transporter (PT) genes (Maeda et al. 2006; Nagy et al. 2005). The direct pathway for Pi uptake via root hairs and epidermis may be, in some cases, suppressed by AM colonization (Chen et al. 2007; Grunwald et al. 2009; Javot et al. 2007). Despite the reciprocal nutritional benefit, the plant growth response to AM colonization can range from positive to negative according to a mutualism-parasitism continuum (Johnson 2010). Mutualistic benefits of delivered P are predicted to be the greatest in soils that are characterized by high N and low P availability (Johnson 2010). By contrast, when neither N nor P is limited, fungal growth is primarily limited by C, so the fungal C demand can increase to the point where it may depress plant growth and generate fungal parasitism (Johnson 2010). Other factors such as fungal genotype, competition, or complementarity can influence as well the AM symbiotic outcome (Angelard et al. 2010; Engelmoer et al. 2014; Jansa et al. 2008; Maherali and Klironomos 2007).
The study of mutants and transgenic plants altered in phytohormone metabolism or perception has provided major insights into their role in the regulation of AM symbiosis. The arbuscule formation vital to the net benefits of AM symbiosis is regulated positively by abscisic acid (ABA), via a dual ethylene-dependent⁄ethylene-independent mechanism (Martín-Rodríguez et al. 2011). In contrast to ABA, gibberellic acid (GA) negatively regulates arbuscule formation via degradation of DELLA proteins, which are required for arbuscule formation (Floss et al. 2013; Foo et al. 2013; Yu et al. 2014). Jasmonate positively regulates arbuscule formation but negatively regulates fungal spread inside the roots, possibly by restricting the C allocated to colonized roots or by increasing root defenses (Gutjahr et al. 2015; Wasternack and Hause 2014). Salicylic acid slows down fungal growth without changing final colonization (Herrera-Medina et al. 2003). Absence of brassinosteroids do not appear to affect directly the arbuscule formation but decreases AM hyphal colonization (Bitterlich et al. 2014). Auxin appears to enhance the hyphal colonization, and auxin perception is required for arbuscule formation (Etemadi et al. 2014; Hanlon and Coenen 2011). In pea (Pisum sativum), the auxin effect was partially mediated by strigolactones (Foo 2013), which in turn stimulate the presymbiotic hyphal branching and enhance the number of infection points in the roots (Yoshida et al. 2012). Altogether, it is evident that plants can employ an extensive phytohormone network to regulate their symbiotic interaction with AM fungi.
Much less is known about the regulatory role of CK in AM symbioses. CK are N6-substituted purine derivatives that regulate many fundamental aspects of plant development, including photosynthesis and root uptake of mineral nutrients (Kieber and Schaller 2014; Werner and Schmülling 2009). The positive effects of AM fungi on the CK levels of the host plant (Allen et al. 1980; Baas and Kuiper 1989; Barker and Tagu 2000) appears to be uncharacteristic of pathogenic fungi (van Rhijn et al. 1997) and independent from the increased P supply in roots (Shaul-Keinan et al. 2002; Torelli et al. 2000). Drüge and Schonbeck (1992) observed a strong correlation between increased CK levels, improved photosynthesis, and enhanced growth of AM plants and hypothesized that CK is part of the positive AM effect on plant performance. However, this hypothesis has been contested as the correlation was not always observed (Baas and Kuiper 1989; Danneberg et al. 1993). Similarly, contradictory results have been found in genetic studies. For example, the cre1 mutation in Medicago truncatula, which causes reduced CK perception, had no effects on AM colonization (Laffont et al. 2015). In contrast, an increased AM colonization was observed in CK-deficient 35S:CKX2 transgenic tobacco (Nicotiana tabacum) (Cosme and Wurst 2013) as well as in the CK-overproducing E151 pea mutant (Jones et al. 2015). Thus, CK appears to have an elusive role in AM symbiosis, and it is yet unclear why AM plants generally have enhanced CK levels in both shoots and roots (Barker and Tagu 2000).
Because CK has opposite roles in shoot and root development (Werner et al. 2001, 2003), an adequate genetic approach to study the role of CK in AM symbiosis is to use plants with distinct contents of CK in these organs. A useful tool to generate plants with a lower CK content has been the ectopic expression of cytokinin oxidase/dehydrogenase (CKX) genes (Werner et al. 2001, 2003, 2010). CKX genes code for enzymes that irreversibly degrade CK in a single enzymatic step to biologically inactive molecules (Schmülling et al. 2003). Constitutive expression of CKX genes under the control of the 35S promoter reduced the levels of CK in the whole plant, which positively affects root growth, but strongly reduces shoot growth as well as leaf chlorophyll and sugar content (Werner et al. 2001, 2003, 2010). In order to generate plants with a reduced CK content particularly in roots, enhanced CKX expression has been limited mainly to the roots by using the tobacco root-specific promoter WRKY6 (Werner et al. 2010). Leaves of WRKY6:CKX1 transgenic plants (hereafter designated as W6:CKX1) exhibited levels of bioactive CKs similar to the leaves of wild-type (WT), whereas the levels of bioactive CKs in the roots were reduced by ∼30 % (Macková et al. 2013). Consequently, shoot development of W6:CKX1 plants was very similar to that of the WT, while the size of the root system was increased by 27–39 % (Macková et al. 2013; Werner et al. 2010).
In the present study, we tested whether a reduction of CK levels restricted mainly to the roots influences the plant interaction with AM fungi and whether the shoot CK status affects AM symbiosis as well. To this end, we compared the AM colonization and plant performance of W6:CKX1 transgenic tobacco plants with that of the untransformed WT and two transgenic lines with constitutive reduction of CK levels (35S:CKX1, 35S:CKX2). Furthermore, we tested whether AM fungal strains or their interaction influence the symbiotic outcome by using single and simultaneous inoculation with two different strains of Rhizophagus irregularis (formerly Glomus intraradices). Potential functional mechanisms underlying plant and fungal responses were explored by determining the P, N, and C content in shoots and the transcript levels of PT genes in roots.
Materials and methods
Plant and fungus
Rhizophagus irregularis (Błaszk., Wubet, Renker and Buscot) Walker and Schüßler (former Glomus intraradices) is a widespread AM fungus and the first one that has been used for large-scale transcriptome sequencing (Tisserant et al. 2012). Although it is generally effective in colonizing roots and transferring mineral nutrients to the host plant, R. irregularis symbiotic function may vary with strain genotype (Angelard et al. 2010). To unveil eventual strain effects, we used two different R. irregularis strains (RI and FM) obtained from INOQ GmbH (Soltau, Germany). Inocula of R. irregularis were produced in sand using mixed plant cultures of Plantago lanceolata, Tagetes erecta, and Zea mays, and contained 200 propagules mL−1, consisting of spores, hyphae, and colonized root pieces.
As a host plant, we used tobacco (N. tabacum L. cv. Samsun NN). The untransformed control is referred to as WT. The transgenic lines expressing W6:CKX1 (line W6-CKX1-24), 35S:CKX1 (line 35S:CKX1-50) and 35S:CKX2 (line 35S:CKX2-38) were described previously (Macková et al. 2013; Werner et al. 2001, 2008, 2010). Briefly, the W6:CKX1 tobacco line harbors the CKX1 gene of Arabidopsis thaliana (L.) Heynh. under the transcriptional control of the predominantly root-expressed WRKY6 promoter and has lower levels of bioactive CK mainly in roots (Macková et al. 2013; Werner et al. 2010). The 35S:CKX1 and 35S:CKX2 plant lines harbor two different CKX genes (CKX1 and CKX2, respectively) of A. thaliana under the transcriptional control of the constitutively expressed 35S promoter (Werner et al. 2001). Constitutive reduction of the CK content in 35S:CKX1 and 35S:CKX2 lines causes in addition to root enhancement a reduced shoot growth because CK is a positive regulator of shoot growth. Both lines differ in the expressivity of the phenotypic traits, with 35S:CKX1 expression causing stronger negative effects on shoot growth than 35S:CKX2, which is reflected by reduced photosynthesis and a lower content of soluble sugar (Werner et al. 2001, 2008).
Experimental set up
To test whether the root CK status influences the AM symbiosis, and eventually, if the CK status of the shoot has a role as well and whether AM fungal strains and/or their interaction influence the symbiotic outcome, we conducted a factorial experiment in a glasshouse (16-h light and 20/24 °C night/day temperatures). The factors were the tobacco line (four levels: WT, W6:CKX1, 35S:CKX1, 35S:CKX2); R. irregularis RI (two levels: −, +); and R. irregularis FM (two levels: −, +); which sums up in a full factorial design to 16 treatments, each treatment with 10 independent replicates. The experimental replicate consisted of a plastic pot (2 L) filled with an autoclaved (121 °C, 20 min) soil/sand mixture (1:1, v/v) described previously (Cosme et al. 2014). Briefly, the soil contained 6.9 mg/100 g P (calcium/acetate/lactate) and 0.12 % of N (C/N analyzer). We inoculated the pots according to AM treatment by mixing thoroughly 100 mL of inoculum on the top layer of the soil/sand mixture. Non-AM (NAM) control pots received sterilized inoculum (autoclaved at 121 °C for 20 min), the R. irregularis RI and FM pots received their respective strain inoculum, and the co-inoculated pots received 100 mL of a mixture (1:1, v/v) of both strain inocula. Additionally, the pots received a microbial wash (20-μm sieve) produced from fungal inocula to correct for the potential presence of NAM microbial backgrounds. All tobacco seeds were surface-sterilized in 1.2 % NaClO for 5 min and rinsed with H2O prior use. Each pot was sown with several seeds of the respective tobacco line and immediately after germination the seedlings were thinned, allowing only one single plant to grow in each pot. Plants were watered regularly and fertilized every week with double strength of a modified Hoagland’s solution without P (no. 3 as described by Douds and Schenck 1990) to facilitate AM colonization. After 8 weeks of growth, the number of flowers per plant was counted and all plants were harvested by cutting the shoot at the ground level. The soil was carefully washed away from roots and root sub-samples (0.3 g) were instantly frozen in liquid N2 and stored in −80 °C to analyze transcript levels as described later. The shoots and roots were dried in an oven during 1 week at 60 °C and subsequently, their biomasses were recorded.
AM fungal colonization
To evaluate whether an altered CK content affects AM fungal development, we assessed the percentage of root length colonized by AM hyphae and arbuscules in all experimental plants. To this end, random samples of 10 2-cm-long root fragments were collected from each root system and stained using the ink and vinegar method (Vierheilig et al. 1998). The percent of root length colonization was determined at the microscope (×200 magnification) using the magnified intersections method with 100 intersects per sample (McGonigle et al. 1990).
Content of phosphorus, nitrogen and carbon in shoots
To determine whether altered plant growth following R. irregularis colonization was correlated with an altered nutrient content, we determined the concentration and total content of N and P as well as the concentration of C in shoots. The dried shoots of each plant were homogenized by grinding to fine particles using a ball mill (MM 400, Retsch, Haan, Germany). Sub-samples (ca. 3 mg) of all ground shoots were placed into individual zinc capsules and the percentages of N and C in shoots were determined by standard procedures using a CN Elemental Analyzer (Euro EA, HEKAtech GmbH, Germany), with acetanilide as standard (HEKAtech M.135.17). The concentration of P was determined from ground shoots of five randomly selected plant replicates per treatment, with two technical repetitions (200 mg each) per plant replicate. Technical repetitions were microwave-digested in 5 mL of 65 % HNO3 and 3 mL of 30 % H2O2 using a MARSXpress (CEM GmbH, Kamp-Lintfort, Germany). The digested solution was filtered and diluted with H2O in 50-mL volumetric flasks, and P was measured photometrically following the DIN EN ISO 15681–1 norm and using a FIA modula (Medizin- und Labortechnik Engineering GmbH, Dresden, Germany).
Root transcript levels of phosphate transporter genes
Total RNA was extracted from roots of 8-week-old tobacco plants with the TRIzol method as described by Brenner et al. (2005). RNA was further purified by using RNeasy mini-columns including the on-column DNase digestion as described in the manufacturer’s protocol (appendix D of the QIAGEN RNeasy Mini Handbook, QIAGEN GmbH, Hilden, Germany). Equal amounts of starting material (1 μg of RNA) were used for complementary DNA synthesis using SuperScript III Reverse Transcriptase. Real-time PCR using FAST SYBR Green I technology was performed on an ABI PRISM 7500 sequence detection system (Applied Biosystems Inc., California, USA) and universal “FAST” cycling conditions (10 min at 95 °C, 40 cycles of 15 s at 95 °C and 60 s at 60 °C) followed by the generation of a dissociation curve to check for specificity of the amplification. Gene expression data were normalized against two different reference genes (N. tabacum elongation factor 1α (EF-1α), and L25 ribosomal protein) according to Vandesompele et al. (2002) and are presented relative to the control treatment. Primers used for reference genes and genes of interest are listed in Supplemental Table 1.
We analyzed AM fungal colonization by two-way ANOVA using only inoculated plants with the categorical factors tobacco line (four levels: WT, W6:CKX1, 35S:CKX1, or 35S:CKX2) and AM inoculation (three levels: R. irregularis RI, R. irregularis FM, or both RI and FM), since we did not observe colonization in NAM plants and ANOVA is not valid with zero variances. Plant parameters were analyzed by three-way ANOVA with the categorical factors tobacco line (same levels as earlier), R. irregularis RI (two levels: −, +) and R. irregularis FM (two levels: −, +). Data were tested for normality of errors using Kolmogorov-Smirnov tests and for homogeneity of variances using Levene’s tests. In the case of non-normality and/or unequal variances, data were log or arcsine transformed prior to ANOVA. Multiple comparisons were analyzed by Duncan’s multiple range test. All data were analyzed in R Studio 0.97.332 (www.rstudio.com).
AM fungal colonization
Plant biomass and fitness
As a proxy for plant fitness, we counted the number of flowers in 8-week-old plants. As previously reported, a lowered CK content of the shoots retards the reproductive development of tobacco plants and reduces the overall number of flowers (Werner et al. 2001), which is confirmed by the 35S:CKX1 and 35S:CKX2 NAM plants in our Fig. 2c. As for plant biomass, the effects of AM fungal inoculations on the number of flowers depended on the combination of R. irregularis inoculation and plant genotype (Fig. 2c; Supplemental Table 3). R. irregularis strain RI reduced the number of flowers of WT by 75 %, while the effects of strain FM and co-inoculation of the strains were not significant compared with the NAM WT plants (Fig. 2c). Although the single-strain inoculations had no significant effects on the number of flowers of W6:CKX1 and 35S:CKX2 (Fig. 2c), the co-inoculation with both strains reduced the number of flowers by 87 and 58 % in W6:CKX1 and 35S:CKX2 compared to their NAM control plants, respectively (Fig. 2c). In contrast, the reproductive development of 35S:CKX1 was not affected by AM fungal colonization (Fig. 2c). Taken together, the increased susceptibility of the plants to fungal parasitism observed on the plant biomass was also reflected in altered plant fitness.
Content of phosphorus, nitrogen, and carbon in shoots
The concentration of N in shoots was also altered by the AM fungal inoculations depending on the plant genotype (Fig. 3c; Supplemental Table 4). Strain RI increased the concentration of N in shoots of WT and 35S:CKX2, while the strain FM increased only the concentration of N in shoots of W6:CKX1 (Fig. 3c). Co-inoculation with RI and FM suppressed the positive effect of RI on the concentration of N in shoots of WT, enhanced synergistically the concentration of N in shoots of W6:CKX1, and maintained the positive effects of RI on the concentration of N in shoots of 35S:CKX2 (Fig. 3c). These increases, however, were associated with an unchanged total N content in shoots (Fig. 3d; Supplemental Table 4). Similarly to the results for P, the concentration and total content of N in shoots of 35S:CKX1 remained unaltered across fungal inoculations (Fig. 3c, d). Overall, the AM-mediated increases of P and N were not generally associated with increases of total uptake, except for the P benefit provided by strain RI to WT plants (Fig. 3).
Root transcript levels of phosphate transporter genes
AM fungi can affect the endogenous CK levels in shoots and roots of their host plants. These effects may be either positive (Allen et al. 1980; Baas and Kuiper 1989; Danneberg et al. 1993; Drüge and Schonbeck 1992; Shaul-Keinan et al. 2002; Torelli et al. 2000; Yao et al. 2005), neutral (Danneberg et al. 1993; Jones et al. 2015), or negative (Drüge and Schonbeck 1992; Jones et al. 2015; Torelli et al. 2000). In tobacco, P supply alone had similar positive effects on the CK metabolite levels in leaves as R. irregularis, while in roots the fungus induced specifically a zeatin riboside and increased by 16-fold the induction of a isopentenyl adenosine compared with P supply (Shaul-Keinan et al. 2002). This suggests a high degree of AM specificity in inducing the CK levels in roots. As a lowered CK status in tobacco can increase AM hyphal colonization (Cosme and Wurst 2013), it is plausible that increased levels of CK in roots may cause a negative feedback on further fungal colonization. In our study, the constitutive reduction of CK levels in 35S:CKX1 plants caused a stronger reduction on the shoot than 35S:CKX2 and reduced the hyphal and arbuscule colonization as well as the NtPT4 induction. However, these reductions were not observed in the W6:CKX1 plants that have a lowered CK levels restricted to their roots. This suggests that the reduced colonization and NtPT4 induction in 35S:CKX1 was caused by the lowered CK levels in the shoots but not in the roots. Consistently, it was recently reported that the positive effects of plant CK overproduction on arbuscule colonization in pea was controlled by the shoots (Jones et al. 2015). In our study, although we observed strong plant-fungus interactions, possibly caused by specificities of plant and fungal genotypes, the use of different transgenic tobacco lines, R. irregularis strains, and their co-inoculation unveiled consistent functions of root CK. Root CK prevented root growth depression following R. irregularis colonization, restricted synergistic depressions of the plant growth, the fitness, and the shoot concentration of C following strain co-inoculation, and secured a P benefit when the symbiotic cost on shoot growth and plant fitness was strong. Taken together, our data suggests that shoot- and root-specific alterations of CK levels can both play important functions in AM symbioses.
The comparison of R. irregularis colonization in W6:CKX1, 35S:CKX1, and WT plants revealed a positive impact of shoot CK on AM symbiosis. This positive impact became evident through the reduced AM colonization success in 35S:CKX1 plants which differed from the two other genotypes by a stronger shoot reduction as a consequence of the lowered CK status. Consistently, Jones et al. (2015) used grafting experiments to show that the positive effects of the CK-overproducing E151 pea mutant on the number of arbuscules in roots was regulated only by the shoot CK status. In our study, the difference in AM colonization may be caused by a lower sugar availability derived from source leaves, as the leaves of 35S:CKX1 transgenic tobacco have a 30 % reduction in sugar content compared with the leaves of WT (Werner et al. 2008). In addition, 35S:CKX1 plants accumulate 80 % more starch in sink leaves than the WT (Werner et al. 2008), which represent an aboveground sink that may contribute to restrict further the fungal access to C in roots, and consequently reduce the AM symbiotic development, i.e., decrease hyphal and arbuscules colonization and NtPT4 induction. Consistently, this C restriction protected 35S:CKX1 roots against fungal parasitism as reflected by the neutral effects on plant growth and fitness. The root transcription of PT4 is specifically induced in root cortex cells during arbuscule formation to equip the cell membranes for Pi transport (Chen et al. 2007; Franken et al. 2007) and may require the transcription of an AM fungal monosaccharide transporter (MST) gene, which in turn is induced by sugar availability (Helber et al. 2011). Thus, an indirect negative effect of a low-shoot CK status on root NtPT4 transcription seems likely, i.e., a reduced source of sugars in 35S:CKX1 plants could limit the induction of NtPT4 transcription in response to AM colonization, thus reducing the AM pathway for P uptake (Fig. 6). Altogether, this suggests that the general positive effects of AM fungi on shoot CK (e.g., Allen et al. 1980) may positively feedback on the functioning of AM symbiosis, possibly through an enhanced source of C.
The lowered CK levels in roots of W6:CKX1 and 35S:CKX2 supported higher AM fungal colonization than 35S:CKX1 and were susceptible to AM-mediated root growth depression, while the WT was not. Yet, the induction of NtPT4 transcripts was not significantly affected by root CK, as the induced levels were not significantly different among WT, W6:CKX1, and 35S:CKX2. Furthermore, the plant uptake of P and N was not limited by the AM-mediated root growth depression. A remarkable and surprising result was the genotype-specific effect of fungal co-inoculation on plant growth. Co-inoculation with RI and FM neutralized their negative effects on shoot biomass formation of WT. However, it led to a synergistic reduction of the shoot and root biomasses and C concentration in shoots of W6:CKX1, which suggests that a lowered CK status confined to the roots may facilitate fungal acquisition of C independently of fungal P supply (Fig. 6). In M. truncatula, an extensive growth of intercellular hyphae in roots of della1/della2 mutants and GA-treated WT without formation of arbuscules also suggested that fungal acquisition of C was independent of fungal P supply (Floss et al. 2013). Kiers et al. (2011) suggested that plants can detect, discriminate, and reward the best AM fungal partner with more C to stabilize cooperation in AM symbiosis. Our study, as well as the one of Floss et al. (2013), indicates that individual phytohormones regulate differently distinct components of this nutrient exchange. As the levels of these phytohormones are altered in response to the ever-changing environment (Pozo et al. 2015), this could explain in part why the controlled reciprocal rewards model proposed by Kiers et al. (2011) cannot always be applied (Walder and van der Heijden 2015). Consistent with our results, the levels of CK in roots of the hyper-mycorrhizal CK-overproducing E151 pea mutant dropped down to levels similar to the WT after inoculation (Jones et al. 2015). This might explain also why the lowered CK levels in 35S:CKX2 plants led to enhanced AM hyphal colonization in roots (Cosme and Wurst 2013). Indirect evidence has suggested that the intraradical hyphae can take up C in roots independently from the formation of arbuscules (Smith and Read 2008). Moreover, in contrast to the intracellular arbuscules, the membranes of the intercellular hyphae have a high ATPase activity and are therefore energized for active transport of sugars (Gianinazzi-Pearson et al. 1991) and can express a MST gene (Helber et al. 2011). On the other hand, although the lowered CK status in tobacco roots increased root growth rates (Werner et al. 2001, 2010), their sugar content was reduced presumably due to the rapid metabolic utilization for growth (Werner et al. 2008). This implies that transfer of sugars from the plant to the AM fungus in roots with a lowered CK status is most likely mediated by active hyphal transport, with an AM fungal sink competing effectively with the sink systems of the host plant. Thus, an AM-specific increase of CK levels in tobacco roots (Shaul-Keinan et al. 2002) might be involved in enhancing the C sink capacity of the plant in relation to that of the fungus, which in turn may limit hyphal proliferation in roots (Cosme and Wurst 2013) or avert fungal parasitism.
The relation between CK and growth of AM plants has been so far unclear. A strong correlation between increased CK levels and improved photosynthesis and growth of AM plants led to the hypothesis that CK is part of the positive AM effect on plant performance (Allen et al. 1980; Drüge and Schonbeck 1992). However, this hypothesis has been disputed as a correlation was not always observed (Baas and Kuiper 1989; Danneberg et al. 1993). The AM fungi, however, do not always increase simultaneously the CK levels in shoots and roots and may even reduce it in roots under specific conditions. The CK levels might decrease in AM roots under high P amendment (Torelli et al. 2000) or temporarily during early colonization (Drüge and Schonbeck 1992), which is often associated with plant growth depression (Johnson 2010; Smith and Read 2008). Neutral growth responses in AM plants have been associated with elevated root CK levels combined with small or no changes in shoot CK content (Baas and Kuiper 1989; Danneberg et al. 1993; Shaul-Keinan et al. 2002). A stronger increase of the shoot CK content accompanied by elevated root CK levels were associated with a positive plant growth response to AM symbiosis (Allen et al. 1980; Drüge and Schonbeck 1992; Yao et al. 2005). Our study suggests that both shoot- and root-specific alterations of CK levels play important roles in the relation between CK homeostasis and growth of AM plants. The shoot CK seems to affect positively AM functioning, potentially enhancing the AM pathway for P uptake, while root CK avert fungal parasitism, possibly by limiting the relative C sink capacity of the fungus. Therefore, the general positive effects of AM fungi on the CK levels in both shoots and roots (e.g., Allen et al. 1980) might be required to balance the C for P exchange between symbionts (Fig. 6) and consequently for the growth promotion of AM plants. By using root-specific and constitutive expression of CKX genes, our study provides a model (Fig. 6) illustrating how plants may employ CK in shoots and roots as part of their regulatory network to fine-tune the bidirectional exchange of nutrients with ubiquitous AM fungi.
MC was supported by the doctoral grant SFRH/BD/81785/2011 from Fundação para a Ciência e a Tecnologia, Portugal. This study was partially funded by the Dahlem Centre of Plant Sciences of Freie Universität Berlin, the Ministries of Consumer Protection, Food and Agriculture of the Federal Republic of Germany, the Ministry for Science, Research and Culture of the State of Brandenburg, and the Thuringian Ministry of Infrastructure and Agriculture, Germany. We are thankful to Kerstin Fischer, Monika Fünning, Kerstin Schmidt, and Dominic Schmitz for technical help.
- Brenner WG, Romanov GA, Köllmer I, Bürkle L, Schmülling T (2005) Immediate-early and delayed cytokinin response genes of Arabidopsis thaliana identified by genome-wide expression profiling reveal novel cytokinin-sensitive processes and suggest cytokinin action through transcriptional cascades. Plant J 44:314–333. doi: 10.1111/j.1365-313X.2005.02530.x CrossRefPubMedGoogle Scholar
- Grunwald U, Guo W, Fischer K et al (2009) Overlapping expression patterns and differential transcript levels of phosphate transporter genes in arbuscular mycorrhizal, Pi-fertilised and phytohormone-treated Medicago truncatula roots. Planta 229:1023–1034. doi: 10.1007/s00425-008-0877-z CrossRefPubMedPubMedCentralGoogle Scholar
- Helber N, Wippel K, Sauer N, Schaarschmidt S, Hause B, Requena N (2011) A versatile monosaccharide transporter that operates in the arbuscular mycorrhizal fungus Glomus sp is crucial for the symbiotic relationship with plants. Plant Cell 23:3812–3823. doi: 10.1105/tpc.111.089813 CrossRefPubMedPubMedCentralGoogle Scholar
- Jones JMC, Clairmont L, Macdonald ES, Weiner CA, Emery RJN, Guinel FC (2015) E151 (sym15), a pleiotropic mutant of pea (Pisum sativum L.), displays low nodule number, enhanced mycorrhizae, delayed lateral root emergence, and high root cytokinin levels. J Exp Bot 66:4047–4059. doi: 10.1093/jxb/erv201 CrossRefPubMedPubMedCentralGoogle Scholar
- Kieber JJ, Schaller GE (2014) Cytokinins. In: The Arabidopsis book. The American Society of Plant Biologists, p e0168. doi: 10.1199/tab.0168
- Marschner H (1995) Mineral nutrition of higher plants, 2nd edn. Acadamic, LondonGoogle Scholar
- Martín-Rodríguez JÁ, León-Morcillo R, Vierheilig H, Ocampo JA, Ludwig-Müller J, García-Garrido JM (2011) Ethylene-dependent/ethylene-independent ABA regulation of tomato plants colonized by arbuscular mycorrhiza fungi. New Phytol 190:193–205. doi: 10.1111/j.1469-8137.2010.03610.x CrossRefPubMedGoogle Scholar
- Nagy R, Karandashov V, Chague V et al (2005) The characterization of novel mycorrhiza-specific phosphate transporters from Lycopersicon esculentum and Solanum tuberosum uncovers functional redundancy in symbiotic phosphate transport in solanaceous species. Plant J 42:236–250. doi: 10.1111/j.1365-313X.2005.02364.x CrossRefPubMedGoogle Scholar
- Smith SE, Read DJ (2008) Mycorrhizal symbiosis, 3rd edn. Academic, LondonGoogle Scholar
- van Rhijn P, Fang Y, Galili S et al (1997) Expression of early nodulin genes in alfalfa mycorrhizae indicates that signal transduction pathways used in forming arbuscular mycorrhizae and Rhizobium-induced nodules may be conserved. Proc Natl Acad Sci U S A 94:5467–5472CrossRefPubMedPubMedCentralGoogle Scholar
- Werner T, Motyka V, Laucou V, Smets R, Van Onckelen H, Schmülling T (2003) Cytokinin-deficient transgenic Arabidopsis plants show multiple developmental alterations indicating opposite functions of cytokinins in the regulation of shoot and root meristem activity. Plant Cell 15:2532–2550. doi: 10.1105/tpc.014928 CrossRefPubMedPubMedCentralGoogle Scholar
- Werner T, Nehnevajova E, Köllmer I, Novák O, Strnad M, Krämer U, Schmülling T (2010) Root-specific reduction of cytokinin causes enhanced root growth, drought tolerance, and leaf mineral enrichment in Arabidopsis and tobacco. Plant Cell Online 22:3905–3920. doi: 10.1105/tpc.109.072694 CrossRefGoogle Scholar
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