Involvement of plant endogenous ABA in Bacillus megaterium PGPR activity in tomato plants
© Porcel et al.; licensee BioMed Central Ltd. 2014
Received: 8 October 2013
Accepted: 23 January 2014
Published: 25 January 2014
Plant growth-promoting rhizobacteria (PGPR) are naturally occurring soil bacteria which benefit plants by improving plant productivity and immunity. The mechanisms involved in these processes include the regulation of plant hormone levels such as ethylene and abscisic acid (ABA). The aim of the present study was to determine whether the activity of Bacillus megaterium PGPR is affected by the endogenous ABA content of the host plant. The ABA-deficient tomato mutants flacca and sitiens and their near-isogenic wild-type parental lines were used. Growth, stomatal conductance, shoot hormone concentration, competition assay for colonization of tomato root tips, and root expression of plant genes expected to be modulated by ABA and PGPR were examined.
Contrary to the wild-type plants in which PGPR stimulated growth rates, PGPR caused growth inhibition in ABA-deficient mutant plants. PGPR also triggered an over accumulation of ethylene in ABA-deficient plants which correlated with a higher expression of the pathogenesis-related gene Sl-PR1b.
Positive correlation between over-accumulation of ethylene and a higher expression of Sl-PR1b in ABA-deficient mutant plants could indicate that maintenance of normal plant endogenous ABA content may be essential for the growth promoting action of B. megaterium by keeping low levels of ethylene production.
KeywordsAbscisic acid Bacillus megaterium Ethylene Hormones PGPR Solanum lycopersicum Rhizobacteria
There are numerous reports of plant growth and yield stimulation by beneficial soil microorganisms [1–4]. A wide range of microorganisms which live in the soil are able to establish symbiotic and non-symbiotic associations with their host plants . These microorganisms play important functions in the soil which include: (1) controlling the adverse effects of pathogens on plant growth, (2) alleviating negative effects of soil stresses on plant growth and yield production, (3) biofertilization, (4) enhancing root growth, and (5) rhizoremediation [6–9].
Plant growth-promoting rhizobacteria (PGPR) are among the most effective and best studied soil microorganisms which can promote plant performance. PGPR can be classified as extracellular bacteria (existing in the rhizosphere, on the root surface or in the spaces between cells) and intracellular bacteria (mainly N2 fixing bacteria) . The action mechanisms of PGPR can be also divided into direct and indirect ones. Biofertilization, stimulation of root growth, rhizoremediation and plant stress control are the direct mechanisms. On the other hand, the mechanisms of biological control by which rhizobacteria can promote plant growth indirectly, by reducing the level of disease, include antibiosis, induction of systemic resistance and competition for nutrients and niches . Hormones such as auxins, ethylene, gibberellins, (+)- abscisic acid (ABA) and cytokinins regulate plant growth and development [10, 11]. Plant hormones are chemical messengers that affect the plant’s ability to respond to its environment. They are organic compounds that are effective at very low concentration and are usually synthesized in one part of the plant and transported to another location. Each plant response is often the result of two or more hormones acting together. Because hormones stimulate or inhibit plant growth, they are also referred as plant growth regulators. Plant-growth-promoting bacteria that contain the enzyme 1-aminocyclopropane-1-carboxylate (ACC) deaminase facilitate plant growth and development by decreasing plant ethylene levels. ACC is the precursor for the production of ethylene, whose amounts are increased under stress, affecting adversely plant growth and yield production. Hence, ethylene is one of the hormones regulating plant growth under different conditions including stress . Ethylene is a plant growth regulator essential for normal growth and development in plants. However, apart from this key function, ethylene also acts as a stress hormone when plants are exposed to salinity, drought, waterlogging, heavy metals or pathogens .
ABA plays an important role in many physiological processes in plants. This hormone is necessary for regulation of several events during late seed development and is crucial for the response to environmental stresses such as desiccation, salt and cold. Abscisic acid controls plant growth and inhibits root elongation , which means that there is a negative correlation between growth and the endogenous ABA content of plants . Despite this, ABA-deficient plants are usually smaller than wild-type (wt) plants . It has been reported that some bacterial species that interact with plants or live in the soil, synthesize ABA and other phytohormones such as indole-3-acetic acid (IAA), gibberellic acid, zeatin (cytokinin) and ethylene [16–18]. Some species from the genus Bacillus have been described not only as plant growth promoters but also as a biological control agents of diseases [19, 20]. So far, although impacts of one specific PGPR on ABA relations of Pisum sativum have been studied , no studies have been conducted to explain how endogenous levels of ABA could affect the PGPR function of Bacillus. In our study, tomato was chosen as the host plant. Tomato has a number of well-known ABA pathway mutants and represents an appropriate model for studying the role of endogenous ABA in plants responses to PGPR. The ABA-deficient tomato mutants flacca and sitiens and their near isogenic wild-type parental line were used in this study. Previous research has shown that these mutants have residual ABA levels (no more than 8% of the wild-type plants)  and are unable to increase their ABA levels when plants are exposed to stress .
A PGPR from degraded soil in southern Spain isolated by our group and identified as Bacillus megaterium  has been used in this study. Marulanda et al.  analyzed how this PGPR strain may influence two crucial components of plant salt tolerance such as root hydraulic characteristics and aquaporin regulation in maize plants. Maize plants inoculated with Bacillus megaterium subjected to salt stress, showed higher biomass production, lower necrotic leaf area and higher root hydraulic conductance than non inoculated control plants . In previous studies carried out by the same group it has been showed that this Bacillus megaterium strain was able to increase drought resistance in plants growing under water-limited conditions  and to increase plant growth under nutrient deficiency conditions . The aim of the present study was to determine whether the activity of Bacillus megaterium PGPR is affected by the endogenous abscisic acid (ABA) content of the host plant.
The experiment consisted of a randomized complete block design with two inoculation treatments: (1) non-inoculated control plants and (2) plants inoculated with the PGPR Bacillus megaterium strain which was isolated by Marulanda-Aguirre et al. , and two plant ABA line treatments: wild type and an ABA-deficient line (flacca or sitiens). There were ten replicated plants per treatment (one plant per pot). The plants were cultivated under well watered conditions throughout the entire experiment. Two different sets of experiments were carried out: one with wild type (cv Rheinlands Ruhm) and sitiens plants (from January to March) and the second with wild type (cv Ailsa Craig) and flacca plants (from March to May). All determinations (except biomass production that was measured in samples taken from both experiments) were carried out on samples taken from the second set of experiments.
Soil and biological materials
Peat and vermiculite mixture (1:1, v/v) was sterilized (120°C for 20 min). Seeds of tomato (Solanum lycopersicum) sitiens (LA0574) and its parental isogenic cv Rheinlands Ruhm, as well as flacca (LA3613) and corresponding parental isogenic cv Ailsa Craig, were obtained from the Tomato Genetics Resource Center (TGRC) at the University of California, Davis, CA, USA. The seeds were sterilized in a 70% ethanol solution for 2 min, then 50% sodium hypochlorite solution for 8 min and finally washed several times with sterile water to remove any trace of chemicals that could interfere with seed germination. The seeds were placed on sterile vermiculite at 25°C to germinate and 10-d-old seedlings were transferred to plastic pots containing 500 g of the peat moss/vermiculite mixture (1:1, v/v). A suspension (0.5 mL per seed) of the bacterium Bacillus megaterium (109 cell mL-1) grown in Luria-Bertani medium (LB) was sprinkled over each seedling one and seven days after planting. Non-inoculated control plants received the same number of applications with the same amount of growth medium without bacteria.
Tomato plants were grown for two months in a greenhouse under controlled climatic conditions (18–24°C, with an 18 h/6 h light/dark period and 50-60% relative humidity). A photoperiod of 16 h at a photosynthetic photon flux density (PPFD) of 600 μmol m-2 s-1,as measured with a light meter (model LI-188B; Licor Inc., Lincoln, NE, USA), was maintained throughout the experiment. Water was supplied daily to maintain constant soil water content close to water –holding capacity during the entire experiment.
At harvest (60 d after planting), the root system of 6 samples was separated from the shoot and fresh weight determined. Shoot and root dry weights were measured after drying in a forced draught oven at 70°C for 2 d. Plant height was also determined.
Stomatal conductance was recorded 2 h after dawn with the porometer system (Porometer AP4, Delta-T Devices Ltd., Cambridge, UK) in the last fully expanded leaf of six plants per treatment. Each measurement was repeated three times in each leaf, and the mean of the three measurements was considered in order to diminish variability in this parameter.
Competition assay for colonization of tomato root tip
In order to check the ability of the examined PGPR strain to colonize wild-type and mutant plants and to confirm its presence inside roots, a competition assay for colonization was carried out. The experiment consisted of a randomized complete block design with three plant ABA line treatment: wild type, sitiens and flacca plants and two inoculation treatments: (1) control plants inoculated with LB medium alone and (2) plants inoculated with Bacillus megaterium strain. Six replicates of each were done totaling 36. Sterilized tomato seeds were germinated in MS plates in darkness until plants had a root 1 cm in length. 10-days-old seedlings were transferred to glass bottles containing sterile peat and vermiculite mixture (1:1, v/v). 1 mL seedling-1 of LB medium (control plants) or a suspension (1 mL seedling-1) of Bacillus megaterium (inoculated plants) was sprinkled over each seed at the time of transferring to bottle. Bacillus megaterium was grown in LB medium supplemented with gentamycin 50 μg mL-1 until OD600 = 1.9-2 that correspond to cell density of about 109 cell mL-1. The glass bottles were kept for seven days in a controlled-climate growth chamber (18–24°C, 50-60% relative humidity, 16 h daylight) and the root systems reached an average length of 12 cm. The bacterial growth inside the roots was determined as described by Marulanda et al. . A 1 cm-long distal root segment was cut, cleaned and surface-disinfected (20 min in 30% [v:v] H2O2 followed by washing in five changes of distilled water). After grinding, 100 μL aliquots were suspended in 10 mL of sterile water (dilutions 10-2) and 1 mL of this suspension was serially diluted to each dilution of 10-2 – 10-7. Dilutions were plated in agar nutrient broth medium (8 g L-1) supplemented with gentamycin 50 μg mL-1 and cultivated for 48 h at 28°C. Colonization experiment was repeated twice.
Analysis of endogenous ABA
The concentration of ABA was analyzed in shoot extracts using high performance liquid chromatography-electrospray-mass spectrometry (HPLC-ESI-MS/MS). The extraction and purification of ABA were carried out using the method described by Bacaicoa et al.  with some variations. Frozen 0.5 g sample of plant tissue (previously ground to a powder in a mortar with liquid N) was homogenized with 5 mL of precooled (-20°C) methanol:water (80:20, v/v) and 2.5 mM Na diethyldithiocarbamate (DDTC). The deuterium-labelled internal standard [2H6] (+)-cis, trans-abscisic acid, (from Olchemim, Olomouc, Czech Republic) was added (100 μL of a stock solution of 400 ng mL-1 of standard in methanol) to the extraction medium. After overnight extraction at -20°C, solids were separated by centrifugation at 12000 × g for 10 min at 4°C using a Centrikon T-124 centrifuge with an A8.24 rotor (Kontron Instruments, Cumbernauld, United Kingdom) and re-extracted for 1 h with an additional 4 mL of extraction mixture. Supernatants were passed through a Strata C18-E cartridge (3 cm3, 200 mg) (Phenomenex, Torrance, CA; Ref. 8B-S001-FBJ), preconditioned with 4 mL of methanol followed by 2 mL of extraction medium. After evaporation at 40°C of aqueous phase using a Labconco Vortex Evaporator (Labconco Co., Kansas City, MO), 0.5 mL of 1 M formic acid was added. Then, ABA was extracted with two portions of 5 and 4 mL of diethyl ether, and the organic phase was evaporated to dryness. The residue was redissolved in 250 μL of methanol: 0.5% acetic acid (40:60, v/v). Before the injection in the HPLC-ESI-MS/MS system, the solution was centrifuged at 8000 × g for 5 min.
ABA was quantified by HPLC-ESI-MS/MS using a HPLC device (2795 Alliance HT; Waters Co., Milford, MA) coupled to a 3200 Q TRAP LC/MS/MS System (Applied Biosystems/MDS Sciex, Ontario, Canada), equipped with an electrospray interface. A reverse-phase column (Synergi 4 μm Hydro-RP 80A, 150 × 2 mm; Phenomenex, Torrance, CA) was used. A linear gradient of methanol (A) and 0.5% acetic acid in water (B) was used: 35% A for 1 min, 35% to 95% A in 9 min, 95% A for 4 min and 95% to 35% A in 1 min, followed by a stabilization time of 5 min. The flow rate was 0.20 mL min-1, the injection volume was 40 μL and column and sample temperatures was 20°C. The detection and quantification of ABA was carried out using multiple reaction monitoring (MRM) in the negative-ion mode, employing multilevel calibration curves with deuterated hormone as an internal standard. For further details see Bacaicoa et al. .
Analysis of endogenous ACC content
The extraction and purification of ACC (1-aminocyclopropane-1-carboxylic acid) was carried out using the method described by Mora et al. . Frozen plant tissue (0.25 g) previously ground using mortar and pestle with liquid nitrogen was homogenized with 20 μL of d4ACC (3 μg/mL in acetonitrile/ acetic acid 0.2% (90/10)) and 3 mL of MeOH/H2O/HCOOH (15/4/1, v/v/v) at -20°C. The mixture was vortexed (2000 rpm) for 10 min. After overnight extraction at -20°C, solids were separated by centrifugation (12000 rpm, 10 min, 4°C). Supernatants were purified using a Strata C18-E cartridge (Ref 8B-S001-FBJ, Phenomenex, Torrance, CA, USA) preconditioned with 4 mL of methanol and 2 mL of MeOH/H2O/HCOOH (15/4/1, v/v/v). The eluent was evaporated at 40°C until methanol was removed (Vortex evaporator mod. 432–2100 from Labconco Corporation, Kansas City, MO, USA). The residue was re-dissolved with 2 mL of MeOH/H2O/HCOOH (15/4/1) and stored at -20°C. After 1 h, the extract was newly centrifuged (12000 rpm, 10 min, 4°C). Supernatants were purified using the same Strata C18-E cartridge. After evaporation to near dryness, the residue was re-dissolved in 2 mL of formic acid 1 M, and applied to an Oasis MCK column (Ref. 186000254, Waters Co., Milford, MA) preconditioned with 4 mL of methanol and 2 mL of formic acid 1 M. The column was washed successively with 1 mL of formic acid 1 M and 1 mL of methanol. ACC was eluted with 1 mL of 0.35 M NH4OH. This eluted fraction was evaporated to dryness in the vortex evaporator and re-dissolved in 500 μL of acetonitrile/acetic acid 0.2% (90:10). Finally the eluted fraction was centrifuged (10000 rpm, 8 min) and injected in the LC/MS/MS systems.
ACC was quantified by HPLC linked to a 3200 QTRAP LC/MS/MS system (Applied Biosystems/ MDS Sciex, Ontario, Canada), equipped with a turbo ion spray interface. Detection and quantification were performed by multiple-reaction-monitoring (MRM) in the positive-ion mode, employing a multilevel calibration graph with deuterated d4ACC as internal standards. For further details see Mora et al. .
Analysis of ethylene production in plant tissues
Intact plants were enclosed in sealed acetate cylinders which were incubated at room temperature for 24 h. Samples of 500 μL were withdrawn from each acetate cylinder with a syringe and the ethylene content was quantified with a Hewlett Packard model 5890 gas chromatograph equipped with a Poropak-R column and a hydrogen flame ionization detector as described Porcel et al. .
RNA isolation and synthesis of first strand cDNA
Total RNA was isolated from tomato leaves from 3 different plants of each treatment by phenol/chloroform extraction method . DNase treatment of total RNA and cDNA synthesis was performed according to Qiagen’s protocol (Quantitect Reverse Transcription KIT Cat#205311, Qiagen, CA).
Quantitative real-time RT-PCR
The expression of Solanum lycopersicum 1-Amynocyclopropane-1-carboxylic acid oxidase (Sl-ACO4), 1-Aminocyclopropane-1-caboxylic acid synthase (Sl-ACS7), pathogenesis-related 1b (Sl-PR1b), 9-cis-epoxycarotenoid dioxygenase (Sl-NCED), and SlLE16 genes was studied by real-time PCR by using iCycler (Bio-Rad, Hercules, California, USA).
Primers used in this study
5′ - TCACCACCACTGCTGAACGGGA-3′
5′ - TGGGCAACGGAACCTCTCAGC -3′
5′ - GGGAGGGCAGCCGTGCAATT -3′
5′ - TGCAACGTGCCCGACCACAA -3′
5′ - TTCGCGCTCACACGGATGCT -3′
5′ - CACCTCTAGCTGATCGCCGAGG -3′
5′ - CGGTCTCCCCGGTTTTCGCA -3′
5′ - GTGGCCGCGGAGACAACCAT -3′
5′ - ACAGCCGACCCACGAGTCCA -3′
5′ - GGTGTCCGGCGGTTGGTTCA -3′
5′ - TCCCTTATCTCGAGGGTCGC -3′
5′ - CGCTGTCTTCCGGTCTTCTG -3′
Each 23 μL reaction contained 3 μL of a dilution 1:10 of the cDNA, 10.5 μL of Master Mix (Bio-Rad Laboratories S.A, Madrid), 8.6 μL of deionised water and 0.45 μxL of each primer pair. The PCR program consisted in 3 min incubation at 95°C to activate the hot-start recombinant Taq DNA polymerase, followed by 32 cycles of 30 s at 95°C, 30 s at 58°C and 30 s at 72°C, where the fluorescence signal was measured. The specificity of the PCR amplification procedure was checked with a heat dissociation protocol (from 70–100°C) after the final cycle of the PCR.
Four independent biological replicates were used and each real-time PCR reaction was done in triplicate. These values were then normalized using the threshold cycle (CT) value for the tomato household gene Sl-actin. The relative levels of transcription were calculated by using the 2-∆Ct Method . Negative controls without cDNA were used in all PCR reactions.
The data were processed by the two-way analysis of variance (ANOVA) with PGPR inoculation and plant genotype as sources of variation, using the SPSS 12.0 statistical software package, (SPSS Inc., Chicago, IL, USA). The means were considered to be significantly different at P <0.05 after the LSD test. The gene expression data were analyzed using Student’s unpaired t test (P < 0.05) in order to compare inoculated plants with their respective non-inoculated controls. To analyze the results of competition assay for colonization of tomato root tip, the data were subjected to the Duncan’s honestly significant difference test.
Finally, total plant dry weight was higher in inoculated wt plants than in the corresponding non-inoculated ones (13% cv Ailsa Craig and 20% cv Rheinlands Ruhm). In contrast, in mutant plants the opposite effect was observed. Inoculation had a negative effect on total dry weight both in flacca and sitiens plants (Figures 1C, 2C).
Two-way analysis of variance (ANOVA)
Significance of sources of vatiation
Competition assay for colonization of tomato root tip
We carried out a competition assay for colonization in order to check the presence of Bacillus megaterium and its ability to colonize root wild-type and ABA-deficient mutant plants. As expected, in control non-inoculated plants we confirmed that there was no presence of Bacillus in roots. However, in inoculated plants, although it was present in all plants (wild-type, sitiens and flacca), the presence of B. megaterium was significantly lower in sitiens plants. Root sitiens plants showed 3.0, wt showed 7.4 and flacca plants 9.5 cfu 106 cm1 root. Due to the similarity of results concerning biomass production and stomatal conductance, and the lower colonization of B. megaterium in sitiens plants, from now on, the following determinations were done only in flacca plants, where the decrease of biomass by inoculation was more pronounced.
ABA and ACC concentration and production rate of ethylene
Since we studied whether the activity of Bacillus megaterium PGPR was affected by the endogenous ABA concentration of the host plant, we analyzed ABA and ACC concentration and ethylene production rate in leaves.
In leaves of wt plants, ACC concentration increased by 90% as a result of inoculation with Bacillus megaterium, while in leaves of mutant plants there were no significant differences as a consequence of inoculation. However, leaves of flacca plants showed higher intrinsic ACC concentration than wt plants (Figure 4B). ANOVA showed highly significant (P < 0.01) effects of both genotype and genotype × PGPR interaction on ACC concentration in tomato leaves (Table 2).
Ethylene production rate was increased nearly 300% in leaves of flacca mutants when inoculated with the PGPR. PGPR inoculation did not change significantly the ethylene production rate of wt leaves. There were no significant differences in ethylene production between non-inoculated leaves of both plant lines (Figure 4C). ANOVA also showed highly significant (P < 0.001) effects of PGPR inoculation on ethylene production rate (Table 2).
Quantitative real-time RT-PCR
ANOVA showed very significant effects (P < 0.001) of both genotype and genotype × PGPR interaction on Sl-PR1b, Sl-ACS7 and Sl-NCED gene expression (Table 2).
Plant growth-promoting rhizobacteria are found in soil and when they are in association with the plant roots can stimulate the growth of the host . One of the mechanisms involved in this effect is the production or degradation of hormones that regulate plant growth and development. It is known that PGPR affect root hormone concentration, and can also alter root-to-shoot long-distance signalling to mediate shoot hormonal status . Several rhizobacteria produce ABA in culture media or regulate plant ABA status . In fact, although the biochemical mechanisms by which ABA is produced in planta have been well characterized , there are no studies concerning the role of endogenous plant ABA on PGPR activity. Herrera-Medina et al.  by comparative analysis of two ABA-deficient tomato mutant plants showed that there were both quantitative and qualitative differences in the pattern of arbuscular mycorrhization colonization. ABA deficiency induced ethylene production, suggesting that one of the mechanisms used by ABA to determine susceptibility to fungal infection is through negative modulation of the ethylene pathway.
In this study, we used ABA-deficient tomato mutants (flacca and sitiens) together with their near-isogenic wt parent to study how endogenous ABA can interfere with PGPR function. Sitiens and flacca are blocked in the final step of the ABA biosynthetic pathway, where the enzyme AAO catalyses the oxidation of abscisic aldehyde to ABA [35, 36]. Sitiens is known to have a mutation in the AAO enzyme and mutant leaves contain only c. 11% of the wild-type ABA levels [35, 37]. The mutant flacca has a mutation in a MoCo cofactor required for the activity of AAO and mutant leaves contain c. 33% of the wild-type ABA levels [37, 38]. The poor growth and strong leaf epinasty shown in the tomato mutants notabilis, as well as flacca and sitiens has been shown to occur even under non-wilting conditions and has been attributed, at least partially, to an excess of ethylene . However, our results have shown that there are no significant differences in ethylene production rate between ABA-deficient mutant and its near-isogenic wt parental. Marulanda et al.  showed that the same Bacillus megaterium strain that was used here, had a positive effect on Trifolium repens growth. In the present study, this positive effect was observed in wt plants but not in flacca or sitiens ones. ABA-deficient plants showed a significant decrease in biomass production as previously demonstrated , indicating that endogenous ABA probably has an important role in keeping plant growth. In the same way, inoculated flacca and sitiens mutant plants showed lower heights than inoculated wt plants. Therefore, the low levels of ABA in these mutant plants switched the effect of the B. megaterium strain used here from plant growth promoting rhizobacteria to plant growth inhibiting rhizobacteria.
Although B. megaterium was present in all plants (wild-type, sitiens and flacca), the presence of this PGPR was significantly lower in sitiens plants. It is possible that the lower ABA may be inhibiting the root colonization. Therefore, a minimal content of ABA should be required for B. megaterium colonization. Similar results were found for arbuscular mycorrhizal symbiosis .
It has been proposed that restriction of ethylene production may be a widespread function of ABA. In fact, it is well known that ethylene and ABA act antagonistically to modulate development , shoot growth  and disease resistance in plants . In addition, there is some evidence that ABA and ethylene antagonistic interaction could interfere with arbuscular mycorrhizal formation . Thus, it appears that the B. megaterium strain used in this study may increase ethylene production of the host plant. Since flacca plants have lower amounts of ABA, the production of ethylene by the PGPR inoculation was exacerbated and even a reduction of the ABA levels took place.
There is a negative correlation between growth and the endogenous ABA concentration of plants  but not under stress conditions . As we expected, ABA-deficient mutant plants showed much lower ABA concentration than wt plants, however inoculation with PGPR in these plants decreased considerably the ABA concentration in leaves, correlating with the decrease in the expression of the ABA-biosynthesis gene Sl-NCED. We observed a direct correlation between growth and the endogenous ABA content in flacca mutant plants. The hormonal response of flacca plants to the PGPR inoculation resembles the plant response to a pathogen, a dramatic increase in ethylene contents .
The PR1b gene is considered an indicator of plant responses to pathogens . Induction of plant systemic acquired resistance (SAR) correlates with the expression of pathogenesis-related (PR) genes [47–49]. Among PR genes, PR1 expression is a paradigm for the coregulation of PR genes during SAR . The interactions between ABA and ethylene in responses to plant pathogens are poorly understood. Whereas several reports have shown an inverse correlation between ABA levels and resistance to pathogens with different lifestyles in several plant species, others have suggested a positive role of this hormone in activation of defence gene expression and pathogen resistance . In ABA-deficient tomato and maize ABA-biosynthesis mutants, exogenous ABA application suppresses ethylene production [41, 52, 53]. Consistent with this, Anderson et al.  found an antagonistic interaction between ethylene and ABA signalling mutants in vegetative tissues. Here, we found that in flacca plants with lower levels of ABA a dramatic increase in ethylene occurs with a concomitant increase in the expression of the pathogenesis-related gene Sl-PR1b. The results of this study are in line with the recent studies suggesting that beneficial microbes can also act as pathogens. This has been reported not only for microbes that induce systemic acquired resistance (SAR), but also for induced systemic resistance (ISR) inducers (see [54, 55]). Since several studies have shown that there is a strong antagonism between ABA and salicylic acid (SA) signalling [56, 57], other alternative explanation for PGPR reduction of growth in flacca plants could be that the ABA-deficient mutants could recognize Bacillus by a possible microbe-associated molecular pattern (MAMP) and could trigger a strong SA-dependent defence, leading to growth retardation.
In wt plants a significant increase in ACC concentration was observed after inoculation with PGPR, while no significant differences were observed in flacca mutant plants as a result of inoculation, most probably because almost all the ACC molecules were converted to ethylene in flacca plants. In fact, only ABA-deficient mutant plants showed a significant increase (6 times) of Sl-ACS7, encoding for an enzyme involved in the ethylene synthesis  when they were inoculated with PGPR.
Positive correlation between over accumulation of ethylene and a higher expression of Sl-PR1b in ABA-deficient mutant plants could indicate that plant endogenous ABA may be essential for the growth-promoting effect of PGPR by maintaining low ethylene production levels.
This work was supported by the Spanish Ministry of Economy and Competitiveness Project AGL2011-25403. We thank to Janusz J Zwiazek (University of Alberta, Canada) for revising the final text.
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