Aina Baró
Pasquale Saldarelli
Maria Saponari
Emilio Montesinos
Laura Montesinos- 1Institute of Food and Agricultural Technology-CIDSAV-XaRTA, University of Girona, Girona, Spain
- 2Institute for Sustainable Plant Protection, National Research Council (CNR), Bari, Italy
Transient expression of genes encoding peptides BP134 and BP178 by means of a Potato virus X (PVX) based-vector system, and treatment with synthetic peptides by endotherapy, were evaluated in the control of Xylella fastidiosa infections, in the model plant Nicotiana benthamiana. Transient production of BP178 significantly decreased disease severity compared to PVX and non-treated control (NTC) plants, without adverse effects. Plants treated with synthetic BP134 and BP178 showed consistently lower levels of disease than NTC plants. However, the coinfection with PVX-BP134 and X. fastidiosa caused detrimental effects resulting in plant death. The levels of X. fastidiosa in three zones sampled, upwards and downwards of the inoculation/treatment point, significantly decreased compared to the NTC plants, after the treatment with BP178, but not when BP178 was produced transiently. The effect of treatment and transient production of BP178 in the induction of defense-related genes was also studied. Synthetic BP178 applied by endotherapy induced the expression of ERF1, PR1a, PAL, PALII and WRKY25, while the transient expression of BP178 overexpressed the Cath, Cyc, PR4a, 9-LOX and Endochitinase B genes. Both treatments upregulated the expression of PR1, PR3, PR4 and CycT9299 genes compared to the NTC or PVX plants. It was concluded that the effect of BP178, either by endotherapy or by transient expression, on the control of the X. fastidiosa infections in N. benthamiana, was due in part to the induction of the plant defense system in addition to its bactericidal activity reported in previous studies. However, the protection observed when BP178 was transiently produced seems mainly mediated by the induction of plant defense, because the levels of X. fastidiosa were not significantly affected.
1 Introduction
Xylella fastidiosa is a Gram-negative bacterium that inhabits the xylem vessels of near 600 plants from 85 taxonomic families (EFSA, 2020). Apart from Pierce’s Disease of grapevines, which is one of the oldest known diseases caused by X. fastidiosa worldwide, the pathogen causes losses of economic importance in other crops, such as almond (Prunus dulcis), citrus (Citrus spp.) and olive (Olea europaea) (Baldi and La Porta, 2017; EPPO, 2019).
Up to now, there is no efficient cure for infected hosts (Kyrkou et al., 2018). Thus, X. fastidiosa-related diseases are still important threats to agriculture all over the world, mainly due to its high genetic plasticity, its xylem-limited nature, and the fact that host plants do not show symptoms during the first stages of the disease. Over the past decades, among several chemical compounds and plant extracts, antimicrobial peptides (AMPs) have been proposed as potential pesticides for disease control (Montesinos E, 2007; Jung and Kang, 2014; Breen et al., 2015). Advantages of their use include the existence of lytic peptides with potent antimicrobial and/or antibiofilm activities, defense elicitor peptides or even multifunctional peptides with reduced cytotoxicity and good biodegradability profiles (Badosa et al., 2022).
In addition, many of these AMPs have been used to create transgenic plants, some of them showing enhanced resistance to bacterial and fungal pathogens (López-García et al., 2012; Breen et al., 2015; Montesinos L. et al., 2017). The application of this technology is especially useful in controlling xylem and phloem-limited bacteria, as the expression of AMPs can be targeted into the vessel’s lumen, which is difficult to access using conventional pesticides. One example is the production of grapevine lines expressing a neutrophil elastase and cecropin B, which conferred increased tolerance and trans-graft protection to Pierce’s Disease (Dandekar et al., 2019).
Even though, as far as we know, there are no pesticides or transgenic plants based on AMPs commercialized up to date. The careful design, selection and evaluation of suitable peptides is essential for their improved development as novel and sustainable alternatives to synthetic chemical pesticides (Montesinos E. et al., 2012; Van Esse et al., 2020). BP178, a derivative peptide from the leader peptide BP100 (syn. BP134) that was designed for being expressed in plants (Badosa et al., 2013), has been successfully produced in rice seed endosperm, and conferred resistance to bacterial and fungal infections (Montesinos L. et al., 2017). Moreover, synthetic BP178 has been described as highly active against X. fastidiosa in vitro (Baró et al., 2020), and recently we confirmed its efficacy in controlling X. fastidiosa infections in almond plants (Moll et al., 2022). Synthetic BP178 was also capable of eliciting the innate immune system of tomato and almond plants (Montesinos L. et al., 2021; Moll et al., 2022). However, it is not known if the production of BP178 by transgenic host plants could protect them from X. fastidiosa infections.
A transient-expression system based on Potato virus X (PVX) has extensively been used in N. benthamiana plants to produce a wide range of proteins (Saitoh et al., 2001; Dickmeis et al., 2015; Röder et al., 2018), and specifically for screening AMPs against plant pathogens (Visser et al., 2012). This system has the advantage that N. benthamiana is a susceptible host for X. fastidiosa (Randall et al., 2009; EFSA, 2022), being a reliable pathosystem for testing the antimicrobial efficacy of BP178 when transiently expressed by this viral vector.
The specific aims of the present work were (i) to validate the N. benthamiana system as a model plant host for X. fastidiosa, (ii) to develop PVX plasmid constructs to produce the peptide BP178 and its parent peptide BP134 in N. benthamiana plants inoculated with X. fastidiosa IVIA 5387.2, and (iii) to study the effect of the application of the peptides by endotherapy or transient production in the population dynamics of the pathogen and in controlling infections, as well as in eliciting defense-response in the plants.
2 Materials and methods
2.1 Growth of plants and greenhouse conditions
4-week-old N. benthamiana plants were used for the experiments. All plants were maintained in 0.8 l pots in an environmentally controlled greenhouse at 25 ± 2 °C (day) and 18 ± 2 °C (night), with a minimum relative humidity of 60%, and with a photoperiod of 16 h light and 8 h dark. Prior to and during the experiments, plants were watered to saturation every three days, and fertilized with a 200 ppm solution of NPK (20:10:20) once a week. Also, all along the experiments, standard treatments with insecticide and acaricide were performed to avoid presence of vector insects or pests.
2.2 Synthesis of peptides
Peptides BP134 (KKLFKKILKYL-OH) and BP178 (KKLFKKILKYL-AGPA-GIGKFLHSAK-KDEL-OH) were synthesized (LIPPSO laboratory, Girona, Spain) using the solid phase procedure previously described (Badosa et al., 2013; Caravaca-Fuentes et al., 2021). Briefly, a Fmoc-Rink-MBHA resin (0.55 mmol/g) was used for the synthesis of BP134, and a PAC-ChemMatrix resin (0.66 mmol/g) for the synthesis of BP178. Peptides were synthesized with purity above 95% and characterized by ESI-MS (Badosa et al., 2013; Montesinos L. et al., 2021). Lyophilized peptides (acetate salts) were solubilized in sterile Milli-Q water to a stock concentration of 20 mM and filter sterilized through a 0.22 μm pore Whatman filter. Dilutions of peptides were prepared in sterile Milli-Q water to obtain the final desired concentrations.
2.3 PVX plasmid construction and evaluation of transient expression in plants
2.3.1. pCXI BP134 and pCXI BP178 plasmid construction and N. benthamiana inoculation
The pCXI scaffold (Cruz et al., 1996; Lee et al., 2014; Shukla et al., 2014), containing the PVX genome sequence under the Ca35S promoter was engineered to fuse the BP134 and BP178 peptide sequences to the viral coat protein (CP) via the foot and mouth disease virus (FMDV) 2A sequence. Primers CX1 BP134 2A and CX1 BP178 2A (Table 1) were coupled with the downstream primer CX1uni to amplify the entire PVX CP from pCXI. Amplifications were carried by using 1 unit of Phusion High Fidelity DNA polymerase (ThermoFisher Scientific) in a 50 μl reaction mix containing 0.5 μM reverse and forward primers, 200 μM dNTPs, 50 ng pCXI in 1x Phusion HF buffer. Cycling conditions were: 98°C for 30” followed by 25 cycles at 98°C 30”, 54°C 30”, 72°C 45” and a final elongation step of 72°C for 10’. The obtained amplicons were digested with EagI/SpeI and ligated to a similarly restricted pCXI to obtain the plasmids pCXI BP134 and pCXI BP178 by transformation in Escherichia coli strain DH5α. N. benthamiana plants at the 6-8 leaf stage were inoculated with pCXI BP134, pCXI BP178 (two different plasmids) and pCXI by Celite abrasion of three leaves with 5 μg of purified plasmid DNA, and plants were maintained in controlled greenhouse conditions.
Table 1 Primer sequences used to engineer the PVX viral vector for the expression of the BP134 and BP178 gene peptides.
Only in the case of PVX – BP134 plants, virus particles were partially purified from 100 g of N. benthamiana leaf tissues (Lee et al., 2014). Briefly, tissues were homogenized in 200 ml cold phosphate buffer and the slurry filtered with gauze and centrifuged at 7,800 g for 20 min at 4°C. The supernatant was added to 1% (v/v) Triton X-100, stirred for 1 h at 4°C and again clarified by centrifugation at 5,500 g for 10 min at 4°C. Virus particles, precipitated from the supernatant by NaCl/PEG stirring and centrifugation at 7,800 g for 10 min at 4°C, were resuspended in 10 ml 0.5 M phosphate buffer pH 7.2 and finally concentrated by high speed centrifugation in a swinging bucket rotor at 104,000 g for 75 min at 4°C. Pellet was resuspended in 0.2 ml of the same buffer.
2.3.2. Western blot analysis of pCXI BP134 and pCXI BP178 inoculated plants
Two weeks after the inoculation, 500 mg N. benthamiana leaf tissues were ground in 0.5 ml of extraction buffer [EB: 50 mM Tris, 10 mM potassium acetate, 1 mM sodium EDTA, 10 mM dithiothreitol, 0.5 mM phenylmethylsulfonyl fluoride (PMSF), 10% sucrose, pH 7.4] and successively centrifuged at 4,000 rpm to separate the supernatant. Proteins were fractionated in 12% SDS-polyacrylamide gels (Laemmli, 1970) and transferred to PVDF membrane (Millipore, Bedford) (Towbin et al., 1979). Membranes were preincubated in blocking buffer [1× TBS (0.01 M Tris-HCl pH 8.0, 0.15 M NaCl), 0.05% Tween 20,5% non-fat dried milk] and probed with the antibodies raised against the PVX and the peptides (GenScript Crop, Piscataway, USA), each at the 1:1,000 dilution in the same buffer. After overnight incubation at 5°C, the membranes were washed with 1× TBS-0.05% Tween and exposed to an anti-rabbit IgG alkaline phosphatase conjugate diluted at 1:2,000. Reactions were revealed by incubation with bromo-4-chloro 3-indolyl phosphate and nitroblue tetrazolium.
2.4 X. fastidiosa
X. fastidiosa subsp. fastidiosa strain IVIA 5387.2 (ST 1) first isolated from an almond tree in Mallorca (Spain) (Moralejo et al., 2019) and reisolated in our facilities from a N. benthamiana infected plant, was used within the different experiments. The strain was maintained at - 80°C in Pierce’s Disease 2 (PD2) broth supplemented with 30% glycerol. When required, cryoconserved stock cultures were plated on buffered charcoal yeast extract (BCYE) solid medium and grown at 28°C for two passages of 5 days each.
2.5 Inoculation of X. fastidiosa
The inoculation of X. fastidiosa was performed by microinjection applied to the main stem as described previously (Baró et al., 2021; Moll et al., 2022). Briefly, a pathogen suspension, at 108 CFU/ml (OD600 ≅ 0.3) confirmed by plate counting, was prepared in phosphate buffered saline (PBS), pelleted (10 min at 13,000 rpm) and resuspended in PD2 broth 1x, to avoid cell aggregation inside the syringe during injection and to ensure cell viability. Inoculations were performed using a high precision microinjector (NanoJet, Chemyx, Stafford, TX, USA) provided with a Hamilton 250 µl syringe including a thin needle with bevel tip (Bondaluz, Switzerland). The needle end was introduced into approximately one half the plant stem diameter to directly access the vascular system, as described previously. Three inoculations of X. fastidiosa suspension of 10 µl each (30 µl of total inoculum/plant, 3x106 CFU/plant) were applied at the same side of the stem in a section of 3 cm at around 10 cm above the soil level (Figure 1).
Figure 1 Scheme of pathogen inoculation, peptide application points, and the leaves transfected with PVX constructs, and details of inoculation/delivery process in the stem of the plant. The location of each sampling zone is also indicated: Upwards zones (U1 and U2) and downwards zone (D).
Inoculated plants were cultivated in a Biosafety level II+ quarantine greenhouse authorized by the Plant Health Services, according to EPPO recommended containment conditions (EPPO, 2006), taking into consideration the quarantine status of X. fastidiosa in the EU (EFSA PLH Panel et al., 2018).
2.6 Endotherapy treatments
Endotherapy treatments with synthetic BP134 or BP178 were performed following the same procedure as described for pathogen inoculation. Briefly, three applications of 10 µl each of the stock solution at 20 mM (30 µl of peptide/plant, corresponding to 1.94 mg of BP178 or 0.84 mg of BP134 per plant) were performed at the same side of the stem in a section of 15 cm at around 5 cm above the substrate level (Figure 1).
2.7 Effect of treatments on plant infection
The effect of transient expression of BP134 and BP178 using the PVX system was compared with that of preventive treatments with synthetic BP134 and BP178 applied by endotherapy. In a first experiment, the effect was evaluated on the disease severity. Nine plants were used for each treatment: (i) non-treated control (NTC), (ii) synthetic BP134, (iii) synthetic BP178, (iv) PVX, (v) PVX expressing BP134, and (vi) PVX expressing BP178. Treatments, either with synthetic peptides, PVX systems or inoculations with X. fastidiosa suspension, were performed as described above. Preventive treatments of synthetic BP178 and BP134 were performed 24 h prior to X. fastidiosa inoculation, while the inoculation with PVX systems to the two selected basal leaves (Figure 1) was carried out one week before the inoculation of X. fastidiosa. Disease severity was assessed at 30 days post-inoculation of the pathogen (dpi) using the severity scale adapted from the one already described for grapevines (Clifford et al., 2013). The scale was the following 0 = no symptoms, 1 = from one to five leaves just beginning to show decay, 2 = from five to ten leaves showing significant decay, 3 = one-half or more of the leaves showing decay and few showing necrosis, 4 = all the leaves showing decay and one-half or more showing necrosis, 5 = dead plant.
In a second experiment, the effect of BP178 on the disease severity and population levels of X. fastidiosa was evaluated using four sets of 15 plants each: (1) NTC, (2) synthetic BP178, (3) PVX and (4) PVX expressing BP178. The procedure for treatments and inoculation of X. fastidiosa were the same as in the previous experiment, and the severity score was evaluated using the already mentioned severity scale. Three plants were assessed for disease severity and sampled for population levels at 7, 14, 21, 30 and 40 dpi. The movement and the population levels of X. fastidiosa in xylem tissue were determined by qPCR as described in Baró et al., 2021. Briefly, the bark was removed from the stem samples and the xylem tissue was placed in extraction bags (Bioreba AG, Switzerland) with sterile PBS (ratio 1 ml PBS/0.2 g plant tissue). Homogenization was performed using a hammer followed by the Homex 6 semi-automated homogenizer (Bioreba AG, Switzerland). Bags were incubated at 4°C for 20 min prior to obtain the pelleted cells by centrifugation of 180 µl of homogenate. GeneJET Genomic DNA Purification Kit (Thermo Fisher Scientific, USA) was used for DNA extraction. Three plants for each dpi were analyzed and upward 1 (U1, 8 cm above the inoculation point), upward 2 (U2, 8 cm above U1) and downward (D, 8 cm below the inoculation point) zones were sampled individually for each plant (Figure 1). The number of cells present in the stem was expressed as log10 CFU/g by interpolating the CT values of each sample in the standard curve (y=-3.42+44.77, R2 0.9997).
2.8 Effect of treatments on the induction of defense-related genes in plants
The expression levels of defense-related genes in N. benthamiana leaves in response to the treatments with synthetic BP178 and of PVX expressing BP178 were examined. Nine plants were used for each treatment. In addition, a NTC set in which distilled water was applied by endotherapy, and a set of plants expressing empty PVX construct alone, were also included. Treatments with either synthetic BP178 or PVX systems were performed as described above, 24 h and 1 week before sampling, respectively. The experiment was performed twice.
Leaf samples were collected and processed to extract RNA for reverse transcription quantitative real-time PCR (RT-qPCR) assays as described in Oliveras et al., 2018. Plant material was ground to a fine powder, and total RNA was extracted from leaves using PureLink Plant RNA Reagent (Invitrogen, Life Technologies). The RNA was solubilized in RNAse free water and was routinely subjected to DNAse treatment (Ambion® Turbo DNA-free™, Life Technologies). First-strand of complementary DNA (cDNA) was generated from total RNA using reverse transcriptase (High-Capacity cDNA Reverse Transcription Kit, Applied Biosystems).
To analyze gene expression in treated N. benthamiana plants, a quantitative real-time PCR (qPCR) was carried out in a fluorometric thermal cycler (qPCR Quant Studio 5, Applied Biosystems) by using SYBR®Green PCR Master Mix (Applied Biosystems) as described in Badosa et al., 2017.
Specific oligonucleotides used for the quantification of the target genes involved in plant defense mechanisms are described in Supplementary Table 1. For each gene system, the concentration of the primer pair was optimized to prevent non-specific reactions or artefacts that could hide the result, and the linearity within a range of number of copies of each gene was evaluated as well as the efficiency for each curve was calculated (efficiencies ranging from 80 to 98.8%, R2 ≥ 0.98). Melting curve analysis was performed after each amplification to verify amplification specificity. A constitutive gene (actin gene) was used as reference control.
The total reaction volume was 20 µl and the reaction mixture contained 1x SYBR®Green PCR Master Mix (2x), the optimized concentration of primers (either 100, 200 or 300 nM), and 2 µl of cDNA (RT reaction). The qPCR conditions were previously described by Badosa et al., 2017.
Relative quantification of gene expression was done using the ΔΔCT method (Livak and Schmittgen, 2001), and the relative expression values were normalized against the actin gene as an internal control.
2.9 Data analysis
To test the effect of endotherapy and transient expression of BP134 and BP178 on the population levels of X. fastidiosa and disease severity in N. benthamiana plants, a one-way analysis of variance (ANOVA) was performed. Means were separated according to the Tukey’s test at a P value of ≤ 0.05. The statistical significance of the gene expression data was determined using the REST2009 Software (Pfaffl et al., 2002). Expression levels higher than 2-fold change were considered differentially expressed.
3 Results
3.1 Transient expression of peptides BP134 and BP178 with the PVX system
The PVX viral vector system (Lee et al., 2014) was used to transiently express the BP134 and BP178 peptides in N. benthamiana. Engineered peptide gene sequences were fused to the viral coat protein (CP) via the foot and mouth disease virus (FMDV) 2A sequence, which allows the expression of free and CP-fused peptides by a ribosomal skip leading mechanism (Donnelly et al., 2001). About two weeks after the inoculation, upper leaves of plants infected with pCXI BP134 and pCXI BP178 showed mild chlorosis and deformation (not shown). Western immunoblot analysis demonstrated that both chimeric viruses correctly replicate in N. benthamiana (Figure 2), since a band recognized by the anti PVX antibody was present in transfected plants. A protein band of the same size was recognized by a mixture of anti BP134 and BP178 antibodies in the same protein extracts. In addition, anti PVX and anti BP antibodies recognized the PVX CP-BP134 fusion proteins in purified viral particles from infected plants (Figure 2A). Even though it is described that the FMDV 2A sequence also allows the expression of free peptides, they were not detected in any of the protein extracts.
Figure 2 Western immunoblot analysis of PVX CP-BP134 and PVX CP-BP178 fusion proteins in total protein extracts from Nicotiana bentamiana leaf tissues. WT indicates protein extracts from leaves of non-transfected plants. (A) Extracts from PVX-BP134 and WT lines. Purified viral particles of PVX CP-BP134 were also analyzed. (B) Extracts from PVX-BP178 lines 1-2 and WT line. Immunodetection was performed using specific polyclonal anti-BP178/antiBP134 or antiPVX antibodies and NBT/BCIP colorimetric detection by alkaline phosphatase-conjugated antibodies.
Two different pCXI BP178 plasmids were tested, which are indicated as extract 1 and 2 in Figure 2B. Since the PVX CP-BP178 protein was barely visible in one of them, it was decided to further continue the experiments using the plasmid expressing the highest amount of fusion protein (Figure 2B). No reactions were visible in protein extracts from wild-type plants (WT).
3.2 Symptoms development
The effect of preventive treatments with the synthetic peptides, as well as their transient expression using the PVX system was assessed on the disease severity caused by X. fastidiosa IVIA 5387.2 in N. benthamiana plants at 30 dpi. Both synthetic peptides, BP134 and BP178, as well as the transient expression of BP178 significantly decreased disease severity compared to the NTC and PVX control plants, with an efficacy of 69.7%, 76.4% and 73.8%, respectively (Figure 3). NTC and PVX plants showed high levels of disease, and no significant differences in disease severity were observed between them. However, the highest disease severity was observed in plants transiently expressing the peptide BP134. In a second transfection experiment, the preventive treatment with BP178 and the production of PVX CP-BP178 in N. benthamiana plants confirmed the previously observed efficacy in controlling X. fastidosa infections.
Figure 3 Effect of endotherapy with BP178 or BP134, and by heterologous production of the peptides on Xylella fastidiosa infections in Nicotiana benthamiana plants. The treatments were: PVX, empty vector; PVX-134, vector with BP134 gene; PVX-178, vector with BP178 gene; BP134, synthetic peptide; BP178, synthetic peptide; and NTC, non-treated control. Values are the means of nine plants (three replicates of three plants per each treatment), and error bars represent the standard deviation of the mean. Different letters between treatments correspond to statistically significant differences between treatments (Tukey’s test, p ≤ 0.05).
3.3 Dynamics of X. fastidiosa
The population of X. fastidiosa IVIA 5387.2 in N. benthamiana plants preventively treated or transiently expressing BP178 is presented in Figure 4.
Figure 4 Effect of peptide treatment on Xylella fastidiosa subsp. fastidiosa population levels of Nicotiana benthamiana plants over a period of 40 days after pathogen inoculation. From top to bottom graph, X. fastidiosa population levels were estimated in the upward zones 1 (U1) and 2 (U2) and in the downward zone (D). Treatments correspond to non-treated control plants (white circle); endotherapy with BP178 (black circle); PVX transfection (white triangle); PVX-BP178 transfection (black triangle). Error bars represent the standard deviation of the mean. Different letters between treatments at specific sampling zones denote statistically significant differences between X. fastidiosa population levels (Tukey’s test, p ≤ 0.05).
The preventive treatment with the synthetic peptide was the most effective in reducing X. fastidiosa cell number, with a maximum decrease of 2.4 to 3 log in all zones analyzed, compared to the NTC. Specifically, a reduction was observed in the U1 zone from 7 to 40 dpi, compared to NTC plants, and being maximum at 21 dpi. In the U2 zone, X. fastidiosa cells were not detected until 30 dpi (detection limit 103 CFU/g). After this time point an increase in the X. fastidiosa population levels was observed in the U2 zone, but they were significantly lower in BP178 plants than those in the control plants. In the D zone, even though a slight reduction was observed compared to the other treatments, the difference was not as significant as in upward zones, except at 30 dpi, where a clear decrease in population levels is observed, with a reduction of 3 logs.
There was no significant difference in the dynamics of the X. fastidiosa population between NTC, PVX and PVX- BP178 plants, which increased from 7 to 30 dpi and remained stable until 40 dpi in all plant parts analyzed.
3.4 Induction of plant-defense related genes
The ability of BP178 to induce the expression of defense-related genes was assessed in N. benthamiana plants using both strategies, endotherapy and transient expression. The expression of 24 genes is presented in Figure 5 by comparison of the levels of expression when applied by endotherapy (BP178 synthetic) or transiently expressed (PVX-BP178). Both treatments significantly upregulated the expression of PR1, PR3, PR4 and CycT9299 genes. When transiently expressed, Cath, Cyc, PR4a, 9-LOX and Endochitinase B, genes were also upregulated. Synthetic BP178 also induced the expression of ERF1, PR1a, PAL and PALII and WRKY25.
Figure 5 Expression levels of defense genes in Nicotiana benthamiana plants in response to endotherapy with synthetic BP178 or transient expression with PVX-BP178, using RT-qPCR analysis. Black line, cut-off values for genes with > 2-fold change value (log10, 0.3) (Relative quantification method using ΔΔCT method). Each BP178 treatment was compared to its appropriate control (i.e., PVX-BP178 compared to PVX control; BP178 applied by endotherapy compared to non-treated control plants, where plants were treated with water by endotherapy). Asterisks indicate significant values of fold-change.
The effect of PVX and PVX-BP178 compared to the NTC plants is shown in Supplementary Figure 1. In both, PVX and PVX-BP178 treatments, PR2, PR3, PR5, plastocyanin, PR1a and PR1 genes were upregulated, while genes Cyt C, PR4a, Endochitinase B and PR4 were only upregulated when BP178 was transiently expressed.
4 Discussion
BP134 and BP178 peptides have potent antibacterial activity against several bacterial plant pathogens, including X. fastidiosa (Badosa et al., 2013; Baró et al., 2020), and are very effective in protecting plants of agronomic interests from infections caused by bacterial and fungal plant pathogens (Badosa et al., 2017; Montesinos L. et al., 2021). Recently we confirmed that BP178 applied by endotherapy and spray to almond plants was able to control infections caused by X. fastidosa (Moll et al., 2022). In the present work, we validated N. benthamiana as a model plant host for the study of X. fastidiosa and evaluated the effect of the transient expression of BP134 and BP178 in controlling infections in this model plant compared to the preventive application of the synthetic AMPs by endotherapy.
We demonstrated that N. benthamiana plants produce BP134 and BP178 when transiently expressed using a PVX-derived vector system. This agrees with the reports of stable genetic transformation and expression of BP178 in rice using endosperm specific promoters (Montesinos L. et al., 2017). On the contrary, constitutive expression of BP134 in rice plants had strong negative impact on rice fitness (Nadal et al., 2012). No yield quantification was performed in our study because when peptides are expressed using a virus-based vector system, transient production levels of heterologous peptides differ between plants, as it depends on physical factors influencing the viral vector infection, environmental conditions, and the physiological state of each plant (Sindarovska and Kuchuk, 2021). In the present study, absence of self-cleavage of the FMDV 2A sequence to obtain the free AMPs was also observed (Kovalskaya et al., 2011), which can be due to the amino acid sequence, as the ratio of fused CP and non-fused viral CP depends on it (Dickmeis et al., 2015). Even so, BP178 fused to the viral CP seems to maintain its activity when transiently produced in N. benthamiana, as it reduced X. fastidiosa disease severity with an efficacy of 74%. This observed activity agrees with the fact that BP178 has already been produced in the endosperm of rice seeds, showing a protective effect against the bacteria Dickeya sp. and the fungus Fusarium verticillioides (Montesinos L. et al., 2017).
Contrarily, PVX-BP134 transfected plants and inoculated with X. fastidiosa showed the highest severity index among all treatments, although the heterologous production of BP134 in non-pathogen inoculated N. benthamiana plants had no detrimental effect. We expected that the large fusion protein (CP-BP134) should not present toxicity because of the large size of the coat protein compared to BP134 (11 amino acids), as it was reported when the BP134 gene alone was constitutively expressed in rice (Nadal et al., 2012). A possible explanation could be related to the effect of the coinfection itself. PVX infection leads to the synthesis of VSR HcPro in Nicotiana tabacum, a viral protein that suppress the plant PAMP Triggered Immunity (PTI), facilitating the multiplication of the pathogen (Navarro et al., 2008; Zvereva et al., 2016). Also, coinfection of rice with Rice yellow mottle virus and Xanthomonas arboricola pv. oryzicola, was reported to increase bacterial specific symptoms and bacterial load, compared to the bacterial infection alone (Tollenaere et al., 2017). Then, suppression of PTI by PVX together with the detrimental effects of coinfection could explain our results of an increase of symptoms during coinfection of the PVX and X. fastidiosa, compared to the X. fastidiosa infection alone. In addition, the coinfection of the PVX-BP134 and X. fastidiosa increased even more the disease symptoms observed with PVX and X. fastidosa coinfection. This should be considered together with the fact that, contrary to BP178, peptide BP134 did not have a significant induction of the plant immune system (Oliveras et al., 2018). In addition, we cannot discard that the synthesis of CP-BP134 fusion may induce tylose overproduction or other gene products that promoted and exacerbated the symptoms of the disease, but we have not analyzed tylose formation and transcriptomic profiling of PVX-BP134 plants.
Endotherapy with BP134 or BP178 reduced X. fastidiosa infections in N. benthamiana with efficacies of at least 70%, the same order as compounds used in the field to control diseases caused by this pathogen. For example, N-acetyl cysteine (NAC) applications reduced X. fastidiosa symptoms between 75 and 80% in infected sweet orange plants under greenhouse conditions (Muranaka et al., 2013), and in olive orchards with initial X. fastidiosa incidence, but without showing a decrease in the pathogen population levels by qPCR (Dongiovanni et al., 2017). Endotherapy treatments using oxytetracycline in infected almond trees also showed a significant reduction of disease symptoms, around 73%, related with a low infectivity percentage in leaves detected by DAS-ELISA (Amanifar et al., 2016). In terms of reduction of the levels of X. fastidiosa, the microinjection of BP178 was effective compared to NTC plants. This agrees with the in vitro bactericidal activity already reported for this functional peptide (Baró et al., 2020). Nevertheless, one single preventive application of the BP178 was not enough to prevent disease in N. benthamiana plants, as remaining live cells were still able to grow after 20 dpi. This agrees with the results obtained in almond plants, where increasing the number of AMP applications resulted in a higher reduction of the bacterial population and, consequently of disease severity (Moll et al., 2022).
In contrast, when BP178 was transiently produced, the population levels of X. fastidiosa did not decrease compared to the NTC plants, despite the observed reduction of disease severity. This was associated with a higher tolerance of these plants to the pathogen due to an elicitation of the plant immune system triggered by the production of BP178 peptide, with no direct action against the pathogen, due to the upregulation of PR1, PR3, PR4, PR4a, CycT9299, Cath, Cyc, 9-LOX and Endochitinase.
It has been reported that tolerance to plant pathogens does not necessarily affect its growth and virulence on the host (Pagan and Garcia-Arenal, 2020). For example, salicylic acid (SA) and ethylene mediate symptom development in Arabidopsis plants infected with Xanthomonas and Pseudomonas, without affecting the growth of both bacterial plant pathogens (Bent et al., 1992; O’Donnell et al., 2001).
We reported that genes coding endochitinase B, PR4 and PR1 proteins were induced in N. benthamiana PVX-BP178 plants. However, the endochitinase B and PR4 gene products do not act directly on bacteria because they are antifungal, as confirmed in many plant species including N. tabacum, and have been involved in abiotic stresses such as cold, salinity or wound stress (Ali et al., 2018). In addition, PR1 has been involved in plant growth and development (Breen et al., 2017). Then, none of these gene products are expected to influence the growth of X. fastidiosa. Among the upregulated genes in N. benthamiana, we observed two cyclophilin genes, known for their role in growth and development of plants, hormone signaling (i.e., auxin signaling) and drought tolerance, but not directly related to pathogen multiplication (Singh et al., 2020). Also, cathepsin B was induced, and in the case of N. benthamiana it was reported to be required for disease resistance to bacterial pathogens, and for induction of SA-related genes (van der Linde, 2012a, b). In fact, the induction of cathepsin gene is required for the induction of 9-LOX gene to promote cell death (Christensen et al., 2015), which also is being overexpressed in our PVX-BP178 plants. It should be considered that here we have paid attention to only 24 genes in N. benthamiana, but many other genes may be implicated in the plant response. Upon treatment with BP178 in tomato (microarray) or almond (RNA seq) we have identified around 100 upregulated/downregulated genes (Montesinos et al., 2021; Moll et al., 2022). Unfortunately, these extensive transcriptomic studies have not been done with PVX-BP178 N. benthamiana plants.
Considering our results and the possible role of tyloses in limiting pathogen progression, the overproduction of tyloses is not compatible with the spread of X. fastidosa we have observed within the PVX-BP178 plants. Interestingly, Ingel et al. (2020) reported that tylose formation in xylem of grapevine affected by Pierce's Disease is related to upregulation of genes associated to ethylene-signaling, cell wall biogenesis and drought stress, whereas several genes related to photosynthesis and carbon fixation were downregulated. In our case, ERF1 (ethylene transcription factor) and Cyt C (when compared to PVX) that are involved in the ethylene pathway, were not overexpressed in PVX-BP178. Unfortunately, we have not analyzed the tylose formation, and we cannot discard an effect of the peptide treatment on its formation.
Regarding the effect of BP178 in other plants like almond or tomato, MYB transcription factors, osmotin, zinc fingers, terpens or PAL genes were upregulated, whereas in Pierce’s diseased grapevine plants, these genes were downregulated (Ingel et al., 2020).
Globally, we consider that transient expression of BP178 could have specific effects in the transcriptome of N. benthamiana that somehow compensates the negative effect of X. fastidiosa in host plants, but without affecting its population levels.
Since PVX is a plant pathogen, mainly affecting Solanaceae (Lico et al., 2015), inoculation with PVX alone induced the expression of several plant defense genes (PR1, PR1a, PR2, PR3, PR5 and plastocyanin), compared to NTC plants. However, this effect was unable to prevent infections caused by X. fastidiosa. On the contrary, practically no symptoms were observed in PVX-BP178-infected plants in which, in addition to the induction of the genes induced by PVX alone, more genes like Endochitinase B, Cyt C, and two PR4 genes, were overexpressed when comparing to NTC plants. The mechanism by which PVX promote this effect is still not well known. Virus presence in the xylem is poorly investigated although PVX was detected in the vessels of infected N. benthamiana (Betti et al., 2012). However, the low number of viable cells in the xylem which is mainly limited to parenchyma associated cells, makes PVX replication and AMP release in the xylem not quantitative, which could explain the lack of decrease of X. fastidiosa levels in PVX-BP178-infected plants.
Activation of the plant immune system is a strategy that has reported promising results in the control of X. fastidiosa. For example, the application of menadione, a plant defense activator, reduced Pierce´s Disease symptoms between 40 and 50%, (Zhang et al., 2019). Also, the foliar and drench application of abscisic acid to potted vines significantly reduced Pierce´s Disease severity compared to control plants, but only when applied in the fall (Meyer and Kirkpatrick, 2011). So, the capacity of AMPs to activate the plant immune system in addition to their antimicrobial activity, and their possibility to be successfully expressed into the lumen of xylem vessels (Agüero et al., 2005; Dandekar et al., 2012; Dandekar et al., 2019), make them of high interest for the control of systemic plant diseases.
Several plant models have been used to study X. fastidiosa. After the first report of X. fastidiosa in Catharanthus roseus (Ueno et al., 1998), its potential as a plant model was studied (Monteiro et al., 2001). The first symptoms appeared on some of the plants two months after inoculation with X. fastidosa subsp. pauca 9a5c, and in all the plants after four months. Similar times to symptom development were observed when Medicago sativa was inoculated with X. fastidosa subsp. pauca DeDonno (Kubaa et al., 2019), but in this case limited systemic colonization was observed and a low number of non-inoculated shoots showed presence of the pathogen. Similarly, some ecotypes of A. thaliana have been used as a plant model, with colonization of distal tissues such as floral shoots and roots and population levels around 106 CFU/g already at 7 days post-inoculation (Pereira et al., 2019). However, no typical symptoms of necrosis or leaf scorch have been observed using this model plant (Rogers, 2012). Nicotiana tabacum was also described as a potential model (Lopes et al., 2000) and showed the first symptoms of leaf scorch between 6-8 weeks after inoculation and population levels of X. fastidiosa from 104 to 108 CFU/g tissue, but this system appears to be difficult to reproduce (Lopes et al., 2000; Alves et al., 2008; Francis et al., 2008; De La Fuente et al., 2013).
In our study with N. benthamiana, the strain IVIA 5387.2 causing ALS in Mallorca, showed high population levels of 108 CFU/g tissue at 3-4 weeks post-inoculation in the three plant zones analyzed and, in all plants, with a rapid development of symptoms and a low variability. Thus, N. benthamiana is proposed as a suitable model for the study of efficacy of compounds against X. fastidiosa and for other studies, with advantages over the previously used plant models.
The present study gives new insights into the potential of AMPs to control diseases caused by X. fastidiosa, more specifically using the expression of BP178 in plant hosts. It also emphasizes the importance of the plant model N. benthamiana to perform in planta screening of functional peptides (and eventually other compounds) against X. fastidiosa.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Author contributions
EM, PS and MS obtained the financial support. AB, PS, LM, MS, and EM designed the research, analyzed the data, and wrote the paper. AB, PS and LM conducted and performed the experiments. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by grants from the European Union XF-ACTORS (Ref. 727987) and BeXyL (Ref. 101060593) projects. AB was recipient of a research grant from the Secretaria d’Universitats i Recerca, Departament d’Economia i Coneixement, Generalitat de Catalunya (Ref. 2018 FI B00334).
Acknowledgments
We thank Héctor Saravia and Gemma Roselló for participating in various tasks related to preparation and maintenance of the plant material. We also thank Professor Ulrich Commandeur and Dr Juliane Röder from RWTH Aachen University for their precious advices about the PVX skipping mechanism.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2022.1061463/full#supplementary-material
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Keywords: bifunctional peptide, bactericidal, plant defense elicitor, plant infections, nicotiana benthamiana, Xylella fastidiosa
Citation: Baró A, Saldarelli P, Saponari M, Montesinos E and Montesinos L (2022) Nicotiana benthamiana as a model plant host for Xylella fastidiosa: Control of infections by transient expression and endotherapy with a bifunctional peptide. Front. Plant Sci. 13:1061463. doi: 10.3389/fpls.2022.1061463
Received: 04 October 2022; Accepted: 11 November 2022;
Published: 01 December 2022.
Edited by:
Vittoria Catara, University of Catania, ItalyReviewed by:
Giorgio Mariano Balestra, University of Tuscia, ItalySteven Earl Lindow, University of California, Berkeley, United States
Copyright © 2022 Baró, Saldarelli, Saponari, Montesinos and Montesinos. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Laura Montesinos, laura.montesinos@udg.edu