1. Introduction
The use of chemical fungicides is a simple strategy to protect grapevines from phytopathogens. However, at present, vine growers face several risks posed by the emergence of chemical fungicide-resistant phytopathogen populations. For example,
Plasmopara viticola, which causes grape downy mildew, is a high-risk pathogen because of its high potential to acquire chemical fungicide resistance [
1]. Some
P. viticola populations in European vineyards have acquired resistance to quinine outside inhibitor (QoI) fungicide [
2] and carboxylic acid amide (CAA) fungicide [
3]. In Japan, QoI fungicide resistance was detected in 2009 in certain
P. viticola populations [
4]. Although CAA fungicide-resistant
P. viticola isolates have not been reported in Japan, a single point mutation at codon 1105 of the cellulose synthase gene
PvCesA3, which confers resistance to CAA fungicides [
5], was found in heterozygotes of Japanese
P. viticola populations [
6].
Interest in eco-friendly alternatives to chemical fungicides for pest management has intensified in viticulture. One of the alternative pest management strategies is the induction of plant defense response by treatment with abiotic or biotic elicitors [
7]. For example, hordenine, a phenethylamine alkaloid found in barley, suppressed grape downy mildew through the activation of plant defense response in grapevine [
8]. Biological control agents also induce plant defense response in grapevine.
Trichoderma harzianum T39 activated plant defense response in grapevine, resulting in the reduction of downy mildew severity in the grapevine without the direct inhibition of
P. viticola [
9]. Integrated pest management (IPM) has seen an upsurge of interest in viticulture. The introduction of practical techniques for inducing plant defense response in viticulture would contribute to suppressing the emergence of chemical fungicide-resistant phytopathogens by reducing chemical fungicide application.
Our objective in this study was to investigate the applicability of electrical stimulation as an abiotic elicitor in the grapevine. In our previous studies, we found that grapevine subjected to electrical stimulation using solar panels exhibited an increase in the content of resveratrol, which is one of the phytoalexins in grapevine [
10], in berries compared with control grapevines [
11]. Through microarray analysis, we demonstrated that electrical stimulation upregulated the transcription of genes related to stilbenoid biosynthesis in grape cells [
11]. From these results, we formulated the hypothesis that electrical stimulation enhances plant defense response in grapevine as an abiotic elicitor. As far as we know, there are no studies of the effect of electrical stimulation on the incidence of fungal disease in crops. Here, we report the effect of electrical stimulation on the incidence of fungal diseases, including downy mildew in grapevine. We also demonstrate that the salicylic acid (SA)-dependent defense pathway is involved in plant defense response triggered by electrical stimulation.
3. Discussion
Since field-grown grapevines have different physiological properties, including growth stages with
Arabidopsis plants, electrical stimulation may induce different physiological changes between field-grown grapevines and
Arabidopsis plants. Electrical stimulation increased resveratrol contents in berries of grapevines relative to those of control grapevines and electrode-treated grapevines [
11], while we could not demonstrate any positive results related to physiological changes in
Arabidopsis plants subjected to electrical stimulation. Future studies employing
Arabidopsis pathosystem would reveal the accurate signaling pathways for plant defense response triggered by electrical stimulation in plants.
Two steel screws or needles were inserted into the trunks of grapevines or the inflorescences of Arabidopsis plants, wounding them. Grapevines and Arabidopsis plants exposed to electrical stimulation exhibited higher plant defense responses than those treated by the electrode. The result suggested that wounding by inserting steel screws or needles into plants as electrodes is not responsible for plant defense response. Therefore, electrical stimulation by solar panels might be indispensable for the induction of plant defense response in plants.
Plant defense response was not triggered by electrical stimulation in SA-insensitive
Arabidopsis mutants. Grape cells in trunk tissue may recognize electrical stimulation through an unknown mechanism and generate SA. SA is involved in plant defense response [
16]. Because SA can migrate long distances into the phloem, the transported SA may induce systemic acquired resistance (SAR) in the plant [
17]. SA generated by electrical stimulation may be transported to bunches and leaves from the phloem to enhance plant defense response. Thus, electrical stimulation acts as an abiotic elicitor of plant defense response in the grapevine. In the SA-dependent defense pathway, NONEXPRESSOR OF PATHOGENESIS-RELATED GENES 1 (NPR1) is transported to the nucleus in response to SA, thereby upregulating the defense gene expression, such as PR1 and β-1,3-glucanase [
18]. As β-1,3-glucanase shows direct antimicrobial activity against
B. cinerea [
19],
C. gloeosporioides [
20], and
P. viticola [
21], the inhibition of fungal diseases in bunches and leaves by electrical stimulation seems reasonable.
How does electrical stimulation activate SA biosynthesis in grapevines? So far, we do not have the answer to this question. Studies have shown that electrical signals generated in plants by mechanical damage and wounding systemically induce a broad range of plant defense responses [
22,
23]. However, those studies did not examine the possibility that electrical signal induces second messengers, such as SA and JA. Electrode treatment (wounding without electrical stimulation) did not decrease disease incidence in field-grown grapevines and induced plant defense response in grapevines and
Arabidopsis plants, suggesting that electrical stimulation induced second messengers. Although future studies to detect second messengers are required, our study is the first to demonstrate crosstalk between an electrical signal and a messenger molecule in plants. Although whether or not electrical stimulation activates SA biosynthesis remains to be elucidated, the experiments on
Arabidopsis mutant demonstrated that SA generated by electrical stimulation might be responsible for systemic plant defense response. Further investigations are necessary to elucidate whether SA generates at tissues exposed to electrical stimulation and transports into the phloem of grapevine as well as how grapevine cells recognize electrical current and how the recognition activates SA biosynthesis.
Electrical stimulation worked well to suppress several fungal diseases in the field tests. However, it is not a fast-acting tool for suppressing plant diseases. Electrical stimulation induced the expression of a gene encoding β-1,3-glucanase 20 days after treatment in potted grapevine seedlings, although we could not exclude the possibility that the intensity of the electrical stimulation applied to the plants affects the timing of expression of plant defense response. The slow action of electrical stimulation in plant disease control may be one of the problems of using electrical stimulation in the field. Under such circumstances, electrical stimulation would be suitable as a disease-preventing tool in viticulture but not as a tool for treating disease symptoms. Further investigations of combinations of electrical stimulation with common plant disease control techniques, including fungicide application in vineyards, may potentially decrease the frequency of chemical fungicide, copper, and sulfur applications and yield a new practical technique for IPM in viticulture.
In the future, eco-friendly plant disease control is expected to predominate in viticulture due to concerns over environmental pollution generated by chemical fungicides. In this study, we focused on electrical stimulation as an innovative tool for IPM in viticulture. Electrical stimulation activated the SA-dependent defense pathway and systemically suppressed fungal diseases in berries and leaves of field-grown grapevines. The voltage applied to a field-grown grapevine by electrical stimulation was oscillated by illuminance [
11]. One important question that remains to be clarified is whether other environmental factors, including soil composition, weather, training system, and grapevine cultivars, affect the physiological responses related to electric stimulation. To explore further the applicability of electrical stimulation to disease control in viticulture, field tests on a number of vineyards having different environmental conditions and cultivars, adjustments of starting time and conditions for electrical stimulation, and development of a universal electrical stimulation apparatus are required.
4. Materials and Methods
4.1. Plant Materials
Vitis vinifera cv. Merlot was cultivated in the experimental vineyard of The Institute of Enology and Viticulture, the University of Yamanashi, Japan. The grapevines were approximately 30 years old and trained to the Guyot-style system.
Self-rooted V. vinifera cv. Cabernet Sauvignon seedlings were also cultivated in pots for approximately 2 months and then used for electrical stimulation.
Seeds of wild-type
Arabidopsis thaliana (Col-0) and SA-insensitive mutant
npr1-5 (CS3724) [
14] were obtained from The Arabidopsis Information Resource (TAIR), sown on rockwool blocks, and then incubated at 22 °C in an incubator (11.8 Wm
−2 for 16 h in a day). The seedlings were planted in soil, and 38-day-old plants were used for electrical stimulation.
4.2. Electrical Stimulation of Field-Grown Grapevines and Grapevine Seedlings
Six grapevines were prepared for electrical stimulation. Electrical stimulation was carried out on 20 May 2016 and 12 May 2020 (approximately two weeks before flowering; BBCH55-57) according to a previously described method with slight modification [
11]. Briefly, two electrodes (steel screws, 40 mm length, 3.3 mm diameter) were entirely screwed on one grapevine trunk (at 20 and 60 cm above ground) and connected to a solar panel (upper, negative electrode; lower, positive electrode;
Figure 1A). The solar panels were located 2.5 m above ground. The solar panel had the following electrical characteristics: maximum voltage 11.6 V ± 5%, maximum current 100 mA ± 5%, and working temperature −35 °C to 85 °C. Grapevines with only electrodes (without solar panel) or without any treatment were prepared as controls. Each grapevine received the same treatment in both years. Electrical stimulation was performed from BBCH55-57 to BBCH89 in both years.
Three grapevine seedlings with 4–5 expanding leaves at BBCH14-15 were subjected to electrical stimulation. A positive electrode (steel nail, 4 mm length, 1 mm diameter) was entirely pricked on the grapevine trunk, and a negative electrode (steel needle, 2 mm length, 0.4 mm diameter) was entirely pricked on a shoot (
Figure 2A). The electrodes were connected to a solar panel. The seedlings were cultivated at 27 °C for 10 d and 20 d in an incubator (11.8 Wm
−2 for 16 h in a day). Seedlings with only electrodes (without solar panel) or without any treatment were prepared as controls. The third to the fifth leaves of the grapevines were detached and frozen immediately in liquid nitrogen for real-time RT-PCR. Electrical stimulation was performed 20 days after the treatment. Three independent experiments were performed.
4.3. Electrical Stimulation of Arabidopsis Plants
Three 38-day-old
Arabidopsis plants were subjected to electrical stimulation. A positive electrode (steel needle, 1 mm length, 0.4 mm diameter) was entirely pricked on the base of the inflorescence, and a negative electrode (steel needle, 1 mm length, 0.4 mm diameter) was entirely pricked on the inflorescence at the distance of 15–20 cm from the positive electrode (
Figure 3A). The electrodes were connected to a solar panel. The
Arabidopsis plants were cultivated at 22 °C for 12 h, 24 h, and 48 h in an incubator (11.8 Wm
−2 for 16 h in a day).
Arabidopsis plants with only electrodes (without solar panel) or without any treatment were prepared as controls. Electrical stimulation was performed 48 h after treatment. Rosette leaves of the
Arabidopsis plants were detached and frozen immediately in liquid nitrogen for real-time RT-PCR. Three independent experiments were performed.
4.4. Disease Assessment
Disease assessment of bunches and leaves was conducted at harvest (BBCH89) on 9 September 2016 and 17 September 2020, respectively. All bunches were collected, and the number of bunches infected with Botrytis cinerea and/or Colletotrichum gloeosporioides was counted manually. All leaves on each grapevine were assessed for downy mildew. The number of leaves infected with P. viticola was counted manually. Disease incidences were calculated using the following formula:
Incidence (%) = number of infected bunches or leaves/total number of bunches or leaves on one grapevine × 100
4.5. Real-Time RT-PCR
Total RNA was extracted from leaves of grapevine and Arabidopsis with a Fruit-mate for RNA Purification (Takara, Otsu, Japan), and this was followed by isolation and purification on a NucleoSpin RNA Plant (Takara) according to the manufacturer’s instructions. First-strand cDNA was synthesized from total RNA using a PrimeScript RT Reagent Kit with gDNA Eraser (Takara). Real-time RT-PCR was performed with SYBR Premix Ex Taq II (Takara). PCR amplification was performed for 40 cycles at 95 °C for 5 s and at 60 °C for 1 min after an initial denaturation at 95 °C for 30 s. The nucleotide sequences of the primers used for real-time RT-PCR were as follows: V. vinifera class IV chitinase primers (5′-CAATCGGGTCCTTGTGATTC-3′ and 5′-CAAGGCACTGAGAAACGCT-3′, GenBank accession no. U97522); V. vinifera β-1,3-glucanase primers (5′-GAATCTGTTCGATGCCATGC-3′ and 5′-GCATTATCAACCGTAGTCCC-3′, GenBank accession no. DQ267748); V. vinifera β-actin primers (5′-CAAGAGCTGGAAACTGCAAAGA-3′ and 5′-AATGAGAGATGGCTGGAAGAGG-3′, GenBank accession no. AF369524); A. thaliana PR1 primers (5′-CCTGGGGTAGCGGTGACTT-3′ and 5′-CGTGTTCGCAGCGTAGTTGT-3′, GenBank accession no. NM_127025); A. thaliana PDF1.2 primers (5′-TCACCCTTATCTTCGCTGCTC-3′ and 5′-ACCATGTCCCACTTGGCTTC-3′, GenBank accession no. AY063779); and A. thaliana actin primers (5′-GCCGACAGAATGAGCAAAGAG-3′ and 5′-AGGTACTGAGGGAGGCCAAGA-3′, GenBank accession no. NM_179953). Data were analyzed using Thermal Cycler Dice RealTime System Single Software ver. 3.00 (Takara) according to the manufacturer’s instructions. Each actin was used for data normalization. The dissociation curves for each sample were evaluated to verify the specificity of the amplification reaction. Using the standard curve method, the expression levels of each gene were determined as the number of amplification cycles needed to reach a fixed threshold. Relative gene expression was expressed as relative values to actin expression values at each sampling time.
4.6. Statistical Analysis
Data are presented as means ± standard deviations. Statistical analysis was performed by using Excel statistics software 2012 (Social Survey Research Information, Tokyo, Japan). Disease incidence on bunches was subjected to the chi-square test. Disease incidence on leaves and the expression levels of genes tested were subjected to the parametric Tukey’s multiple comparison test.