Dual Effect of the Cubic Ag₃PO₄ Crystal on Pseudomonas syringae Growth and Plant Immunity

Abstract

We previously found that the antibacterial activity of silver phosphate crystals on Escherichia coli depends on their structure. We here show that the cubic form of silver phosphate crystal (SPC) can also be applied to inhibit the growth of a plant-pathogenic Pseudomonas syringae bacterium. SPC pretreatment resulted in reduced in planta multiplication of P. syringae. Induced expression of a plant defense marker gene PR1 by SPC alone is suggestive of its additional plant immunity-stimulating activity. Since SPC can simultaneously inhibit P. syringae growth and induce plant defense responses, it might be used as a more effective plant disease-controlling agent.

Since antiquity, silver due to its antibacterial activity has been diversely used in commercial products and medical applications (Klaine et al., 2008). Recently, it has been revealed that the silver ion (Ag⁺) can induce the production of reactive oxygen species (ROS) by disrupting metabolic pathways and increases membrane permeability by inhibiting disulfide bond formation in bacteria, which leads to bacterial cell death (Morones-Ramirez et al., 2013). However, due to the higher cytotoxicity of Ag⁺, particle-embedded silvers are preferentially studied and used as antibacterial agents.

Effect of silver either as an ionic or a nano-sized particle form has been also investigated in plants. It has been reported that both Ag⁺ and silver nanoparticles (AgNPs) have a contrasting effect on plant growth: stimulatory at low concentration but inhibitory at high concentration (Vannini et al., 2014; Wang et al., 2013). Transcriptomic and proteomic analyses by Ag⁺ and AgNP have revealed that they mostly control the expression of stress-related genes (Kaveh et al., 2013; Vannini et al., 2014). However, the presence of non-overlapping genes changed by Ag⁺ and AgNP indicates that nanoparticle itself used to encage silver has its own specific effect on plants (Kaveh et al., 2013; Vannini et al., 2013; Vannini et al., 2014). We previously found that the cubic silver phosphate (Ag₃PO₄) crystal (SPC) with six facets had a greater effect on inhibiting Escherichia coli growth than the rhombic dodecahedral one with twelve facets (Yeo et al., 2015). Since any particle effect can be ruled out by using SPC, we therefore tested whether or not it could be applied for controlling a plant disease caused by phytopathogenic bacteria.

We synthesized SPC and checked its structure by powder X-ray diffraction and scanning electron microscopy (SEM) as described previously (Fig. 1A, inset) (Yeo et al., 2015). We then started to grow the Arabidopsis-pathogenic Pseudomonas syringae DC3000 bacterium with 0.06 Absorbance at 600 nm (A₆₀₀) in the presence or absence of SPC. P. syringae DC3000 grown at 28°C without SPC almost reached plateau at 1 d post inoculation (Fig. 1A). However, at the same time point, we detected no significant bacterial growth in the presence of SPC (Fig. 1A). Although bacterial growth with 0.5 μg/ml of SPC reached the comparable level to that without SPC after a longer incubation period (6 d post inoculation), bacteria with 5 μg/ml of SPC completely failed to grow (Fig. 1A). To further test the effect of SPC on bacterial growth, we additionally counted bacterial numbers by counting colonies in the growth medium containing or not SPC. Similar to results obtained by measuring optical density (Fig. 1A), numbers of bacteria in the presence of SPC were significantly reduced compared to those without SPC (Fig. 1B). Interestingly, we still detected bacterial colonies even in the presence of 5 μg/ml of SPC with which bacterial population never increased (Fig. 1B). This implies that SPC suppresses bacterial cell division rather than kills bacteria. Taken together, our data indicate that as in the case of E. coli SPC can also effectively inhibit the growth of phytopathogenic P. syringae DC3000 bacterium. This also suggests a potential agrochemical activity of SPC to control a bacterial disease in plants.

Fig. 1.

Inhibition of P. syringae DC3000 growth by SPC. Overnight-grown bacteria were diluted and aliquoted into new tubes with A₆₀₀ = 0.06. They were further grown with or without the indicated amounts of SPC. Bacterial growth was then analyzed at the indicated time points by measuring values of A₆₀₀ (A) or by counting bacterial colonies (B). Data represent mean±SD from three biological replications. (inset in A) The cubic structure of synthesized SPC was analyzed by SEM. Bar, 1 μm.

To test whether SPC has any additional disease-controlling activity in plants, we then examined bacterial growth inside plant tissues. We first treated 10 d-old Arabidopsis plants grown in liquid medium with different amounts of SPC for 2 d and liquid-inoculated those plants with P. syringae DC3000. To exclude the direct growth-inhibiting effect of SPC on P. syringae DC3000, SPC-treated plants were extensively washed to remove surface SPC and transferred to new liquid medium followed by bacterial inoculation. At 3 d post inoculation, we found that bacterial growth was significantly reduced in plants pretreated with 5 and 50 μg/ml of SPC compared to that in non-treated plants (Fig. 2A). This suggests that SPC may directly increase plant immune responses to diminish bacterial multiplication. Therefore, we then investigated the expression of PR1 which is the best representative marker gene of elevated plant immunity. In plants treated with 50 μg/ml of SPC, we found that the expression of PR1 was enhanced in a time-dependent fashion compared to non-treated ones (Fig. 2B). Since simple mechanical stress by solid SPC can affect the expression of PR1, we additionally examined the expression of CAF1a whose transcription is induced by mechanical wounding (Walley et al., 2010). However, we found that unlike PR1 the expression of CAF1a was not increased by SPC (Fig. 2C). This indicates that SPC has an additional role in specifically boosting plant immune responses.

Fig. 2.

Induction of plant immune responses by SPC. (A) SPC inhibits the in planta growth of P. syringae DC3000 in a dose-dependent manner. Ten day-old plants were treated with the indicated amounts of SPC for 2 d and liquid-inoculated with P. syringae DC3000 with A₆₀₀ = 0.02. At 4 h (grey bar) or 3 d (black bar) after inoculation, bacterial numbers inside plants were counted. (B and C) SPC induces the expression of PR1 (B) but not CAF1a (C). Ten day-old plants were treated with or without 50 μg/ml SPC for the indicated time. RNA extracts were then subject to realtime RT-PCR analysis with a LightCycler^® Nano System (Roche). Primers used were; 5′-TTCTTCCCTCGAAAGCTCAA and 5′-AAGGCCCACCAGAGTGTATG for PR1, 5′-TGATGTTAACGGTAACCTCCCAGAC and 5′-GCCGACGAAGCAACTCGATCGAATC for CAF1a, and 5′-ATGGAATCTGCTGGAATCCAC and 5′-TTTGCTCATACGGTCAGCGAT for Actin2. Relative transcript amounts of PR1 and CAF1a were normalized against Actin2. Bar, mean±SD from three biological replications. *, P<0.05; **, P<0.01 in comparison to non-treated plants.

In summary, we here show that SPC has a dual activity to inhibit the growth of a plant-pathogenic P. syringae DC3000 and to elevate plant immune responses. It is not surprising that SPC could affect the growth of P. syringae DC3000, because we previously found that it inhibited the growth of E. coli. Our previous analysis on SPC structure suggested that Ag⁺ in the cubic form is better outward exposed than the rhombic dodecahedral one (Yeo et al., 2015). Hence, the increased exposure of Ag⁺ in the cubic SPC is thought to inhibit the growth of P. syringae DC3000 as well as E. coli. However, the plant immunity-elevating activity of SPC was not expected. To rule out a direct bactericidal activity of remaining SPC itself, we washed treated plants. In addition, the side length of SPC that we synthesized is between 1.5 and 2.5 μm (Fig. 1A, inset), which makes it difficult to enter plant leaf tissue via stomata. More importantly, PR1 expression was dramatically elevated in plants treated with SPC only (Fig. 2B). Although an exact mechanism to induce plant immune responses by SPC is currently unknown, one possibility is that Ag⁺ can induce ROS generation by disrupting metabolic pathways in plants as in bacteria (Morones-Ramirez et al., 2013). It has been reported that the plant immune hormone salicylic acid (SA) and ROS form a positive feedback loop in plant immunity (Bartsch et al., 2006). Since SPC is not likely to enter plant tissues due to its size, SPC-induced ROS generated from epidermal cells is suggested to stimulate the SA-associated immune responses in plants. Although we extensively washed SPC-treated plants, it is still possible that a small fraction of treated SPC remains on leaf surface. Since we liquid-inoculated plants with bacteria, therefore, it cannot be ruled out that remained SPC inhibits at least in part the epiphytic bacterial growth.