Biological control agent Rhizobium (=Agrobacterium) vitis strain ARK-1 suppresses expression of the essential and non-essential vir genes of tumorigenic R. vitis.

OBJECTIVE: To gain insights into the virulence suppressive mechanism of a nonpathogenic strain of Rhizobium vitis ARK-1, we co-inoculated ARK-1 with a tumorigenic (Ti) strain of R. vitis to examine the expression of two essential virulence genes (virA and virG) and one non-essential gene (virD3) of the Ti strain at the wound site of grapevine.
RESULTS: Co-inoculation of ARK-1 with a Ti strain VAT03-9 at a 1:1 cell ratio into grapevine shoots resulted in significantly lower expression of the virulence genes virA, virD3, and virG of VAT03-9 at 1 day after inoculation compared with those when shoots were inoculated only with VAT03-9. ARK-1 was not able to catabolize acetosyringone, which is the plant-derived metabolites inducing the entire vir regulon in Ti strains, suggesting the direct effect of ARK-1 on the induction of broad range of vir genes of R. vitis Ti strains.

Introduction

Grapevine (Vitis vinifera L.) crown gall is caused mainly by Rhizobium vitis (Ti) [syn. Agrobacterium vitis (Ti)], where “Ti” means “tumorigenic”. To avoid confusion, we follow the nomenclature for Rhizobium species adopted by Young et al. [1]. Crown gall is one of the most important diseases of grapevine around the world [2, 3]. Infected vines generally lose their productivity, and rapid decline can be associated with the infection of young vines.

The virulence (vir) genes and transfer DNA (T-DNA) are located mostly in large tumor-inducing plasmids (pTi). Rhizobium Ti strains transfer T-DNA and several virulence effector proteins into plant host cells, and this infection pathway is mediated by a bacterial type IV secretion system [4, 5]. The plant phenolics acetosyringone (AS) and α-hydroxyacetosyringone induce the entire vir regulon in Rhizobium as well as the formation of T-DNA intermediate molecules [4]. T-DNA transfer and processing require products of the several vir genes, which are named as virA to virE, and virG and located outside of the T-DNA coding region [4-7].

Previously, we have reported that a nonpathogenic R. vitis strain VAR03-1, which was isolated from grapevine in Japan and strongly inhibited tumor formation in tomato, grapevine, rose, sunflower, and apple [8-11]. Moreover, we isolated and identified nonpathogenic R. vitis strain ARK-1, which performed much better than VAR03-1 at inhibiting tumor formation in grapevine in greenhouse and field trials, as a new antagonistic strain [12-16]. ARK-1 is also endophytic in grapevine [12]. When grapevine shoots were inoculated with a Ti strain that was not affected by ARK-1 in the antibiosis assay, ARK-1 was able to suppress tumor formation. [13]. In addition, dead cells of ARK-1 (autoclaved) and the culture filtrate (CF) of ARK-1 (without cells) were not able to inhibit tumor formation in grapevine [15]. When ARK-1 and a Ti strain was co-inoculated, the number of colony-forming unit (cfu) of the Ti strain was not affected from 1 to 5 days after inoculation (dai), but it was significantly reduced at 7 dai [13, 14].

Saito et al. [17] have reported that the suppressive activity of antagonistic and non-pathogenic R. vitis strain VAR03-1 on the virulence gene expression of Ti was found to be its CF in vitro. Consistent with our speculation, the cfu of Ti strain was temporarily reduced after incubation of CF prepared from the growth medium of VAR03-1. Interestingly, the suppressive activity was detected in the high molecular weight fraction (> 100 kDa) of CF, suggesting that the antagonistic effects of VAR03-1 on Ti are mediated by large particles released in the culture media [17]. On the other hand, the CF of ARK-1 did not show suppressive effect on both the tumor formation and the expression of vir genes in planta experiments [14].

Two different mechanisms (antibiotic compounds or quorum-sensing) of biological control of plant crown gall disease using antagonistic bacteria have been reported [8–10, 17–23], but disease suppression mechanism of ARK-1 is different from these two mechanisms [13, 14, 16]. The biological control activity of ARK-1 is likely based on the suppression of some essential virulence genes [14, 16]. Two Rhizobium proteins, VirD2 and VirE2 expressed by virD and virE, respectively, are directly associated with the T-strand [4-6]. Co-inoculation of grapevine shoots with ARK-1 and Ti strain at a 1:1 cell ratio resulted in significantly lower expression of the virulence genes virD2 and virE2 of Ti strain at 1 dai than expression levels of these genes by a Ti strain inoculated by itself [14, 16]. When a non-pathogenic R. vitis strain VAR06-30, which is neither antagonistic against R. vitis (Ti) nor limit the development of crown gall of grapevine, was co-inoculated with a Ti strain, expression levels of virD2 and virE2 were not affected (Additional file 1: Table S1), [14].

At this moment, it remains unclear if ARK-1 suppresses the expression of the other vir genes including essential or non-essential genes. Two Rhizobium proteins, VirA and VirG are directly associated with the T-strand as essential vir genes. VirA molecule works as the sensor protein to recognize the plant signal molecule AS. VirG protein works as the response regulator, which activates all genes in the regulon [4-6]. On the other hands, there are some non-essential genes such as virD3 in vir regulon, which are not required for tumorigenicity on plants [24].

To gain insights into the virulence suppressive mechanism of ARK-1, we co-inoculated ARK-1 with a Ti strain to examine the expression of two essential virulence genes (virA and virG) and one non-essential gene (virD3) of the Ti strain at the wound site of grapevine.

Main text

Methods

Detection of vir genes’ mRNA using the RT-qPCR

Cell suspensions of the non-pathogenic strains ARK-1 (antagonistic and non-pathogenic), VAR06-30 (non-antagonistic and non-pathogenic), and VAT03-9 (tumorigenic) (Additional file 1: Table S1) were prepared from 48-h-old cultures on potato sucrose agar medium slants [12, 14, 15]. Supernatant of these cultures was discarded, then the surface of the slant was washed with distilled water to obtain a cell suspension. Cell concentration was adjusted to approximately 108 cells mL−1. Two mixed cell suspensions at a cell ratio of 1:1 (ARK-1 plus VAT03-9, VAR06-30 plus VAT03-9), and a VAT03-9 suspension were prepared. An inoculation method was followed the needle-prick method using grapevine seedlings grown from a seed (2 years old, cv. ‘Neo Muscat’, seeds obtained from grape clusters cultivated in NARO, Japan) [14]. Each seedling (one plant per pot) was inoculated once with one of the mixed cell suspensions or with only VAT03-9. Seedlings inoculated with sterile distilled water were used as the negative control. We grew the seedlings in a greenhouse at 20 to 35 °C with natural sunlight and collected the shoot samples that included the one wound site. One sample, which was 0.2 g fresh weight, was obtained per plant from five plants (i.e., n = 5) at 1 dai.

The basic information for the RT-qPCR procedures, which followed the methods of Bustin et al. [25] and Kawaguchi [14], are summarized in Table 1 and the Additional file 2: Table S2. A housekeeping gene pyrG of Ti strain VAT03-9 was amplified to be used as both for the standardization of amplified products and an internal control [14]. To amplify the pyrG gene of VAT03-9 alone and to not amplify the same gene of strains ARK-1 and/or VAR06-30, specific primers and probe were designed and confirmed that these primers/probes worked well [14].

Table 1

Oligonucleotide primers and probes used in the RT-qPCR analyses

Name	Primer or probe	5′-3′ nucleotide sequence	Target DNA	Reference	Accession no.	Design or supplier
virA-F	Primer	CTC GAC TGA AAG AAG GAC ATA CTC A	virA	This study	CP000637	Licensed Dual-Labeled Probes for qPCR (Sigma-Aldrich)
virA-R	Primer	CGC AAG AAG GTC TAT CAT AAG GAA G	virA	This study	CP000637	Licensed Dual-Labeled Probes for qPCR (Sigma-Aldrich)
virA-P	Probe	AAT GGT TCC GCT CGC AAG CAC CTT G	virA	This study	CP000637	Licensed Dual-Labeled Probes for qPCR (Sigma-Aldrich)
virD3-F1P	Primer	GTC AAC TCG GGG AAG TCG T	virD3	This study	CP000637	ProbeFinder (Roche Diagnostics)
virD3-R1P	Primer	CAG TTC AGT TCG ATC GCT TG	virD3	This study	CP000637	ProbeFinder (Roche Diagnostics)
virD3-P	Probe	TTC CTC TG	virD3	This study	CP000637	Universal ProbeLibrary probe #6 Cat. no. 04685032001 (Roche Diagnostics)
virG-F	Primer	CTG TCT CGG ATG CGA GTA CG	virG	This study	CP000637	Licensed Dual-Labeled Probes for qPCR (Sigma-Aldrich)
virG-R	Primer	CGG AGT ATC TAA CGA TCC ACG C	virG	This study	CP000637	Licensed Dual-Labeled Probes for qPCR (Sigma-Aldrich)
virG-P	Probe	TGA CCG CCG TAT CCG ATA GTC AGC AAT T	virG	This study	CP000637	Licensed Dual-Labeled Probes for qPCR (Sigma-Aldrich)
VAT03-9pyrG-F-2	Primer	GGT GAA GTC TTC GTC ACC GAC	pyrG	[14]	AB272142	Licensed Dual-Labeled Probes for qPCR (Sigma-Aldrich)
VAT03-9pyrG-R-2	Primer	CGC CCT GTG AAG CGT TCA TAG	pyrG	[14]	AB272142	Licensed Dual-Labeled Probes for qPCR (Sigma-Aldrich)
VAT03-9pyrG-P-2	Probe	CGG CGC AGA GAC CGA CCT TGA TCT TG	pyrG	[14]	AB272142	Licensed Dual-Labeled Probes for qPCR (Sigma-Aldrich)

Relative quantification of the virA, virD3, and virG genes’ mRNA concentrations was carried out using the ΔΔCt method [26] by the Ct values of pyrG gene’s mRNA as reference points [14] across three independent technical replications. Relative expression rate of each vir gene in grapevine inoculated with ARK-1 plus VAT03-9 and VAR06-30 plus VAT03-9 was reported as percentage of the expression of each gene in grapevine inoculated with only VAT03-9 strain. All measurements were taken at 1 dai. The means of five biological replicates were used as a measured relative expression level.

The effect of treatment, gene, and their interaction on the median adjusted gene expression rate was examined using the linear mixed model ANOVA [packages ‘car’ and ‘lme4’ in R, ver. 3.5 (http://www.r-project.org/)]. In the model, treatment, gene, and their interaction were considered as fixed effects, and experimental replication was considered as a random effect. For the effect of treatment, Tukey’s HSD (package ‘emmeans’ in R) was used as a post hoc multiple comparison method.

Catabolism test of AS

Cell suspensions (2 mL each) of ARK-1, VAR06-30, and VAT03-9 were prepared from 24-h-old cultures on King’s B medium [27] in a shaking incubator at 28 °C. The tubes with each culture were centrifuged at 4000 rpm for 15 min. A supernatant of these strains was discarded and the surface was washed with distilled water to obtain a cell suspension, which was suspended in AT minimal media solution [28-30] with 0.2% mannitol as a carbon source (called ATM) with supplemental biotin (2 μg mL−1). The cell concentration was adjusted to approximately 2 × 108 cells mL−1. Two millilitre of cell suspensions were prepared in three tubes per strain. Three tubes containing 2 mL of ATM were also prepared as a negative control. The 2 μL of AS (Sigma-Aldrich, Germany) was dissolved in dimethyl sulfoxide (DMSO) to produce a 10 mM stock solution. The 2 μL of the stock AS solution was applied to each tube of ARK-1, VAR06-30, VAT03-9, or the negative control. Each tube was incubated in a shaking incubator at 28 °C for 24-h. Then, 1 mL of culture supernatant was obtained from each culture after centrifugation with 13,000 rpm for 5 min. Then, concentration of AS in each culture fluid was measured at UV 296 nm after 1.95 min using the high-performance liquid chromatography (HPLC, HITACHI LaChrom Elite, Japan) equipped with Kinetex 2.6 μm Biphenyl column (150 × 4.6 mm) (Phenomenex, USA). The experiment was repeated three times. The effect of treatment on the concentration of AS was examined with a linear mixed model ANOVA as described above.

Results

Suppressive effect on expression of the vir genes of the Ti strain by co-inoculation with ARK-1 in grapevine plants

The treatment factor significantly affected the median adjusted expression rate (F = 21.9, P < 0.01), but the effect of gene (F = 1.0, P = 0.38) and treatment and gene interaction (F = 0.09, P = 0.98) were not significant. The median adjusted expression rate of virA, virD3, and virG genes were significantly suppressed (P ≤ 0.05) by co-inoculation of ARK-1 with VAT03-9 (Fig. 1). On the other hand, no significant difference (P > 0.05) in the adjusted median expression rate of virA, virD3, and virG were observed when co-inoculation of VAR06-30 with VAT03-9 and inoculation of VAT03-9 alone were compared (Fig. 1).

Fig. 1

Relative expression rate of the virA, virD3, and virG genes in bacterial cells of the Rhizobium vitis Ti strain in grapevine plants measured using the reverse transcriptase quantitative polymerase chain reaction (RT-qPCR). Values (%) represent the relative expression rate of the vir genes at 1 day after inoculation (dai) compared with the value when only Ti strain VAT03-9 was inoculated (“Ti strain alone”), which had a value of 100%. Each cell suspension or mixture (ARK-1 plus a Ti, VAR06-30 plus a Ti, and a Ti alone) at cell ratios of 1:1 was inoculated onto the stems of grapevine plants after wounding. Stem samples were harvested at 1 dai. The center bar of the boxplot is the median, the lower and upper horizontal bars are 25th and 75th percentile, and whiskers show 95% range. Boxes labeled with different letters indicate a significant difference from the other bars in same gene expression (P ≤ 0.05, Tukey’s HSD test)

Catabolization of AS by ARK-1

There were no significant differences in the concentrations of AS among each R. vitis strain (F = 2.2, P = 0.19). No significant reduction of AS content was observed compared with the negative control (Fig. 2).

Fig. 2

The concentration of acetosyringone (AS) after incubation Rhizobium vitis Ti strain (VAT03-9) and non-pathogenic strains (ARK-1 and VAR06-30) with AT medium (ATM) or only ATM without a bacterial strain as negative control. The center bar of the boxplot is the median, the lower and upper horizontal bars are 25th and 75th percentile, and whiskers show 95% range

Discussions

In our study, treatment with ARK-1 suppressed the expression of virA, virD3, and virG by the Ti strain in grapevine. In comparison, VAR06-30, a non-antagonistic and non-pathogenic strain, did not suppress the expression of these genes. With results from this and a previous study [14], ARK-1 has shown to be able to suppress the expression of at least five different vir genes: virA; virD3; virG (this study); virD2; and virE2 [14]. ARK-1 suppresses both essential (virA, virD2, virE2, and virG) and non-essential (virD3) virulence genes of R. vitis Ti strains. Since ARK-1 suppresses the expression of virA and virG, which are the first two triggers of expression of all other vir genes in Rhizobium Ti strains [4-6], there is a possibility that all subsequent expression of vir genes can be suppressed.

We previously demonstrated that ARK-1 suppressed the expression of vir genes of Ti when the expression was triggered by AS in a liquid culture medium [14]. However, there was a possibility that the suppression of these vir genes was a consequence of quick catabolization of AS by ARK-1, thus, the sensor protein VirA was not able to detect AS to trigger subsequent vir gene expressions [4-6].

In catabolization test, however, all the tested R. vitis strains including ARK-1was not able to catabolize AS (Fig. 2). This result indicates that ARK-1 is not capable of metabolizing AS to interfere with a Ti strain’s vir genes. Therefore, ARK-1 has an ability to suppress the expression of vir genes via other mechanism(s).

Conclusions

ARK-1 suppressed expression of the virulence genes virA, virD3, and virG of a Ti strain at the wound site without catabolizing AS. The suppressive effect of ARK-1 was not specific to the essential virulence genes.

Limitations

We have carried out the inoculation with grapevines seedlings, not adult trees.

Additional file 1: Table S1. Bacterial strains used in this study.

Additional file 2: Table S2. Experimental condition used in reverse-transcriptase quantitative real-time polymerase chain reaction (RT-qPCR) based on MIQE requirements.