Development of Specific Markers for Identification of Biovars 1 and 2 Strains of Pseudomonas syringae pv. actinidiae

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Abstract

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Pseudomonas syringae pv. actinidiae (hereafter called PSA) is the causal agent of bacterial canker of kiwifruit. This bacterium causes dark brown angular spots surrounded by yellow haloes, cankers with white or reddish exudation on twigs and trunks, wilting, and eventually plant mortality (Bastas and Karakaya, 2012; Koh et al., 2010; Vanneste et al., 2011). This pathogen was first described in Japan in 1989 (Takikawa et al., 1989) and was subsequently isolated in Korea (Koh et al., 1994) and Italy (Scotichini, 1994) in 1992. The Japanese and Korean populations of PSA have been reported to diverge evolutionarily. While Japanese strains produced phaseolotoxin, Korean strains synthesized coronatine as a phytotoxin (Han et al., 2003). Only a few reports are available on the situation of PSA in China where Actinidia plants are endemic species (Liang et al., 2000). In Italy, bacterial canker on kiwifruit caused by PSA was not a destructive disease when first reported in 1992 despite causing occasional leaf spot and twig dieback. However, PSA strain associated with more severe symptoms has been isolated from central Italy since 2008 (Ferrante and Scortichini, 2009). This strain has rapidly spread to other kiwifruit-producing regions in Italy and has been reported from other European countries, including Portugal (Balestra et al., 2010), Spain (Balestra et al., 2011), France (Vanneste et al., 2011), and Turkey (Bastas and Karakaya, 2012). In other continents, this pathogen has also been detected in New Zealand (Everett et al., 2011) and Chile (European Plant Protection Organization, 2011) in 2010. Bacterial canker caused by PSA has become the most serious limiting factor for cultivating kiwifruit worldwide.

The genetic relationships between PSA populations with different geographic origins have recently been investigated using various molecular methods. Ferrante and Scortichini (2010) used rep-PCR and multi-locus sequence analysis (MLSA) and found that PSA strains isolated in Italy during 2008–2009 are distinct from those previously reported in Japan and Italy. The unique characteristics of PSA populations isolated from recent outbreaks in Italy were confirmed by a random amplified polymorphic DNA (RAPD) analysis, which produced different profiles from those of previously isolated strains (Mazzaglia et al., 2011). Chapman et al. (2012) performed MLSA of housekeeping and type III effector genes in PSA strains from Japan, Korea, Italy, New Zealand, Australia, and Chile and demonstrated that at least four PSA MLSA groups, designated Psa 1–4 (biovar 1–4), are present globally. Biovar 1 includes strains isolated from Japan and Italy in 1992. Korean strains isolated since the late 1980s belong to biovar 2. Strains causing recent outbreaks in European countries, including Italy, New Zealand, and Chile, belong to biovar 3 (Mazzaglia et al., 2012). Strains belonging to biovar 3 are considered to cause more serious disease based on their aggressiveness and rapid spread (Scortichini et al., 2012; Young, 2012). Strains belonging to biovar 4 have been detected in New Zealand and Australia, apparently causing only leaf spots but no canker symptoms. Recently, biovar 4 has been shown to be a distinct and different pathovar of P. syringae, and it was assigned a new name of pv. actinidifoliorum (Cunty et al., 2015; Ferrante and Scortichini, 2015; McCann et al., 2013).

In Korea, biovar 2 strains have been isolated since the late 1980s causing severe economic losses to A. deliciosa cv. Hayward as well as A. chinensis cv. Hort16A (Koh et al., 1994, 2010). However, strains belonging to biovar 3 have also been isolated since 2011 (Koh et al., 2012). These strains display identical molecular characteristics with biovar 3 strains isolated from recent outbreaks (Koh, et al., 2014).

PCR primers have been developed to detect PSA or distinguish populations with different geographic origins. One of the primer pairs was designed within the 16S–23S rDNA intertranscribed spacer (ITS) region of PSA strains after comparison with other related species and pathovars (Rees-George et al., 2010). However, this primer set could not distinguish PSA from the phylogenetically similar pv. theae. Balestra et al. (2013) developed PCR primer sets based on genome sequences of PSA strains available from the GenBank database. They designed a primer pair to specifically detect PSA but not any P. syringae pathovar, including pv. theae, as well as three additional primer sets to distinguish PSA populations originating from Europe, China, and Japan/Korea. However, the Japan/Korea primer set could not distinguish biovar 1 from biovar 2.

In this work, biovar 1 and 2-specific primer sets were developed based on RAPD analyses. Twelve PSA strains, including four biovar 1, three biovar 2, and five biovar 3 strains, were used for RAPD analyses and for primer validation (Table 1). Bacterial strains were cultured at 28°C in peptone-sucrose (20 g of peptone, 20 g of sucrose per 1 liter) medium. Total DNA was isolated from bacteria using an AccuPrep genomic DNA extraction kit (Bioneer, Korea).

Table 1

Bacterial strains used in this work

The existence of genes related to phytotoxin production were tested in order to confirm that the four strains isolated in Japan belong to biovar 1 and the three strains isolated in Korea belong to biovar 2. While biovars 1 and 2 each produce phaseolotoxin and coronatine, respectively, biovar 3 produces neither (Ferrante and Scortichini, 2010; Han et al., 2003). PCR amplification procedures have been applied to detect coronatine- or phaseolotoxin-producing P. syringae pathovars. The PCR primer set OCT-F/R, based on the argK sequence encoding phaseolotoxin-resistant ornithine carbamoyltransferase, has been used for specific detection of phaseolotoxin-producing P. syringae pathovars (Sawada et al., 1997). The PCR primer set CFL-1/2, derived from cfl gene encoding coronafacate ligase, has been used to detect coronatine-producing P. syringae strains (Bereswill et al., 1994). As shown in Fig. 1, the OCT-F/R primer set amplified a 1,098-bp fragment with four strains isolated from Japan and Italy in 1992. Three strains isolated in Korea amplified an expected 655-bp fragment using the CFL-1/2 primers. However, no PCR products were produced when these primer sets were applied to biovar 3 strains.

Fig. 1

PCR amplification products obtained with DNA of Pseudomonas syringae pv. actinidiae strains and primers, OCT-F/R (A) and CFL-1/2 (B). Lane M, 100-bp marker (Bioneer); lane 1, CJW7; lane 2, KBE9; lane 3, KBE29; lane 4, KW11; lane 5, SUPP 319; lane 6, SUPP 320; lane 7, NCPPB 3871; lane 8, SYS1; lane 9, P1; lane 10, 155; lane 11, CFBP 7286; lane 12, ICMP 18708.

The first primer set was designed to specifically detect biovar 1 strains, but not biovar 2 or biovar 3 strains. RAPD amplification was carried out throughout this work in 50-μl reaction mixtures containing 30 ng of genomic DNA, 5 μl of 10× reaction buffer, 5 μl of 10 mM dNTP mix, 20 pmol of single primer, and 2.5 U of Top DNA polymerase (Bioneer, Korea). The random primer OPA-2 (Operon Biotechnologies, USA) amplified a distinct band of approximately 650 bp present in four biovar 1 strains (data not shown). The differential RAPD band was excised from 2.0% agarose gel, and the DNA was purified using an AccuPrep gel purification kit (Bioneer, Korea). The DNA eluted from the band was ligated into pGEM-T Easy vector (Promega, USA) and then transformed into competent Escherichia coli JM109. The inserted DNA fragment was sequenced by SolGent Co. (Korea). Nucleotide sequence revealed that the exact nucleotide length of the specific amplicon was 641 bp, including 10-mer random primers at each end. This sequence showed 93% homology with the PPHGI-1 genomic island sequence of P. syringae pv. phaseolicola retrieved from the National Center for Biotechnology (NCBI) database using the BLAST algorithm. The amplified region is located within the nucleotide sequence of the genomic island between base pairs 16717 and 17353 of GenBank accession number AJ870974.1. The biovar 1-specific primer set PsaJ-F/R was designed using primer3 software (Untergasser et al., 2012) based on internal sequences of the RAPD marker. This primer set amplified 481-bp fragment only from DNA of biovar 1 strains of PSA (Fig. 2A).

Fig. 2

Agarose gel showing PCR amplification products using biovar 1-specific primer pair, PsaJ-F/R (A) and biovar 2-specific primer pair, PsaK-F/R (B). Lanes are the same as Fig. 1.

The same methods used to design biovar 1 were applied to develop biovar 2-specific primers. The random 10-mer primer OPA-16 produced an approximately 450-bp biovar 2-specific band. Sequencing showed that the size of this fragment was 462 bp but did not detect any significant homology to known sequences available from the NCBI database. PCR primers PsaK-F/R were designed from the nucleotide sequences of the biovar 2-specific RAPD marker. This primer pair amplified a 413-bp region present only in the genome of biovar 2 of PSA (Fig. 2B). The nucleotide sequences, annealing temperatures, and amplicon sizes of the primers used in this work are listed in Table 2.

Table 2

List of primers used in this work

Amplifications were carried out in a DNA Thermal Cycler (Takara Shozo, Japan) under the following conditions: an initial denaturation at 95°C for 5 min, followed by 30 cycles of a denature step of 95°C for 30 s, annealing for 30 s, extension at 72°C for 30 s, and final extension at 72°C for 7 min.

Two primer sets, PsaJ-F/R and PsaK-F/R, were validated with an additional five biovar 1 and twenty biovar 2 strains of PSA. The 481-bp biovar 1 fragment and 413-bp biovar 2 amplicon were produced with corresponding primer sets and DNA from PSA strains isolated from Japan and Korea, respectively (data not shown). In order to verify the specificity of the designed primer sets, both primer sets were tested on 15 bacterial strains, including 10 P. syringae pathovars; P. syringae pv. glycinea, pv. syringae, pv. tabaci, pv. viridiflava, pv. maculicola, pv. tomato, pv. atropurpurea, pv. phaseolicola, pv. morsprunorum and pv. theae, and five plant pathogenic bacteria; P. fluorescens, P. veronii, P. rhodesiae, Xanthomonas campestri pv. pruni, and Acidovorax valerianellae. No signal was obtained from these 15 bacterial strains when using the two primer sets, confirming the reliability of these primers in discriminating between biovar 1 and 2 strains of PSA (Fig. 3A, B). However, when we performed PCR with OCT-F/R primer set, 1,098-bp fragments were amplified from not only biovar 1 strain but also P. syringae pv. phaseolicola and pv. tabaci (Fig. 3C). In the case of PCR performed with CFL-1/2 primer set, the expected fragments of 655 bp were amplified from P. syringae pv. glycinea and pv. atropurpurea together with the biovar 2 strain of PSA (Fig. 3D).

Fig. 3

Specificity of PCR assay using biovar 1 primer pair, PsaJ-F/R (A), biovar 2 primer pair, PsaK-F/R (B), OCT-F/R (C), and CFL-1/2 (D). Ten Pseudomonas syringae pathovars and five plant pathogenic bacteria were used to test specificity of the designed primer pairs. Lane M, 100-bp marker (Bioneer); lane 1, Pseudomonas syringae pv. glycinea; lane 2, P. s. pv. syringae; lane 3, P. s. pv. tabaci; lane 4, P. s. pv. viridiflava; lane 5, P. s. pv. maculicola; lane 6, P. s. pv. tomato; lane 7, P. s. pv. atropurpurea; lane 8, P. s. pv. phaseolicola; lane 9, P. s. pv. morsprunorum; lane 10, P. s. pv. theae; lane 11, P. fluorescens; lane 12, P. veronii; lane 13, P. rhodesiae; lane 14, Acidovorax valerianellae; lane 15, Xanthomonas campestri pv. pruni; lane 16, P. syringae pv. actinidiae KW11 (A, C) or P. syringae pv. actinidiae CJW7 (B, D).

These biovar 1 and 2-specific primers can be used to determine the biovar group of PSA strains together with biovar 3-specific primers, which were reported in the previous study (Koh et al., 2014). The PCR assay developed in this study may serve as a useful tool for identification of biovars of PSA and will consequently be helpful in monitoring the migration of PSA strains.

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