Transposon Mutagenesis of Pseudomonas syringae Pathovars syringae and morsprunorum to Identify Genes Involved in Bacterial Canker Disease of Cherry

Bacterial canker of Prunus, affecting economically important stone fruit crops including cherry, peach, apricot and plum, is caused by the plant pathogen Pseudomonas syringae (P.s.). Strains from two pathovars—P.s. pv. syringae (Pss) and P.s. pv. morsprunorum race 1 (PsmR1) and 2 (PsmR2)—in three phylogenetically distant clades have convergently evolved to infect Prunus. The bacteria enter woody tissues through wounds and leaf scars, causing black necrotic cankers. Symptoms are also produced on blossom, fruit and leaves. Little is known about the mechanisms P.s. uses to colonise tree hosts such as Prunus. Here, we created transposon (Tn) mutant libraries in one strain of P.s. from each of the three clades and screened the mutants on immature cherry fruit to look for changes in virulence. Mutants (242) with either reduced or enhanced virulence were detected and further characterised by in vitro screens for biofilm formation, swarming ability, and pathogenicity on leaves and cut shoots. In total, 18 genes affecting virulence were selected, and these were involved in diverse functions including motility, type III secretion, membrane transport, amino acid synthesis, DNA repair and primary metabolism. Interestingly, mutation of the effector gene, hopAU1, led to an increase in virulence of Psm R2.


Introduction
Pseudomonas syringae (P.s.) is a bacterial plant pathogen made up of over 60 pathovars (pv) which cause disease in over 180 plant species including many important crops. Bacterial canker caused by P.s. is the leading cause of disease in cherry and there are as yet no effective control measures [1]. Bacterial canker of Prunus which attacks the economically important crop species cherry, peach, apricot and plum is caused by members of at least three clades of P.s., P.s. pv. syringae (Pss) and P.s. pv. morsprunorum race 1 (Psm R1) and 2 (Psm R2). The Rsm races are found in two different phylogroups (R1 in P3, R2 in P1) [1]. Bacterial canker has been reported to result in tree losses of up to 75% [2] and is an annual problem. The pathogens occupy two niches including an epiphytic phase where the bacteria remain on the surface of the plant, and an endophytic phase in the intercellular spaces within plant tissues [3]. To reach the intercellular space in woody tissue, the bacteria enter through wounds and leaf scars in the winter and lie dormant until the spring when black necrotic cankers develop [4]. Blossom, fruit and leaves are all affected by the disease and display a range of necrotic symptoms [1,5]. The long-term goal of research into bacterial canker of Prunus is to identify the genes essential for host colonisation and symptom development during the different phases of the bacterial infection cycle [5]. In the pathovars of P. syringae, it has been established that effector proteins secreted into plant cells by the type III secretion system (T3SS) and also lowmolecular-weight toxins have key roles in the suppression of the plant's immune responses, allowing successful colonisation of the apoplast to take place [6][7][8]. The identification of the T3SS was achieved by transposon mutagenesis of P.s. pv phaseolicola and complementation analysis of mutants recovered that had lost the ability to induce a hypersensitive reaction as well as pathogenesis [9].
The mutant screening approach has been the cornerstone of genetic dissection of pathogenicity and has been used with numerous plant pathogenic bacteria [10,11]. In addition to effectors and toxins, many other genes with less clearly defined roles in virulence have been found to influence disease outcomes. For example, in a study of P. cannabina pv. alisalensis (P. cal), Sakata et al. [12] tested 1040 Tn5 mutants by dip inoculation onto cabbage plants. P. cal causes bacterial blight of Brassicaceae, an economically important crop which includes plants such as cabbage, broccoli, cauliflower and mustards. A total of 53 mutants showed decreased virulence and further tests revealed that 31 of these mutants also exhibited decreased virulence on oat seedlings. The potential virulence factors identified included not only genes encoding the T3SS, but also membrane transporters and enzymes involved in amino acid metabolism. Manoharan et al. [13] selected 106 out of 1920 Tn mutants from P.s. pv. phaseolicola using an in vitro screen looking for changes in motility, colony formation, and adhesion, which were proxies for infection, microcolony formation and cell adhesion. A number of mutants with altered motility bearing mutations in genes encoding various parts of the flagellum were found to lose pathogenicity. However, a mutation in a gene encoding an unidentified conserved hypothetical protein caused a positive increase in bacterial multiplication in planta.
A new approach to mutagenesis, allowing rapid identification of genes improving pathogenic fitness, is transposon sequencing (Tn-seq). This method is based on recent developments in high-throughput sequencing platforms and involves creation of a saturated Mariner transposon insertion library followed by deep-sequencing of populations of bacteria to identify the genes maintained during infection [14]. The application of Tn-seq has allowed genome-wide identification of genes in P.s. pv. syringae B728a required for fitness during colonisation of the bean leaf surface and inside the plant [15]. Genes within the functional categories of amino acid and polysaccharide biosynthesis contributed most to fitness, both on the leaf surface (epiphytic) and in the leaf interior (apoplast), while genes involved in the T3SS and also syringomycin toxin synthesis were important in the apoplast. Of the secreted type III effectors, disruption of hopAB1 had the greatest effect on intercellular colonisation. Numerous other genes that had not been previously associated with in planta growth were also required for maximum epiphytic or apoplastic fitness. In short, mutagenesis experiments have shown that there is more to the life of a plant pathogen than the T3SS, effectors, and toxins.
The inoculation of immature cherry fruit provides a rapid test of P.s. pathogenicity that is well suited for mutant screening experiments [1]. Here, we describe experiments using the fruit assay as a primary screen of Tn mutants of each of the major cherry canker pathogens Pss, Psm R1 and Psm R2. Mutants with reduced and also enhanced virulence recovered from the fruit assay were further characterised by in vitro growth parameters including biofilm formation [13] and leaf and cut shoot pathogenicity tests. The mutated genes in a selection of mutants with altered pathogenicity were identified by sequencing and complementation experiments. Intriguingly, mutation of the effector hopAU1 in Psm R2 was found to lead to increased symptom development in all assays.

Bacterial Strains and Growth Conditions
Bacterial strains and plasmids used in this study are listed in Table 1. Escherichia coli strains were grown at 37 • C in Lysogeny Broth (LB, Difco, Detroit, MI, USA) medium supplemented with 15 g/L Bacteriological No.1 agar (Oxoid, Altrincham, Cheshire, UK) and Pseudomonas strains were grown at 25 • C on Kings medium B (KB, Difco, Detroit, MI, USA) or in LB broth. Selected mutants were grown on M9 minimal media supplemented with 20% glucose to test for auxotrophy. Antibiotics were used at the following concentrations (µg/mL): gentamycin (Gm) 10, kanamycin (Km) 50, rifampicin (Rif) 10, and nitrofurantoin (NF) 100.

Transposon Insertion Library Construction
Libraries of transposon (Tn) mutants were generated using Psm strains MH001 and 5244 and Pss strain 9644 (recipient strains) following bi-parental mating with E. coli S17-1 λpir carrying IS-Ω-Km/hah (donor strain) [17]. Essentially, 500 µL of an overnight culture was inoculated into 10 mL of LB broth and incubated for 2 h (donor strain) or 4 h (recipient strain). Following incubation, 30 µL of donor was mixed with 100 µL of an overnight culture of the required recipient strain and the mixture transferred to the centre of a LB plate before incubation at 30 • C for 48 h. This conjugation mixture was then diluted, plated on KB + Km + NF or Rif and incubated at 25 • C for 72 h. Single-transformation mutants were selected and inoculated on KB + Km in a 48 colony grid pattern and numbered. The locations of transposons in the genome were identified using Arbitrary Primed (AP)-PCR and DNA sequencing (Eurofins Genomics) [13] (see Table S1 for primer sequences). The resulting sequences were analysed using the BLAST programme from the NCBI.

Pathogenicity Testing
The initial screen was performed on detached unripe cherry (Prunus avium) fruit, as described in Hulin et al. [1]. Green cherry fruit, cultivar Sweetheart, were inoculated with individual colonies from 48 colony replica plates using a sterile cocktail stick. The fruit were placed on boards with~200 pre-drilled holes and incubated at 23 • C, 80% humidity, 16/8 h light/dark cycle in a growth cabinet. The fruits were scored by eye for symptoms and photographed after 5 days. Scoring was as follows: wild type (WT, +), no lesions other than the inoculation wound (-), lesion formation less than in the wild type (-), increased symptoms (++), increased symptoms with signs of spread (+++). Detached 1-2-week-old leaves of cherry cultivar Sweetheart obtained from NIAB EMR were syringe infiltrated with 2 × 10 8 CFU/mL bacterial suspension from an overnight broth culture. Six replicate leaves were inoculated per strain and leaves were placed in plastic trays on water agar For in planta growth analyses, dormant cherry shoots of susceptible cultivar Van were obtained from NIAB EMR. Shoots were sterilised in 5% hypochlorite for 5 min before being washed 3 times in tap water and then air dried overnight. Shoots were cut to 10 cm in length and a sterile scalpel used to carve an 'I' shape into the bark, which was then peeled back and the shoot inoculated with 8 × 10 7 cfu/mL bacterial suspension. This was allowed to soak in for 5 min before the bark was folded back down and the wound wrapped in parafilm. The shoots were stood in 2 cm water and incubated at room temperature for 5, 10 and 14 days. A sterile scalpel was then used to harvest the inoculated area (10 mm long by 10 mm wide and 3 mm down into the tissue), and this was homogenised in 1 ⁄4 Ringers solution before being diluted and spread plated onto KB plus appropriate antibiotic selection. Colonies were counted after three days.

Colony Morphology
Tn libraries were replica plated onto KB agar with the WT control strain in position one. Each library plate was tested in triplicate and plates were incubated at 25 • C for three days before visual observation of the colony phenotypes.

Biofilm Attachment
The biofilm attachment assay was modified from Spiers et al. [19]. Tn library plates were replica plated into a 96-well microtiter plates containing 200 µL LB broth + Km. The WT control was tested without Km in plate position one. Plates were incubated at 25 • C for seven days without shaking. After seven days, the bacteria attached to the microtiter plates were stained with 1% crystal violet (CV). The density of the eluted CV was determined at OD 570 using a microtiter plate reader (FLUOstar OPTIMA, BMG Labtech, Ortenberg, Germany). To test individual mutants, strains were incubated in 10 mL of LB broth + Km static at 25 • C for seven days. After seven days, attached bacteria were stained as described above with 1 mL of 1% CV.

In Vitro Growth Rate
Initial growth assays were carried out in 96-well plates containing 200 µL LB broth, inoculated directly from plate culture with a replica plater and incubated for 8 h shaking. The cell density was determined at OD 600 using a microtiter plate reader (FLUOstar OPTIMA, BMG Labtech, Ortenberg, Germany). Any mutants that showed a statistically significant growth rate compared to their respective WT strain as determined by Student's t-test (p < 0.05) were repeated in triplicate. Individually selected mutants were grown overnight in LB broth + Km and diluted to 8 × 10 8 CFU/mL (OD 600 1.0). Cells (100 µL) were subcultured into 10 mL fresh LB broth and the optical density measured and recorded. All cultures were incubated at 25 • C with shaking (10 g) and their optical densities measured and recorded after 8 h.

Swarming Ability
Selected mutants were tested for swarming motility individually. Mutants and WT strains were spotted into the centre of a 0.3% LB agar plate. Each mutant was tested in triplicate and plates were incubated at 25 • C for 72 h before visual observation and measurement of the colonies' swarming motility.

Cloning and Complementation
Ectopic complementation of selected Tn mutants was carried out following PCR amplification of the disrupted genes including both start and stop codons and a 100 bp region upstream of the start codon to include likely promotor sequences (see Table S1 for primer sequences) and insertion of the resulting fragment into TOPO pCR2.1 (Invitrogen) by TA cloning following the manufacturer's instructions. The resulting construct was partially digested with EcoR1 and the fragment of the correct size was ligated into broad host range vector pBBR1MCS-5, allowing expression from the Tn3 or Tn7 promoters [18]. These constructs were introduced into their respective mutant strain via electroporation, as described by Keen et al. [20]. An empty vector was also transformed into the mutants as a control.

Pathogenicity Screening of Pseudomonas syringae Transposon Mutants
Libraries of transposon mutants were made of the three pathogenic strains-Pss 9644, Psm 5244 and Psm MH001. Due to the relative inefficiency of the conjugation process, and a desire to test the proof of principle of this approach, 940 Tn mutants per library were chosen. The libraries were screened for changes in pathogenicity on unripe detached cherry fruit. Each insertion mutant was picked directly from a colony using a sterile cocktail stick and stabbed into fruit. Each mutant was tested three times and the symptoms scored and photographed after five days incubation at 23 • C. Symptoms were scored compared to WT, Figure 1 illustrates the range of symptoms observed.
A total of 76, 53 and 113 mutants of Pss 9644, Psm 5244 and Psm MH001, respectively, showed changes in pathogenicity compared to WT. Numbers of individual Tn mutants that show changes in pathogenicity are given in Table 2.

Cloning and Complementation
Ectopic complementation of selected Tn mutants was carried out following PCR amplification of the disrupted genes including both start and stop codons and a 100 bp region upstream of the start codon to include likely promotor sequences (see Table S1 for primer sequences) and insertion of the resulting fragment into TOPO pCR2.1 (Invitrogen) by TA cloning following the manufacturer's instructions. The resulting construct was partially digested with EcoR1 and the fragment of the correct size was ligated into broad host range vector pBBR1MCS-5, allowing expression from the Tn3 or Tn7 promoters [18]. These constructs were introduced into their respective mutant strain via electroporation, as described by Keen et al. [20]. An empty vector was also transformed into the mutants as a control.

Pathogenicity Screening of Pseudomonas syringae Transposon Mutants
Libraries of transposon mutants were made of the three pathogenic strains-Pss 9644, Psm 5244 and Psm MH001. Due to the relative inefficiency of the conjugation process, and a desire to test the proof of principle of this approach, 940 Tn mutants per library were chosen. The libraries were screened for changes in pathogenicity on unripe detached cherry fruit. Each insertion mutant was picked directly from a colony using a sterile cocktail stick and stabbed into fruit. Each mutant was tested three times and the symptoms scored and photographed after five days incubation at 23 °C. Symptoms were scored compared to WT, Figure 1 illustrates the range of symptoms observed.
A total of 76, 53 and 113 mutants of Pss 9644, Psm 5244 and Psm MH001, respectively, showed changes in pathogenicity compared to WT. Numbers of individual Tn mutants that show changes in pathogenicity are given in Table 2.

In Vitro Screening of Transposon Mutants
Transposon insertions may have had an impact on bacterial metabolism, affecting growth or the ability to colonise and/or attach to the plant cell within the apoplast, thus the libraries of mutants from each pathogen were tested for in vitro growth characteristicscolony size, biofilm formation and growth rate in liquid culture. A number of alterations from the wild type were recorded for each strain. Results from a selection of mutants, illustrating the variations observed in mutants of each pathogen, are shown in Figures 2 and 3. Mutations of Psm MH001 only produced mutants with an increased adherence ability.  The numbers of mutants with each phenotype from in vitro assessment and pathogenicity scores were compared determine whether changes in pathogenicity related to changes in phenotype (Table 2). Mutants with higher or lower growth rates in vitro were similarly more or less pathogenic in the cherry fruit assay. A similar trend was noted for biofilm formation, although there were exceptions, for example, of the three Psm 5244 mutants with reduced biofilm formation, two recorded increased symptom scores. Results recorded for all the assays for each mutant can be found in Table S2.

Selection of Transposon Mutants for Further Analysis
From the results of the phenotypic screens, 18 mutants were selected for further analysis ( Table 3). The focus was on mutants with altered virulence and included twelve (two Pss 9644 and 10 Psm MH001) that produced no disease symptoms on cherry fruit, but displayed WT colony morphology. Genomic analysis of the selected genes between strains showed that some of the genes are present in all three strains but some are only present in one or two strains (Table S3). Six mutants that displayed hypervirulence on cherry fruit were also selected for further analysis (four Pss 9644, one Psm 5244 and one Psm MH001).

Swarming Ability of Selected Transposon Mutants
The chosen 18 transposon mutants were subjected to a further phenotypic test to determine whether the insertions had affected their motility and hence their ability to disperse throughout the apoplast, which is expected to be an important factor in successful colonisation of the plant. Mutant and WT strains were spotted individually onto 0.3% soft LB agar plates and incubated for 72 h at 25 • C, before being visually compared and measured (Table 3). Swarming ability was altered in five out of the 18.

Identification of Disrupted Genes in Selected Transposon Mutants
The gene disrupted in each mutant was identified by AP-PCR and sequencing using primers located in the transposon and semi-random primers for the chromosome ( Table 3). As a number of mutations were identified in genes involved in metabolism all 18 mutants were tested for growth on M9 minimal medium. Absence of growth on M9 minimal medium was observed for 9644 mutant strain 3.15 (Tn located in a serine hydroxymethyltransferase 2) and MH001 mutant strain 4.02 (Tn located in an ornithine carbamoyltransferase).
Taken together, even within the small sample of mutants analysed in depth, the mutations affecting virulence were found to be in genes involved in diverse functions including membrane transport, amino acid metabolism, DNA repair and primary metabolism. In addition, we found examples of mutations in genes involved in the T3SS (hrcS) and flagellar assembly (fliK) that led to loss of pathogenicity. By contrast, an insertion in the effector encoding gene hopAU1 led to increased virulence.

Complementation of Transposon Mutants
To determine whether the wild-type phenotype could be restored, complementation experiments were carried out. Primers designed to include putative promoter regions, start and stop codons were used to amplify the genes from WT DNA of each strain. Functional copies of the disrupted gene were cloned into a broad host range vector pBBR1MCS-5 and electroporated into the matching Tn mutant. An empty vector was also transformed into all the mutants tested and used as a control. The WT, mutants, complemented strains and controls were then inoculated onto both detached cherry fruit and detached cherry leaves of cv. Sweetheart and incubated for five and ten days, respectively, at 23 • C. Figure 4 shows six examples of the observed phenotypes. In all 18 cases, the WT disease phenotype was restored by complementation in fruit and leaves. The empty vector control did not affect the mutant phenotype in any strain (data not shown). Mutants that showed no disease symptoms (-) on cherry fruit but displayed wild-type (WT) characteristics in all other phenotypic assays, along with several mutants that displayed hypervirulence (+++) on cherry fruit were selected for complementation. The disrupted genes (3.17, dnaJ; 7.43, hrcS; 5.18, glycosyl transferase 1; 9.46, hopAU1; 11.18, nhaA; 20.17, argE) were cloned into a broad host range vector and transformed into their respective mutant strain. The WT, Tn mutant (M) and complemented strains © were tested on cherry fruit and cherry leaves to confirm restoration pathogeniciy in the complemented strains. Images displayed show 6 of the 18 complemented strains. However, in all cases, pathogenicity was restored on both fruit and leaves. Images of 9644-11.18 and 5244-20.17 are composites of three photographs.
Bacterial multiplication at inoculation sites was examined in all 18 mutants and their complemented strains using woody shoots of cherry cv. Van (this was the only susceptible cultivar available for use at the time). The complementation apparent in the fruit and leaf assays was reflected by restoration of bacterial populations to those recorded for the wild-type strains ( Figure 5) for all except 9644-12.36 (arginine-ornithine antiporter) where the complementation failed to restore WT population levels in woody tissue.

Discussion
The development of disease-resistant cherry tree varieties is a central approach to reducing yield losses and securing fruit supply for the future. Key to developing such varieties is an understanding of how pathogens cause disease and trigger resistance, especially when there is diversity in pathogen genotypes. To examine this, we used random transposon (Tn) mutagenesis in combination with a series of screens to identify mutants with altered phenotypes potentially associated with virulence in cherry canker pathogens Pss and Psm. Overall, we screened 940 colonies from each of three Tn libraries of Pss 9644, Psm R1 5244 and Psm R2 MH001. Combining the results of the various tests, we chose 18 mutants to focus on, including six that appeared to be hypervirulent on cherry fruit. When comparing the 18 genes to two other small-scale Tn screens in P. syringae [13] and P. cannabina [12] as well as a more in-depth Tn screen [15], we were able to see overlaps in the general classes of genes observed to be important (e.g., amino acid metabolism and transport, T3SS, cofactor metabolism) as well as some specific matches (e.g., glyA, dnaJ, acetolactate synthase). These demonstrate some commonalities in genes that play important roles in virulence as well as the expected diversity observed due to the influence of host and environment on pathogen evolution.
Of the six mutants that showed an increase in disease symptoms on cherry fruit, five also showed increased multiplication in planta. These include Pss 11.18 and 12.36, which had WT colony morphology and WT in vitro growth, and the mutated genes encoding for Na(+)/H(+) antiporter NhaA and an arginine-ornithine antiporter ArgE, respectively. An antiporter is a membrane protein that actively transports two or more different molecules through the plasma membrane in opposite directions. Na+/H+ antiporters catalyse the efflux of Na+ in exchange for H+ in order to regulate intracellular pH. Most bacteria contain between five and nine different Na+(K+)/H+ antiporters [21], which may explain how mutation of nhaA did not lead to a reduction in growth in vitro. Herz et al. [22] created a triple mutant of three Na+/H+ mutants in Vibrio cholerae and found no significant reduction in exponential growth in high pH environment. One theory to explain this phenomenon is that the bacterium may employ alternative regulatory strategies, for example functional redundancy or compensatory upregulation mechanisms, to rescue negative effects caused by the single-antiporter gene disruptions [23]. Three mutants involved in arginine metabolism were observed-two showing hypervirulence and one loss of virulence. Notably, arginine metabolism genes (argA and argB) were identified in a transposon mutagenesis screen of the olive knot pathogen, P. savastanoi pv. savastanoi [24]. As with olive, we know nothing about the cherry metabolome and the status of arginine levels, unlike tomato apoplast where levels are very low [25]. Together, these observations indicate a deeper metabolome analysis of cherry is warranted that examines how the pathogen interacts with arginine and how it influences disease. By contrast, Pss 6.08 (Pyridoxine/pyridoxamine 5 -phosphate oxidase) and Psm 5244 20.17 (Acetylornithine decacetylase) showed an increase in disease symptoms and an increase in in planta growth but also had a larger than WT colony morphology and Psm 5244 20.17 also had higher in vitro growth than WT but, by contrast, a reduced swarming ability (65 ± 6). Pyridoxine/pyridoxamine 5 -phosphate oxidase is part of the vitamin B6 biosynthesis pathway and acetylornithine decacetylase is an enzyme in step 1 of the sub-pathway that synthesises L-ornithine from N(2)-acetyl-L-ornithine (linear).
An increase in disease symptoms and multiplication in planta was also recorded for Psm MH001 9.46 but this mutant had WT in vitro characteristics. The transposon located Psm MH001 9.46 disrupts the type III effector hopAU1 which is present in most strains of PsmR1 and R2, but not the Pss strains pathogenic to cherry [1]. The function of HopAU1 has not been determined but the protein has been shown to be localised to the plant cytoplasm and excluded from the nucleus in Psa [26]. It is also necessary for growth at later stages of infection by Pph strain 1448A in bean [27]. Why a disruption in the genes responsible for a type III effector, metabolic enzymes and the antiporter genes discussed above would lead to increased in planta growth and enhanced disease symptoms is unclear but highlights the complexity of the control of virulence in these pathogens. It may be that deletion of these genes leads to advantage as a plant pathogen under laboratory conditions but would be detrimental to the bacterium in the field. There is likely to be a delicate balancing act between being a more aggressive pathogen and surviving under other circumstances. It may also be possible that the presence of a functional HopAU1 protein and the production and release of other metabolites from the cell activates some level of host resistance that reduces pathogen fitness in planta and this may help to explain why hopAU1, for example is absent from certain cherry pathogens like Pss. This suggests a further analysis using experimental evolution approaches may help to understand the nuances underpinning selective pressure to maintain this gene in Psm in the face of reduced fitness, especially if it reveals a weak but quantifiable host resistance.
In contrast to the above mutants the final hypervirulent mutant Pss 9644-1.38 showed increased symptoms on cherry fruit but no increase in multiplication in woody tissue. The mutation in 1.38 is within an adenine DNA glycosylase, a member of a family of enzymes involved in base excision repair. The increased symptom development caused by the mutant may be due to increased toxin or degradative enzyme production or activity, but the outcome clearly does not improve overall fitness of the pathogen as measured by growth.
Of the 12 mutants that produced no disease symptoms on cherry fruit but displayed WT colony morphology and WT in vitro growth, only four (all Psm MH001) showed decreased growth in cherry stems. One of these Psm MH001 7.43 encodes the T3SS protein HrcS. HrcS codes for an inner membrane-spanning protein of the T3SS and is crucial for pathogenicity [28], so we would expect disruption of it to cause a decrease in disease. Another mutant causing no disease is Psm MH001 5.42, which encodes for a DNA ligase D (LigD), an ATP-dependent enzyme that joins breaks in the phosphodiester backbone of DNA that occur during replication and recombination and as such they are essential for DNA replication and repair in all organisms. Psm MH001 4.14 is a phosphoglycerate mutase (PGM), an enzyme that catalyses step 8 of glycolysis. PGM catalyses the internal transfer of a phosphate group from C-3 to C-2, which results in the conversion of 3phosphoglycerate (3PG) to 2-phosphoglycerate (2PG) through a 2,3-bisphosphoglycerate intermediate. Morris et al. [29] demonstrated that functional PGM is essential for the growth and pathogenicity of P.s. pv. tomato on its host as a mutation in PGM renders the strain unable to grow and elicit disease symptoms on tomato seedlings. Psm MH001 15.32 is a disruption to the flagellar hook-length protein FliK [30]. Flagella confer motility to a number of bacteria [31] and discovery that flagellar genes are involved in virulence to the plant is not unexpected as it has been recorded in a number of plant pathogens [32,33]. FliK has previously been identified in another P. syringae Tn screen as a mutant that had a reduced ability for swarming in the Pph strain 1448A bean screen [13]. Four of the mutants that produced no disease also showed a reduced swarming ability-these were 9644-3.15, a serine hydroxymethyltransferase 2, and the three MH001 mutants discussed above (4.14, 5.42 and 15.32). 15.32 was particularly reduced in swarming (32 ± 3%) as could be expected of a flagellar mutant. Three of the 12 mutants-9644 3.15, a serine hydroxymethyltransferase 2; 9644-5.18, glycosyl transferase family 1; and MH001-3.17, molecular chaperone DnaJ-were also identified by Helmann et al. [15] as genes that when disrupted reduced the fitness of Psy B728a in apoplastic fluid by <−2.
In all 18 cases, the WT disease phenotype was restored in fruit and leaves by complementation and 17 of the complemented mutants restored their growth in woody tissue also. However, we failed to restore the WT woody tissue growth phenotype in mutant 9644 12.36, indicating that the insertion may be having a polar effect on a surrounding gene. The IS-Ω-Km/hah transposon carries a strong nptII promotor on its inside end (IE) [17]. The location of the insertion in mutant 12.32 indicates that the nptII promotor may be activating the adjacent gene BKM12_0040 an arginine deiminase, which may explain why complementation was not possible in the stem inoculations.
Although this study used a small sample size, it has identified a number of genes of potential interest with widely different functions. An unexpected observation was that the mutation of six genes caused the parent strain to become hypervirulent on cherry fruit and leaves, four of which became hypervirulent in woody tissue as well. Hypervirulence has been observed following single-gene deletions in a range of pathogenic microorganisms. Brown et al. [34] identified 112 hypervirulent mutations from 37 pathogen species using the pathogen-host interaction database. The 112 genes identified were from across kingdoms, in many cases conserved and came from a number of molecular, biochemical and cellular pathways. If hypervirulence mutations can be selected for in a population without any subsequent cost to the bacteria, it is possible that more virulent forms of these pathogens could evolve. Thus, understanding the potential barriers and drivers of this process becomes important to ensure that management approaches do not inadvertently promote the emergence of more pathogenic strains.
Supplementary Materials: The following are available online at https://www.mdpi.com/article/ 10.3390/microorganisms9061328/s1, Table S1: PCR primers used in this study; Table S2: Screening results for all Tn mutants; Table S3: Presence of selected mutant genes in the other strains used in this study.