Eucalyptus globulus Leaf Aqueous Extract Differentially Inhibits the Growth of Three Bacterial Tomato Pathogens

As available tools for crop disease management are scarce, new, effective, and eco-friendly solutions are needed. So, this study aimed at assessing the antibacterial activity of a dried leaf Eucalyptus globulus Labill. aqueous extract (DLE) against Pseudomonas syringae pv. tomato (Pst), Xanthomonas euvesicatoria (Xeu), and Clavibacter michiganensis michiganensis (Cmm). For this, the inhibitory activity of different concentrations of DLE (0, 15, 30, 45, 60, 75, 90, 105, 120, 135, and 250 g L−1) was monitored against the type strains of Pst, Xeu, and Cmm through the obtention of their growth curves. After 48 h, results showed that the pathogen growth was strongly inhibited by DLE, with Xeu the most susceptible species (15 g L−1 MIC and IC50), followed by Pst (30 g L−1 MIC and IC50), and Cmm (45 and 35 g L−1 MIC and IC50, respectively). Additionally, using the resazurin assay, it was possible to verify that DLE considerably impaired cell viability by more than 86%, 85%, and 69% after Pst, Xeu, and Cmm were incubated with DLE concentrations equal to or higher than their MIC, respectively. However, only the treatment with DLE at 120 g L−1 did not induce any hypersensitive response in all pathogens when treated bacterial suspensions were infiltrated onto tobacco leaves. Overall, DLE can represent a great strategy for the prophylactic treatment of tomato-associated bacterial diseases or reduce the application of environmentally toxic approaches.


Introduction
Nowadays, to meet the increasing food demand of an ever-growing population, agrifood production needs to step up considerably using progressively fewer resources [1]. To make matters worse, climate change is imposing additional challenges for crop growth, not only by directly restricting plant growth due to abiotic stress factors, such as high temperatures, water shortages, and salinity, but also by increasing the incidence and severity of pests and diseases [2,3].
Solanum lycopersicum L. (the tomato plant) is one of the most valuable crops worldwide, representing more than 15% of the world's total vegetable production [4] and playing an important role in both human nutrition and the socio-economic activities of the main producing countries. However, its production has been severely impacted by bacterial diseases, among which are bacterial speck, bacterial spot, and bacterial cancer, caused by Pseudomonas syringae pv. tomato Okabe (Pst), Xanthomonas euvesicatoria ex Doidge (Xeu), and Clavibacter michiganensis spp. michiganensis Smith (Cmm), respectively [5]. While the first aeruginosa [12,20], Salmonella sp. [20], Staphylococcus aureus [18][19][20][21][22], Bacillus sp. [18,19], Klebsiella pneumoniae [12,19], and Listeria sp. [22,23]. Accordingly, the only study exploring the antimicrobial properties of aqueous extracts of E. globulus leaves focus on human pathogens, leaving much to clarify regarding their antibacterial activity against phytopathogens [24]. Actually, to the best of our knowledge, only Sabir, et al. [25] has investigated the antibacterial activity of E. globulus leaf essential oils against a phytopathogenic bacterial species, namely Pst, having verified that they presented an interesting bactericidal activity against Pst DC3000.
In this sense, E. globulus leaf extracts could represent a more practical, affordable, and feasible approach to harnessing the bioactivity of eucalyptus specialized metabolites. A previous work [26] extensively characterized the phytochemical profile of aqueous extracts prepared with fresh and dried leaves of young and mature E. globulus trees, suggesting potential applications for these plant extracts. This study revealed that aqueous extracts prepared with dried leaves of young trees were rich in hydroxybenzoic acids, flavonoids, and organic acids, three chemical classes whose ability to disrupt bacterial membranes has already been described, thus having strong antibacterial properties [27][28][29].
The present study aims at evaluating the antimicrobial activity of aqueous extracts prepared from dried leaves of young E. globulus trees against three important tomato phytopathogens, Pst, Xeu, and Cmm. For this, the inhibitory effect of different concentrations of the aqueous eucalyptus extract was monitored on the type strains of the three bacterial species by determining their MIC, IC 50 , and bactericidal effect by addressing their viability and hypersensitive response on tobacco leaves.

Antibacterial Activity of the Dried Leaf Extract (DLE) against Pst, Xeu, and Cmm
After exposing Pst, Xeu, and Cmm for 48 h to different concentrations of the dried leaf extract (DLE), the results revealed that the eucalyptus leaf aqueous extract inhibited bacterial growth in a dose-dependent manner ( Figure 1). While Xeu growth was inhibited by the lowest DLE concentration tested (15 g L −1 ), slightly higher doses were required to suppress Pst and Cmm growth (30 and 45 g L −1 , respectively) ( Figure 1; Table 1). For Pst, the half-maximal inhibitory concentration (IC 50 ) of DLE was very close to the minimal inhibitory concentration (MIC), but for Cmm the IC 50 was lower than that (35 g L −1 ) ( Table 1). On the other hand, it was not possible to calculate the IC 50 for Xeu since the lowest DLE concentration tested (15 g L −1 ) inhibited microbial growth by more than 85%. Overall, the growth data indicates that the three phytopathogenic strains present different susceptibilities to DLE, being Xeu the most susceptible species, followed by Pst and Cmm, the most tolerant phytopathogens.

MIC IC 50
Pst At the end of the 48 h incubation of the phytopathogens with DLE, an aliquot of each suspension from microplate wells was spread in Nutrient Agar (NA) medium to determine the minimal bactericidal concentration (MBC) for each strain. Since the exposure of the three type strains to DLE concentrations higher than their MIC, except for DLE at 250 g L −1 , resulted in the formation of bacterial colonies indicating bacterial recovery after 48 h (data not shown), and thus not allowing the determination of the MBC, a resazurin-based assay was performed to quantify the percentage of viable cells (Figure 2). The cell viability of Pst, Xeu, and Cmm exposed to DLE concentrations corresponding to their MICs (30, 15, and 45 g L −1 , respectively) was drastically reduced by 97%, 99%, and 69%, respectively, compared to the negative control ( Figure 2). For Pst and Xeu, their MICs induced the highest reduction of cell viability, affecting this parameter in a similar way to that of streptomycin (ca. 98%). In contrast, the highest inhibition of the percentage of cellular viability (approximately 88%) for Cmm was registered after the 48 h incubation with DLE at 90 and 105 g L −1 , in comparison with the negative control ( Figure 2). catoria LMG 905 (Xeu), and Clavibacter michiganensis michiganensis LMG 7333 (Cmm).

Cellular Viability of Pst, Xeu, and Cmm upon 48 h of Exposure to Different DLE Concentrations
At the end of the 48 h incubation of the phytopathogens with DLE, an aliquot of each suspension from microplate wells was spread in Nutrient Agar (NA) medium to determine the minimal bactericidal concentration (MBC) for each strain. Since the exposure of the three type strains to DLE concentrations higher than their MIC, except for DLE at 250 g L −1 , resulted in the formation of bacterial colonies indicating bacterial recovery after 48 h (data not shown), and thus not allowing the determination of the MBC, a resazurinbased assay was performed to quantify the percentage of viable cells ( Figure 2). The cell viability of Pst, Xeu, and Cmm exposed to DLE concentrations corresponding to their MICs (30,15, and 45 g L −1 , respectively) was drastically reduced by 97%, 99%, and 69%, respectively, compared to the negative control ( Figure 2). For Pst and Xeu, their MICs induced the highest reduction of cell viability, affecting this parameter in a similar way to that of streptomycin (ca. 98%). In contrast, the highest inhibition of the percentage of cellular viability (approximately 88%) for Cmm was registered after the 48 h incubation with DLE at 90 and 105 g L −1 , in comparison with the negative control ( Figure 2). Streptomycin (Strept) was used as a control for growth inhibition (50 µg mL −1 ). Different letters above the bars denote significant differences (p ≤ 0.05), according to Tukey's post-hoc test.

Hypersensitive Response (HR) on Tobacco Leaves of the Phytopathogens Treated with DLE
To evaluate the impact of DLE on the virulence of the three phytopathogens, the HR on tobacco leaves was analysed. For that purpose, Nicotiana tabacum L. leaves were infiltrated with each one of the three bacterial species, after these being treated for 1 h with DLE at its respective MIC (Table 1) and with a higher concentration that significantly affected the growth and viability of the tree pathogens (120 g L −1 ; Figures 1 and 2). After 48 h, the incubation of the three bacterial strains with DLE at 120 g L −1 did not produce any HR on tobacco leaves, presenting a very similar appearance to that of the negative control ( Figure 3). In opposition, the infiltration of the three pathogens treated with the respective MIC (Table 1) induced an HR identical to that of the positive control ( Figure 3). Streptomycin (Strept) was used as a control for growth inhibition (50 µg mL −1 ). Different letters above the bars denote significant differences (p ≤ 0.05), according to Tukey's post-hoc test.

Hypersensitive Response (HR) on Tobacco Leaves of the Phytopathogens Treated with DLE
To evaluate the impact of DLE on the virulence of the three phytopathogens, the HR on tobacco leaves was analysed. For that purpose, Nicotiana tabacum L. leaves were infiltrated with each one of the three bacterial species, after these being treated for 1 h with DLE at its respective MIC (Table 1) and with a higher concentration that significantly affected the growth and viability of the tree pathogens (120 g L −1 ; Figures 1 and 2). After 48 h, the incubation of the three bacterial strains with DLE at 120 g L −1 did not produce any HR on tobacco leaves, presenting a very similar appearance to that of the negative control ( Figure 3). In opposition, the infiltration of the three pathogens treated with the respective MIC (Table 1) induced an HR identical to that of the positive control ( Figure 3). Plants 2023, 12, x FOR PEER REVIEW 6 of 13

Discussion
The limited existing tools for bacterial disease management in agricultural contexts have motivated several scientific studies to investigate effective and sustainable alternatives [30]. One of the most explored approaches consists of taking advantage of the specialized metabolism of different plants, such as Thymus sp., Satureja sp., and Origanum sp. to control the growth of crop-related disease causal agents (reviewed by Raveau, et al. [31]). Accordingly, the leaves of E. globulus are characteristically rich in terpenes, flavonoids, and phenolic acids, whose antibacterial activities have already been described [28,32,33], and for that reason, eucalyptus leaf extracts can constitute a great antimicrobial strategy. As a matter of fact, a previous study has reported strong inhibitory properties of E. globulus extracts against human-pathogen bacteria, such as P. aeruginosa [24]. However, the antibacterial potential of eucalyptus extracts against phytopathogens remains unclear, since, as far as we know, only the antibacterial activity of eucalyptus essential oils has been tested against Pst DC3000 [25]. Based on their data, eucalyptus essential oils showed bactericidal properties, thus presenting a great potential to become a new biobactericide. In this way, this study aims to assess, for the first time, the antimicrobial properties of a eucalyptus leaf aqueous extract against three major phytopathogens causing economically important diseases in tomato plants-bacterial speck, spot, and cancer caused by Pst, Xeu, and Cmm, respectively. For this purpose, the impact of the exposure of the type strains of these bacterial species to different concentrations of the dried leaf eucalyptus extract was assessed, by monitoring their growth, quantifying their cellular viability, and analysing their HR on N. tabacum leaves.
The growth of Pst, Xeu, and Cmm was differentially inhibited by DLE, resulting in distinct susceptibilities to the plant extract. A recent report from our group, which analysed the metabolomic profile of aqueous extracts of eucalyptus leaves, revealed that DLE-the one prepared with dried leaves of young E. globulus trees -, in comparison with those prepared with fresh leaves of juvenile and mature trees and dried leaf extracts of mature trees, presented appreciable amounts of phenolic acids, more specifically, gallic acid, digalloylglucose I, IV, and V, and galloylglucose I and II [26]. Due to their great

Discussion
The limited existing tools for bacterial disease management in agricultural contexts have motivated several scientific studies to investigate effective and sustainable alternatives [30]. One of the most explored approaches consists of taking advantage of the specialized metabolism of different plants, such as Thymus sp., Satureja sp., and Origanum sp. to control the growth of crop-related disease causal agents (reviewed by Raveau, et al. [31]). Accordingly, the leaves of E. globulus are characteristically rich in terpenes, flavonoids, and phenolic acids, whose antibacterial activities have already been described [28,32,33], and for that reason, eucalyptus leaf extracts can constitute a great antimicrobial strategy. As a matter of fact, a previous study has reported strong inhibitory properties of E. globulus extracts against human-pathogen bacteria, such as P. aeruginosa [24]. However, the antibacterial potential of eucalyptus extracts against phytopathogens remains unclear, since, as far as we know, only the antibacterial activity of eucalyptus essential oils has been tested against Pst DC3000 [25]. Based on their data, eucalyptus essential oils showed bactericidal properties, thus presenting a great potential to become a new biobactericide. In this way, this study aims to assess, for the first time, the antimicrobial properties of a eucalyptus leaf aqueous extract against three major phytopathogens causing economically important diseases in tomato plants-bacterial speck, spot, and cancer caused by Pst, Xeu, and Cmm, respectively. For this purpose, the impact of the exposure of the type strains of these bacterial species to different concentrations of the dried leaf eucalyptus extract was assessed, by monitoring their growth, quantifying their cellular viability, and analysing their HR on N. tabacum leaves.
The growth of Pst, Xeu, and Cmm was differentially inhibited by DLE, resulting in distinct susceptibilities to the plant extract. A recent report from our group, which analysed the metabolomic profile of aqueous extracts of eucalyptus leaves, revealed that DLE-the one prepared with dried leaves of young E. globulus trees -, in comparison with those prepared with fresh leaves of juvenile and mature trees and dried leaf extracts of mature trees, presented appreciable amounts of phenolic acids, more specifically, gallic acid, digalloylglucose I, IV, and V, and galloylglucose I and II [26]. Due to their great affinity for lipids, phenolic acids, a class of specialized metabolites with notorious antibacterial properties, can easily cross membranes, causing cytoplasmic acidification and consequently inducing membrane disruption [32]. For this reason, gram-negative bacteria are usually more susceptible to phenolic acids than gram-positive bacteria, thus correlating the outcomes of this study, in which Pst and Xeu, both gram-negative bacteria, were the most sensitive phytopathogens to DLE. In addition, this extract had rich contents in protocatechuic acid, a benzoic acid that had been reported to inhibit the growth of Pseudomonas spp., besides Listeria monocytogenes, Mannheimia haemolytica, Pasteurella multocida, Escherichia coli, and strains of Salmonella spp. [32] and Staphylococcus strains mainly by inducing membrane lysis [34]. Accordingly, Pereira, Dias, Vasconcelos, Rosa, and Saavedra [24] found that the growth of P. aeruginosa isolates was inhibited by an aqueous extract prepared with E. globulus leaves, which registered lower MIC values than those observed for Pst in this study. Similar results were obtained by Morales-Ubaldo, et al. [35], which reported that Xanthomonas campestris presented a greater susceptibility to hydroethanolic extracts of Larrea tridentata aerial parts in relation to P. syringae and Cmm. Yet, these two species presented identical MIC values [35]. In contrast, X. campestris and Cmm were the most susceptible species to methanolic and ethanolic extracts of Artemisia nilagirica leaves, with Pst being the most tolerant species with the highest MIC values [36]. In addition, the study of Körpe, et al. [37], which explored the antibacterial properties of aqueous and methanolic extracts of Urtica dioica and Urtica pilulifera seeds, leaves, and roots against multiple food-borne and phytopathogenic bacteria, including Cmm, Pst, and Xeu, concluded that Cmm was more affected by U. dioica seed and U. pilulifera leaf methanolic extracts than Xeu and Pst. Additionally, the MICs of both extracts for Cmm, Pst, and Xeu were lower than those registered in the present work for DLE. When assessing the antibacterial activity of Allium sativa and Ficus carica extracts against Pst, Xeu, and Cmm, Balestra, Heydari, Ceccarelli, Ovidi, and Quattrucci [5] found that Pst presented a higher susceptibility to these extracts than Xeu and Cmm in both in vitro and in planta experiments.
This outcome diversity can be the result of multiple factors, including the type of solvent and plant species selected to obtain the botanical extracts. Indeed, the extraction of plant biomass with solvents of different polarities results in the recovery of specialized metabolites with distinct chemical properties and, thus, bioactivities [37]. Furthermore, the type of plant species selected and even the developmental stage can exert a great influence on the resultant antimicrobial activity since the pool of phytochemicals retrieved, each with distinct modes of action, will also vary.
The MIC of DLE for Pst, Xeu, and Cmm induced a remarkable reduction of the percentage of cellular viability but did not interfere with the virulence of the few that remained viable, as shown by the similar intensity of the hypersensitive response of MIC infiltration on tobacco leaves for the three types of strains in comparison with the positive control. However, the treatment of bacterial species for 1 h with higher concentrations of DLE, such as 120 g L −1 , did not induce any HR on the leaves of N. tabacum, showing that, at this concentration, DLE highly compromised their virulence. In addition, as hypothesized by Mariz-Ponte, et al. [38] for the treatment of Pseudomonas syringae pv. actinidae with antimicrobial peptides (AMPs), the absence of HR after the infiltration of bacteria treated with DLE at 120 g L −1 can also be related to the reduction of cell density. In fact, despite the different incubation periods of pathogens with DLE at 120 g L −1 employed in the determination of the percentage of cellular viability and in HR analysis, the 48 h incubation of the bacteria with this DLE concentration induced a large reduction in the percentage of cellular viability, suggesting that it can also have contributed to the absence of infection symptoms on tobacco leaves.
Despite this potent inhibition of bacterial growth, the MBC for each phytopathogen was not possible to ascertain, as colony formation was always recorded. In agreement, Pereira, Dias, Vasconcelos, Rosa, and Saavedra [24] were also unable to determine the MBC for aqueous and organic solvent extracts of E. globulus leaves or for eucalyptus essential oils when they evaluated the antimicrobial potential of these extracts and essential oils against respiratory tract P. aeruginosa isolates. Still, the great reductions in cell viability induced by DLE concentrations equal to or greater than the MIC for each phytopathogen can possibly indicate that the inhibitory effects of DLE could be useful in the treatment of bacterial spot, speck, and cancer. Furthermore, the eco-friendly and low-cost nature of DLE also makes it an excellent candidate for pruning tools' sanitizing, as suggested by Sabir, El Khalfi, Errachidi, Chemsi, Serrano, and Soukri [25] for eucalyptus leaf essential oils, as well as to reduce the application of other innovative but expensive and pollutingt treatments, as is the case with AMPs and organic solvent-based plant extracts, respectively [36][37][38].
In comparison with other approaches, like AMP or other single-molecule therapies, the acquisition of bacterial resistance to plant extracts, as in the case of DLE, is less likely to occur, as they comprise a complex mixture of different compounds with distinct modes of action. In fact, as mentioned earlier, DLE is composed of many phenolic acids like gallic acid, galloylglucose digalloylglucose and the benzoic acid protocatechuic acid, which induce membrane disruption, organic acids such as arabinaric and tartaric acids, and flavonoids like quercetin [26]. Organic acids have the ability to cross membranes and can disrupt ATP production and induce cytoplasmic acidification [29], whereas flavonoids display multiple modes of action in bacterial cells, as they can inhibit biofilm formation, bacterial virulence, and nucleic acid, cell envelope, and peptidoglycan synthesis, besides disrupting membrane permeability [28]. In addition, flavonoids have the ability to inhibit cell efflux pumps, a property that can be of great interest to reverse bacterial antibiotic resistance [28]. Besides, DLE had very high levels of amino acids like methylserine hexoside [23]. Nonproteogenic amino acids can act as defence compounds and are usually toxic in nature, since their structures can be similar to those of proteogenic amino acids and be mistakenly incorporated during protein biosynthesis and disrupt this process [39].
Furthermore, the application of DLE could be of particular interest in terms of integrated pest management as, in a recent publication from our group, it also showed a potent herbicidal activity against a model weed species, Portulaca oleracea L., when foliar-applied at the highest concentration (250 g L −1 ) [11]. So, to attain a more sustainable agronomic production, DLE could be applied in low doses to treat tomato plants-associated bacterial diseases, and in the maximum concentration to control weed proliferation. However, before its implementation, the environmental safety of this strategy should be addressed, by carefully evaluating its non-target impacts on crops, soil microorganisms and invertebrates, and even human health. Ongoing studies focused on evaluating the effects of DLE application on the physiological performance of crops are being carried out.
For the evaluation of the antibacterial activity of the eucalyptus extract, synchronized cultures of each bacterial species were used. For this, a pure colony of each phytopathogen was selected, individually cultured on liquid Mueller-Hinton medium (MH), a non-selective and non-differential medium widely used for antimicrobial testing (MH; Liofilchem, Téramo, Italy), and incubated at 28 • C in a shaking incubator set for 220 rpm (Orbital Shaker, Model 3500 L, VWR ® , Radnor, PA, USA). To obtain synchronous cultures, the strains were subcultured three times when at the exponential phase. Then, the optical density at 600 nm (OD 600 ) of the bacterial suspensions was adjusted to 0.1.
To analyse the hypersensitive response in tobacco leaves, a pure colony of each phytopathogen was cultured on liquid MH medium and incubated overnight, at 28 • C in a shaking incubator set for 220 rpm.

Determination of the MIC and IC 50 of the Dried Leaf Extract (DLE)
To assess the MIC and the IC 50 of DLE for each phytopathogen, different concentrations of DLE (0, 15, 30, 45, 60, 75, 90, 105, 120, 135, and 250 g L −1 ) were prepared by diluting in liquid MH medium (22 g L −1 ) a stock solution, obtained by dissolving 0.22 g of MH in 10 mL of DLE (250 g L −1 ). In sterile 96-well microplates, 10 µL of the synchronized bacterial suspensions (three different suspensions for each pathogen) with an OD 600 adjusted to 0.1 were added to 140 µL of MH medium, and each DLE concentration. Streptomycin (50 µg mL −1 ) served as an antimicrobial control in this experiment. Microplates were incubated in Multiskan™ GO (Thermo Fisher Scientific, Waltham, MA, USA) with constant shaking for 48 h at 28 • C and hourly readings of the OD 600 .

Assessment of the Cell Viability upon Exposure to DLE
The viability of the bacterial cells incubated for 48 h with different concentrations of DLE and streptomycin was evaluated using the resazurin method, essentially as described by Lee and Jain [40]. Briefly, when viable cells come into contact with resazurin (bluish with absorbance at 570 nm), they metabolize it and produce a pink product, the resorufin (pink with absorbance at 600 nm). By quantifying the absorbance at 570 (Abs 570nm ) and 600 nm (Abs 600nm ) at the beginning end of the incubation period (t 0 and t 4 , respectively), the percentage of viable bacterial cells can be estimated. So, at the end of the 48 h incubation of each microplate, the content of each well was centrifuged for 5 min at 5800× g, to eliminate the interference imposed by DLE colour in absorbance readings. After carefully discarding the supernatant, the pellet was resuspended in sterile phosphate buffer saline (PBS; 8 g L −1 NaCl; 0.2 g L −1 KCl; 2.9 g L −1 Na 2 HPO 4 ·12H 2 O; 0.2 g L −1 KH 2 PO 4 ; pH 7.0) for the same final volume (150 µL). The suspensions were distributed in new microplates, to which 10 µL of 1 mM resazurin solution (resazurin sodium salt; Sigma-Aldrich, St. Louis, MO, USA) prepared in PBS buffer were added. As control situations, wells containing 160 µL of sterile PBS and 150 µL of PBS to which 10 µL of the resazurin solution were added were both considered. The microplates were incubated for 4 h at 28 • C with constant agitation in the microplate reader Multiskan™ GO and the Abs 570nm and Abs 600nm were read at t 0 and t 4 . The percentage of viable cells was calculated according to the following formula [40]: Percentage of viable cells ε resazurin_600nm ×Abs 570nm t4 − ε resazurin_570nm ×Abs 600nm t4 ε resorufin_600nm ×Abs 600nm t0 − ε resorufin_570nm ×Abs 570nm t0 where ε resazurin_600nm and ε resazurin_570nm is the extinction molar coefficient of resazurin at absorbances of 600 and 570 nm ; ε resorufin_600nm and ε resorufin_570nm is the extinction molar coefficient of resorufin at absorbances of 600 and 570 nm; Abs 570nm_t0 and Abs 570nm_t4 represents the absorbance at 570 nm at the beginning and at the end of the incubation period, respectively; Abs 600nm_t0 and Abs 600nm_t4 represents the absorbance at 600 nm at the beginning and at the end of the incubation period, respectively.

Analysis of the HR in Tobacco Leaves
Although tomato plants are the primary hosts of the studied phytopathogen species, tobacco plants were used as a model species to assess the effect of DLE on pathogens' virulence. So, after sowing tobacco seeds (Nicotiana tabacum cv. havana) in peat substrate (Siro, Mira, Portugal), seedlings were transferred to plastic pots containing 600 mL of this substrate. Before infiltrating the different treatments in their leaves, plants grew for a month in a growth chamber at 23 • C under a photoperiod of 16 h/8 h light/dark, 50% relative humidity, and photosynthetically active radiation (PAR) of 120 mmol m −2 s −1 , where the hypersensitive response assay was carried out.
The HR of tobacco leaves exposed to each phytopathogen treated with the corresponding MIC, shown in Table 1, and a concentration that presented antimicrobial activity against all tested bacterial species (120 g L −1 DLE) were analysed following the protocol of Mariz-Ponte, Regalado, Gimranov, Tassi, Moura, Gomes, Tavares, Santos, and Teixeira [38]. The incubation period of bacterial cells in different situations was optimized in the preliminary assays. Briefly, before infiltration on tobacco leaves, bacterial suspensions were incubated with the selected situations for 1, 2, 4, 6, 8, and 16 h, using Pst as a model (data not shown). Results revealed that all incubation periods produced similar results, and for that reason, we selected the minimum incubation period (1 h) to perform the final assay (data not shown).
A pure colony of each phytopathogen was cultured on liquid MH medium and incubated overnight at 28 • C in a shaking incubator set for 220 rpm. Afterwards, the bacterial suspensions were centrifuged at 2500 rpm (Thermo Scientific centrifuge bucket 75003655, Mega Star 1.6 R, VWR ® , Radnor, PA, USA) for 5 min at room temperature. After removing the supernatant, the pellet was resuspended in PBS until the OD 600 reached 0.2. Then, each bacterial suspension was added in a 1:1 proportion to PBS, DLE at twice the concentration of the MIC of each phytopathogen (30 g L −1 for Xeu, 60 g L −1 for Pst, and 90 g L −1 for Cmm), and 240 g L −1 DLE. These concentrations of DLE were prepared by diluting DLE in PBS. Sterile PBS was used as a negative control. The suspensions were incubated at room temperature in a shaking incubator set to 115 rpm (Orbi-Shaker, Benchmark, Sayreville, NJ, USA) for 1 h. To eliminate the possible interference of DLE in the HR, suspensions were centrifuged at 2500 rpm (Thermo Scientific centrifuge bucket 75003655, Mega Star 1.6 R, VWR ® , Radnor, PA, USA) for 5 min at room temperature, and the pellet was resuspended in PBS buffer for the same final volume. Finally, 1 mL of the following situations was infiltrated on three different leaves of tobacco plants containing two pairs of fully expanded leaves: The HR was photographically recorded 24 h and 48 h post infiltration. This experiment was performed three times for each phytopathogen.

Statistical Analysis
The results were expressed as mean ± standard deviation (SD) and all experimental situations comprised at least three experimental replicates (n ≥ 3). The homogeneity and normality of the data were verified using the Brown-Forsythe and Shapiro-Wilk tests, respectively. Whenever needed, data were transformed to meet the analysis of variance (ANOVA) assumptions. To determine the MIC for each phytopathogen, a one-way ANOVA, followed by the Tukey post-hoc test, was applied to the values corresponding to the end of the exponential growth phase (28 h for Pst, 34 h for Xeu, and 47 h for Cmm). The MIC corresponded to the lowest concentration of DLE that was capable of significantly inhibiting bacterial growth (p ≤ 0.05). In turn, the IC 50 for each phytopathogen, i.e., the concentration of DLE that caused a decline of 50% of the bacterial population, was calculated by linear regression, using the values of growth corresponding to the end of the exponential growth phase. To assess the effect of different concentrations of DLE on the percentage of viable cells for each pathogen species, a one-way ANOVA followed by the Tukey post-hoc test was used, considering statistically significant differences at p ≤ 0.05. Statistical analyses were performed using GraphPad Prism ® 7.0 software (GraphPad Software, San Diego, CA, USA).

Conclusions
This study characterized for the first time the antibacterial activity of an aqueous extract of E. globulus leaves against phytopathogenic species, namely, the ones affecting tomato production-Pst, Xeu, and Cmm. Dried eucalyptus leaf extracts presented bacteriostatic activity, severely inhibiting the growth and the cellular viability of the type strains of these pathogens, which showed different susceptibilities to the extract-Cmm was the most tolerant species, followed by Pst and Xeu, which was the most susceptible species. Additionally, the treatment of these phytopathogen strains with a high concentration of DLE inhibited the hypersensitive response on N. tabacum leaves. For these reasons, DLE can have a great potential to be used in the prophylactic treatment of tomato-associated diseases, in the disinfection of pruning tools, or even to complement other effective but expensive or environmentally toxic approaches, allowing the reduction of their application.