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versión impresa ISSN 0100-204X
Pesq. agropec. bras. vol.47 no.3 Brasília mar. 2012
Antibacterial activity of essential oils on Xanthomonas vesicatoria and control of bacterial spot in tomato
Atividade antibacteriana de óleos essenciais sobre Xanthomonas vesicatoria e controle da mancha-bacteriana do tomateiro
Gilvaine Ciavareli LucasI; Eduardo AlvesI; Ricardo Borges PereiraII; Fabiano José PerinaI; Ricardo Magela de SouzaI
IUniversidade Federal de Lavras, Departamento de Fitopatologia, Caixa Postal 3037, CEP 37200-000 Lavras, MG, Brazil. E-mail: firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com
IIEmbrapa Hortaliças, Caixa Postal 218, CEP 70359-970 Gama, DF, Brazil. E-mail: firstname.lastname@example.org
The objective of this work was to evaluate the effects of plant essential oils (EOs) on the growth of Xanthomonas vesicatoria, on bacterial morphology and ultrastructure, and on the severity of tomato bacterial spot. EOs from citronella, clove, cinnamon, lemongrass, eucalyptus, thyme, and tea tree were evaluated in vitro at concentrations of 0.1, 1.0, 10, and 100% in 1.0% powdered milk. The effect of EOs, at 0.1%, on the severity of tomato bacterial spot was evaluated in tomato seedlings under greenhouse conditions. The effects of citronella, lemongrass, clove, and tea tree EOs, at 0.1%, on X. vesicatoria cells were evaluated by transmission electron microscopy. All EOs showed direct toxic effect on the bacteria at a 10%-concentration in vitro. Under greenhouse conditions, the EOs of clove, citronella, tea tree, and lemongrass reduced disease severity. EOs of clove and tea tree, and streptomycin sulfate promoted loss of electron-dense material and alterations in the cytoplasm, whereas EO of tea tree promoted cytoplasm vacuolation, and those of citronella, lemongrass, clove, and tea tree caused damage to the bacterial cell wall. The EOs at a concentration of 0.1% reduce the severity of the disease.
Index terms: alternative control of plant disease, cell ultrastructure, pathogenic bacteria.
O objetivo deste trabalho foi avaliar o efeito de óleos essenciais (OEs) no crescimento de Xanthomonas vesicatoria, na morfologia e na ultraestrutura bacteriana, e na severidade da mancha-bacteriana do tomateiro. OEs de citronela, cravo-da-índia, canela, capim-limão, eucalipto, tomilho e árvore-de-chá foram avaliados in vitro nas concentrações de 0,1, 1,0, 10 e 100% em leite em pó a 1,0%. O efeito dos OEs, a 0,1%, na severidade da mancha-bacteriana do tomateiro foram avaliados em plantas de tomateiro em casa de vegetação. Os efeitos dos óleos de citronela, capim-limão, cravo-da-índia e árvore-de-chá, a 0,1%, nas células de X. vesicatoria foram avaliados por meio de microscopia eletrônica de transmissão. Todos os OEs apresentaram efeito tóxico direto sobre as bactérias na concentração de 10% in vitro. Em casa de vegetação, os OEs de cravo-da-índia, citronela, árvore-de-chá e capim-limão reduziram a severidade da doença. Os OEs de cravo-da-índia e árvore-de-chá, e o sulfato de estreptomicina promoveram perda de material eletro-denso e alterações no citoplasma, enquanto o OE de árvore-de-chá promoveu vacuolização do citoplasma, e os de citronela, capim-limão, cravo-da-índia e árvore-de-chá causaram danos à parede celular bacteriana. Os OEs, na concentração de 0,1%, reduzem a severidade da doença.
Termos para indexação: controle alternativo de doenças de plantas, ultraestrutura celular, bactéria fitopatogênica.
Diseases of tomato (Solanum lycopersicum L.) are responsible for significant yield losses. Bacterial spot, caused by a number of species of bacteria of the genus Xanthomonas (Dowson) (Jones et al., 2000), is among the most important of these diseases.
Several studies have shown that it is possible to use essential oils to control plant diseases (Pereira et al., 2011). Medicinal plants contain substances that are able to play an important role in plant-pathogen interaction, by activating plant defense mechanisms (Schwan-Estrada et al., 2003; Lucas et al., 2012). Antifungal substances, similar to fungicides, may also be present in those plants, acting directly on the pathogens (Rosato et al., 2007). Medice et al. (2007) observed that essential oils from eucalyptus [Corymbia citriodora (Hook.) K.D.Hill & L.A.S. Johnson], thyme (Thymus vulgaris L.), neem (Azadirachta indica A. Juss.), and citronella [Cymbopogon nardus (L.) Rendle.] completely inhibited the germination of urediniospores of Asian soybean rust (Phakopsora pachyrhizi Syd. & P.Syd.) and reduced the severity of the disease in greenhouse trials. Ranasinghe et al. (2002) reported the fungitoxic and fungistatic activity of the essential oils of clove [Syzygium aromaticum (L.) Merr. & L.M. Perry] and cinnamon (Cinnamomum zeylanicum Blume) on Colletotrichum musae (Berk. & M.A. Curtis) Arx, Lasiodiplodia theobromae (Pat.) Griff & Maubl., and Fusarium proliferatum (Matsush.) Nirenberg. Lucas et al. (2012) found that clove essential oil reduced the severity of tomato bacterial spot and induced an increase in activities of β-1,3-glucanase, chitinase, and peroxidase.
In an ultra-structural study, Rasooli et al. (2006) showed that the essential oils of Thymus eriocalyx (Ronniger) Jalas and T. x-porlock provoke severe damage to the walls, membranes, and cell organelles of Aspergillus niger spores, when in direct contact, causing morphologic alterations in the hyphae, rupture of the plasma membrane, and mitochondrial destruction.
Researchers have used ATP production in the cell, bacterial mobility, and cationic exchange to evaluate the action of essential oils on bacteria. However, Gustafson et al. (1998) observed, by transmission electron microscopy, that the electron-dense material of Escherichia coli bacteria exposed to the essential oil of tea tree (Melaleuca alternifolia Cheel) was lost, which indicates cell wall loss. In spite of previous research, little is known about the mode of action of these compounds on plant-pathogenic bacteria.
The objective of this work was to evaluate the effect of plant essential oils on the growth of X. vesicatoria, on bacterial morphology and ultrastructure, and on the severity of tomato bacterial spot.
Materials and Methods
The experiments were carried out from January 2008 to December 2010, at the Universidade Federal de Lavras, MG, Brazil. The essential oils of all species used in the experiments were acquired from Brasil Portrait (Sorocaba, SP, Brazil), and the isolate of X. vesicatoria used was 89T, from a culture collection of Embrapa Hortaliças, DF, Brazil.
X. vesicatoria was stored at -80ºC in glycerol-peptone (15% v v-1). The bacterium was streaked into 523 medium (Kado & Heskett, 1970) and grown at 28ºC for 24 hours. To confirm the pathogen virulence, the bacterial pathogen was inoculated on healthy plants before every experimental setup. For the experiments, the bacterium was isolated from the previously infected tomato leaves in 523 medium. The inoculum was prepared by soaking the bacterial colony with distilled water, scraping it, and adjusting the concentration to A600 = 0.30 (5.0x108 CFU mL-1). Inoculation was done by spraying the suspension over tomato plants until runoff.
The direct inhibitory potential of the essential oils on the growth of X. vesicatoria was evaluated by in vitro assay. The essential oils of clove, citronella, tea tree, thyme, eucalyptus, cinnamon, and lemongrass (Cymbopogon citratus Stapf) were assessed at concentrations of 0.1, 1.0, 10, and 100% in 1.0% powdered milk. Powdered milk was used as an emulsifier for the oil-based treatments. The essential oils were added separately to a previously autoclaved powdered milk solution (sterile distilled water + powdered milk) and agitated on a vortex mixer for 10 s. Control treatments with streptomycin sulfate 25 mg mL-1, Recop 2.0 mg mL-1 (a copper fungicide), 1.0% powdered milk, and sterilized water were also evaluated. The experimental design was a completely randomized block, with four replicates and parcels of six Petri dishes. Previously autoclaved filter paper disks (3.0-micron porosity), with 6.0 mm in diameter, were soaked in 20 µL of each evaluated treatment, dried at room temperature, and distributed in Petri dishes with 523 medium containing 100 µL of the X. vesicatoria suspension (5.0x108 CFU mL-1). The presence and the diameter of inhibition halos were determined 48 hours after incubation in a growth chamber at 28ºC, under a 12-hour photoperiod. Data were subjected to analysis of variance, and means were compared by the Scott-Knott test, at 5% probability. The SAS software (SAS Institute, 2001) was used for data analysis.
The efficiency of essential oils in reducing the severity of tomato bacterial spot was evaluated. Tomato seedlings of the cultivar Santa Cruz Kada (Hortec, Bragança Paulista, SP, Brazil), susceptible to X. vesicatoria, were grown under greenhouse conditions in trays (128 wells), at 25±5ºC, with daily irrigation. Fifteen days after sowing, the seedlings were transplanted to 5.0-kg pots containing commercial substrate consisting of expanded vermiculite, organic materials, and macro- and micronutrients. Fertilization was done primarily with (NH4)2SO4, P2O5, and KCl, according to the necessity of the culture, until the end of experiment. The experiment was conducted in a randomized complete block design, with five replicates and three plants per plot. Essential oils of thyme, clove, eucalyptus, cinnamon, citronella, tea tree, and lemongrass, at 0.1% concentration, were used. For all the oil-based treatments, 1.0% powdered milk was used as an emulsifier. Other additional treatments were: the control (plants sprayed with water); a 1.0%-powdered milk control; a resistance induction treatment, with acibenzolar-S-methyl 0.2 mg mL-1; and a copper treatment (Recop 2.0 mg mL-1).
Three treatment periods were evaluated: tomato plants were treated before pathogen inoculation (B), after pathogen inoculation (A), and with weekly applications, during the entire cultivation period, before and after pathogen inoculation (BA). The B treatment and the first application in the BA treatment were carried out 23 days after sowing, whereas the A treatment took place only 37 days after sowing. All plants were inoculated 30 days after sowing. For inoculation, plants previously exposed to a moisture chamber for 24 hours were used. The concentration of the bacterial suspension used was prepared as described above and adjusted in a spectrophotometer to A600 = 0.30 (5.0x108 CFU mL-1). Inoculation was done by foliar spray to the point of runoff. Subsequently, plants were exposed to a new moisture chamber for 24 hours. The evaluations began seven days later. Five evaluations of severity were carried out using the Mello disease assessment key (Lobo et al., 2005), and the efficiency of the treatments was calculated by the formula adapted from Abbott (1925): EF = (Mtr - Mte)/(100 - Mte), in which EF is the percentage of treatment efficiency; Mtr is the percentage of treatment severity; and Mte is the percentage of control severity.
Data were subjected to analysis of variance, and means were compared by the Scott-Knott test, at 5% probability. For data analysis, the software SAS (SAS Institute, 2001) was used.
The effects of essential oils on X. vesicatoria cells were evaluated by transmission electron microscopy. The essential oils of citronella, lemongrass, clove, and tea tree at 0.1% were selected by in vivo assay. Powdered milk at 1.0% was used as an emulsifier for the oil-based treatments, and streptomycin sulfate 25 mg mL-1 was used as a standard treatment.
The essential oils were added separately to a previously autoclaved powdered milk solution (sterile distilled water + powdered milk) and agitated on a vortex mixer for 10 s. The solution was then added to Erlenmeyer flasks (one of each treatment) containing 100 mL of liquid 523 medium (Kado & Heskett, 1970) and X. vesicatoria cells at a concentration of 5x108 CFU mL-1 previously cultivated in liquid 523 medium, for 24 hours, at 28°C, under a 12-hour photoperiod. The Erlenmeyer flasks were maintained in a rotating orbital Table incubator at 100 rpm, at 28°C, under a 12-hour photoperiod, for 24 hours. Then, 2.0-mL aliquots of these solutions were put in microcentrifuge tubes and pre-fixed in a modified Karnovsky solution (glutaraldehyde 2.5%, paraformaldehyde 2% in sodium cacodylate buffer 0.05 mol L-1, CaCl2 0.001 mol L-1 , pH 7.2) for 24 hours. The microcentrifuge tubes were centrifuged for 5 min at 6,000 rpm, and the supernatant were discarded. A total of 0.5 mL of 1.0% agarose gel (50 to 55°C) was added to the microcentrifuge tubes, for the formation of a pellet, on which the bacteria were adhered. Fragments of these pellets with the bacteria were transferred to 0.05 mol L-1 of sodium cacodylate buffer solution, washed three times for 10 min, and post-fixed in 1.0% osmium tetroxide for 1 hour. Later, the fragments were washed twice in distilled water for 15 min, en-bloc stained in 0.5% uranyl acetate solution for 12 hours, at 4°C, and washed again in distilled water. The samples were dehydrated in graded acetone series (once at 25, 50, 75, and 90% and three times at 100%) and infiltrated in an increasing Spurr/acetone gradient of 30% (8 hours), 70% (12 hours) and 100% twice, for 24 hours each. The specimens were mounted in molds, embedded in pure Spurr resin, and were polymerized in an oven at 70°C, for 48 hours.
For ultramicrotomy, the blocks obtained were taken to the trimming apparatus for removal of the excess of resin. Afterwards, thick (0.85 µm) and thin (<100 nm) sections were cut, using an ultramicrotome Ultracut, Reichrt-Jung, (Leica, Wetzlar, Germany) equipped with a diamond knife. The thick sections were collected with a gold ring, put on glass slides, stained with toluidine blue (1.0 g toluidine blue, 1.0 g sodium borate, and 100 mL water), filtered in a 0.22 µm cellulose membrane, and permanently mounted in Permalt medium. The thin sections were picked up on gold slot grids and left to dry on Formvar-coated aluminum racks (Rowley & Moran, 1975). The sections were post-stained with uranyl acetate, followed by lead citrate for 3 min each. Then, the samples were examined using a transmission electron microscope EM 109, (Zeiss, Oberkochen, Germany) operating at 80 Kv and at a 9-mm distance. The images generated were digitally recorded and edited in the Photopaint software of the Corel Draw 13 package (Corel Corporation, Ottawa, Canada).
Results and Discussion
None of the essential oils inhibited the growth of X. vesicatoria in vitro, at the concentration of 0.1% (Table 1). At the concentration of 1.0%, the essential oils of thyme, clove, and cinnamon partially inhibited the growth of the bacterium. The other oils did not have any effect on bacterial growth. However, at the concentrations of 10 and 100% all of the essential oils inhibited bacterial growth. Bacterial growth was observed on sterilized water, Recop, and powdered milk, whereas total bacterial inhibition occurred on streptomycin sulfate. Huang & Laksman (2010) also observed antibacterial activity of clove oil against seven different species of plant pathogenic bacteria: Agrobacterium tumefaciens, Erwinia carotovora pv. carotovora, Pseudomonas syringae pv. syringae, Ralstonia solanacearum, X. campestris pv. pelargonii, Rhodococcus fascians, and Streptomyces spp. Both Gram-positive and Gram-negative bacteria tested were sensitive to clove essential oil (0.1 and 0.5%), with R. solanacearum being the most sensitive one. Martins et al. (2009) reported the inhibitory effects of citronella in concentrations of 2.0, 4.0, 8.0, and 100%, and of lemongrass in concentrations of 1.0, 2.0, 4.0, 8.0, and 100% on the in vitro development of the bacterium R. solanacearum.
In the assay conducted in the greenhouse, no phytotoxicity symptom was observed as a result of applying essential oils. However, there was a significant interaction between the application periods and the products used.
Among the plants sprayed only before inoculation, acibenzolar-S-methyl was the most efficient treatment in controlling the progress of tomato bacterial spot, with 89% control, followed by the oils of tea tree, lemongrass, clove, citronella, and cinnamon (Figure 1 A). The essential oils of thyme and eucalyptus, and the fungicide Recop were statistically equal to the powdered milk control.
Among the plants sprayed before and after inoculation, acibenzolar-S-methyl was also the most efficient treatment in controlling the disease, with 89% efficiency, followed by the essential oils of lemongrass, clove, citronella, fungicide, and tea tree (Figure 1 B). The essential oils of cinnamon, eucalyptus, and thyme showed lower efficiency, being statistically equal to the powdered milk control (13%).
Among the plants sprayed only once after inoculation, the fungicide and the essential oils of eucalyptus, citronella, tea tree, lemongrass, and thyme were the best treatments for disease control (Figure 1 C). Cinnamon oil, acibenzolar-S-methyl, and clove oil did not differ in comparison to the control.
Several works have shown that plant-derived products, such as essential oils, induce resistance in plants (Schwan-Estrada et al., 2003; Lucas et al., 2012). Kessmann et al. (1994) reported that, to be considered resistance inducers, chemical or biological agents should not have direct inhibitory activity on the plant-pathogenic microorganism. However, this concept is currently more flexible, and various compounds that are considered resistance inducers also exert direct action on the pathogens. Active compounds of the oils act directly on the pathogens or induce host resistance through the production of phytoalexins, increased PRP activity, synthesis of structural compounds, and biochemical plant defense (Schwan-Estrada et al., 2003), resulting in disease reduction (Paul & Sharma, 2002). Reduction in the severity of the disease was observed at a concentration of 0.1% of essential oils. This indicates that, besides the induction of resistance, other factors may contribute to a greater effect of the essential oils in vivo than in vitro, such as variation of the optimum temperature of bacterial growth and the presence of microorganisms in the plant surface (Halfeld-Vieira et al., 2004).
The efficiency of the oils used in the present study confirms the results obtained by other authors. Abreu (2006) observed reductions of 26, 62, and 95% in the incidence of tomato black spot in plants treated with the essential oil of cinnamon. In the field, reductions of 12.5 and 32.8% were observed in the incidence of diseases of tomato plant leaflets treated with the essential oil of cinnamon, at the concentrations of 3,000 and 5,000 µL L-1 (0.3 and 0.5%). According to Abreu (2006), increasing the concentration of the essential oil of cinnamon and decreasing the application intervals boosts the efficiency of the oil in controlling the disease. However, in the present study, the essential oil of cinnamon promoted 49% protection when applied once before inoculation; 21% protection when applied once after inoculation; and 27% protection when applied weekly, during the entire cultivation period, before and after inoculation, indicating that decreasing the application intervals did not increase the efficiency of the oil in controlling the disease.
In another study, Medice et al. (2007) observed a reduction in the severity of Asian soybean rust, in cultivars treated with the essential oils of thyme (0.3%), citronella (0.5%), eucalyptus (1.0%), and neem (1.0%), seven days before inoculation. In a field experiment with Asian soybean rust and in a greenhouse experiment with coffee plant rust, respectively, Medice et al. (2007) and Pereira et al. (2012) obtained results similar to the ones observed in the present study. The essential oils of tea tree, eucalyptus, and citronella promoted control of the disease similar to that of the fungicide. Furthermore, Pereira et al. (2012) observed protection of 54.3% when using clove oil (0.1%) against coffee plant rust, which is similar to the result found in the present work.
The essential oils of clove, lemongrass, citronella, and tea tree at 0.1% caused damage to the structure of X. vesicatoria cells (Figure 2). All of the evaluated essential oils caused degradation of the cell wall, which was also observed in the bacterial cells exposed to streptomycin sulfate, the antibiotic normally used as a standard in in vitro experiments with bacteria. Alterations in the cytoplasm density, known as electron-dense material loss, were also observed in bacterial cells exposed to the essential oils and to streptomycin sulfate. This can be attributed to cytoplasmic vacuolation, clearly observed in bacterial cells exposed to the essential oil of tea tree (Figure 2 F).
Although essential oils of clove, lemongrass, citronella, and tea tree at 0.1% did not cause bacterial growth inhibition in vitro, they caused severe damage to the structure of the bacterial cell. As observed in the in vitro assay (Table 1), even the oils at 100% were not able to completely inhibit X. vesicatoria bacterial growth, indicating that some cells remained viable and promoted the multiplication of the bacteria in vitro. According to Hammer et al. (1999), results obtained by different methods may differ, since many factors vary between assays. These factors include differences in microbial growth, exposure of microorganisms to plant oil, oil solubility and components. In the assay using transmission electron microscopy, for example, the contact of the bacteria with the essential oil was direct, due to the liquid medium. For in vitro assay, the diffusion of the essential oils in the lowest concentrations in the solid medium could occur in a heterogeneous form or not occur at all. In this case, the bacteria could not be affected by the essential oil. These results were also observed in other microorganisms (Carson et al., 1995; Piper et al., 2001), indicating the potential use of essential oils in plant pathogen control.
There are few known studies on the antibacterial activity mechanism of the components present in essential oils (Bagamboula et al., 2004; Gill et al., 2006). However, Carson et al. (1995) reported that the essential oil of tea tree can kill a variety of microorganisms (Gram-negative and Gram-positive bacteria, and yeasts), through alterations in the cell membrane structures by disinfectant agents that actively denature the proteins, leading to cytoplasm leakage, lyses, and cell death. Electron-dense material losses and alterations in the cytoplasm density were also observed by Carson et al. (2006) in E. coli cells treated with tea tree essential oil, indicating the loss of cellular constituents and cell wall breakdown. According to Piper et al. (2001), substances present in essential oils, when in contact with microorganisms, affect the integrity of the cell membranes, causing representative cytoplasm extravasations. The loss of electron-dense material was also observed by Gardner & Peel (1991) in bacteria subjected to disinfectant agents, such as chlorhexidine and quaternary ammonium compounds.
Amaral et al. (2005) evaluated the growth and development of fungi in rice, soy, corn, and bean seeds treated with the essential oil of clove and reported that it possibly acted on the cell wall of the fungus, consequently provoking cell extravasations. In previous works, Blaszyk & Holley (1998) demonstrated that active eugenol, one of the main compounds in clove oil, had antimicrobial activity on E. coli and Listeria monocytogenes. Several studies showed that eugenol has an important function in the membrane of microorganisms, including the inhibition of specific processes or cellular enzymes (Walsh et al., 2003).
Ultee et al. (1999) found that the hydrophobic component of carvacrol, another compound present in the essential oil of clove, interacts with the cell membranes of Baccilus cereus, altering the permeability for H+ and K+ cations. This alteration harms several essential cell processes, such as the inhibition of enzymes by the loss of those ions, the loss of turgidity, the alteration in DNA synthesis, and the reduction of metabolic activities.
There are currently no known reports on the effect of the essential oils of citronella and lemongrass on the ultrastructure of bacterial cells. However, it is believed that their mode of action is similar to that observed in electron micrographs of bacteria treated with the essential oils of tea tree, clove, and glycerol, as shown in this study.
Understanding the action mechanism of these essential oils and their effects on the morphology and physiology of the plant pathogenic bacterium will allow the rational use and the development of alternative methods of plant pathogen control.
1. Concentrations above 10% of the essential oils of cinnamon, clove, citronella, tea tree, lemongrass, thyme, and eucalyptus are necessary for in vitro growth inhibition of Xanthomonas vesicatoria; however all essential oils tested, at 0.1% concentration, are able to reduce the severity of tomato bacterial spot, indicating the existence of other factors influencing the action of essential oils in vivo.
2. Citronella, lemongrass, clove and tea tree essential oils cause loss of integrity of the bacterial cell wall in vitro, which results in various morphological and physiological changes leading to cell death.
To Embrapa Hortaliças and Dr. Alice Quesado-Duval, for making available the bacterial isolate; to Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, for scholarship granted; to Fundação de Amparo à Pesquisa do Estado de Minas Gerais, for financial support; and to the Laboratory of Electron Microscopy and Ultrastructural Analysis of Universidade Federal de Lavras, for support.
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Received on October 17, 2011
Accepted on February 17, 2012