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Brazilian Journal of Microbiology

versão impressa ISSN 1517-8382

Braz. J. Microbiol. vol.42 no.2 São Paulo abr./jun. 2011

http://dx.doi.org/10.1590/S1517-83822011000200023 

ENVIRONMENTAL MICROBIOLOGY

 

Quick adaptation of Ralstonia Solanacearum to copper stress to recover culturability and growth in water and soil

 

 

Sergio Daniel Moreira AscarrunzI, *; Tomohide NatsuakiII; Hitoshi HonjoII; Ryo FukuiII

IUnited Graduate School of Agricultural Science, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu, Tokyo 183-8509, Japan
IIDepartment of Bioproductive Science, Faculty of Agriculture, Utsunomiya University, 350 Mine, Utsunomiya, Tochigi 321-8505, Japan

 

 


ABSTRACT

Cells of Ralstonia solanacearum were exposed to Cu in distilled water, and the resulting Cu-stressed non-culturable cells were inoculated to natural (non-pasteurized) and pasteurized soils in order to examine their culturability and recovery. Exposing the cells to 20 µM CuSO4 produced transitory non-culturable cells, which exhibited a remarkable recovery in culturability after incubation in the solution for 36 h, reaching a density near the initial level by 108 h. To determine whether such non-culturable cells actually "resuscitated" or multiplied after adapting to Cu toxicity, growth curves were constructed in order to contrast the rates of increase in culturable cell numbers between Cu-stressed or non-stressed inocula. Additionally, fresh non-stressed cells were exposed to CuSO4 in the presence of nalidixic acid by adding the antibiotic at different times after the onset of Cu stress to verify any cell multiplication during the population increase. The results revealed that the non-culturable cells surviving Cu toxicity adapted very quickly to Cu and began multiplying within 12 h, because only the Cu-stressed cells that were increasing in the exponential growth phase, but not those in the stationary phase, were killed by the antibiotic. Such cells exhibited an apparent tolerance to this metal when inoculated to a freshly prepared solution of CuSO4, and also detoxified the ion in the solution in which they grew. The presence of nutrients greatly counteracted the effect of Cu in water microcosms, since culturable cells were detected and increased in number even when exposed to 40 µM CuSO4. In contrast, when inoculated to non-pasteurized soil, Cu-stressed cells showed no such recoveries. However, when the soil was pasteurized before inoculation or added with nutrients, culturable cells were recovered and increased in number. This indicates that increased nutrient availability in soil allows Cu-stressed cells to quickly overcome the stress and increase in culturable populations.

Key words: Ralstonia solanacearum, non-culturable cells, adaptation to copper, survival, detection


 

 

INTRODUCTION

The bacterial wilt pathogen, Ralstonia solanacearum (Race 1), is a widely distributed soil inhabiting bacterium and affects a wide variety of crops, representing a serious threat to crop production in the areas where the disease has been reported as well as in the areas free of the pathogen (17). Coupled with its wide host range, it is very difficult to eliminate it from soil once established due to its great ability to survive in soil.

For detection of this pathogen, the most recent approaches utilize PCR-based detection methods due to their specificity, and relatively quick results. Various genus and species, or even biovar-specific primers, have been designed and employed in many studies involving detection and identification (2, 4, 9, 11, 16, 22, 23, 27, 28, 35, 37). However, such an advanced technology is not always available for researchers in developing countries. Furthermore, PCR theoretically cannot distinguish virulent populations of the pathogen from less virulent or non-pathogenic populations, which include the severely stressed or inviable cells that are not capable of infecting host plants any longer (25). Thus, in these cases, a semi selective agar medium specifically developed for detection may still be useful providing circumstantial evidence for the presence of the pathogen due to its lower cost and availability for being used on site. As a matter of fact, such a medium as SMSA has been and still is recommended in Europe (33) and in South America (18). Ideally, both types of methods should be used simultaneously to achieve the best reliable detections.

Nonetheless, detection methods based on use of agar media also have disadvantages. Since these methods depend on culturability, the pathogen can not be detected if it does not grow on the medium for some reason. It is known that Cu is widely used to control not only fungal but also bacterial plant diseases (1), and it has been reported that the presence of Cu can induce non-culturable cells of R. solanacearum (20). In addition, it has been suggested that Viable-But-Non-Culturable (VBNC) cells of R. solanacearum may be involved in infection of tomato and potato (20, 41).

Given that the VBNC state of R. solanacearum can greatly complicate its detection by various means, a study of the physiological responses of the pathogen to stresses that induce this state is justified in order to precisely understand how and when non-culturable cells are induced under different environmental conditions. Such knowledge would be particularly valuable in predicting and anticipating the presence of non-culturable cells in soil or plant samples as well as understanding their ecology and importance for plant health (40). 0The objectives of this study were to examine the effects of Cu on activity and culturability of R. solanacearum, and to examine survival and recovery of non-culturable cells in distilled water as well as natural and pasteurized soil.

 

MATERIALS AND METHODS

Strain and inoculum preparation

The strain of R. solanacearum used in this study was the rifampicin-resistant spontaneous mutant strain 22R6, derived from strain MAFF301522 (race 1, biovar 3) obtained from the Gene Bank of the Japanese Ministry of Agriculture, Forestry and Fisheries, initially isolated from tomato. Before use, strain 22R6 was streaked on plates of BGT medium (36) supplemented with 50 µg ml-1 of rifampicin (Sigma Chemical Co., St. Louis, MO, USA) and incubated for 48 h at 28°C to obtain single colonies. The colonies were transferred onto plates of BGT medium without TZC (2,3,5-triphenyl tetrazolium chloride, Sigma Chemical Co., St. Louis, MO, USA) (BGA medium) and incubated for 48 h at 28 °C. After incubation, cells were suspended in sterile distilled water to prepare inocula with desired cell concentrations according to their turbidity at 590 nm measured with a Biolog turbidimeter (Biolog, Inc, Hayward, CA, USA).

Cu treatment for induction of non-culturable cells

Two and a half milliliters of the cell suspension (OD590 = 0.5; approx. 8.0 log CFU ml-1) dispensed into triplicate tubes were mixed with an equal volume of a filter sterilized CuSO4 solution to obtain the desired final concentration of CuSO4 (20 and 40 µM) in the mixture. These concentrations were chosen after a series of preliminary tests on the responses of 22R6 to Cu stress (data not shown), which showed that recovery in culturable cell numbers was observed typically at 20 µM CuSO4. Sterile distilled water was mixed with the cell suspension for the control without CuSO4. The tubes were incubated without shaking at 28°C.

Examination of non-culturable cells

Cell density of strain 22R6 was enumerated in three different parameters every 12 h: (a) the total cell counts, (b) the number of culturable cells, and (c) percentage actively respiring cells. The total cell counts represent the numbers of all intact cells regardless of their viability and culturability. The number of culturable cells denotes colony forming units (CFU) enumerated on an agar medium. Actively respiring cells represent those having a functional electron transport system capable of oxidizing NADH or NADPH. (a) Enumeration of total cell counts: A Bacterial Counting Chamber (Sunlead Glass Co., Saitama, Japan) was used to enumerate the total cell counts, by optimizing the manufacturer's instructions. Briefly, a few drops (approx. 25 µl) of a sample cell suspension were pipetted onto the chamber, which then was mounted and observed under a light microscope at a magnification of 600X. Cells in 40 squares of 50 µm × 50 µm were counted, and the cell count was expressed as the logarithm of cell numbers per milliliter. (b) Enumeration of culturable cells: The number of culturable cells was determined by dilution plating on selective BGT medium supplemented with 50 mg ml-1 of rifampicin, and incubating the plates at 28°C. Colonies of 22R6 developing on this selective medium, verified by their colony morphology to be typical of R. solanacearum, were enumerated after 2 - 3 days, and the number of culturable cells was expressed as the logarithm of CFU per milliliter. The detection limit was 1.0 log CFU ml-1, and the value of 1 log CFU ml ml-1 was used for samples below the limit of detection. (c) Determination of percentage of actively respiring cells: Reduction of an artificial electron acceptor, 2 - (p - iodophenyl) - 3 - (p - nitrophenyl) - 5 - phenyl tetrazolium chloride (INT, Sigma Chemical Co., St. Louis, MO, USA), used by Fukui et al. (19) to measure metabolic activity of pseudomonads in sugar beet spermosphere, was employed with some modifications. The bacterial suspension to be assayed (100 µl) was mixed with an equal volume of filtered-sterilized INT solution (0.5 mg ml-1 in 50 mM Tris buffer at pH 7.5 ), and incubated at room temperature on a rotary shaker at 50 r.p.m. in the dark for 1 h. After incubation, 50 µl of 18% formaldehyde were added to the suspension to stop the reaction, and the mixture was stored overnight at 4°C. Droplets of this suspension were placed on a water agar (WA) plate and then air-dried. These sections were then cut out and mounted on a glass slide with a cover slip and observed under the light microscope at a magnification of 1500X. For each replicate tube, more than 400 cells were counted and the percentage of INT - positive cells (i.e. cells with a visible INT formazan crystal inclusion) was determined (with three or four replicates), yielding a total of more than 1200 - 1600 cells counted per sample. Since the data for total cell numbers enumerated visually were available in pairs with the corresponding data for percentage INT - positive cells, the numbers of actively respiring cells were extrapolated and expressed as the logarithm of cells per milliliter.

The effect of different concentrations of CuSO4 (5, 10, 20 and 40 µM) on culturability of strain 22R6 was evaluated following the protocol described previously. A control treatment without CuSO4 was also included in this trial. This range of concentrations was used because it reflects successive 2-fold dilutions of the concentration that induced total loss of culturability (40 µM) and the concentration that induced the recovery observed initially (20 µM). For this test, only culturability was determined every 12 h by dilution plating during incubation at 28°C.

Survival of Cu-stressed cells in soil microcosms as compared to survival in water

Upland loam soil (Haplic Andosols) without any histories of previous cropping for years was collected from a field in the University Farm of Utsunomiya University (Mooka, Tochigi).

Some soil properties were as follows: pH (H2O) = 4.50, EC = 0.194 dS m-1, CEC = 36.75 cmolc Kg-1 dry soil, total C = 112.62 g Kg-1 dry soil, total N = 6.50 g Kg-1 dry soil, C/N = 17.33 (Hirai, H., personal communication). The original Cu content of the soil was the following: Total Cu = 52.65 mg Kg-1 dry soil, soluble Cu(0.1M HCl) = 0.17 mg Kg-1 dry soil (26).

Composite soil samples were collected from approx. 10 random locations at a given site in the field to a depth of 10 - 15 cm, and transported to the campus. After lumps of soil were pulverized by crushing them with a clean shovel, the soil was passed through a 2.0-mm sieve to homogenize and stored in 50-L plastic containers with plastic lids that allowed aeration, in a cool, shady place to maintain soil moisture.

The inocula used were the cells of 22R6 taken freshly from BGA medium and those exposed to 20 or 40 µM of Cu, by mixing the cell suspension prepared at approx. 8.0 log CFU ml-1 4 h prior to inoculation with an equal volume of CuSO4 solution at 0, 40 or 80 µM. The inoculum cell suspensions were added to the soil microcosms directly to wet up the soil. Immediately prior to inoculation, the inocula were enriched with peptone and glucose to obtain a concentration of 0.2% for each nutrient in soil water. The inocula without addition of the nutrients were used as the controls.

Soil microcosms were prepared as follows: Samples of 100 g of soil (with its water content pre-determined) were placed into 93-mm-diameter plastic cups (approx. 300-ml capacity). Then, 5 ml of each inoculum suspension were poured over the soil, and the cup was gently tapped to level the soil surface. If necessary, additional distilled water was added to the suspension to achieve the soil water content (37%) equivalent to -10 KPa in the soil microcosms. Triplicate soil microcosms were prepared for each treatment. To maintain soil moisture and avoid anaerobic conditions during incubation, the cups were covered with screw-capped lids having several holes that were covered with oxygen-permeable (260 ml m-2 h-1 at 1 atm, 30°C) parafilm (Novix-II, Asahi Technoglass, Tokyo, Japan). The microcosms then were incubated at 28°C, and the numbers of CFU in the soil were determined after 0, 3, 7 and 14 days of incubation by the method described below.

For the enumeration of culturable cells in soil, five grams of wet soil were sampled from the soil microcosm and suspended in 95 ml of distilled water. The soil suspension was mixed well by shaking on a rotary shaker for 30 min. at 75 r.p.m. to homogenize soil particles thoroughly, and dilution-plated on BGT medium supplemented with 50 µg ml-1 of rifampicin and 100 µg ml-1 of cycloheximide (Sigma Chemical Co., St. Louis, MO, USA). After 48 hours of incubation at 28 °C, typical R. solanacearum colonies were counted, and the numbers of culturable cells were expressed in log CFU per gram of dry soil. The detection limit in this assay was 2.5 log CFU g-1 dry soil, and the value of 2 log CFU g-1 dry soil was used for the data below the detection limit.

A comparative test was also employed simultaneously in distilled water by using the same inocula inoculated into the soil microcosms. To 5 ml of each Cu-treated inoculum cell suspension dispensed in triplicates in the test tubes, 1 ml of 1/10-strength BG broth was added as the nutrient source. For the controls, 1 ml of distilled water was added. The tubes then were capped and incubated at 28°C. The number of CFU was determined by dilution plating on BGT medium supplied with rifampicin after 0, 1, 2, 3, 5 and 7 days of incubation.

A separate experiment was also made with pasteurized soil microcosms. Twenty four hours before use, soil was heated in a water bath at 55°C - 65°C or at 75°C - 85°C for 30 min. to be pasteurized. These temperatures were chosen according to the differential sensitivity to heat manifested by fungi and bacteria. It has been reported that soil fungal populations decrease at lower temperatures than bacterial populations (8, 15). Accordingly, the first soil pasteurization temperature was mainly directed to reduce fungal populations and the second to reduce bacterial populations. The triplicate microcosms were prepared with these pasteurized soils as well as non-pasteurized natural soil using only Cu-stressed inocula exposed to 20 or 40 µM of Cu. The test was done as described above.

Statistical analysis

Data of survival experiments using natural and pasteurized soils were analyzed by ANOVA with a factorial completely randomized design. Cu concentration, presence or absence of nutrients and, when applicable, pasteurization of soil were considered as the main effect factors and sampling day was considered a repeated measures factor. When significant differences were detected by the ANOVA, means were compared with the protected LSD test.

 

RESULTS

Cu treatment and culturability of Cu-stressed cells

When the cells of 22R6 were exposed to 20 µM CuSO4, no CFU was detected by either 12 h or 24 h. After 36 h, however, 1.97 log CFU ml-1 was detected and thereafter CFU increased progressively over time, reaching nearly the initial CFU by 108 h (Fig. 1A). The percentage of INT-positive cells also dropped sharply but only to approx. 30% of the initial cell numbers by 12 h, and remained at about a half of the corresponding total cell number (Fig. 1B). Throughout the incubation, the total cell number remained nearly constant. Therefore, after 108 h of incubation, the number of CFU was only 0.6 log-unit lower than the log number of INT-positive cells (Fig. 1B). In contrast, exposure to 40 µM CuSO4 clearly showed a long-lasting toxic effect of Cu on strain 22R6. By 12 hours, no CFU was detected but about 25% of the cells remained INT-positive cells (Fig. 1C). The total cell number remained above log 8.0 cells ml-1 throughout the incubation.

Effect of different concentrations of Cu on culturability and recovery of Cu-stressed cells

The effect of Cu on culturability was dependent on Cu concentration (Fig. 2). The decline in culturable cell numbers 12 h after inoculation was observed in all treatments but it was less pronounced at 5 and 10 µM CuSO4. As before, the subsequent recovery of culturable cell numbers was not observed for the inoculum exposed to 40 µM CuSO4. In none of the treatments where recovery was observed did the final culturable cell number exceed the initial population size; both 5 and 10 µM-stressed cells approached approx. log 8.0 CFU ml-1 while 20 µM-stressed cells approached 7.0 CFU ml-1.

 

 

Characterization of recovered culturable cells following Cu stress

Resistance to Cu of culturable recovered Cu-stressed cells: In order to examine if Cu-adapted cells survive the initial stress of Cu treatment and multiply in the 20 µM CuSO4 solution, the cells recovered from this solution and fresh cells taken from 48 h-old BGA plates were inoculated in triplicates to newly prepared solutions of CuSO4 by adjusting the concentrations of CuSO4 to 10 µM and 20 µM. The culturability of the cells was monitored by dilution-plate counting at various times. When actively growing cells taken from BGA medium and those cells that had been exposed to 20 µM CuSO4 over 108 h were transferred to a freshly made solution of 20 µM CuSO4 and incubated at 28°C, most of the fresh unstressed cells became undetectable by dilution plating by 12 h (Fig. 3). In contrast, previously exposed cells did not show any significant drop during the entire period of incubation.

 

 

Increase in culturable cell numbers in distilled water and under Cu stress: In order to construct growth curves for culturable population in water, an initial cell suspension of approx. log 4.0 CFU ml-1 and four serial 4-fold dilutions of the suspension were prepared in distilled water. The suspensions were incubated at 28°C and culturability was determined periodically. For the curves in 20 µM CuSO4, equal volumes of 40 µM CuSO4 and fresh inocula were mixed in order to obtain cell suspensions of different concentrations and culturable cells were counted every 12 h by dilution plating. The curves showing the dynamics of culturable populations of strain 22R6 in distilled water and in 20 µM CuSO4 with time are shown in Fig. 4A and 4B, respectively. Additionally, the initial numbers of visually verifiable cells under the light microscope were determined in order to compare them with the maximum CFU numbers attained by the increase of culturable cells (Fig. 4). In distilled water, and despite a different initial cell density in each water microcosm, the culturable cell numbers in the five microcosms reached a cell density near log 7.0 log CFU ml-1 after 48 h of incubation, and these culturable cell densities did not decrease until the end of incubation. These final CFU numbers were well above the theoretical maximum of initial total cell number estimated by visually counting the cells under the microscope (<log 4.0 cells ml-1) (Fig. 4A). The doubling time in culturable populations was calculated by the equation: log 2 (t2 - t1)/(log N2 - log N1), where t1 and t2 are the earliest and latest time points, respectively, during log growth phase; and N1 and N2 are the corresponding numbers of CFU per milliliter. The doubling times of these growing culturable cells in distilled water were calculated to be between 1.86 h and 2.32 h. For the Cu-stressed inocula, only the highest initial concentration inoculum (approx. log 8.0 CFU ml-1) retained culturability and showed the typical initial decline and subsequent increase of culturable cells after 24 h of incubation (Fig. 4B). In this case, the final CFU number (log 7.5 CFU ml-1) was lower than the initial total cell number counted under the microscope (log 8.1 cells ml-1). The "doubling time" calculated for these increasing culturable cells in the Cu solution was 2.83 h. The inocula at lower initial concentrations (< log 7.7 CFU ml-1) did not show any recovery or adaptation following Cu stress and culturable cells were not detectable even at 12 h after stress onset (Fig. 4B).

Biological availability of Cu in the solution after recovery of Cu-stressed cells: Biological availability or bioavailability of Cu in the context of this study is defined as the amount of Cu effectively acting upon strain 22R6 in contrast to the total amount of Cu present in the solution (molar concentration), since the biologically unavailable portion may be chelated or otherwise bound to extracellular molecules.

With the objective of clarifying the biological availability of Cu in the 20 µM CuSO4 solution following the observed recovery, fresh cells (approx. log 8.0 CFU ml-1) were inoculated to three triplicate sets of tubes containing equal volume of solutions of CuSO4 to obtain final concentrations of 0, 20 and 40 µM of CuSO4 in each triplicate set. After 1 week of monitoring culturability, the remaining suspensions were filter-sterilized and new fresh cells were inoculated into these remaining solutions. Culturable cells were then monitored by dilution plating. As observed earlier, culturable cell numbers decreased from approx. log 8.0 CFU ml-1 to log 2.6 CFU ml-1 when the fresh cells were first exposed to 20 µM of Cu (Fig. 5A). The subsequent recovery of culturable cell number after 24 h was also observed. At 40 µM CuSO4 the total loss of culturable cells was observed as previously. After 96 h, strain 22R6 cells at 20 µM CuSO4 had a final culturable cell concentration 10-fold lower than that of the control without Cu stress. The control showed a slight increase in culturable cell numbers during the first 24 h and thereof no evident variation throughout the experiment (Fig. 5A).

When fresh cells were then inoculated into filter-sterilized solutions from the initial cell suspensions, the bioavailability of Cu for 22R6 in the 20 µM CuSO4 solutions was apparently much less, and comparable to that of the distilled water control since no decrease in culturability was observed (Fig. 5B). At 40 µM CuSO4, on the other hand, the culturable cell number decreased after 9 h to 2.94 log CFU ml-1 and then increased to the level of approx. log 7.5 CFU ml-1 after 46 h (Fig. 5B). Also in this case, the final number of culturable cells did not exceed the initial number.

Effect of nalidixic acid on the recovery of Cu-stressed cells: Since the nature of the observed recovery of culturability in water was not obvious after the previous experiments, nalidixic acid was used to discriminate "resuscitating" cells from multiplying Cu-adapted cells that might have arisen from the original population. Nalidixic acid inhibits DNA replication by blocking the activity of DNA-gyrase, and the hypothesis tested was as follows: If the increase in culturable cells was due to "resuscitation" from non-culturable cells, nalidixic acid should not stop or influence this population increase in any manner. But if cell division and hence cell multiplication were involved in the increase, nalidixic acid should affect the increase in an observable manner. A similar approach has been previously used in R. solanacearum in order to inhibit multiplication of viable cells (3, 20).

Fresh cell inoculum was prepared as explained previously and inoculated into triplicate tubes with an equal volume of CuSO4 solutions in order to obtain final Cu concentrations of either 20 µM or 40 µM. Nalidixic acid was added to a final concentration of 25 µg ml-1 at either 0, 12, 24 or 36 h after inoculation. The concentration of the antibiotic was determined in preliminary tests as the minimum concentration capable of inhibiting growth of 22R6 cells. Addition of nalidixic acid at different times after inoculation and Cu-stress onset was tested in order to observe the effect of the antibiotic on cells at different stages of the population increase. Triplicate tubes of control treatments without nalidixic acid were also prepared for each Cu concentration.

The effect of nalidixic acid was clearly more dependent on the time of antibiotic addition than on Cu concentration. When added at the same time of inoculation and the stress onset, a remarkable masking of the Cu stress at both concentrations was observed as the reduction of culturable cells was negligible (Fig. 6). Culturable cells stayed at approx. 8.0 CFU ml-1 during the whole duration of the experiment. When nalidixic acid was added into 20 µM CuSO4 (Fig. 6A) at 12 h after inoculation, the increase of culturable cells observed in the control and in previous experiments was completely prevented, resulting in a drop in culturable population below detection levels by 48 h. Addition of nalidixic acid at 24 h also interrupted the increase of culturable cells and resulted in a non-culturable population by 48 h. When the antibiotic was added at 36 h however, its effect was indiscernible. Culturable cells had already recovered and reached a near-maximum number by the time of the antibiotic addition, but only a small reduction in culturable cell numbers to 6.57 CFU ml-1 was observed at 96 h. At 40 µM CuSO4 (Fig. 6B), on the other hand, the addition of nalidixic acid at 12 h did not allow either the decline of culturable cell numbers below detection at 12 h, as it occurred in the control and in previous experiments, or any possible recovery from the stress. The culturable cell number dropped to approx. 3.0 CFU ml-1 at 12 h and steadily decreased until eventually becoming undetectable by the end of the experiment. The antibiotic added at 24 h or 36 h after inoculation did not affect the already undetectable cells stressed by 40 µM CuSO4, which stayed undetected until the end of the experiment.

Survival of Cu-stressed cells in soil microcosms as compared to that in water: The previous experiments were all conducted in distilled water in order to isolate the effect of Cu on culturability of strain 22R6. Thus, the partial physiological characterization of some aspects of the cells with recovered culturability after Cu stress was performed without the interference of their response to nutrients or of other microbes present in the medium. However, it is natural to assume that these two factors could have significant roles in the ecology of these cells in natural environments. In order to test this hypothesis, experiments in which Cu-stressed cells were inoculated into natural soil and distilled water in the presence of nutrients were executed. In addition, the influence of microorganisms present in soil was studied in an experiment in which natural soil and soil pasteurized at two different temperatures were inoculated with Cu-stressed cells in the presence or absence of nutrients.

When the cells exposed to CuSO4 at 20 or 40 µM were inoculated into natural soil, culturable populations remained low (near or less than 3.0 log CFU g dry soil -1) throughout 14 days of incubation (Fig. 7B and 7C). When the inocula were enriched with nutrients, however, culturable populations increased dramatically; culturable populations for the cells treated with 20 µM CuSO4 were not significantly different from those for non-treated cells (Fig. 7A and 7B), and the populations for the cells treated at 40 µM were only less than 1.0-log unit lower than those for the controls (Fig. 7A and 7C).

When the cells exposed to 20 or 40 µM were incubated in distilled water at 28°C, the culturable population again dropped sharply and was not detected after 1 day of incubation (Fig. 8B and 8C). However, as observed in the previous experiments, the cells treated with 20 µM CuSO4 regained culturability thereafter and rapidly increased in number to reach approx. 7.0 log CFU ml -1 by 5 days of incubation (Fig. 8B). Yet, such recovery and increase in culturable population were not observed for the cells treated with 40 µM of CuSO4 (Fig. 8C). On the other hand, when both Cu-treated inocula were enriched with nutrients, high numbers of culturable populations (>7.0 log CFU ml -1) were detected after 3 days even though the populations initially dropped to some extent. When the cells were not treated with Cu, culturable population remained at high levels (>8.5 log CFU ml -1) and nutrient enrichment had virtually no effects on the population (Fig. 8A).

The data presented in Fig. 9 show the survival of cells stressed with 20 µM CuSO4 (Fig. 9A) or with 40 µM CuSO4 (Fig 9B) in natural soil and in the same soil pasteurized at 55°C - 65°C or at 75°C - 85°C. As observed previously, the Cu-stressed cells did not increase notably when inoculated to the non-pasteurized natural soil, but attained high culturable populations (>8.0 log CFU ml-1) when the same inocula were enriched with the nutrients. Soil pasteurization produced a more than 100-fold increase of culturable cells after 3 days in the soil inoculated with non-enriched inocula, regardless of the concentration of Cu in the soil. This effect of soil pasteurization was more pronounced when the soil was treated at 75°C - 85°C than at 55°C - 65°C. The presence of nutrients in pasteurized soils caused the culturable numbers to be 2 - 3 log units higher than the corresponding numbers for non-enriched inocula. This difference increased dramatically when using the natural non-pasteurized soil: the presence of nutrients considerably reduced the difference in culturable cell numbers between the pasteurized and natural soils for both concentrations of Cu.

 

 

DISCUSSION

This study revealed that Cu-stressed cells of R. solanacearum induced by exposure to the borderline cytotoxic concentration of Cu were able to respond quickly to overcome the toxicity of Cu and multiply in the absence of external nutrients. When the cells were incubated in distilled water with 20 µM CuSO4, the Cu-stressed cells once became non-culturable or nearly non-detectable but remained viable. Then, they soon showed a remarkable recovery in culturability in a matter of a day (Fig. 1B). Subsequently, the number of culturable cells increased and nearly reached the number of INT-positive cells.

The effect of Cu on strain 22R6 was apparently transient and dose-dependent (Fig. 2), providing an evidence for quick adaptation of the strain to this heavy metal. This suggests that Cu-stressed cells may recover eventually even at higher Cu concentrations if incubated under different conditions. In fact, the cells exposed to 40 µM of Cu were apparently not recovering in distilled water (Fig. 8C), but quickly did so when enriched with nutrients. In contrast, Grey and Steck (20) were able to produce VBNC cells of R. solanacearum with concentrations of CuSO4 as high as 500 µM, but they did not report any recovery of culturability even at 5 µM. Van Overbeek, cited by Van Elsas et al. (40), reported that a strain of R. solanacearum biovar 2 resisted Cu concentrations up to 25 mM for over 3 weeks. These differences may indicate that the Cu effect is also strain-dependent or such strains differed in nutritional status. It is clear also that the cells that had been exposed to Cu in this study were less sensitive in a freshly prepared Cu solution (Fig. 3), indicating that some mode of adaptation/tolerance was developing quickly. Thus, previous exposure(s) of some strains to Cu may explain the strain-dependent effect of Cu. In fact, such adjustments are not unconceivable in bacteria. Cu is an important trace element but toxic at high concentrations due to an unspecific uptake system for heavy metals mediated by P-type ATPases (31). As a consequence, it requires what is thought to be a chromosomally encoded homeostasis system in bacteria, from which a plasmid-borne resistance mechanism may have evolved (13, 31).

Detoxification or chelation of Cu molecules is one likely mechanism by which R. solanacearum copes with its cytotoxic effect. It has been reported previously that siderophores, metal binding proteins, and even polysaccharides can bind to Cu and reduce its bioavailability (21). It has also been suggested that pseudomonads have the ability to compartmentalize Cu ions in the periplasm and the outer membrane (13). If this is the case, the concentration of biologically active Cu ions in the solution must decrease as the number of culturable cells increases during incubation. Thus, it seems valid to speculate that the recovery of culturability by strain 22R6 is a secondary effect of the reduced bioavailability of Cu in the solution. Once the amount of free Cu ions in the solution is reduced to a certain level by the aforementioned compartmentalization mechanism, some still viable cells can multiply and reflect in the recovery observed. To test this hypothesis, a 2-stage experiment was performed by reinoculating fresh cells to Cu solutions in which inoculated cells had previously recovered their culturability and then been removed (Fig. 5). As a result, Cu was apparently not much available in the filtrate anymore for the second inoculum. In contrast, toxicity of Cu was still evident if no recovery had taken place. In order to confirm that Cu is detoxified by the bacterium, a bio-sensor bacterial strain (30) genetically engineered to specifically react to Cu ions by expressing reporter genes may be an effective tool to measure and monitor the concentration of biologically active Cu in the culture, understood as the concentration capable of affecting bacterial metabolism as opposed to the Cu concentration that might not be all available to affect the cells.

INT by itself does not affect the viability of the cells, and the percentage of INT-positive cells remained constantly low (around 30%) while the number of culturable cells increased progressively (Fig. 1B). This indicates that the metabolic activity, represented by the percentage of respiring cells, did not increase during recovery of culturability, implying that multiplication of the cells was not involved in the event. However, the latter event cannot be ruled out, since the number of culturable cells in the Cu solution was nearly equal to the number of INT-positive cells after 108 h of incubation, and the percentage of INT-positive cells decreased even in the absence of Cu (data not shown). In fact, the lack of correlation between culturability and respiration has been reported earlier, and it has even been indicated that tetrazolium salts could be reduced by quiescent redox systems, questioning their suitability for viability evaluation (7). On the other hand, Yamamoto (44) stated that respiratory activity is a more stringent indicator of viability than, for instance, membrane integrity. In general, respiratory activity may not be the only reliable parameter for evaluating bacterial activity, considering that it also depends sometimes on experimental conditions (45) or the response of the bacteria to the addition of nutrients (29). Besides, any significant changes in respiratory activity could not be detected by measuring percentage INT-positive cells if such changes were occurring in very small portions of the total cell populations.

A typical pattern of cell growth was observed when non-stressed cells were incubated in distilled water despite the total absence of nutrients: the final CFU number was higher than the theoretical initial total cell number, which should not have been surpassed, had only "resuscitation" taken place (Fig. 4A). Culturable cell numbers in Cu solutions did not exceed the theoretical total cell number present initially in the culture (Fig. 4B) but the doubling time of non-treated cells was not substantially different from the doubling time calculated for Cu-treated cells. In the past, this approach was used to prove the presence of non-culturable cells in V. vulnificus and E. amylovora (34, 43) and this phenomenon has also been reported for R. solanacearum (14, 40). It seems apparent that those increasing culturable populations exceeding the initial total cell number are actually multiplying (Fig4A), and rational to assume that those reaching but not eventually surpassing the initial cell density (Fig. 4B) represent the populations that are only recovering culturability, since the increase in culturable cells does not accompany an increase in metabolic activity (i.e. respiration). However, nalidixic acid clearly interrupted the increase of culturable cells after the onset of Cu stress (Fig. 6A). Previous studies using this antibiotic to demonstrate the viability of bacterial cells (20, 29) reported the strong dependence of this antibiotic on nutrient enrichment in order to affect bacterial cells. Additionally, it is known that this antibiotic acts on actively multiplying cells by affecting their DNA replication machinery. In this study, nalidixic acid did not affect culturability of cells when added 0 h or 36 h after the addition of copper, indicating that such cells were not in the mode of multiplication. Thus, the results demonstrate that the apparent increase in culturable cells was a result of multiplication and such cells have enough nutrient reserves to multiply. Nonetheless, in order to have a more conclusive evidence of multiplication, it might be necessary to quantify the number of DNA copies during this "recovery". This may be possible by real time PCR, in which any increase of DNA due to cell multiplication may be quantified by selecting a proper sequence. The fact that cells did not suffer the Cu effect when nalidixic acid was added at the same time as Cu (0 h) can be explained by the ability of nalidixic acid, a quinolone, to chelate Cu and other metals to form complexes, as has been studied extensively (39).

If we accept the possibility of cell multiplication in oligotrophic environments as suggested by the test with nalidixic acid, one likely explanation to this is that such cells undergo cell division in the absence of nutrients by reducing their size. It has been well documented that bacterial cells in the nutrient-depleted environments are smaller than those found in the nutrient-rich environments (10) and they become dwarf cells under stressful conditions (24). The dwarf cells are less than 0.3 µm in size, and such extremely small cells are found abundantly in soil (5). However, these extremely small cells could not be observed either in this study due to the limitation in the methodology employed (i.e. light microscope) or in previous studies (42). Another possibility is that the cells multiplied in distilled water by utilizing what was left in their cellular reserve or extracellular polysaccharide capsule. Nevertheless, an intriguing phenomenon observed was that the populations of culturable cells typically plateaued at approx. 7.0 log CFU ml-1 in all cases (Figs. 1A, 2, 4B, 5A, 8B). No explanation to this is available at this point. It seems that this definite number may have some significant biological relevance or may be determined simply by the size of tubes used in the in vitro tests. In all, the biological functions of culturability and the number and size of the cells in a given bacterial population need to be studied in great detail to fully understand the behavior of R. solanacearum.

Another significant finding in this study is the distinctive differences in the responses of Cu-stressed cells when inoculated to the soil versus water (Fig. 7 and Fig. 8). Non-culturable cells induced by 20 µM CuSO4 regained culturability in the water microcosms as observed in the previous tests, but the same was not observed in soil. Furthermore, the increase in culturability was pronounced at both high and low Cu concentrations when the inocula were enriched with nutrients. These results suggest that the availability of nutrients is the limiting factor for the Cu-stressed cells to recover in soil. It is likely that the increased availability of nutrients enabled the cells to produce more peptides with sulfhydryl group, to which Cu binds to reduce its toxicity (38). It was also demonstrated that various nutrients bind Cu ions to diminish the deleterious effect of Cu (32, 34). It is noteworthy that, although no culturable cells were detected in the solution containing 40 µM CuSO4, some residual culturable populations were detected when those non-culturable cells were inoculated to the soil. This may indicate that the soil actually contained a minute amount of nutrients to be used by the non-culturable 22R6 that otherwise remained non-culturable in the total absence of nutrients in distilled water.

The test in pasteurized soil showed that recovery of culturability was hindered by the presence and activity of other soil microorganisms competing for nutrients (Fig. 8). In fact, even without addition of nutrients, culturable cell numbers of strain 22R6 increased in pasteurized soil but not in non-pasteurized, natural soil. This indicates that deactivation and death of soil microorganisms by pasteurization increased nutrient availability in the soil, triggering non-culturable cells to regain their culturability and start to multiply as they were in distilled water. Soil fungi as well as soil bacteria seemed to prevent the non-culturable cells of 22R6 from regaining their culturability and multiplying, since soil fungi are in general more sensitive to heat than soil bacteria (8, 15) and soil pasteurization at both temperatures had similar effects on the non-culturable cells. This might be an exclusive phenomenon of Cu-stressed cells of R. solanacearum, since soil amendment with organic substances has previously been reported to reduce the pathogen population of fresh, unstressed cells when inoculated into natural soil (6), probably due to the increase of antagonists already present in that soil. This may be an important discrimination to be made when studying this pathogen's ecology, since we have demonstrated that Cu-stressed cells have at least some physiological differences with fresh unstressed cells.

In all, we have showed that survival of Cu-stressed R. solanacearum in water is superior to that in bulk soil. This has implications on the epidemiology of the pathogen and directly affects control methods based on exclusion of inoculum. It is clear that, as long as nutrients are available, R. solanacearum can survive very well in soil even in the presence of Cu. This suggests that the efficacy and reliability of culture-dependent detection can be improved by incubating soils with nutrients prior to the assay, since this would increase the threshold of detection when detection is based on the plus/minus basis. The soil enrichment should also increase the sensitivity of culture-independent methods by increasing the minimum threshold population for detection in various types of soil. In water, on the other hand, the lack of nutrients does not necessarily limit survival and population growth of the pathogen. We feel that the epidemiology of this bacterium in water is affected not only by low temperature (12) but also by toxic metals and compounds, and the latter effects should receive more attention. This is of great importance, for instance, in tropical regions where Cu is frequently used to control various plant diseases while heavy rains may wash contaminated soils in and out of farming fields. Further studies on the survival of non-culturable R. solanacearum in water in conjunction with the effects of toxic metals and other environmental substances should provide valuable information to improve the efficacy and reliability of culture-dependent methods for detecting the pathogen.

 

ACKNOWLEDGEMENTS

This research was possible thanks to the financial support of The Japanese Government Scholarship (Monbukagakusho). We also thank the Japanese Ministry of Agriculture, Forestry and Fisheries (MAFF) for providing the strain used in this study.0We are grateful to Steve E. Lindow for reviewing the manuscript and for his valuable suggestions.

 

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Submitted: August 03, 2010; Returned to authors for corrections: October 14, 2010; Approved: January 13, 2011.

 

 

* Corresponding Author. Mailing address: United Graduate School of Agricultural Science, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu, Tokyo 183-8509, Japan.; Tel: +81-28-649-5421 Fax: +81-28-649-5401.; E-mail: sermoreira@yahoo.com

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