Several Salmonella enterica outbreaks have been traced back to contaminated tomatoes. In this study, the internalization of S. enterica Typhimurium via tomato leaves was investigated as affected by surfactants and bacterial rdar morphotype, which was reported to be important for the environmental persistence and attachment of Salmonella to plants. Surfactants, especially Silwet L-77, promoted ingress and survival of S. enterica Typhimurium in tomato leaves. In each of two experiments, 84 tomato plants were inoculated two to four times before fruiting with GFP-labeled S. enterica Typhimurium strain MAE110 (with rdar morphotype) or MAE119 (without rdar). For each inoculation, single leaflets were dipped in 109 CFU/ml Salmonella suspension with Silwet L-77. Inoculated and adjacent leaflets were tested for Salmonella survival for 3 weeks after each inoculation. The surface and pulp of ripe fruits produced on these plants were also examined for Salmonella. Populations of both Salmonella strains in inoculated leaflets decreased during 2 weeks after inoculation but remained unchanged (at about 104 CFU/g) in week 3. Populations of MAE110 were significantly higher (P<0.05) than those of MAE119 from day 3 after inoculation. In the first year, nine fruits collected from one of the 42 MAE119 inoculated plants were positive for S. enterica Typhimurium. In the second year, Salmonella was detected in adjacent non-inoculated leaves of eight tomato plants (five inoculated with strain MAE110). The pulp of 12 fruits from two plants inoculated with MAE110 was Salmonella positive (about 106 CFU/g). Internalization was confirmed by fluorescence and confocal laser microscopy. For the first time, convincing evidence is presented that S. enterica can move inside tomato plants grown in natural field soil and colonize fruits at high levels without inducing any symptoms, except for a slight reduction in plant growth.
Citation: Gu G, Hu J, Cevallos-Cevallos JM, Richardson SM, Bartz JA, et al. (2011) Internal Colonization of Salmonella enterica Serovar Typhimurium in Tomato Plants. PLoS ONE 6(11): e27340. doi:10.1371/journal.pone.0027340
Editor: Jacques Ravel, Institute for Genome Sciences, University of Maryland School of Medicine, United States of America
Received: June 3, 2011; Accepted: October 14, 2011; Published: November 9, 2011
Copyright: © 2011 Gu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by Institute of Food and Agricultural Sciences, University of Florida. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Fruits and vegetables, in particular leafy greens and fruit that are consumed raw, are increasingly recognized as vehicles for transmission of human enteric pathogens. Despite the increased importance of fresh produce as a source of enteric pathogens for humans, there is currently limited knowledge about contamination points in the supply chain or about the mechanism by which human pathogens colonize and survive on or in fruits and vegetables .
Salmonella enterica is the most frequently encountered pathogen associated with foodborne illness in the United States , . Consumption of contaminated produce has been implicated in many of the salmonellosis outbreaks in recent years . In particular, Salmonella-contaminated tomatoes have led to several multistate and international outbreaks, each involving hundreds of cases , , , , . Contamination of produce may occur in the processing stage but sources of contamination have also been associated with certain production fields , , . However, little is known about the routes of contamination and potential internalization in plants .
During crop production, irrigation water, particularly if applied overhead, could be an important source of contamination of plants with Salmonella , . Foliar applications of fertilizers or pesticides where contaminated water was used to dilute the formulated products could also contaminate plants. Many pesticide formulations include surfactants, which enable the spray suspension to spread more uniformly over waxy plant surfaces. Surfactants differ chemically and in their abilities to reduce the surface tension of water and penetrate into plant surfaces. Surfactants that enhance penetration of aqueous solutions into plant surfaces, like trisiloxanes, are commonly used in herbicide formulations . Silwet L-77, an organo-silicone surfactant based on trisiloxane ethoxylate, is considered a “super spreader” due to its effect on the water/cuticle interface. This surfactant is a component for many agro-chemical products on the market, including herbicides, insecticides, fungicides, plant growth regulators, fertilizers and micronutrients, at a concentration of 0.025% to 0.1% . Some trisiloxane surfactants were shown to enhance the dispersal of foliar bacterial diseases to a greater extent in a simulated citrus nursery than did several other spreader/ stickers . In contrast, Tween 20™ (polyoxyethylene sorbitan monolaurate) is a non-ionic surfactant that is widely used in agricultural applications, but appears to be just a spreader. It does not appear to enhance penetration of plant surfaces by aqueous solutions . The effects of surfactants such as the trisiloxane products on the risk of contamination of crops plants with S. enterica have been insufficiently documented thus far.
S. enterica can colonize seeds , , sprouted seeds , leaves , , ,  and fruit ,  of a variety of plant species. The interaction with plants can depend on the particular serovar . For example, while S. enterica Typhimurium, Enteritidis and Senftenberg adhered efficiently to leafy vegetables, others (Arizona, Heidelberg and Agona) did not .
The surface morphology of different strains of Salmonella appears to affect their survival and multiplication on plants. Pilus curli (also known as fimbriae), encoded by agfB, seemed to play an important role in adhesion of serovars Enteridis and Newport to alfalfa sprouts . Curli and cellulose can also play a role in attachment of serovar Typhimurium to parsley . Besides curli, the O antigen capsule (encoded by yihO) and cellulose synthesis (encoded by bcsA) have been implicated in adhesion of serovar Enteritidis to alfalfa sprouts . Curli, cellulose and capsules are all regulated by agfD which contributes to the formation of bacterial rdar morphotype, which forms distinct, rough and dry colonies . The wild type Salmonella rdar morphotype is not phenotypically stable and is highly dependent on environmental conditions, like lower temperature (<30°C), nutrient limitation or low osmolarity , , . Previous researchers concluded that the rdar morphotype was important for environmental persistence with increased resistance to desiccation and antimicrobial agents , , , , .
In comparison to bacterial attachment to plant surfaces, the internal movement and translocation of Salmonella in plants have not been investigated in detail. Inoculation of tomato plants with Salmonella by dipping whole seedlings in a suspension with a cocktail of strains resulted in surface contamination of fruits on plants irrigated by automated drip tubes , but systemic translocation in the plants was not investigated. Several serovars of Salmonella were able to invade root tissues and spread into shoots , , but again, systemic translocation was not demonstrated.
In this study, we investigated the internalization of S. enterica Typhimurium into tomato plants via leaves, and evaluated the effects of surfactants and the bacterial rdar morphotype on internalization.
Bacterial strains and plant preparation
S. enterica Typhimurium strains MAE110 (PagfD1, rdar: aggregate/multicellular phenotype) and MAE119 (ΔagfD101, saw: smooth colony morphology) were kindly provided by Dr. Ute Romling , . These strains carry kanamycin resistance and green fluorescent protein (GFP) genes on the chromosome and were derived from MAE52 and MAE51, respectively, after transformation with the PAG408 mini-transposon . Different from their wild type strain S. enterica Typhimurium ATCC 14208, MAE110 constantly presents the rdar morphotype, whereas MAE119 has completely lost the rdar morphotype and develops shiny and smooth colonies , , , . Bacterial cultures were stored in Luria-Bertani (LB) broth containing 25% glycerol at −80°C. For each experiment, a loopful of the stored culture was added to shake cultures (150 rpm) of LB broth (50 µg/ml kanamycin), grown for 18 to 20 h at 37°C. The cultures were harvested by centrifugation. The pellets were suspended in sterile distilled water (SDW) to an optical density of 0.46, which approximates 109 CFU/ml.
Tomato seeds (Solanum lycopersicum ‘Florida Lanai’, a small-fruited compact variety, not commercially available) were kindly provided by Dr. Jane Polston at the University of Florida. These seeds were surface disinfected with 1 M HCl for 30 min. Seeds were germinated in potting mix. At 2 weeks post-seeding, seedlings were transplanted to sandy loam soil in 15-cm diameter pots placed on a saucer to collect runoff water. Sandy loam soils were collected from the Plant Science Experiment Station of the University of Florida at Citra, Florida, with typical fertilizer, fungicide, insecticide and herbicide application schedules (conventional soil) and from a certified organic farm where vegetables were grown organically in the past five years (organic soil). The soil organic matter content was 1.33% in the conventional soil and 2.33% in the organic soil and the pH was 6.5 in both soils. In this paper, the results obtained for both soils are lumped. Water was applied to the pots at a 2-day interval and fertilization was applied every 2 weeks as 150 ml half-strength Hoagland solution (pH 6.8). Plants were grown in a biological safety level 2 greenhouse equipped with ridge vents, a cooling air conditioning unit and a gas heater. For the first experiment red and blue LED lights (LGL Technologies, Inc., Barnesville, MD) were used with a 14/10 day/night cycle. For the second experiment, plants were exposed to natural light only. The temperature fluctuated between 23°C and 33°C, with an average temperature of 28°C.
Inoculation of tomato leaves with S. enterica Typhimurium with or without surfactants
The effect of surfactants on penetration and colonization of leaves by Salmonella was examined prior to tests on Salmonella internalization and possible translocation in tomato plants. Tween 20™ and Silwet L-77 (Sigma Chemical Co., St. Louis, MO) were added to suspensions of Salmonella prior to leaflet dip inoculation. Eighteen 8-week-old tomato plants were inoculated with a S. enterica MAE110 (109 CFU/ml) suspension containing 0.025% (v/v) Tween 20 ™, Silwet L-77 or SDW and placed on a greenhouse bench in a completely randomized design. For inoculation, three leaflets on each of two branches per plant were dipped into one of the three Salmonella suspensions for 30 s. At 7 and 14 days post inoculation, inoculated leaflets were immersed in 70% alcohol for 20 s and then 0.6% sodium hypochlorite for 10 s and rinsed 3 times by SDW to eliminate surface populations of bacteria. One 12-mm leaf disc was taken with a sterile cork borer from each leaflet and ground in 1 ml SDW and plated on LB plates (50 µg/ml kanamycin) after preparing a ten-fold dilution series. Samples (100 µl) of appropriate dilutions were spread onto LB agar plates containing 50 µg/ml kanamycin. The Petri plates were incubated at 37°C overnight. Numbers of S. enterica Typhimurium colonies on each Petri plate were determined by counting green fluorescent CFU's using a UV lamp (UVGL-25, Entela Inc., USA). All plates were checked under UV light to exclude the possibility of counting colonies that were not the gfp-marked Salmonella strains. Very few unidentified bacterial colonies were found on the LB agar with kanamycin; these did not show green fluorescence under UV light.
Inoculation of tomato leaves with S. enterica Typhimurium for the internalization experiments
Salmonella internalization experiments were conducted twice in 2 years using a randomized complete block design. In each experiment, 126 tomato plants were evenly divided over seven blocks located on three greenhouse benches. Eighteen plants in each block were randomly inoculated with GFP labeled S. enterica Typhimurium strain MAE110, MAE119 or with SDW as control (six plants per treatment per block). Inoculation was carried out by dipping three leaflets on each of two branches per plant into 109 CFU/ml Salmonella suspension with 0.025% (v/v) Silwet L-77 for 30 s. Control plants were inoculated with the same amount of SDW with 0.025% (v/v) Silwet L-77. Tomato plants were inoculated in weeks 5 and 10 after planting seeds in year 1, and in weeks 5, 8, 9 and 10 in year 2.
Leaf sampling and testing procedure
In year 1, inoculated tomato leaflets were sampled 7 days after inoculation. In year 2, inoculated leaflets and non-inoculated adjacent leaflets were sampled 3 h, 1, 3, 5, 7, 14, 21 days after each inoculation. At each sampling time, two inoculated leaflets and one non-inoculated adjacent leaflet were removed from three randomly selected plants of each treatment in each block. Two 12-mm leaf discs were taken with a sterile cork borer from each inoculated leaflet. One of the two leaf discs was treated to eliminate surface populations of bacteria by dipping the disc in 70% alcohol for 20 s and then in 0.6% sodium hypochlorite for 10 s. Thereafter, leaf discs were rinsed 3 times by SDW. Both of the two discs with or without the surface treatment were ground in 1 ml SDW, the extract was diluted 10-fold in phosphate buffered saline (PBS) and 0.1 ml aliquots of the appropriate dilutions were spread over LB plates (50 µg/ml kanamycin) after preparing a 10-fold dilution series. Adjacent non-inoculated leaves were ground and enriched in LB broth (50 µg/ml kanamycin) overnight at 37°C. The number of Salmonella colonies was counted as described above.
Fluorescence and confocal laser microscopy
In year 2, three inoculated leaflets were sampled 1 day after the second inoculation from each of the eight plants inoculated with Salmonella and eight control plants. Five days later, three non-inoculated adjacent leaves and one adjacent stem from each of the eight plants were also collected for fluorescent microscopic analysis as described previously . In brief, the plant tissues were fixed overnight in 10% Neutral Buffered Formalin (Fisher Scientific Company, Middletown, VA) and then washed in PBS (pH 7.4) and soaked in 20% sucrose solutions (w/v) in PBS overnight at 4°C. Next, the samples were embedded in Tissue-Tek OCT compound (Miles, Elkhart, IN). About 40 tissue sections of 15 µm or 30 µm thickness were cut horizontally or vertically from each sample with a cryostat (Microm HM 500 O; Microm Laborgerate GmbH, Waldorf, Germany) at −20°C. The samples were transferred to slides and mounted in anti-fade mounting medium (Vector Laboratories).
GFP-labeled Salmonella cells in the tissue sections were observed with a fluorescence microscope (Leika DM4000 B; Leika, German) and a confocal laser scanning microscope (Olympus IX81-DSU; Olympus, Japan). The tissue sections were scanned for fluorescent bacteria under light with an excitation wavelength of 488 nm and a BA505-525 emission filter (GFP). Use of an excitation/emission wavelength of 541/572 nm (TRITC) enabled distinction of Salmonella cells from chlorophyll and vascular tissue auto-fluorescence under the GFP filter. Time lapse microscopy of a single field was employed.
Fruit sampling and testing procedure
Ripe (fully red in color) tomatoes were picked by hand, placed in a plastic zip-lock bag and transported to the lab. Each tomato was placed in a sterile plastic bag with 30 ml of 0.1% sterile peptone water. Potential surface populations were dislodged by sonicating the bags for 5 min in an ultrasonic cleaner (Bransonic 5200, Branson Ultrasonics Corp., Danbury, CT). The Salmonella population in the peptone wash suspension was enriched and enumerated as described above. The fruit samples were then immersed in 70% alcohol for 2 min and then rinsed twice in SDW. Each fruit was vertically cut into halves with a sterile knife. Tomato halves were placed directly with cut-side-down for 1 min on LB agar plates supplemented with 50 µg/ml kanamycin. The halves then were removed from LB plates. The plates were incubated at 37°C overnight. S. enterica Typhimurium colonies on each Petri plate were determined by counting green fluorescent CFUs using a UV lamp. The pulp of Salmonella contaminated tomato fruits in ziplock bags was crushed by hand to form a pulp slurry, and then transferred into a 50-ml centrifuge tube and vortexed for 3 min. Thereafter, 1 ml of the slurry was used to establish tenfold dilution series with 0.1% peptone water. Aliquots (100 µl) of appropriate dilutions were spread onto LB agar plates containing 50 µg/ml kanamycin. The plates were incubated at 37°C overnight. Numbers of Salmonella colonies were counted as described above.
Injection of S. enterica Typhimurium into peduncles
54 pink fruits with about 0.5 cm long peduncles were picked by hand from non-inoculated healthy plants. The weight of these individual tomatoes ranged from 27 to 44 g. Suspensions of S. enterica Typhimurium strains MAE110 and MAE119 were prepared separately as described above. Ten µl inoculum suspensions with a density of 104 CFU/ml were injected into peduncles about 0.4 cm deep with the aid of sterile syringe needles (0.46 mm O.D., 13 mm Length). The opening caused by the needle was sealed with molten paraffin immediately after inoculation. Tomatoes were individually placed in zip-lock bags, stored in the greenhouse and sampled from 0 to 15 days post inoculation. At each sampling point, 3 tomatoes of each treatment were submerged in 70% alcohol for 30 s, 0.6% sodium hypochlorite for 20 s and finally rinsed with SDW twice. The pulp of the tomatoes was extracted and analyzed for S. enterica Typhimurium CFUs as described above.
Growth of S. enterica Typhimurium at a range of pH levels
Experiments were conducted to determine the pH values at which S. enterica Typhimurium MAE110 and MAE119 could grow at room temperature. The experiments used 50 ml of liquid LB in 250 ml flasks as a base medium and were repeated twice on different dates. Hydrochloric acid was used to adjust the pH of the media to a range between 2.2 and 7 with a 0.4 unit interval as described previously . Each strain was replicated in three flasks in each experiment. The inoculum of S. enterica Typhimurium was prepared as described above. Fifty µl suspension (104 CFU/ml) was added into each flask. After 3-day incubation at room temperature, 0.5 ml of medium suspension was transferred from each flask to determine the CFU of Salmonella. The dilution series and plating were the same as described above.
Plant dry weight measurements
Aboveground dry weights of tomato plants, after removal of fruits, were measured as described previously . In brief, plants were removed from the soil and any loose soil was washed off; the plants were then blotted to remove any free surface moisture and dried in an oven at 37±2°C for 4 days. The dry weights were measured after the plants cooled in zip-lock bags.
The number of colonies per plate was converted to CFU/ml or CFU/g (fresh weight) and log-transformed to obtain normal distributions for statistical analysis. The surface disinfection effect and the effect of bacterial rdar morphotype on the internal persistence of S. enterica Typhimurium in tomato leaves at the inoculation site was evaluated by fitting log-transformed data (separately for each replication) to the exponential decay model with asymptote: Ct = A+(M − A)e−Rt+Et , in which C = S. enterica Typhimurium concentration (log (CFU/g)), A = asymptote (log (CFU/g)), M = initial bacterial concentration (log (CFU/g)), R = growth rate (day−1), t = time (day) and E = Error term. Estimated values of the parameters were subjected to multivariate analysis of variance (MANOVA). Similarly, log-transformed data of Salmonella concentration in tomato fruits through peduncle injection were fitted to the Gompertz equation: Yt+Et, in which Y = S. enterica Typhimurium concentration (log (CFU/g)), A = upper asymptote (log (CFU/g)), B = growth displacement (dimensionless), C = growth rate (day−1), t = time (day) and E = Error term. Statistical analyses (ANOVA, MANOVA, nonlinear regressions, and t tests) were performed using SAS (SAS release 9.2, SAS Institute Inc., Cary, NC).
Plant surface disinfection efficiency
On average, 6.60×104±1.10×104 S. enterica serovar Typhimurium CFU were recovered after the alcohol/hypochlorite washes of the inoculated leaves, whereas 1.36×108±0.28×108 CFU were obtained in the absence of the leaf disinfection treatments. Thus, the treatment reduced counts by about 2000 times (3.3 logs), and the surface disinfection efficiency was about 99.95% (±0.21%). The surface disinfection efficiencies for S. enterica Typhimurium strains MAE110 and MAE119 were not significantly different (P>0.05).
Effect of surfactants on S. enterica Typhimurium colonization in tomato leaves
Seven and 14 days after inoculation, the population of S. enterica Typhimurium MAE110 in the tomato leaves inoculated with a suspension plus Silwet L-77 (4.53±0.09, 4.16±0.07 Log (CFU/g)) was significantly higher than that in leaves inoculated with a suspension with Tween 20™ (4.06±0.14, 3.45±0.11 Log (CFU/g)) or a suspension in SDW (3.59±0.17, 3.04±0.10 Log (CFU/g), Fig. 1). Thus, the application of Silwet L-77 to leaves may enhance the initial internalization or survival of Salmonella in tomato leaves.
Figure 1. Survival of Salmonella enterica Typhimurium inside tomato leaves after Salmonella inoculation with or without surfactants.
SDW: Sterile distilled water.doi:10.1371/journal.pone.0027340.g001
Surface and internal colonization of tomato leaves by S. enterica Typhimurium
Three hours after inoculation, the Salmonella concentration on non-disinfected leaves was about 108 CFU/g, which was about 3 logs higher than the concentration in disinfected leaves (~105 CFU/g) (Fig 2). Based on the disinfection efficiency described above, most of the bacteria (99.9%) were attached to the leaf surface at that time. After 1 day, the Salmonella concentration in disinfected leaves remained the same while the concentration of non-disinfected leaves significantly decreased. Additionally, the decrease rate of the Salmonella populations on non-disinfected samples was about two times as high as that in disinfected samples (Table 1). These results suggest that Salmonella survived better after internalization when compared to surface colonization.
Figure 2. Survival of Salmonella enterica Typhimurium on/in tomato leaves with/without surface disinfection.
Pdis and Pnon are the predicted regression curves based on an exponential decay model with asymptote for the survival of Salmonella with and without surface disinfection, respectively.doi:10.1371/journal.pone.0027340.g002
Table 1. Statistical analysis of parameter estimates for the exponential decline of Salmonella enterica Typhimurium concentrations on/in tomato leaves over a 21 day period.doi:10.1371/journal.pone.0027340.t001
Two weeks post inoculation, the Salmonella concentration in disinfected leaves decreased to about 104 CFU/g, which was about 0.5 to 1 log less than that of the non-disinfected leaves. The population on the surface was at least 2 times higher, and over 65% of Salmonella existed on the surface.
No Salmonella was detected in the control plants.
Effect of bacterial rdar morphotype on the persistence of S. enterica Typhimurium inside tomato leaf tissues
In year 1, levels of S. enterica Typhimurium strain MAE110 (4.37±0.09 Log (CFU/g)) were significantly higher than those of strain MAE119 (3.84±0.17 Log (CFU/g)) at 7 days post inoculation (Fig 3a). In year 2, leaves were sampled several times between day 1 and day 21 to confirm the result obtained in the first year (Fig. 3b). The populations of both Salmonella strains in surface disinfected leaves decreased during the first 2 weeks after inoculation but remained unchanged in week 3. The exponential decay model used to describe survival of Salmonella in each sample had a mean square error of 0.257 and a coefficient of variation (R2) of 0.974. With respect to estimates of R (rate), A (asymptote) and M (initial bacterial concentration), the two strains were significantly different, with an overall Wilk's Lambda significance value of 0.0228 (Table 1). The R and A values of MAE110 were significantly higher than those of MAE119 (P<0.05), while M was not significantly different. Thus, S. enterica Typhimurium strain MAE110 with rdar morphotype persisted longer inside tomato leaves than the saw morphotype strain MAE119.
Figure 3. Population of Salmonella enterica Typhimurium strains MAE110 and MAE119 in tomato leaves after surface disinfection.
Population of Salmonella strains MAE110 and MAE119 in inoculated tomato leaves 7 days after inoculation in year 1 (a); Survival trends of Salmonella strains MAE110 and MAE119 in inoculated tomato leaves in year 2 (b). P110 and P119 are the predicted regression curves based on the exponential decay model with asymptote for the survival of Salmonella strains MAE110 and MAE119.doi:10.1371/journal.pone.0027340.g003
Internalization and movement of S. enterica Typhimurium in tomato plants
In year 2, Salmonella was detected in adjacent non-inoculated leaves of eight tomato plants at 5 days post first inoculation (five plants inoculated with strain MAE110 and three with strain MAE119) (Table 2). To confirm the internalization and movement of S. enterica Typhimurium in tomato plants, plant tissues were sampled from these 8 tomato plants after the second inoculation. Salmonella cells were observed on the leaf surface, frequently associated with the trichomes and sometimes harbored by stomata at a rate of about 2–3% of the stomata (Fig. 4 A and B). One day after inoculation, Salmonella cells had ingressed into tomato leaves, moved into midrib veins of leaves (Fig. 4 C and D) and sometimes entered the vascular system, in particular the xylem (Fig. 4 E and F). As expected, Salmonella cells were also found inside non-inoculated leaflets adjacent to the inoculated leaflets on the eight plants where non-inoculated adjacent leaflets had tested positive for Salmonella (Fig. 5, Table 1). In addition, Salmonella was detected in the adjacent non-inoculated stems, including inside the phloem (Fig. 6). The frequency of Salmonella detected in non-inoculated adjacent leaves and stems was not very high (leaf cross section slides: 11 positive out of ~960; stem slides: 5 positive out of ~240). The presence of Salmonella cells as projected images of several Z section-overlaid fluorescence images from different layers (Fig. 4 F, Fig. 5 B, Fig. 6 B and D) indicated that the bacterial cells were located inside the plant tissues (Figures S2, S4, S6, S8), and that the presence of GFP fluorescent cells was not caused by contamination during manipulation. In addition, the observation of the Salmonella cells in the images obtained under a GFP filter (green fluorescence), and absent under a TRITC filter (red auto-fluorescence of chloroplasts and vascular tissues) confirmed that they were GFP labeled bacterial cells instead of plant tissues with auto-fluorescence (Figures S1, S3, S5, S7). All these microscopic results supported the internal movement of S. enterica Typhimurium in tomato plants. Salmonella cells were not detected in samples of control plants.
Figure 4. Microscopy of inoculated tomato leaf tissue sections colonized by Salmonella enterica Typhimurium.
Fluorescence microscopic images of GFP-tagged Salmonella (green) showing both diffuse and stomata-associated attachment on inoculated leaves. Red fluorescence is the autofluorescence of plant chloroplasts (A and B). Endophytically present Salmonella was observed in the mid-rib vein of inoculated tomato leaves (C and D) and inside the vascular system (E and F). Image F as merged image under GFP and TRITC filters (Figure S1) was obtained by projecting 15 Z section overlaid fluorescence images of different layers (Figure S2) with 1 um interval into one combined image. Fluorescence and confocal microscopic images were labeled with magnification and scale bars, respectively.doi:10.1371/journal.pone.0027340.g004
Figure 5. Microscopy of non-inoculated tomato leaf tissue sections colonized by Salmonella enterica Typhimurium.
Salmonella was observed inside the non-inoculated leaves close to the veins. Image B as merged image under GFP and TRITC filters (Figure S3) was obtained by projecting 15 Z section overlaid fluorescence images of different layers (Figure S4) with 1 um interval into one combined image. Fluorescence and confocal microscopic images were labeled with magnification and scale bars, respectively.doi:10.1371/journal.pone.0027340.g005
Figure 6. Confocal microscopy of non-inoculated tomato stem tissue sections colonized by Salmonella enterica Typhimurium.
Salmonella was located in the phloem of non-inoculated stems in vertical plant tissue cross sections (A and B) and horizontal sections (C and D). Images B and D as merged images under GFP and TRITC filters (Figure S5, S7) were obtained by projecting 15 Z section overlaid fluorescence images of different layers (Figure S6, S8) with 1 um interval into one combined image.doi:10.1371/journal.pone.0027340.g006
Table 2. Salmonella enterica Typhimurium contamination in tomato plants.doi:10.1371/journal.pone.0027340.t002
Colonization of fruit pulp by S. enterica Typhimurium
In the first year experiment, a total of 810 tomato fruits collected from the 126 (84 inoculated with Salmonella and 42 with SDW) tomato plants were tested for the presence of Salmonella on the surface of fruit or in tomato pulp. S. enterica Typhimurium was not detected in the wash water after enrichment, indicating that the fruit were not externally contaminated. One of the 42 MAE119-inoculated plants was systemically infected by S. enterica Typhimurium (Table 1). All nine fruits collected from that plant were internally colonized at high concentrations while no symptoms were observed (Fig. 7 A1 and A2). In year 2, a total of 750 tomato fruits were tested for the presence of Salmonella on the surface of fruits and in tomato pulp. Again, S. enterica Typhimurium was not detected in the wash water after enrichment. Two of seven harvested tomatoes of one plant and five of six harvested tomatoes from another plant were found Salmonella-positive, and both of these two plants were inoculated with strain MAE110. Both of these plants also tested positive for Salmonella in adjacent non-inoculated leaves (Table 1). Six of these contaminated fruits from the two Salmonella-positive plants were located at lower positions on the plants, closer than 5 cm from the inoculated leaves. Only one colonized fruit was collected from the top of one systemically infected tomato plant suggesting that Salmonella may not have moved very far up in the plants. The average concentration of S. enterica Typhimurium in the colonized tomato fruits was 6.3×105±1.9×105 CFU/g. The lack of visible symptoms and the distributions of the bacterial cells in the pulp are shown in Fig. 7, where A1 and B1 are the cut fruits from Salmonella strains MAE119 and MAE110 contaminated plants, respectively. A2 and B2 show the Salmonella colonies recovered from the corresponding fruits shown in A1 and B1 on LB plates with 50 µg/ml kanamycin, the GFP-labeled Salmonella colonies showed green fluorescence under a UV lamp (B2). Fig. 7 C1 and C2 show controls.
Figure 7. Tomato fruit contamination of Salmonella enterica Typhimurium.
A1 and B1 are the cut fruits from Salmonella strains MAE110 and MAE119 contaminated plants, respectively. A2 and B2 present the Salmonella colonies recovered from corresponding fruits shown in A1 and B1 on LB plates with kanamycin; GFP labeled Salmonella colonies showing green fluorescence under UV lamp (B2). C1 and C2 are controls.doi:10.1371/journal.pone.0027340.g007
S. enterica Typhimurium reached the interior of the fruit that were inoculated in the peduncle and multiplied inside the pulp to concentrations of about 107 CFU/g pulp (fresh weight). The Gompertz model for growth of Salmonella in MAE110 and MAE119 of inoculated fruit had mean square errors of 0.2582 and 0.1653 and R2 values of 0.994 and 0.995, respectively. Estimates of A (asymptote), B (growth displacement) and C (growth rate for the two strains were not significantly different with an overall Wilk's Lambda significance value of 0.1383 (Fig. 8, Table 3). The population of Salmonella reached over 106 CFU/g in LB media when the pH was above 4 (Fig. 9). There was no significant difference between the log(CFU/ml)s of two Salmonella strains at each pH condition. These results support the ability of Salmonella to multiply inside harvested tomato fruits, no matter where it was located inside the fruits.
Figure 8. Growth of Salmonella enterica Typhimurium strains in tomato fruits after injection through peduncles.
P110 and P119 are the predicted regression curves based on the Gompertz equation for the growth of Salmonella strains MAE110 and MAE119.doi:10.1371/journal.pone.0027340.g008
Figure 9. Growth of Salmonella enterica Typhimurium strains MAE110 and MAE119 at low pH levels.
The concentrations of strains MAE110 and MAE119 were determined 3 days after inoculation.doi:10.1371/journal.pone.0027340.g009
Table 3. Statistical analysis of parameter values for a Gompertz growth curve of Salmonella enterica Typhimurium in tomato fruits after peduncle injection.doi:10.1371/journal.pone.0027340.t003
Effect of S. enterica Typhimurium inoculation on aboveground dry weight of tomato plants
Aboveground parts of tomato plants were collected at the end of the second experiment (5 months growth) and dried for weight measurements (Fig. 10). Compared to the plants treated with SDW containing 0.025% (v/v) Silwet L-77, the aboveground dry weights of the plants inoculated with Salmonella were significantly decreased, indicating that Salmonella inoculation could reduce the aboveground plant biomass. During the experiment, the inoculated tomato leaves turned yellow, wilted and finally dropped. While the leaves inoculated with SDW with 0.025% Silwet L-77 remained healthy. Thus, the reduction in biomass may be partially due to the drop of inoculated leaves.
The main results obtained from this research were that S. enterica Typhimurium entered tomato plants via the leaves (possibly through stomates) and moved through petioles and stems into non-inoculated leaves and fruits, although the rate of internal fruit contamination was low. The rdar mophotype of S. enterica Typhimurium enhanced the ingress and internal persistence in tomato leaves at the inoculated sites. This is the first time to confirm that S. enterica can be transported inside tomato plants to contaminate fruits internally, possibly by moving through phloem, the main means of transportation of liquid and sugars into the fruit . Previous studies demonstrated that the inoculation of flowers and stems with S. enterica can result in the contamination of tomato fruits , and that inoculation of leaves can result in surface contamination of tomato fruits . However, the internal movement of Salmonella from leaves into tomato fruits has not been reported.
To investigate the presence of S. enterica Typhimurium inside plant tissues, the Salmonella cells on the plant surface must be removed efficiently without killing the bacteria inside the plant. For this purpose, the efficiency of 70% ethanol and 0.6% sodium hypochlorite was evaluated for surface disinfection of the leafy parts of plants that were dip-inoculated with S. enterica Typhimurium. The decrease of the Salmonella population after the disinfection treatment was about 3.3 logs which is higher than the 2.7 logs reduction shown by Klerks , mainly due to the longer disinfection time and additional treatment with sodium hypochlorite in this experiment.
The Salmonella rdar mophotype is important for the attachment to plant surfaces ,  and the persistence in environments outside of animal hosts , , but it may not be critical to the persistence within tomato fruits . In this study, the results indicated that Salmonella stain MAE110, permanently containing the rdar morphotype, survived better in inoculated tomato leaves compared to the rdar deficient mutant strain MAE119. However, the contamination rate in adjacent leaves and fruits (Table 2) was not significantly higher for strain MAE110. A possible explanation may be that characteristics associated with the rdar morphotype protected the bacteria from stress on the surface and just below the surface of inoculated leaves, but these character traits were less important once the cells had completely entered the plants and were sheltered from external stress factors. Another explanation may be that the Salmonella rdar mophotype may have a different function in tomato leaves than in fruits. Further molecular biological studies should be conducted to investigate the mechanism how the rdar mophotype affects the survival of Salmonella inside plant leaves, stems and fruits.
During our microscopic observations, we noticed that S. enterica Typhimurium was frequently observed at the base of leaf trichomes (data not shown), similar to a previous report on the distribution of a mixture of strains of S. enterica (not including serovar Typhimurium) on tomato leaf surfaces . In that report, S. enterica cells were not found in stomates. We observed that S. enterica Typhimurium cells were located in stomates and that inoculation did not result in stomatal closure, similar to the colonization of S. enterica Typhimurium on iceberg lettuce . Thus, Salmonella cells could have entered through these “open gates” (Fig. 4 A and B). In our study, 2–3% of the stomata of inoculated leaves contained S. enterica Typhimurium cells. So, besides wounds, stomata may be an important pathway for Salmonella ingress into tomato leaves.
Although Salmonella cells were observed in the vascular system of inoculated leaves, they were not found in the xylem vessels of non-inoculated plant tissues. Yet, they were observed in the phloem of non-inoculated tissues. These results suggest that phloem is more conducive for presence of Salmonella when compared to xylem, probably due to the high levels of sugars and nutrients in the phloem. When lettuce or Medicago truncatula plants were grown in contaminated manure-amended soil or were inoculated on agar media, S. enterica infected the plants as a plant pathogen, invoking host defense responses , . Similar to the findings of Klerks et al. , inoculated leaves became chlorotic and the biomass of inoculated plants was reduced in our experiments. This indicates that S. enterica Typhimurium had some pathogenic effect on tomato plants. However, the rare occurrence of Salmonella cells in the phloem of inoculated plants indicated that Salmonella was an exogenous bacterium in tomato plants, mainly colonizing the apoplast of the tissues . Nevertheless, it could enter the vascular system in inoculated leaves, survive and move in the sieve tissues of the phloem and thus result in internal contamination of tomato fruits, although at a low rate (5 in 240 microscopic slides from 8 Salmonella positive plants). Unlike plant pathogens, which could produce hemicellulase and pectinases to degrade plant cell walls, the mechanism how Salmonella cells enter and survive inside the phloem is still unclear. One possibility for the rare occurrence of S. enterica Typhimurium in the phloem is that the primary sugar transported by the phloem in tomatoes is sucrose which could not be digested by Salmonella . Another hypothesis is that the high concentration of sugars and other nutrients in phloem provides a negative osmotic pressure to the bacteria and limits water absorbability. Further studies would need to be conducted to answer these questions.
To confirm the possibility of internal growth of S. enterica inside tomato fruits, young pink fruits (pH 4–4.5) in this experiment were harvested and injected with low concentrations of S. enterica Typhimurium through the peduncle, and the growth of S. enterica Typhimurium was tested in vitro at a range of pH levels. S. enterica Typhimurium entered the fruit through the peduncle and multiplied inside the pulp. Similar as reported previously , Salmonella could grow when the pH was above 4. Although it is not exactly known whether Salmonella was in the symplast or apoplast inside the fruit and the pH values of various tissues in tomato fruits differ, a low pH value of any tissue in the tomato fruits would not be a limitation for Salmonella multiplication. Further studies would be needed to investigate the exact location of Salmonella in contaminated tomato fruits.
Based on the fruit contamination rate (Table 2), internal contamination is a low chance event, even though we set up a worst case scenario. To maximize the possibility of internalization, we inoculated tomato leaves two or four times before fruit set with a suspension of S. enterica Typhimurium at a high concentration (109 CFU/ml) including the surfactant Silwet L-77, which could facilitate entry of bacteria into plant leaves . The contamination rates of adjacent non-inoculated leaves and fruits were 9.5% and 1.8%, respectively, and the chance to detect contaminated fruits after inoculation was less than 1.5%. Nevertheless, due to the very large numbers of tomatoes produced in the USA, about 4 million metric tons in North America in 2003 , this low probability event would have a chance to occur, especially in large tomato fields with a high plant density (about 2×104 plants / ha). Because the probability of internal movement of Salmonella in tomato plants is low, a high concentration of inoculum was necessary to obtain positive results for this fundamental research to investigate if internal movement was at all possible. In environmental samples such as manure that can be used to amend soil, Salmonella can be present in levels up to 106 CFU/g  and grow to levels above 109 CFU/g if microbial competitors are not present . However, these conditions and high inoculum levels of Salmonella would be hard to reach in natural environments. A probabilistic microbial risk model would need to be developed to assess the contamination probability in a practical tomato production chain .
Another important point of this study is that all tomato plants were grown in agricultural soils collected from farms with a long cropping history. Unlike commercial potting mix, which usually contains more nutrients for plant growth and has excellent drainage properties , the agricultural soil we used reflected the conditions of a regular field, possibly providing a higher chance for survival and ingress into the plant and internal contamination of the fruit by Salmonella , . Moreover, natural soil may also provide the right conditions for seed contamination, as the seeds extracted from the contaminated fruits in these experiments were internally contaminated by Salmonella (Gu and van Bruggen, to be published). Further studies to see if S. enterica Typhimurium could be transmitted from these internally contaminated seeds to seedlings, plants and fruits in the second generation are currently underway.
Similar as reported for lettuce , the biomass of tomato plants was reduced after inoculation of Salmonella. Further studies are needed to assess the mechanisms of plant biomass reduction by Salmonella compared with other bacteria.
The practical implication of this work may be that application of surfactants, especially Silwet L-77, could enhance the entrance of bacterial pathogens into leaf tissues (this work and ), although internal movement of Salmonella in tomato plants was not enhanced by surfactants. Additional experiments would be needed to investigate if a reduction in the application of fungicides, insecticides and herbicides containing surfactants could lower the risk of contamination with S. enterica.
This work resulted in two major findings, viz. that S. enterica Typhimurium can reach tomato fruit via internal translocation from leaves through stems and that phloem tissue is a potential conduit. The chance of internal movement is low, but once Salmonella cells reach a fruit they can multiply to high densities within that fruit. Additional findings were that the rdar morphotype and surfactants enhanced initial colonization of leaf tissues.
Images of the same inoculated leaf section as in Figure 4F taken with GFP, TRITC filters and their combination. White arrows point at the locations of Salmonella cells shown with the GFP filter, and absence with the TRITC filter.
Images of the same inoculated leaf section as in Figure 4F obtained from different layers of a Z section. White arrows point at the locations of Salmonella cells inside the plant tissues.
Images of the same inoculated leaf section as in Figure 5B taken with GFP, TRITC filters and their combination. White arrows point at the locations of Salmonella cells shown with the GFP filter, and absence with the TRITC filter.
Images of the same inoculated leaf section as in Figure 5B obtained from different layers of a Z section. White arrows point at the locations of Salmonella cells inside the plant tissues.
Images of the same inoculated leaf section as in Figure 6B taken with GFP, TRITC filters and their combination. White arrows point at the locations of Salmonella cells shown with the GFP filter, and absence with the TRITC filter.
Images of the same inoculated leaf section as in Figure 6B obtained from different layers of a Z section. White arrows point at the locations of Salmonella cells inside the plant tissues.
Images of the same inoculated leaf section as in Figure 6D taken with GFP, TRITC filters and their combination. White arrows point at the locations of Salmonella cells shown with the GFP filter, and absence with the TRITC filter.
Images of the same inoculated leaf section as in Figure 6D obtained from different layers of a Z section. White arrows point at the locations of Salmonella cells inside the plant tissues.
We would like to thank Dr. Joyce Merritt for helpful critique of this manuscript; Dr. Jorge Giron, Dr. Jeff Jones and Dr. Jeri Barak for insightful comments during the research phase and the preparation of the manuscript.
Conceived and designed the experiments: GG JH JAB AHCvB. Performed the experiments: GG JH JMC-C SMR. Analyzed the data: GG JH JMC-C. Wrote the paper: GG JH AHCvB.
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