Downy mildew disease promotes the colonization of romaine lettuce by Escherichia coli O157:H7 and Salmonella enterica
© Simko et al.; licensee BioMed Central. 2015
Received: 1 October 2014
Accepted: 22 January 2015
Published: 4 February 2015
Downy mildew, a plant disease caused by the oomycete Bremia lactucae, is endemic in many lettuce-growing regions of the world. Invasion by plant pathogens may create new portals and opportunities for microbial colonization of plants. The occurrence of outbreaks of Escherichia coli O157:H7 (EcO157) and Salmonella enterica Typhimurium (S. Typhimurium) infections linked to lettuce prompted us to investigate the role of downy mildew in the colonization of romaine lettuce by these human pathogens under controlled laboratory conditions.
Whereas both EcO157 and S. Typhimurium population sizes increased 102-fold on healthy leaf tissue under conditions of warm temperature and free water on the leaves, they increased by 105-fold in necrotic lesions caused by B. lactucae. Confocal microscopy of GFP-EcO157 in the necrotic tissue confirmed its massive population density and association with the oomycete hyphae. Multiplication of EcO157 in the diseased tissue was significantly lower in the RH08-0464 lettuce line, which has a high level of resistance to downy mildew than in the more susceptible cultivar Triple Threat. qRT-PCR quantification of expression of the plant basal immunity gene PR-1, revealed that this gene had greater transcriptional activity in line RH08-0464 than in cultivar Triple Threat, indicating that it may be one of the factors involved in the differential growth of the human pathogen in B. lactucae lesions between the two lettuce accessions. Additionally, downy mildew disease had a significant effect on the colonization of EcO157 at high relative humidity (RH 90-100%) and on its persistence at lower RH (65-75%). The latter conditions, which promoted overall dryness of the lettuce leaf surface, allowed for only 0.0011% and 0.0028% EcO157 cell survival in healthy and chlorotic tissue, respectively, whereas 1.58% of the cells survived in necrotic tissue.
Our results indicate that downy mildew significantly alters the behavior of enteric pathogens in the lettuce phyllosphere and that breeding for resistance to B. lactucae may lower the increased risk of microbial contamination caused by this plant pathogen.
Biotrophic and necrotrophic fungi that cause post-harvest decay have been shown in several instances to enhance the colonization of fruit and vegetables by enteric pathogens. Glomerella cingulata infection of apple fruit promoted proliferation of Listeria monocytogenes and EcO157, likely due to a change of pH from 4.0 to 7.0, whereas the reverse effect was observed with Penicillium expansum [13,14]. Alternaria alternata and Cladosporium spp. had a positive effect on S. enterica colonization of tomato fruit  and Fusarium spp. prolonged the survival of EcO157 on tomato under storage conditions but not that of L. monocytogenes . These observations suggest that the effect of pathogenic fungi on enteric pathogens in plant tissue may vary depending on several factors in this tri-partite association.
Despite the endemic nature of downy mildew disease in lettuce fields in California and other regions in the United States, and the increased appearance of disease symptoms on plants near harvest maturity i.e. not long prior to the lettuce crop reaching the consumer, the role of B. lactucae infection in the behavior of EcO157 on lettuce has not been investigated. B. lactucae requires free water on the phylloplane for spore germination and invasion of plant cells, a condition that also promotes the survival and multiplication of EcO157 on lettuce [17,18]. Additionally, lesions caused by B. lactucae are known to act as portals to necrotrophic plant pathogens, such as Botrytis cinerea, which colonize the broken tissue as secondary invaders . Our study investigates the potential of downy mildew lesions to serve as a portal for EcO157 and to create a habitat where the human pathogen may thrive opportunistically by gaining protection from environmental insults within the plant tissue.
Results and discussion
Effect of downy mildew disease on EcO157 and S. enterica under wet conditions
Lettuce leaves are rich in a variety of carbohydrates, including sucrose, glucose, fructose, galactose and mannose [20,21]. EcO157 rapidly activates multiple carbohydrate transport systems and utilization pathways upon exposure to lysates of romaine lettuce leaves . Although it is likely that the oomycete itself acquires a large share of the nutrients present in plant cells, the collapsed leaf tissue at advanced stages of the disease such as that inoculated in this study probably supports high rates of multiplication of the human pathogens without overall significant competition by the plant pathogen. Another possibility is that at advanced stages of the disease, the oomycete scavenges plant components, the degradation of which makes substrates available to EcO157. It is noteworthy that leaf damage caused by phytopathogens does not de facto promote colonization by enteric pathogens. For example, S. enterica levels in lettuce shoots also inoculated with lettuce mosaic virus (LMV) were not different than in non-LMV-infected plants and even decreased in infected plants grown under water stress . Additionally, EcO157 cell density on spinach was unaffected by its co-inoculation with Pseudomonas syringae DC3000, a plant pathogen that caused necrotic lesions on the leaves . Thus, factors additional to leakages of substrates from infected cells are at play in the interaction of enteric pathogens with plant pathogens.
Localization of EcO157 by microscopy
Role of plant susceptibility to downy mildew in EcO157 growth
Reports on the role of plant genotype in the microbial community composition of the lettuce phyllosphere have been inconsistent [26,27]. Numerous lettuce cultivars have been developed in order to minimize crop yield losses incurred from plant disease, including downy mildew. Given the highly hospitable environment of downy mildew lesions to EcO157, as illustrated in Figure 2, we investigated the role of plant susceptibility to B. lactucae infection in lettuce colonization by this human pathogen. A commercially released lettuce cultivar Triple Threat and a newly developed lettuce breeding line RH08-0464 were selected to test this hypothesis. Triple Threat is highly susceptible to infection by B. lactuacea [28,29], whereas RH08-0464 has high field resistance to this pathogen that is inherited from the stem-type lettuce Balady Banha .
Effect of romaine lettuce susceptibility to downy mildew on the multiplication of EcO157 in leaf tissue in three replicate experiments
Log-10 increase in EcO157 population size on leaf tissue of two lettuce accessions a
Experiment 1 b
Importantly, the EcO157 population increase in diseased tissue in our study was significantly lower on lettuce line RH08-0464 than on the more susceptible cultivar Triple Threat in all three replicate experiments (P < 0.05) (Table 1). This suggests that a plant factor linked to the dynamics or amount of tissue infection by B. lactucae affects the ability of the human pathogen to fully exploit these lesions for multiplication. The nature of this plant factor remains unclear. It is unlikely that the plant gene(s) that contribute(s) to the resistance of RH08-0464 to B. lactucae infection directly inhibited the growth of EcO157 in the lesions because this type of resistance is expected to be specific to B. lactucae-lettuce interactions. Recently, chromosomal regions associated with broad-spectrum quantitative disease resistance to plant pathogens were identified [32,33]. It would be of great interest to determine if broad-spectrum disease resistance may be involved not only in plant interaction with plant pathogens but may be of use also to reduce plant colonization by human enteric pathogens.
Expression of PR-1 in lettuce accessions
Because basal immunity contributes to protection of plants against a broad range of insults, we tested the expression of the gene encoding the antimicrobial PR-1 protein in two lettuce accessions infected with B. lactucae. PR-1 is a major marker of the salicylic acid-mediated pathway of basal defense against microbial infection  that is induced in plants also in response to oomycete infection [35,36]. Both healthy and chlorotic leaf tissue were tested for PR-1 expression in the resistant line RH08-0464 and in the susceptible cultivar Triple Threat. Necrotic lesions do not yield sufficient mRNA to allow for transcript measurement by qRT-PCR.
Lesion-mediated protection of EcO157 from desiccation
Our study is the first to determine the effect of downy mildew, an endemic disease of lettuce in a major vegetable production region of the USA, on the behavior of EcO157 on this crop and to assess various factors that may enhance its persistence in infected leaves. Given the great potential for multiplication and survival of EcO157 in B. lactucae lesions on wet and dry leaves, respectively, and considering that large fluctuations in water availability to bacterial cells likely prevail on lettuce in the field, downy mildew disease may represent an important risk factor of microbial contamination. The higher prevalence of downy mildew on lettuce plants approaching harvest maturity may compound the risk of contamination associated with this disease. Although most of the old lettuce leaves infected with downy mildew are trimmed off during harvest, a fraction of B. lactucae lesions escape visual detection. Additionally, the proliferation and enhanced survival of EcO157 in the infected tissue may create a reservoir from which the pathogen is disseminated or vectored to other sites in the field, as well as contribute to the persistence of the human pathogen in crop debris in the field. Further investigation of the role of downy mildew in the colonization of lettuce by enteric pathogens under field conditions is warranted. Additionally, our observation that EcO157 survives and multiplies at different rates in comparable B. lactucae lesions of two accessions indicates that variability in lettuce gene pool may be explored to develop cultivars that are less hospitable to human enteric pathogens. Such cultivars would be a vital part of an integrated strategy to minimize EcO157 illness linked to lettuce contamination.
The massive proliferation of EcO157 (and S. Typhimurium) under wet conditions in downy mildew lesions on lettuce leaves, and its enhanced persistence in this diseased tissue under conditions of lower RH, suggest that infection of lettuce by B. lactucae may increase the risk of microbial contamination of this crop. Given that differences in EcO157 colonization of diseased tissue were observed in two lettuce accessions with different levels of resistance to downy mildew, breeding lettuce for resistance to this disease may be worth exploring to decrease the burden of enteric illness due to contamination of lettuce.
Strains and media
E. coli serovar O157:H7 strain ATCC 43888, a natural strain that does not produce shiga toxin 1 and 2, and S. enterica serotype Typhimurium strain SL1344, were used in this study. A spontaneous rifampin-resistant strain of E. coli O157:H7 43888 was obtained by selection on Luria Bertani (LB) amended with rifampin at 100 μg/ml. The spontaneous mutant and parental strain were compared in LB throughout all phases of culture and did not show any difference in fitness. S. Typhimurium strain SL1344 is naturally resistant to streptomycin. The strains were grown to stationary phase at 28°C in Luria Bertani broth - half salt (0.5% NaCl), the cells were washed twice in potassium phosphate buffer (KP) (10 mM, pH 7.0), and then resuspended in KP buffer (1 mM, pH 7.0) at the cell concentration specified below for each experiment.
Lettuce (Lactuca sativa L.) plants were grown in the field at the USDA, ARS experimental station in Salinas, CA. The crop was cultivated using standard cultural practices for the area except that no fungicide treatment was applied in order to allow for natural infection by B. lactucae and development of downy mildew. At harvest maturity, when a full head had formed, naturally infected plants were transplanted into plastic pots (27 cm in diameter, 24 cm height) and transported to the USDA, ARS in Albany, California for experimentation. Two cultivars and one breeding line of romaine lettuce with different levels of field resistance to B. lactucae were used in experiments: susceptible cultivar Triple Threat with a low level of resistance, cultivar Green Towers with an intermediate level of resistance, and breeding line RH08-0464 with a high level of resistance [28,29]. Green Towers is one of the main cultivars used for commercial production in the USA. Because naturally occurring infection was used, races of B. lactucae that infected the plants were not controlled for. However, based on recent data from the same lettuce growing area, the most frequently detected avirulence genes in B. lactucae were Avr17, Avr37, Avr38, and Avr36 .
Inoculation and incubation of inoculated lettuce leaves
Immediately before inoculation with enteric pathogens, leaves that had symptoms of downy mildew at the chlorotic and necrotic stages of the disease were harvested from the potted plants. Each replicate detached leaf was inoculated individually by holding it at its base and immersing it upside down in the inoculum suspension for 3 sec and then briefly draining the excess inoculum suspension, as we previously described .
Comparison of EcO157 and S. Typhimurium proliferation on healthy and diseased lettuce tissue was conducted only on the cultivar Green Towers and under conditions of free water on the leaf surface in order to assess the overall effect of downy mildew on their colonization of lettuce; all other experiments in this study were performed with EcO157 only. For comparison of S. Typhimurium and EcO157, the leaves were inoculated with single strains in a suspension of 106 cells/ml. For comparison of colonization of various lettuce accessions by EcO157, leaves were also inoculated in a suspension of 106 cells/ml. In both types of experiments, the leaves were then incubated horizontally in a single layer in a large plastic tub lined with wet paper towels and covered with a plastic bag, which promoted the presence of free water on the leaves. The tub was then placed in an incubator at 28°C. This experimental set up was devised to test the maximum growth potential of the enteric pathogens on healthy tissue, and on chlorotic and necrotic tissue due to infection by B. lactucae.
In order to investigate the effect of relative humidity on the persistence of EcO157 on healthy and diseased tissue, the leaves were inoculated in a suspension of 2 × 105 and 107 cells/ml for incubation under high and low relative humidity (RH), respectively. Then, the lettuce leaves were incubated upright in a small container with water at the bottom to maintain leaf turgidity. Half of the containers were covered with a plastic bag tightened with a rubber band around the bottom of the container and the other half remained uncovered. All of the containers were placed in a chamber maintained at 28°C and 65-75% RH. This set up resulted in the leaves in the covered containers being exposed to 90-100% RH, whereas those in the uncovered containers experienced 65-75% RH. By the end of the experiment, free water was absent macroscopically on the leaves under low RH, whereas leaves under high RH still harbored free water at rare locations. RH and temperature in the chamber were monitored with a Dickson TH8P5 Chart Recorder equipped with a remote sensor (Dickson, Addison, IL). Four, eight and six replicate discs were used in the first, second and third replicate experiment, respectively.
Recovery of bacterial cells from leaf tissue and population measurement
Immediately after inoculation and at indicated times, discs 9 mm in diameter of healthy, chlorotic, and necrotic tissue, as illustrated in Figure 1 were sampled from the inoculated leaves with a cork borer #5. Sampling was performed at random from a total of 15 replicate leaves; the three types of tissue were not necessarily taken from the same leaf. The number of replicate discs varied from three to eight depending on the type of experiment and is indicated in figure legends.
To recover bacteria from leaf tissue, each disc was homogenized with a mortar and pestle in 2 ml KP buffer (10 mM, pH 7.0). The homogenate and dilutions were plated onto LB agar containing rifampin (100 μg/ml) or streptomycin (30 μg/ml) for bacterial counts of EcO157 and S. enterica, respectively. For experiments under low RH conditions and in which the population size of EcO157 declined over time, the entire disc homogenate was plated and thus, the detection limit for measurement of population size was one cell per disc of leaf tissue. The plates were incubated at 37°C overnight and colonies counted to assess population sizes per disc of leaf tissue.
Small discs of healthy and necrotic lettuce tissue were sampled from the leaves at 48 h post-inoculation as described above and mounted with AquaPolymount (Polysciences, Warrington, PA) for visualization with a Leica SP5 confocal microscope (Leica Microsystems, Wetzlar, Germany). The green fluorescent signal was obtained from GFP-EcO157 43888 transformed with pGT-KAN, a stably maintained plasmid expressing gfp constitutively from the kanamycin resistance gene promoter , which was used in EcO157 in our previous studies [17,40]. The red fluorescent signal was obtained from the autofluorescence of B. lactucae and from the chloroplasts of the leaf tissue. In one instance, the far-red autofluorescent signal of the B. lactucae hyphae was pseudocolored in blue in order to better distinguish them from the GFP-EcO157 cells that colonized some of the hyphae infecting the leaves.
Expression of the basal plant defense gene PR-1 was quantified in romaine lettuces Triple Threat and RH08-0464. Discs from uninoculated and nonincubated leaves with natural infection of B. lactucae from the field were harvested from the same plants that were sampled for leaf inoculation. The discs were frozen in liquid nitrogen and stored in the −80°C freezer until used for qRT-PCR. Six discs from each type of tissue were sampled at random from ten leaves. The discs were ground individually using a mortar and pestle in liquid nitrogen before RNA was extracted using the Ambion® TRIzol® reagent and PureLink® RNA kit (Life Technologies, Carlsbad, CA). The RNA was tested for absence of DNA and analyzed by qRT-PCR with the Stratagene Brilliant II SYBR Green kit as described previously [22,41]. Expression of ACT7 was used to normalize the data between samples based on the method by Pfaffl . The sequences of the primers, based on Lactuca sativa nucleotide sequences in GenBank, were: PR-1-F 5′TCGCCACAAGACTTTGTTAATG, PR-1-R 5′GAGGCAAGATTTTCACCATAGG, ACT7-F 5′GCAATTCAAGCCGTTCTTTC, and ACT7-R 5′GATCCAAACGGAGGATAGCA.
All experiments were replicated at least twice with plants harvested from the field at different times. Analysis of variance (ANOVA), t-test, and descriptive statistical analyses were performed with the software JMP v. 11.1.1 (SAS Institute, Cary, NC, USA). Significant differences for multiple comparisons were determined using the Tukey-Kramer HSD (honest significant difference) procedure.
We thank A. Atallah for technical assistance with field experiments and R. Hayes for providing plants used in preliminary experiments. Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture. This research was supported by the United States Department of Agriculture, Agricultural Research Service CRIS projects 5325-42000-046 and 5305-21220-005.
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