An efficient method for visualization and growth of fluorescent Xanthomonas oryzae pv. oryzae in planta
© Han et al; licensee BioMed Central Ltd. 2008
Received: 25 April 2008
Accepted: 30 September 2008
Published: 30 September 2008
Xanthomonas oryzae pv. oryzae, the causal agent of bacterial blight disease, is a serious pathogen of rice. Here we describe a fluorescent marker system to study virulence and pathogenicity of X. oryzae pv. oryzae.
A fluorescent X. oryzae pv. oryzae Philippine race 6 strain expressing green fluorescent protein (GFP) (PXO99GFP) was generated using the gfp gene under the control of the neomycin promoter in the vector, pPneo-gfp. The PXO99GFPstrain displayed identical virulence and avirulence properties as the wild type control strain, PXO99. Using fluorescent microscopy, bacterial multiplication and colonization were directly observed in rice xylem vessels. Accurate and rapid determination of bacterial growth was assessed using fluoremetry and an Enzyme-Linked ImmunoSorbant Assay (ELISA).
Our results indicate that the fluorescent marker system is useful for assessing bacterial infection and monitoring bacterial multiplication in planta.
Xanthomonas oryzae pv. oryzae, a yellow-pigmented Gram-negative bacterium, is the causal agent of bacterial blight disease of rice (Oryzae sativa L.) plants. X. oryzae pv. oryzae infection can cause yield loss of up to 50% in tropical Asia . X. oryzae pv. oryzae infects rice leaves through natural openings such as hydathodes and/or wounded sites and then primarily colonizes the vascular tissues by propagating in the xylem. Increased extracellular polysaccharide secretion accompanies bacteria growth, eventually causing a block in the vascular system . The early symptoms therefore start with wilting in the infected leaves and enlargement in length and width of the legions of leaf blight . As the symptom progress, severe necrosis occurs along the interveinal regions. Eventually, the whole leaf becomes whitish and greyish, and then dies [2, 4]. Over the last few decades, the challenge in elucidating biological phenomena has been met by advances in techniques, which have accelerated our understanding of biological events. In particular, useful tools have been developed to evaluate cellular dynamics in vivo. One of the best examples of a technique that has facilitated cell-based studies is marker systems that use fluorescent proteins (FPs). Since the green fluorescent protein (GFP) was first discovered from the jellyfish Aequorea victoria in 1962 , various types of FPs, including red, yellow, and cyanine fluorescent proteins, have been developed and used in fields such as biophysics, biochemistry, and plant pathology [6–8]. The proteins are stable , non-species specific [10, 11], and have no requirement of specific substrate . Therefore, labelling a specific target protein with a FP is a powerful molecular tool for a cell biology study since it provides the ability to visualize, track, and quantify targets in living cells with high spatial and temporal resolution essential features for understanding biology systems . In addition, bimolecular fluorescence complementation (BiFC) analysis using split-FP systems has been successfully applied to determine protein-protein interactions in planta as well as in animals [12, 13]. Recently, FPs have been used for monitoring living organisms such as Lactobacillus sakie, Pseudomonas syringae, X. axonopodis pv. dieffenbachiae, and Xylella fastidiosa in their hosts [14–17].
To determine virulence and pathogenicity of bacterial pathogens in plant-microbe interactions, researchers typically quantify bacterial multiplication in planta by counting the number of bacterial colonies in plate assays of leaf extracts [18, 19]. This method consists of leaf harvesting, tissue maceration, colony plating, incubating, and counting of bacterial cells. These methods are time-consuming and labour intensive, especially for slow-growing bacteria like X. oryzae pv. oryzae. In addition, the results frequently show large amounts of variation depending on experimental conditions.
Here, we provide an improved method for the study of X. oryzae pv. oryzae using a fluorescent marker system. It not only eliminates many of the difficulties of conventional methods but also allows for reliable and rapid monitoring of bacteria in planta prior to the formation of symptoms.
Results and discussion
Generation of X. oryzae pv. oryzaeexpressing GFP
The PXO99GFP strain is useful for studies of X. oryzae pv. oryzaepathogenesis
First, we examined whether the pPneo-gfp vector/plasmid had an affect on the pathogenicity and virulence of X. oryzae pv. oryzae in rice. The leaves from japonica rice varieties Taipei 309 (TP309, susceptible to PXO99) and a transgenic line of TP309 expressing the XA21 resistance protein (TP309-XA21, resistant to PXO99) were inoculated with the PXO99 or PXO99GFP strains using the scissor clipping method . The typical inoculation symptoms were consistent between the PXO99 and PXO99GFP strains. In the susceptible line (TP309), lesions that developed were approximately 17 to 23 cm in length at 12 DPI, while lesions were less than 1 cm in the resistant line (TP309-XA21). (Fig 2A) These results suggest that pPneo-gfp introduction into the PXO99 strain does not affect pathogenicity.
Bacteria have a tendency to lose exogenous plasmids in the absence of antibiotics . We observed that pPneo-gfp in the PXO99 strain was not stable under non-selective conditions on PS medium without kanamycin (data not shown). Population increase was therefore measured on PSA plates containing cephalexin/kanamycin (PXO99GFPKm in Fig. 2B) to examine the stability of pPneo-gfp under host conditions (Fig. 2B). Surprisingly, the populations of the PXO99GFP strain at 12 days did not vary with or without the kanamycin antibiotics, indicating that the pPneo-gfp plasmid is stable during propagation under host conditions. Recently, several reports showed similar phenomena that bacterial pathogens carry plasmid-borne fluorescent proteins in hosts. L. delbrueckii ssp. lactis and L. fructosus expressing GFP on plasmid in chickens allowed to trace it in the gastro-intestinal tract using fluorescence microscopy . Another notable examples is X. axonopodis pv. dieffenbachiae strain containing p519ngfp plasmid . This strain still showed and the fluorescence in the host, anthurium, even at 5 weeks after inoculation . Taken together, although it is poorly understood why bacterial pathogens carry exogenous plasmids under host conditions, plasmid-borne GFP should be useful tool for tracing pathogen in the host.
In order to investigate if there is a difference in the disease progress between the PXO99 and PXO99GFP strains, bacterial growth curves and lesion length development were established at 0, 4, 8, and 12 DAI [see Additional file 1]. Lesion lengths and bacterial populations at 4 and 8 DAI were nearly identical between the strains, indicating that the continuously expressed GFP did not affect disease progress. Tsuge, et al., reported that bioluminescent transconjugants of X. oryzae pv. oryzae were indistinguishable in pathogenicity with the parental strain . To date, continuous fluorescence in bacteria did not alter the pathogenicity and virulence in the hosts. To apply our system with other patho-system, the stability of pPneo-gfp plasmid must be checked in planta growth.
We also confirmed the pathogenicity and virulence of the PXO99GFP strain and the stability of pPneo-gfp in the PXO99GFP strain using resistant and susceptible lines of Kitaake, another japonica cultivar, that has emerged as a model variety for rice genomics analysis . The results from the Kitaake lines were consistent with the results from TP309 lines, showing that PXO99GFP strain had no detectable affect on the pathogenicity and virulence of the bacteria. These results suggest that the PXO99GFP strain can be used with various cultivars. Taken together, our results indicate that the fluorescent X. oryzae pv. oryzae PXO99GFP strain with the pPneo-gfp plasmid is a useful tool for studies of pathogenesis.
Visual observation of PXO99GFP in planta
To test if PXO99GFP xylem colonization is detectable at the leaf surface without using a thin section, we examined the surface of the leaf every five-centimetres from the inoculation site (Fig. 3C and 3D). The fluorescent PXO99GFP strain was detected along the entire length of the leaf of susceptible TP309 lines in both vertical and transverse vascular bundles, even in symptomless regions that are 30 cm away from the inoculation site at 12 DPI (data not shown). However, the fluorescence from the PXO99GFP strain in the resistant line, TP309-XA21, was not detected even in the first five-centimeter region from inoculation site (Fig. 3D). This data shows that GFP can be used for efficient and rapid detection of X. oryzae pv. oryzae in planta. Additionally, we tested bacterial migration along vascular system in TP309 and TP309-XA21 lines at earlier time (4 DAI). Although lesion lengths were almost similar in both lines at 4 DAI, bacterial migrations were clearly different. PXO99GFP strain migrated 8.6 cm and 2.2 cm from inoculation sites in TP309 and TP309-XA21, respectively. These observations indicate that multiplication and localization of X. oryzae pv. oryzae in the rice vascular system occurs before typical disease symptoms, such as wilting and yellowing of leaf blades, can be detected [see Additional file 2]. In other words, although disease symptoms are not clearly apparent at 4 DPI [see Additional file 1], bacterial localization can be determined [see Additional file 2]. This result demonstrates that the PXO99GFP strain can be used to obtain an earlier diagnosis of infection compared to conventional methods.
Quantification of PXO99GFPstrain using a fluoremeter or enzyme-linked immunosorbent assay
The ELISA (enzyme-linked immunosorbent assay) is widely used to quantify a particular protein. This method has been applied as a diagnostic tool to detect specific pathogen proteins in medicine and plant pathology [29, 30]. To quantify the multiplication of the PXO99GFP strain in rice, ELISA was carried out with anti-GFP antibody and the results were compared with the populations of the PXO99GFP strain at the indicated time points (Fig. 4B). PXO99 and PXO99GFP strains were harvested from TP309 and TP309-XA21 at 0, 4, 8, and 12 DAI. While the PXO99 strain showed a background absorbance level at all time points (approximately 0.4 A480 (absorbance at 480 nm)), the PXO99GFP strain showed a temporal-dependent increase of GFP. The level of GFP expression in the resistant rice line was maintained with a gentle increase until 12 DAI. Interestingly, the GFP in the susceptible rice line, TP309, increased after 4 DAI and reached up to 2.0 A480 at 12 DAI. This increase of GFP observed in ELISA correlated well with PXO99GFP population levels (inset in Fig. 4B), indicating that the significant increase of GFP in rice is dependent on bacterial multiplication. Because the fluorescent marker approach does not require diluting, incubating, and counting of bacterial cells, the method is 3 days faster than conventional measurement methods using plate assays. Taken together, these results suggest that measurement of the bacterial fluorescence and GFP quantification by ELISA are sensitive and rapid methods to determine growing bacterial population and host resistance compared to conventional methods.
In this report, we introduce an application of a fluorescent marker system for study of the phytopathogenic bacterium, X. oryzae pv. oryzae. The fluorescent X. oryzae pv. oryzae strain, PXO99GFP, facilitates detection of the invading pathogen. With this fluorescent marker system, bacterial population can be measured in a day, and resistant/susceptible lines can be screened at 4 DPI. This application, which may be used for other patho-systems, can reduce the time and effort required for bacterial growth determination compared to the conventional method.
Bacteria strains, plants and growth conditions
Bacterial strains and plasmids used in this study
Strain or plasmid
Source or reference
F-mcrAΔ(mrr-hsdRMS-mcrBC) φ80/acZΔM15ΔlacX74 deoR recA1 endA1 araΔ139Δ(ara, leu)7687galU galKλrpsL(Spr)nupGλtonA
Xanthomonas oryzae pv. oryzae
Philippine race 6 (PR6) strain, Cpr
PXO99 with pPROBE-NTpNm, Kmr, Cpr
pBBR1 ori, Kmr, broad-host range expression vector
neo (promoter of neomycin resistant gene) cloned into pPROBE-gfp
OriV, OriT, Gmr, pNm (nptll), broad-host range expression vector
For inoculation experiments to test for virulence, two different cultivars of the japonica rice varieties Taipei 309 (TP309) and Kitaake (Kit) were used. Transgenic mutant lines of the cultivars expressing XA21 protein, TP309-XA21 and Kit-XA21, that are resistant to PXO99 strain expressing AvrXA21  were used for avirulence test. The surface was sterilized in 95% ethanol for 5 min, 40% bleach for 30 min with shaking and then three times rinsed with sterilized water. Rice seeds were germinated for three or four days in water at 37°C in water. The germinated seeds were planted onto soil and grown in greenhouse. Six-week-old rice for TP309 line and five-week-old rice for Kit lines were transferred into growth chamber at least two day prior to inoculation. The growth chamber was set on a 16 h light and 8 h dark photoperiod, a 28/26°C temperature cycle, and 90% humidity.
Standard methods described in Sambrook et al.  were used for DNA manipulations during plasmid preparations and digestions with restriction enzymes. All enzymes for construction of plasmid were purchased from Invitrogen. DNA and protein concentrations were measured using the Nanodrop® ND-1000 (Bio-Rad, USA). The Cell-Porator™ system (Gibco BRL, USA) was used for E. coli (≥ 600 DC) and X. oryzae pv. oryzae (≥ 700 DC) transformations under the following conditions; booster: 4, capacitance: 330 μF, charge rate: fast, low α.
Generation of Xanthomonas oryzae pv. oryzae mutant strain carrying green fluorescent protein (gfp) gene
Broad-host-range promoterless probe vector, pPROBE-gfp , was used for generation of X. oryzae pv. oryzae mutant strain constitutively expressing GFP. Neomycin promoter (approximately 400 nucleotide-lengths) cut out with Sal I and EcoR I from pML122 vector  was inserted into the multi-cloning site of the pPROBE-gfp vector linearized with the same enzymes. The construct for constitutively expressing GFP, pPneo-gfp, was introduced into E. coli competent cell, DH10B, and then selected on the LB plates containing 50 μg/ml of kanamycin. The plasmid DNA extracted from the E. coli transformants re-introduced into PXO99 competent cells using electroporation method. The PXO99 mutant strain carrying the pPneo-gfp was (PXO99GFP) selected on the PSA plates containing 20 μg/ml of cephalexin and 50 μg/ml of kanamycin. The transformants also confirmed by observation using a Zeiss Axiophot fluorescence microscope (Jena, Germany) equipped with a fluorescein isothiocyanate filter (excitation filter, 450 to 490 nm; emission filter, 520 nm; dichroic mirror, 510 nm).
Inoculation experiment and bacteria growth in planta
X. oryzae pv. oryzae strains were prepared by culturing on PSA plates containing either cephalexin (for the PXO99) or cephalexin/kanamycin (for the PXO99GFP) for three days at 28°C. Rice leaves were inoculated with the scissor clipping method , using cells suspended in distilled water at a density approaching 1.0 × 108 CFU/ml. Lesion lengths were measured 0, 4, 8, and 12 DAI.
X. oryzae pv. oryzae growth in planta was measured using a modified method from a report by Song et al. . For establishing growth curves, the inoculated rice leaves were harvested at each time point, immediately sliced into small pieces. Sliced rice leaves were incubated in 1 ml sterile water including 15 μg/ml of cephalexin with shaking for 1 h, and then filtered through two layers of cheesecloth. The filtrates were then plated onto PSA plates with cephalexin for PXO99 strain or cephalexin/kanamycin for PXO99GFP strain. Colonies on the plates were counted after three days of incubation at 28°C.
To visualize bacterial infection through leaf veins under microscope, rice leaves were harvested at 12 DAI. To get thin transverse sections (0.1 mm), TP309 and TP309-XA21 leaves inoculated with PXO99GFP were cut using a razor blade. The small pieces of leaf sections were placed on a microscope slide, submerged in immersion oil (Cargille lab, USA), covered with a glass slip and sealed with grease. The fluorescence photographs were taken using a Zeiss Axiophot fluorescence microscope (Jena, Germany) fitted with fluorescein isothiocyanate filters (excitation filter, 450 to 490 nm; emission filter, 520 nm; dichroic mirror, 510 nm). The optimal exposure time was 1 sec. Three biological replicates using leaf blades from each of the three different plants were used for all microscopic analyses.
Fluorimetric measurements of PXO99GFPstrain
X. oryzae pv. oryzae strains were inoculated on 6 weeks old TP309 and TP309-XA21 lines, and to quantify GFP using a fluoremeter, X. oryzae pv. oryzae cells were recovered at 0, and 12 DPI as described in the previous section. The bacteria recovered from the rice leaves were serially diluted until 10-4 with water and 200 μl of cell suspension were transferred in a microtitre plate, MICROTEST™ 96 (Falcon, USA). Fluorescence of the bacteria was directly measured in a fluoremeter, SafireII (Tecan, USA) . GFP fluorescence was measured at a wavelength of 480 nm for excitation and 520 nm for emission, with a bandwidth of 20 nm in both cases.
Enzyme-Linked ImmunoSorbant Assay
Leaves were collected from TP309 and TP309-XA21 at 0, 4, 8, and 12 DAI by PXO99 or PXO99GFP strain. The inoculated rice leaves were harvested at each time point, immediately sliced into small pieces, incubated in 1 ml sterile water including 15 μg/ml of cephalexin with shaking for 1 h, and then filtered through two layers of cheesecloth. The filtrates were precipitated by centrifugation at 15,000 g for 15 min, and the pellets were dissolved in 100 μl of lysis buffer (100 mM Tris-Cl, pH 8.0, 8 M urea, and 100 mM NaH2PO4). Micro-ELISA plates (96-well plate, Fisher Scientific, UK) were coated with 200 μl of PXO99 or PXO99GFP diluted with carbonate-bicarbonate buffer (0.2 M sodium carbonate-bicarbonate, pH9.4). After overnight incubation at 4°C, plates were washed three times with 0.5% Tween-20 in PBS buffer (10 mM phosphate buffer, pH 7.4, 150 mM NaCl, and 0.1% sodium azide; PBST). Plates were treated with 5% skim milk in PBS and washed three times with PBST buffer. Anti-GFP polyclonal IgG antibody (Santa cruz, USA) of 1:500 dilution was added to each well (100 μl/well) and incubated for 1 h at 37°C. After three washings with PBST, a 1: 5,000 diluted horseradish peroxidase linked anti-rabbit IgG antibody (GE healthcare, UK) was added for 1 h at 37°C. The plates were subsequently washed three times with PBST. To detect peroxidase activity, one OPD (ortho-phylenediamine) tablet (Sigma, USA) and one urea hydrogen peroxidase tablet (Sigma, USA) was dissolved in 20 ml of distilled water. 200 μl of substrate was added to each well and incubate the plate in the dark for 20 min at room temperature followed by addition of 50 μl 3 M HCl to stop the reaction. Absorbance of the plate was measured at 480 nm by an ELISA reader, SafireII (Tecan, USA).
Exempt – animal subjects are not used.
We thank Dawn Chiniquy for helpful comments and critical reading of the manuscript. This work was financially supported by USDA grants # 2006-01888, # 2007-01531, and USDA Rice CAP. The work of S.-W. H. was partially supported by a grant for the Graduate Study Abroad Scholarship from the Korean Science and Engineering Foundation. The work of C.-J. P. was partially supported by grant for the Post-doctoral Fellowship Program of Korea Science & Engineering Foundation.
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