Bacterial Leaf Infiltration Assay for Fine Characterization of Plant Defense Responses using the Arabidopsis thaliana-Pseudomonas syringae Pathosystem

Summary

Quantification of pathogen growth is a powerful tool to characterize various Arabidopsis thaliana (hereafter: Arabidopsis) immune responses. The method described here presents an optimized syringe infiltration assay to quantify the Pseudomonas syringae pv. maculicola ES4326 growth in adult Arabidopsis leaves.

Abstract

In the absence of specialized mobile immune cells, plants utilize their localized programmed cell death and Systemic Acquired Resistance to defend themselves against pathogen attack. The contribution of a specific Arabidopsis gene to the overall plant immune response can be specifically and quantitatively assessed by assaying the pathogen growth within the infected tissue. For over three decades, the hemibiotrophic bacterium Pseudomonas syringae pv. maculicola ES4326 (Psm ES4326) has been widely applied as the model pathogen to investigate the molecular mechanisms underlying the Arabidopsis immune response. To deliver pathogens into the leaf tissue, multiple inoculation methods have been established, e.g., syringe infiltration, dip inoculation, spray, vacuum infiltration, and flood inoculation. The following protocol describes an optimized syringe infiltration method to deliver virulent Psm ES4326 into leaves of adult soil-grown Arabidopsis plants and accurately screen for enhanced disease susceptibility (EDS) towards this pathogen. In addition, this protocol can be supplemented with multiple pre-treatments to further dissect specific immune defects within different layers of plant defense, including Salicylic Acid (SA)-Triggered Immunity (STI) and MAMP-Triggered Immunity (MTI).

Introduction

Due to their sessile nature, plants are constantly threatened by a plethora of pathogens exhibiting various lifestyles and nutritional strategies¹. To a first approximation, biotrophic pathogens maintain their host alive to retrieve nutrients, while necrotrophic pathogens actively secret toxins and enzymes to kill host tissue and feed on the dead cells¹. Another group of pathogens, termed hemibiotrophs, begins their infection course with the biotrophic stage and shifts to the necrotrophic stage upon reaching a certain threshold of pathogen accumulation². In order to effectively defend themselves against these microorganisms, plants have evolved a complicated innate immune system equipped with multiple surveillance mechanisms to detect the pathogen attack and trigger localized programmed cell death³ as well as Systemic Acquired Resistance (SAR)⁴. Current research is focused on characterizing the essential signaling components and cross-talks within the plant immune system⁵.

As proposed in the “Zig-Zag” model⁵, the first layer of the plant innate immune response requires the presence of plasma membrane-localized Pattern Recognition Receptors (PRRs) to detect the invasion of a microbe. PRRs are able to recognize Microbe-Associated Molecular Patterns (MAMPs) and establish MAMP-Triggered Immunity (MTI)⁶. Besides inducing a transcriptional upregulation of genes encoding antimicrobial PR proteins⁷, MTI leads to a variety of events that arrest pathogen growth, including the production of Reactive Oxygen Species (ROS) and Reactive Nitrogen Species (RNS), deposition of callose to the cell wall as well as the activation of multiple kinase signaling pathways⁸.

Until now, several MAMPs have been identified to trigger MTI in Arabidopsis, including bacterial flg22⁹ (a 22 amino acid fragment derived from flagellin), elf18¹⁰ (18 amino acids from the bacterial translation elongation factor Tu) and a structural cell wall component peptidoglycans¹¹. To establish a successful infection, some specialized pathogens have evolved the ability to secret virulence effector proteins into the intracellular or intercellular spaces, and consequently repress MTI and trigger Effector-Triggered Susceptibility (ETS)^12,13. For instance, virulence effectors can inactivate Mitogen-Activated Protein Kinase (MAPK) phosphorylation cascades of MTI to induce the disease development within the infected tissue^14-16. During the dynamic co-evolution between hosts and pathogens, plants also developed the counterattack strategy to recognize the effector proteins and attenuate the pathogen virulence molecules¹⁷. This direct or indirect effector recognition is mediated by disease resistance (R) proteins¹⁸. Most of them are members of NB-LRR (Nucleotide Binding and Leucine-Rich Repeats) family¹⁹. The perception of an avirulent effector by an R protein elicits a stronger and broader immune response characterized as Effector-Triggered Immunity (ETI)²⁰. Besides inducing the expression of defense genes²¹ and the production of defense metabolites²², ETI often leads to a rapid localized programmed cell death known as Hypersensitive Response (HR) to restrict the pathogen from spreading into the adjacent tissue³.

In addition to the localized programmed cell death²³, plants are capable of initiating a long-term and system-wide immune response termed Systemic Acquired Resistance (SAR)⁴. Upon challenge with a biotrophic pathogen, plant cells trigger the biosynthesis and accumulation of an endogenous phytohormone salicylic acid (SA) and PR proteins in both local and systemic tissues²⁴. Through this process, a heightened state of preparedness is achieved in the uninfected leaves that allows for mounting faster defense responses during a subsequent infection by a broad spectrum of pathogens²⁴. SA and its synthetic analogs such as benzo-(1,2,3)-thiadiazole-7-carbothioic acid S-methyl ester (BTH) and 2,6-dichloroisonicotinic acid (INA) are capable of chemically inducing Salicylic Acid (SA)-Triggered Immunity (STI) upon external application²⁴. Nonexpressor of Pathogenesis-Related genes 1 (NPR1) is proposed to be one of the SA receptors and functions as a major transcriptional regulator during SA-mediated defense response in both local and systemic tissues^21,25,26. It has been conclusively demonstrated that NPR1 is required for SAR establishment and the loss of NPR1 leads to dramatic susceptibility towards Pseudomonas syringae²⁵.

To extensively characterize the molecular contribution of plant components in the plant-pathogen interactions, multiple bioassays have been developed to measure specific defense events, including ROS burst²⁷, callose deposition²⁸, defense genes expression and accumulation of their protein products²¹. While these individual assays can provide insights into a specific form of the plant immune response, none of them, however, are able to represent the complete defense response on the whole plant level. Conversely, quantification of pathogen growth after infection provides an overall estimation of immune response at the organismal level. Therefore, the development and optimization of a precise and highly standardized pathogen inoculation assay is critical to fuel up the research and discoveries on the Arabidopsis immune responses.

Pseudomonas syringae, a Gram-negative bacterium, was identified as a phytopathogen capable of causing disease in a range of plant hosts including Arabidopsis²⁹. As the model plant-pathogen system, the Arabidopsis - P. syringae interaction has been widely applied to understand the molecular mechanisms underlying plant defense responses²⁹. Until now, over 50 P. syringae pathovars have been identified based on their ability to infect different plant species³⁰ . P. syringae pv. tomato DC3000(Pst DC3000)³¹and P. syringae pv. maculicola ES4326 (Psm ES4326)³² are the two most widely used and extensively characterized virulent strains. Aside from being recognized by the plant and triggering the MTI response, Pst DC3000 and Psm ES4326 are capable of secreting virulent effector proteins to suppress MTI and trigger ETS to favor the pathogen growth^31,33.

To functionally dissect the interaction between Arabidopsis and P. syringae, multiple pathogen infection methods have been developed based on the pathogen delivery approach. For soil-grown plants, pathogen can be delivered by syringe infiltration, vacuum infiltration, dip inoculation and spray inoculation^29,34. Recently, seedling flood-inoculation assay was developed to perform large-scale screens on tissue culture plates-grown young Arabidopsis plants³⁵. Syringe infiltration, as one of the most commonly used approach, manually delivers the pathogen into the apoplast through the natural leaf openings termed stomata²⁹. Through this approach, equal amounts of P. syringae can be infiltrated into the infected leaf and the strength of plant immune response is inversely correlated to the pathogen growth levels. Therefore, quantification of pathogen growth serves as an optimal approach to evaluate the immune function at the whole plant level. In addition, syringe infiltration can distinguish the local and systemic tissue, which can be applicable in characterizing the molecular mechanisms underlying SAR³⁶.

In the following protocol, we describe an optimized syringe infiltration assay with Psm ES4326 to screen Arabidopsis mutants for enhanced disease susceptibility (EDS). This protocol will employ two Arabidopsis genotypes: a wild-type ecotype Columbia-0 (Col-0) plants (control) and npr1-1 loss-of-function mutants (hypersusceptible) that will be infected with virulent bacterial strain Psm ES4326³⁷. The npr1-1 mutant carries a point mutation within the ankyrin-repeat consensus sequence of the NPR1 molecule, which alters the highly conserved histidine to tyrosine and renders the protein non-functional²⁵. In addition, a number of modifications of the syringe infiltration assay are described that allow quantification of defects in the specific layers of immune response, including MTI and STI.

Protocol

The following text describes a stepwise protocol to perform optimized Psm ES4326 syringe infiltration assay in Arabidopsis. Major procedures of this assay are represented in a simplified flowchart (Figure 1).

1. Plant Growth Conditions

1. Sow seeds
   1. Prepare 2 pots (4 in diameter, 3.75 in tall) loosely filled with soil and water pots by soaking them from the bottom O/N before draining the excess water.
   2. Sow 50-100 Arabidopsis seeds, wild-type Col-0 or npr1-1 mutant, on each pot with a folded 70 mm weighing sheet or other paper.
   3. Cover the pot with a water-sprayed transparent dome to increase the relative humidity to 80-90% (Figure 2A).
2. Incubate the pot at 4 °C for 72 hr to allow for complete stratification and synchronous germination.
3. Transfer the pot to the standard growth conditions (12 hr light/12 hr dark, 21 °C, light intensity 100 µmol/m²/sec, relative humidity 40%) to allow the seed to germinate. Crack the dome to generate a 2-3 in opening immediately after transfer to the growth room, which will help avoid water condensation.
4. When the first true leaf reaches the size of 2-3 mm in length, transplant the seedlings from the pot to a 72-wells flat filled with soil.
   1. Use a finger or a 1 ml pipette tip to create a 1-in deep depression in the middle of the soil surface on the flat.
   2. Gently separate individual seedlings with as little root damage as possible. Carefully pick up seedlings that have intact roots with forceps.
   3. Place a single separated seedling together with the adhering soil clump to minimize transplantation shock into the depression and gently pat down the surrounding soil to fill the depression. Discard the extra seedlings and soil into biohazard waste container and dispose in accordance with the local biohazard waste disposal guidelines.
   4. Water transferred seedlings from the top and completely cover the flat with a water-sprayed transparent dome to maintain 80-90% humidity. Keep the dome on for 3 days, then crack the dome in the morning of day 4 and completely remove it by the end of that day.
      Note: Sowing seeds can be alternatively performed by stratifying seeds in 1.5 ml centrifuge tubes containing 1 ml 0.1% agar for 48 hr at 4 °C followed by transferring 2-3 seeds with a glass pipette onto a 72-wells flat filled with soil. Flats need to be covered with a transparent dome that can be removed one week after the germination. Extra seedlings can be removed to leave only one seedling per well.
5. Water plants every two days by soaking flats in 1-in water for 20 min, then drain the excess water.
   Note: The time interval for watering plants depends on the growth room humidity and needs to be determined based on continuous observation of user’s plant growth facility. Check plants daily to make sure they are well watered. If only few spots are drying, water those plants from the top with a squirt bottle.
6. Perform pathogen infection assays (Step 3-5) on plants that are at or near developmental stage # 3.50 (when rosette size is 50% final size), which corresponds to 3-5 weeks old depending on growth conditions (photoperiod, temperature). Do not infect plants after inflorescence emergence (stage # 5) due to onset of age-related resistance^38,39.

2. Preparation of Culture Media and Plates

1. Make 1 L of King’s B (KB) liquid medium. Gently stir 20 g proteose peptone and 2 g potassium phosphate dibasic trihydrate using a magnetic stir bar with 1,000 ml deionized H₂O until there is no visible pellet. Aliquot 100 ml into 150 ml glass bottles and autoclave on a 20-min liquid cycle.
2. Prepare culture plates with KB solid medium.
   1. Gently stir 20 g Proteose Peptone, 2 g Potassium Phosphate Dibasic Trihydrate and 15 g Agar with 1,000 ml deionized H₂O. Autoclave.
   2. Cool down the medium on a magnetic stir plate until it is cool to touch to minimize future condensation and avoid degradation of antibiotics. Add 18 ml sterile 80% Glycerol and 5 ml sterile 1 M MgSO₄ to the medium. Given that Psm ES4326 carries resistance against streptomycin, add streptomycin into the cooled media to a final concentration of 50 µg ml⁻¹.
   3. Pour the plates. Prepare two different sizes of KB media plates: 100 mm x 15 mm and 150 mm x 15 mm Petri dishes. The smaller Petri dish containing medium serves as the primary bacteria culture plate, and the larger Petri dish serves as bacteria counting plate.
      Note: For the bacteria counting plates, rectangular-shaped plates can be used to reduce the consumables cost since twice as many treatments can be plotted per plate compared to traditional round plates.
      1. Pour the plates prior to the infection experiment. Store KB medium plates at 4 °C for up to 2-3 months since streptomycin sulfate gradually loses the antibiotic activity⁴⁰.

3. Enhanced Disease Susceptibility (EDS)

1. Day 1 - Streak bacteria on plate
   1. Two days before the EDS assay, streak Psm ES4326 from -80 °C glycerol stock on a KB-Strep bacterial culture plate and incubate at 28 °C for 24-48 hr.
2. Day 2 - initiate liquid culture and water plants
   1. Initiate the liquid culture in a sterile test tube with 4 ml liquid KB medium containing 50 µg ml⁻¹ streptomycin and shake at 250 rpm, 28 °C O/N.
      Note: For EDS infection assay, using 6 plants per genotype is recommended. For STI and MTI assays, 6 plants per genotype per treatment are recommended. For the bacteria inoculum, it is recommended to use a fresh liquid culture with optical density at λ_600nm between 0.3 and 0.6.
   2. Mark the petioles of leaves number 5 and 6 with a blunt-end waterproof marker for easy identification of infected tissue at sampling (Figure 1). To enhance the opening of stomata and facilitate the entrance of pathogen solution into the leaf, water the plants well by soaking the flat from the bottom for 20 min, then drain the excess water.
      Note: Alternatively, cover the flat with a transparent dome and soak it in water for 2-4 hr to increase the stomatal opening.
   3. Day 3 - Pathogen dilution and syringe infiltration
      Note: Pathogen infection during morning hours is optimal for pathogen proliferation and development of the most pronounced disease symptoms on susceptible genotypes. Make every effort to keep the infection timing consistent to eliminate the effect of circadian rhythms and diurnal gene regulation^41,42, which helps reduce the variation among experimental replications.
      1. Pellet the bacterial culture in a microcentrifuge 1.5 ml tube at 9,600 x g for 2 min at RT and discard the supernatant. Resuspend the bacterial pellet with 1 ml of sterile 10 mM MgCl₂.
         Note: Magnesium cations can enhance the motility and adhesion of P. syringae⁴³. Alternatively, use MgSO₄ at the same concentration. Sterile water is an acceptable substitute for the Mg salt solutions.
      2. Dilute the bacteria suspension with 9 ml of 10 mM MgCl₂ in a 50 ml centrifuge tube and measure the optical density (OD) of bacteria with a spectrophotometer at λ=600 nm. Dilute the bacteria with 10 mM MgCl₂ to the final OD_600nm=0.0002 for EDS infection assay.
      3. Infiltrate the leaf with a 1 ml blunt end needleless syringe (commonly known as the insulin syringe) that contains the diluted bacterial solution.
      4. Do not fill the syringe up to its full capacity. Fill it up with 0.5-0.6 ml to allow for a much better control during the infiltration process.
      5. Expose the lower surface of the leaf on the top of index finger, and then gently adjust the leaf position with the help of thumb. Position the syringe vertically against the leaf surface to ensure that pressure is evenly distributed. Try to avoid the midrib area during the infiltration to reduce leaf damage.
      6. Slowly push the plunger to infiltrate the bacterial solution; liquid entry into the leaf mesophyll will be visualized as indicated by the darker leaf color. Attempt to infiltrate the entire surface of the leaf. If this is not accomplished in a single attempt, choose another infiltration spot and repeat the actions described above until the entire leaf surface is covered.
      7. Once completed, gently blot the leaf with absorbent tissue to remove the extra pathogen solution. Visually inspect the infected leaf tissue for damage.
         Note: The circular syringe impression should not be visible after the infiltration is complete.
      8. Leave the infiltrated plants to dry for 1-2 hr before returning them into their original growth conditions. Next, spray a clear dome with water and cover the infected plants for 2 hr, then crack the dome to generate a 2-3 in opening and leave it on throughout the remainder of the infection experiment.
         Note: Since P. syringae is not an airborne pathogen, there is no risk of spreading the infectious agent to other plants grown in the same facility. However, as an added precaution, avoid physical contact between infected plants and other experimental plants located nearby. Covering the flat with a transparent dome will increase the pathogen virulence and accelerate disease progression. The need for this step and optimal duration of the covering period needs to be determined based on the humidity conditions of the user’s plant growth facility.
   4. Day 5 - Pre-dry the media plates
      1. Take the 150 mm x 15 mm KB plates out of the cold storage unit and dry any pre-existing water condensation on the plate. Dry plates by keeping them at RT for roughly 24 hr. To speed up this process, place them in a laminar flow hood with their lids cracked for 30-60 min.
         Note: This step is critical for the formation of circular droplet on the surface of the plate in the next step.
   5. Day 6 - Quantifying the pathogen growth
      Note: The following pathogen quantification procedure may be performed at earlier time points after the infection to confirm equal amounts of bacteria are delivered into the leaf, especially when plants have altered leaf morphology.
      1. Process the infected tissue after the emergence of chlorosis indicated by the yellowing of the infected tissue in the susceptible genotypes, but before the development of necrotic lesions (Figure 2B).
         Note: Suggested sampling time is three days after the pathogen inoculation. However, since pathogen growth depends on a number of environmental factors, the length of incubation may vary within a range of 2 ½-3 ½ days and needs to be determined by careful observations of the infection progression in user’s plant growth facility.
         1. Prepare 6 grinding tubes for each genotype (Figure 1). Place one stainless steel grinding ball and add 500 µl sterile 10 mM MgCl₂ into the each tube.
         2. Detach the infected leaf from the plant and punch a leaf disc with a 1-hole paper punch (Figure 1).
            Note: To minimize the sampling error, try to punch each sampled leaf at the same position. Sampling of the leaf disc from the top of the leaf is recommended.
         3. Randomly place 2 leaf discs (from two different plants) into each grinding tube using forceps.
         4. Seal the tube and homogenize the tissue with a high-throughput homogenizer at maximum speed (1,600 strokes per minute) for 10 min. Repeat this process if needed until tissue is well homogenized and the solutions turn green due to chlorophyll release from the infected leaves.
      2. While waiting for the homogenization, fill the first 6 rows of a 96-well culture plate with 180 µl 10 mM MgCl₂ using a multi-channel pipette and a pipetting reservoir.
      3. After grinding, transfer 20 µl of ground tissue suspension into the first row of the 96-well plate and mix by repeated pipetting the liquid up and down. If small fragments of tissue clog the tip, clip it by 2-3 mm to help acquire the correct volume of the solution.
         1. To provide enough space for the droplet on the top of the plate, space the tissue from different genotypes in alternative rows (Figure 1). To prepare a ten-fold serial dilution, transfer 20 µl liquid into the second row and repeat this procedure until the sixth dilution.
      4. Transfer 20 µl of the solution from the 96-well plate onto the 150 mm x 15 mm KB plate using divided pipette tips (Figure 1). Work from the most dilute suspension to the most concentrated.
         Note: Proceeding from most diluted to most concentrated makes it unnecessary to change pipette tips between the dilutions. If the plate is well pre-dried, the transferred droplet should stay intact on the top of the medium until absorbed (usually 15-30 min). Drying time varies with the RT and humidity.
      5. Dry the plate at RT with lid cracked. Once no more liquid can be observed on the plate surface, close the lid, invert and incubate the plate at RT or a 28 °C incubator.
      6. Incubate plates for 40-60 hr until the colonies become visible. Confirm that the growth on the plates reflects the predictable 10-fold drop in colony forming units (cfu) (Figure 2C). Count the bacteria before they overgrow and colonies fuse. Determine the number of bacteria in the lowest dilution that does not have overlapping colonies. Usually, the preferred dilution to be counted will contain between 10-50 colonies.
         Note: Variation may be present among technical replicates; therefore, the lowest dilution for each replicate should be determined separately.
      7. To calculate the levels of bacterial proliferation, document the number of the row (R) as well as the number of the bacteria within each technical replicate (T) in writing. Determine the number of colony forming unit – cfu/leaf disc through the formula: cfu/leaf disc = (T × 10^R / 20) × 500 / 2
      8. Type the data in the following spreadsheet template to produce a graph (Figure 1) (for spreadsheet data analysis template file, see Table 2). Each data point is represented as the mean of six technical replicates on a logarithmic scale. Error bars represent 95% confidence interval of the mean (n = 6).
         Note: The calculation of 95% confidence intervals needs to be adjusted based on the number of technical replicates.

4. SA-Triggered Immunity (STI)

1. Day 1: Follow the same procedure as described in step 3.1.
2. Day 2: In addition to watering the plants and initiating the liquid bacterial culture (Step 3.2), induce resistance by external application of SA derivative Sodium Salicylate²¹.
   Note: Pure SA has poor water solubility and requires prior pH adjusting, thus it’s not recommended for this assay.
   1. To induce SA-mediated defenses against P. syringae and prime the plants for future infection^21,24, spray plants with a fine mist of 1 mM Sodium Salicylate or H₂O (as mock) 16-24 h before the pathogen infection.
3. Day 3: Prepare pathogen dilution to OD_600nm=0.001 and push the bacteria into the entire leaf surface by syringe infiltration (Step 3.3).
4. Day 6: For pathogen quantification and counting process, follow the procedure as described for the EDS assay (Steps 3.4 and 3.5). Plate and count the H₂O and Sodium Salicylate – pretreated samples separately. For wild-type Arabidopsis, a 1-2 log reduction in pathogen growth is expected in the Sodium Salicylate – pretreated plants.

5. MAMP-Triggered Immunity (MTI)

Note: In this assay, we use Arabidopsis wild-type Col-0 and mutant fls2 and efr plants. FLS2 and EFR are plasma membrane-localized Pattern Recognition Receptors (PRRs) that can recognize flg22 and elf18, respectively^9,10. Loss of each PRR results in the insensitivity to the specific type of MAMP, which is indicated by the unaltered pathogen growth in the mutant following external MAMP pre-treatment and syringe infiltration with Psm ES4326.

1. Day 1 and 2: Follow the same procedure as described in Step 3.1 and 3.2.
2. Day 3: MAMP pre-treatment and Pathogen infection
   1. To establish the MAMP-Triggered Immunity, prepare 1 µM solution of flagellin epitope flg22 or EF-Tu epitope elf18 and syringe-infiltrate it into the entire leaf surface 4 h before the pathogen infection (Steps 3.3.3-3.3.6). This will allow for induction of MAMP-mediated defenses against P. syringae and prime the plants for future infection^6,37.
      Note: Publicly available microarray data revealed the maximum transcriptional reprogramming of MAMP-responsive genes happens 4 h after flg22 or elf18 treatment^37,44. Thus, 4 hr is the recommended duration of the MAMP pre-treatment that results in achieving a clear difference in the pathogen growth between MAMP-treated Col-0 and fls2 and efr mutants.
   2. Remove the extra MAMP solution with absorbent tissue and leave the plants uncovered to speed the liquid absorption process within the leaf. To account for the wounding effect from syringe pressure infiltration, infiltrate H₂O into the leaves of control plants.
   3. Prepare pathogen dilution to OD_600nm=0.001 and push the bacteria into the entire leaf surface of MAMP/H₂O pre-treated leaf by syringe infiltration (Step 3.3).
3. Day 6: For pathogen quantification and counting process, follow the procedure as described in Step 3.4 and 3.5. Plate and count the H₂O and MAMP–pretreated samples separately. In wild-type Arabidopsis, a 1-2 log reduction in pathogen growth is expected in the MAMP–pretreated plants, with somewhat stronger reduction mediated by flg22 compared to elf18.

Results

The protocol we describe here represents an optimized P. syringae syringe infiltration assay to quantitatively evaluate the immune response in Arabidopsis plants. As illustrated in Figure 1, the syringe infiltration of Psm ES4326 is followed by pathogen extraction and quantification via serial dilutions and colonies enumeration.

As described in Step 3 within the protocol text, Enhanced Disease Susceptibility (EDS) against Psm ES4326 can be a...

Discussion

With decreasing available farmland and increasing population, researchers around the world are challenged with pressing needs for crop improvement. The yield can be greatly influenced by various biotic and abiotic stresses. Among them, pathogen infection is one of the leading causes of crop yield reduction, responsible for approximately 12% losses in the U.S. alone⁴⁵. To resolve this issue, massive research has been conducted in the model Arabidopsis - P. syringae pathosystem to comprehensively charac...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
MetroMix 360	Grosouth	SNGMM360
Large pots	Grosouth	TEKUVCC10TC
12 x 6 Inserts	Grosouth	LM1206
11x 21 Flats with no holes	Grosouth	LM1020
11x 21 Flats with holes	Grosouth	LM1020H
Vinyl propagation domes	Grosouth	CW-221
Proteose Peptone	Fisher Scientific	DF0122-17-4
Potassium Phosphate Dibasic Trihydrate	MP Biomedicals	151946
Agar	Fisher Scientific	A360-500
Streptomycin sulfate	Bio Basic Inc	SB0494
100 x 15 mm Petri dishes	Fisher Scientific	FB0875713
150 x 15 mm Petri dishes	Fisher Scientific	R80150
Rectangular plate	Fisher Scientific	12-565-450
MgCl2 Hexahydrate	Bio Basic Inc	MB0328
Glycerol	Bio Basic Inc	GB0232
MgSO4	Bio Basic Inc	MN1988
1 ml syringe	Fisher Scientific	NC9992493
Kimwipe	Fisher Scientific	06-666-A
Grinding tubes	Denville Scientific	B1257
Caps for grinding tubes	Denville Scientific	B1254
Stainless steel grinding ball	Fisher Scientific	2150
96-well plate	Fisher Scientific	12-556-008
Sodium Salicylate	Sigma Aldrich	s3007-1kg
flg22 (QRLSTGSRINSAKDDAAGLQIA)	Genescript	Made to order
elf18 (Ac-SKEKFERTKPHVNVGTIG)	Genescript	Made to order
Hole puncher	Staples	146308
Biophotometer plus	Eppendorf	952000006
PowerGen High-Throughput Homogenizer	Fisher Scientific	02-215-503
Accu spin micro centrifuge	Fisher Scientific	13-100-675
Multichannel pipette (10-100 µl)	Eppendorf	3122 000.043
Multichannel pipette (30-300 µl)	Eppendorf	3122 000.060
Pipette (20µl)	Eppendorf	3120 000.038
Pipette tips	Fisher Scientific	3552-HR
Sharpie permanent marker	Staples	507130
1.5 ml tube	Eppendorf	22363204
Forceps	Fisher Scientific	08-890