Direct Observation and Automated Measurement of Stomatal Responses to Pseudomonas syringae pv. tomato DC3000 in Arabidopsis thaliana

Summary

Here, we present a simple method for direct observation and automated measurement of stomatal responses to bacterial invasion in Arabidopsis thaliana. This method leverages a portable stomatal imaging device, together with an image analysis pipeline designed for leaf images captured by the device.

Abstract

Stomata are microscopic pores found in the plant leaf epidermis. Regulation of stomatal aperture is pivotal not only for balancing carbon dioxide uptake for photosynthesis and transpirational water loss but also for restricting bacterial invasion. While plants close stomata upon recognition of microbes, pathogenic bacteria, such as Pseudomonas syringae pv. tomato DC3000 (Pto), reopen the closed stomata to gain access into the leaf interior. In conventional assays for assessing stomatal responses to bacterial invasion, leaf epidermal peels, leaf discs, or detached leaves are floated on bacterial suspension, and then stomata are observed under a microscope followed by manual measurement of stomatal aperture. However, these assays are cumbersome and may not reflect stomatal responses to natural bacterial invasion in a leaf attached to the plant. Recently, a portable imaging device was developed that can observe stomata by pinching a leaf without detaching it from the plant, together with a deep learning-based image analysis pipeline designed to automatically measure stomatal aperture from leaf images captured by the device. Here, building on these technical advances, a new method to assess stomatal responses to bacterial invasion in Arabidopsis thaliana is introduced. This method consists of three simple steps: spray inoculation of Pto mimicking natural infection processes, direct observation of stomata on a leaf of the Pto-inoculated plant using the portable imaging device, and automated measurement of stomatal aperture by the image analysis pipeline. This method was successfully used to demonstrate stomatal closure and reopening during Pto invasion under conditions that closely mimic the natural plant-bacteria interaction.

Introduction

Stomata are microscopic pores surrounded by a pair of guard cells on the surface of leaves and other aerial parts of plants. Under ever-changing environments, regulation of the stomatal aperture is central for plants to control the carbon dioxide uptake required for photosynthesis at the expense of water loss via transpiration. Thus, quantification of the stomatal aperture has been instrumental to understanding plant environmental adaptation. However, quantifying the stomatal aperture is inherently time-consuming and cumbersome as it requires human labor to spot and measure stomatal pores in a leaf image captured by a microscope. To circumvent these limitations, various methods have been developed to facilitate the quantification of stomatal aperture in Arabidopsis thaliana, a model plant extensively used to study stomatal biology^1,2,3,4,5,6. For instance, a porometer can be used to measure transpiration rate as a metric of stomatal conductance. However, this method does not provide direct information on the stomatal number and aperture that determine stomatal conductance. Some studies have used confocal microscopy techniques highlighting stomatal pores using a fluorescent actin marker, a fluorescent dye, or cell wall autofluorescence^1,2,3,4,5. While these approaches facilitate the detection of stomata, the cost of both operating a confocal microscopy facility and preparing microscopy samples can be an obstacle to routine application. In a ground-breaking work by Sai et al., a deep neural network model was developed to automatically measure stomatal aperture from bright-field microscopic images of A. thaliana epidermal peels⁶. Yet, this innovation does not exempt researchers from the task of preparing an epidermal peel for microscopic observation. Recently, this obstacle was overcome by developing a portable imaging device that can observe stomata by pinching a leaf of A. thaliana, together with a deep learning-based image analysis pipeline that automatically measures stomatal aperture from leaf images captured by the device⁷.

Stomata contribute to plant innate immunity against bacterial pathogens. The key to this immune response is stomatal closure that restricts bacterial entry through the microscopic pore into the leaf interior, where bacterial pathogens proliferate and cause diseases⁸. Stomatal closure is induced upon recognition of microbe-associated molecular patterns (MAMPs), immunogenic molecules that are often common to a class of microbes, by plasma membrane-localized pattern recognition receptors (PRRs)⁹. A 22 amino acid epitope of bacterial flagellin known as flg22 is a typical MAMP that induces stomatal closure through its recognition by the PRR FLS2¹⁰. As a countermeasure, bacterial pathogens such as Pseudomonas syringae pv. tomato DC3000 (Pto) and Xanthomonas campestris pv. vesicatoria have evolved virulence mechanisms to reopen stomata^9,11,12. These stomatal responses to bacterial pathogens have been conventionally analyzed in assays in which either leaf epidermal peels, leaf discs, or detached leaves are floated on bacterial suspension, and then stomata are observed under a microscope followed by manual measurement of stomatal aperture. However, these assays are cumbersome and may not reflect stomatal responses to natural bacterial invasion that occur in a leaf attached to the plant.

Here, a simple method is presented to investigate stomatal closure and reopening during Pto invasion under the condition that closely mimics the natural plant-bacteria interaction. This method leverages the portable imaging device for direct observation of A. thaliana stomata on a leaf attached to the plant inoculated with Pto, together with the image analysis pipeline for automated measurement of stomatal aperture.

Protocol

1. Growing plants

1. To break dormancy, resuspend A. thaliana (Col-0) seeds in deionized water and incubate them at 4 °C for 4 days in the dark.
2. Sow the seeds on the soil and grow in a chamber equipped with white fluorescent light. Maintain the following growth conditions: temperature of 22 °C, light intensity of 6,000 lux (ca. 100 µmol/m²/s) for 10 h, and relative humidity of 60%.
3. When needed, water the plants with a liquid fertilizer. Refrain from watering from 1 week to 2 days prior to inoculation and water well 1 day prior to inoculation.

2. Preparing bacterial inoculum

1. Streak Pto from glycerol stock on solidified King's B (KB) medium (20 g of Tryptone, 1.5 g of K₂HPO_4, and 15 g of Glycerol for 1 L, 1.5% Agar) with 50 µg/mL rifampicin and incubate at 28 °C for 2 days.
2. Inoculate a single colony to 5 mL of KB liquid medium with 50 µg/mL rifampicin and incubate at 28 °C with shaking at 200 rpm until late logarithmic growth phase.
3. Centrifuge the culture at 6,000 x g for 2 min, discard the supernatant, and resuspend the pellet in 1 mL of sterile water. Repeat this step once again.
4. Remove the supernatant, resuspend the pellet in 1 mL of stomata opening buffer (25 mM MES-KOH pH 6.15, 10 mM KCl), and measure the OD₆₀₀.
5. Dilute the suspension to OD₆₀₀ 0.2 with stomata opening buffer containing 0.04% silicone surfactant.

3. Spray inoculation of bacteria

1. From 1 day before inoculation till the end of the experiment, expose plants to a light intensity of about 10,000 lux (ca. 170 µmol/m²/s).
2. To ensure that most stomata are open, keep plants on a tray covered with a transparent lid under the light for at least 3 h before spray inoculation.
3. Remove the lid and use an airbrush to spray the abaxial side of leaves with 2.5 mL of bacterial suspension per three plants on a single pot.
4. Incubate the inoculated plants on a tray covered with a transparent lid to maintain a relative humidity of around 85%.
5. Acquire images of stomata at 1 h and 3 h after spray inoculation using the method described in section 4.

4. Direct observation of stomata using the portable imaging device

NOTE: The portable stomatal imaging device is equipped with an LED light and a camera module and can acquire 2,592 × 1,944 (height × width; pixels) images with a resolution of about 0.5 µm/pixel.

1. Connect the portable stomatal imaging device to a personal computer (PC) equipped with image acquisition software.
2. Gently but completely remove water droplets from the inoculated leaves with a piece of paper.
3. Open the top cover of the device, place the leaf on the stage, and close the top cover (Figure 1).
4. Adjust the focus of the image by manipulating the adjuster screw, then click the Save Image button on the PC screen. The image will be acquired instantly. Typically, a focused image contains approximately 10 analyzable stomata. To obtain robust results, acquire stomatal images from six leaves of three different plants (two leaves per plant).

5. Manual measurement of stomatal aperture

NOTE: The ImageJ software can be downloaded at https://imagej.nih.gov/ij/download.html

1. Open an image file in the ImageJ.
2. Open the ROI manager by selecting Analyze > Tools > ROI Manager.
3. Use the Straight-Line selection tool to draw a line corresponding to the width of a stoma (Figure 2) and register the ROI by clicking Add in the ROI Manager.
4. Draw a line corresponding to the length of the same stoma (Figure 2A) and register the ROI as described in step 5.3.
5. Click Measure in the ROI Manager to measure the width and length.
6. Divide the width by the length to obtain the stomatal aperture (ratio). For robust quantification, use 60 or more stomata for each treatment and time point. Do not choose premature or obscure stomata for the analysis (Figure 2B, C).

6. Automated measurement of stomatal aperture

NOTE: The image analysis pipeline runs in Google Colaboratory, a cloud Python programming language executable environment. Users must have a valid Google account with a working Google Drive, Google Chrome browser, and a stable internet connection as a prerequisite.

1. Download the Google Colaboratory notebook from Zenodo (https://doi.org/10.5281/zenodo.8062528), and open the notebook.
2. Make a local copy of the notebook to Google Drive by selecting File > Save a copy in Drive. After a new tab appears, safely close the tab of the original notebook.
3. Press the Execute button once below the Environmental Setup section in the notebook without unfolding the cell blocks to import the required libraries.
4. Execute the Directory Settings section to create three folders used for analysis (e.g., example_result, inference_results, and model) in Google Drive.
   NOTE: In this case, the folders named example_result, inference_results, and model are used as the parental directory, storing inference results and trained models, respectively. This notebook shows an example of directory construction as a representative procedure. To change the name, rewrite the pardir, infdir, or modeldir path.
5. According to the Preparation of the Images section, move the acquired images to example_result, grouped in image titles by treatment or sample (e.g., mock_1h_XXXXXX.jpg) for the final graph generation. Sample images are available from Zenodo (https://doi.org/10.5281/zenodo.8062528).
6. Perform the Download Trained Models part to download the ONNX files of the trained models from Zenodo (https://doi.org/10.5281/zenodo.8062528) and place them under the model directory.
7. Run the Inference and Measurement of Stomatal Aperture part to quantify the stomatal aperture from individual images. The result images with overlaid inference and the csv file named example_result.csv will be exported to the inference_results directory.
8. Execute the Graph Generation section to create a graph about the stomatal aperture ratio, exported to the inference_results directory.

Results

Following spray inoculation of Pto, stomata on leaves attached to the inoculated plants were directly observed by the portable stomatal imaging device. Using manual and automated measurements, the same leaf images were used to calculate stomatal aperture by taking ratios of width to length of approximately 60 stomata. Manual and automated measurements consistently indicated a decrease in the stomatal aperture in Pto-inoculated plants compared with mock-inoculated plants at 1 hour post inoculation (hpi) ...

Discussion

Previous studies used epidermal peels, leaf discs, or detached leaves to investigate stomatal responses to bacterial invasions^9,11,12. In contrast, the method proposed in this study leverages the portable stomatal imaging device to directly observe stomata on a leaf attached to the plant after spray inoculation of Pto, mimicking natural conditions of bacterial invasion. In addition, because this method does not involve ...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Agar	Nakarai tesque	01028-85
Airbrush kits	ANEST IWATA	MX2900	Accessory kits for SPRINT JET
Biotron	Nippon Medical & Chemical Instruments	LPH-411S	Plant Growth Chamber with white fluorescent light
Glycerol	Wako	072-00626
Half tray	Sakata	72000113	A set of tray and lid
Hyponex	Hyponex	No catalogue number available	Dilute the solution of Hyponex at a ratio of 1:2000 in deionized water for watering plants
Image J	Natinal Institute of Health	Download at https://imagej.nih.gov/ij/download.html	Used for manual measurement of stomatal aperture
K2HPO4	Wako	164-04295
KCl	Wako	163-03545
KOH	Wako	168-21815	For MES-KOH
MES	Wako	343-01621	For MES-KOH
Portable stomatal imaging device	Phytometrics	Order at https://www.phytometrics.jp/	Takagi et al.(2023) doi: 10.1093/pcp/pcad018.
Rifampicin	Wako	185-01003	Dissolve in DMSO
Silwet-L77	Bio medical science	BMS-SL7755	silicone surfactant used in spray inoculation
SPRINT JET	ANEST IWATA	IS-800	Airbrush used for spray inoculation
SuperMix A	Sakata seed	72000083	Mix with Vermiculite G20 in equal proportions for preparing soil
Tryptone	Nakarai tesque	35640-95
Vermiculite G20	Nittai	No catalogue number available	Mix with Super Mix A in equal proportions for preparing soil
White fluorescent light	NEC	FHF32EX-N-HX-S	Used for Biotron