Combining Histochemical Staining and Image Analysis to Quantify Starch in the Ovary Primordia of Sweet Cherry during Winter Dormancy

Podsumowanie

We present a methodology to quantify the starch content in the ovary primordia in sweet cherry (Prunus avium L.) during winter dormancy by using an image analysis system combined with histochemical techniques.

Streszczenie

Changes in starch in small structures are associated with key events during several plant developmental processes, including the reproductive phase from pollination to fertilization and the onset of fruiting. However, variations in starch during flower differentiation are not completely known, mainly due to the difficulty of quantifying the starch content in the particularly small structures of the flower primordia. Here, we describe a method for the quantification of starch in the ovary primordia of sweet cherry (Prunus avium L.) by using an image analysis system attached to the microscope, which allows relating the changes in starch content with the different phases of dormancy from autumn to spring. For this purpose, the dormancy status of flower buds is determined by evaluating the bud growth of shoots transferred to controlled conditions at different moments in winter time. For the quantification of starch in the ovary primordia, flower buds are sequentially collected, fixed, embedded in paraffin wax, sectioned, and stained with I₂Kl (potassium iodide-iodine). Preparations are observed under the microscope and analyzed by an image analyzer that clearly distinguishes starch from the background. Starch content values are obtained by measuring the optical density of the image that corresponds to the stained starch, considering the sum of the optical density of each pixel as an estimation of the starch content of the frame studied.

Wprowadzenie

Temperate woody perennials adapt to the seasons by modulating their growth and development. While they develop during spring and summer, they stop growing during the autumn to go dormant in winter¹. Although dormancy allows them to survive at low winter temperatures, chilling is a prerequisite for a proper budburst in spring². The important implications of dormancy in temperate fruit production and forestry have led to diverse efforts to determine and predict the dormancy period³. In fruit tree species, empirical experiments transferring shoots to forcing conditions and statistical predictions based on data of flowering are current approaches to determine the date of the breaking of dormancy, which allows researchers to estimate the chilling requirements for each cultivar. However, how to determine the dormancy status based on biological processes remains unclear³.

Flowering in temperate fruit trees, such as sweet cherry (Prunus avium L.), occurs once a year and lasts about a fortnight. However, flowers start to differentiate and develop about 10 months earlier, during the previous summer⁴. Flower primordia stop growing during the autumn to remain dormant inside the buds during winter. In this period, each cultivar needs to accumulate a particular chilling requirement for proper flowering⁴. Despite the lack of phenological changes in the buds during winter, flower primordia are physiologically active during dormancy, and the accumulation of chilling temperatures has been recently associated with the dynamic of starch accumulation or decrease within the cells of the ovary primordium, offering a new approach for dormancy determination⁵. However, the small size and the location of the ovary primordium require a special methodology.

Starch is the major storage carbohydrate in woody plant species⁶. Thus, changes in starch have been related to the physiological activity of the flower tissues, which need carbohydrates to support their development^7,8. Different key events during the reproductive process are also related to variations in starch content in different floral structures, such as anther meiosis⁹, the growth of the pollen tubes through the style or ovule fertilization¹⁰. Histochemical techniques allow the detection of starch in each particular tissue of the flower primordia during dormancy. However, the difficulty remains in quantifying that starch to allow following its pattern of accumulation/decrease over time or comparing the starch content among tissues, cultivars, or years. This is due to the little amount of tissue available for the analytical techniques¹¹. As an alternative, image analysis linked to microscopy¹² allows the quantification of the starch in very small samples of plant tissue¹³.

Approaches combining microscopy and image analysis have been used to quantify the content of different components in plant tissues, such as callose¹⁴, microtubes¹⁵, or starch¹⁶, by measuring the size of the area dyed by specific stains. For starch, it can be easily detected using the potassium iodide-iodine (I₂KI) reaction¹⁷. This method is highly specific; I₂KI intercalates within the laminar structure of starch grains and forms a dark blue or reddish-brown color, depending on the amylose content of the starch¹⁸. Sections stained with I₂KI stain show adequate contrast between starch and the background tissue, allowing an unequivocal starch detection and the subsequent quantification by the image analysis system¹⁹. Although this dye is not stoichiometric, the accumulation of iodine is proportional to the length of the starch molecule, which can highly vary¹⁷. Thus, the size of the stained area expressed as the number of pixels may not reflect accurately the content of starch, since high differences in starch content could be found between fields with stained areas of similar size. As an alternative, the starch content may be evaluated by measuring the optical density of the stained granules on black and white images obtained from the microscope, as it has been reported in different tissues in apricot^8,13,19, avocado^10,20, and olive²¹.

Here, we describe a methodology that combines the experimental determination of dormancy status with the quantification of starch content in the ovary primordium tissue from autumn to spring in sweet cherry, offering a new tool for the understanding and prediction of dormancy based on the study of the biological mechanisms linked with dormancy.

Protokół

1. Dormancy Determination and Plant Material Collection

1. Sample the flower buds in the field. Dormancy studies are long-term experiments and require adult trees big enough to collect buds and shoots all winter without compromising the trees’ development during the next spring. Special orchard management could be required depending on the training system; thus, pruning may be less severe than for fruit production purposes.
   1. Each week, from the start of autumn until the onset of bud break, collect and weigh 10 flower buds.
   2. Fix the flower buds by placing them into a 10-mL glass tube with a cap and soak the samples in a fixative solution of ethanol/acetic acid (3:1) for at least 24 h at 4 °C. Then, discard the fixative and add 75% ethanol, generously ensuring that it covers the samples. The samples can be conserved in this solution at 4 °C until use.
      Note: Vacuum infiltration can be used to remove the air bubbles inside the bud and prevent them from floating. This facilitates the penetration of the fixative into the tissues but could damage the structure of the tissues. Try to avoid it if not necessary.
2. Sample the shoots in the field.
   1. Each week, from the start of autumn until the onset of bud break, take three shoots of 15 - 30 cm in length and 5 mm in diameter, containing at least 10 flower buds each. Place them on water-soaked florist foam in a growth chamber at 22 ± 1 °C with a 12 h light photoperiod.
   2. After 10 days in the growth chamber, pick and weigh 10 flower buds from the shoots.
3. Evaluate the bud growth and determine the dormancy status. The sampling period has to be adjusted to the conditions of the location. In the orchard conditions (Zaragoza, Spain, 41°44’30” N, 0°47’00” W, and 220 m above sea level), the sampling of the shoots was carried out from November 30 until the end of February or the beginning of March.
   1. Weekly evaluate the response of the flower buds to the suitable growth conditions of the chamber, from the beginning of autumn until budburst in the spring, by comparing the weight of the 10 buds picked from the field.
   2. If there are no differences or those differences are less than 30%, consider that the buds have not fulfilled their chilling requirements and are endodormant²². If the differences are more than 30%, consider that the buds have fulfilled their chilling requirements and are ecodormant²².

2. Plant Material Preparation for Starch Quantification

1. Select about six fixed buds from each sampling date (see step 1.1). Depending on cultivars, each sweet cherry flower bud contains up to five flower primordia.
   1. Remove the external bud scales and place the bud on a watchmaker’s glass with 75% ethanol to prevent it from drying out.
   2. Dissect the bud and extract at least one flower primordium per bud with the help of precision forceps and an ophthalmologic scalpel under a stereoscopic microscope. The flower primordium can be conserved in a 10-mL glass tube with 75% ethanol at 4 °C, or proceed immediately to the next step.
2. Dehydrate the samples in a tertiary butyl alcohol series.
   1. Replace the 75% ethanol solution with 10 mL of 75% tertiary butyl alcohol (TBA) to generously cover the samples and incubate them for 1.5 h. A Pasteur pipette can be useful to discard the solution.
   2. Repeat step 2.2.1, adding TBA with rising concentrations (85%, 95%, and 100%, v/v; and 3x with pure TBA) in a drying stove at 30 °C with air extraction, since pure TBA crystalizes at room temperature (< 20 °C) and is very volatile and toxic. If TBA crystalizes with the sample, it would damage the tissues.
3. Embed the samples in paraffin¹⁸.
   1. Melt the paraffin by introducing the paraffin pearls in the drying stove at 60 °C with air extraction the previous day. The paraffin pearls can be also melted on a hotplate, but ensure that the liquid paraffin is at 60 °C and not at a higher temperature, to avoid tissue damage.
   2. Replace the TBA with a mix of TBA and paraffin oil (1:1) and incubate for 24 h inside a drying stove at 60 °C. Then, replace the mix of TBA and paraffin oil with pure melt paraffin and incubate for at least 6 h inside a drying stove at 60 °C. Repeat it 2x and incubate the last change for at least 4 - 6 d.
   3. Place each sample on a small metal base mold over a heat surface, embedded in paraffin wax, and pace the embedding cassette. Place it over a cold surface and remove the block once the wax is solidified.
4. Section and rehydrate the preparations.
   1. Prepare Haupt’s adhesive: dissolve 1 g of plain Knox gelatin in 100 mL of distilled water at 30 °C; then, add 2 g of phenol loose crystals (C₆H₅OH) and 15 mL of glycerol. Spread the Haupt’s adhesive over a glass slide with a brush and add a drop of a 1% formaldehyde solution.
   2. Section each paraffin block at 10 µm in a rotatory microtome and place the sections onto the glass slide covered with Haupt’s adhesive.
   3. Place the glass slides with the sections over a heat surface at 35 - 40 °C until dry; then, move the glass slides to a slide rack.
   4. Prepare the dewax and rehydration solutions. Place 200 mL of Histoclear II in three glass-staining dishes, another one with Histoclear II:ethanol (1:1, v/v), an ethanol series (100%, 70%, 40%, v/v), and a final distilled-water wash.
   5. Dewax the sections with three washes, each 5 min, in Histoclear II and in Histoclear II:ethanol (1:1, v/v). Place the slide rack inside the glass-staining dishes, ensuring that the solution completely covers the slides, and, then, move the slide rack from one solution to the next.
   6. Rehydrate the sections by the following series of 2-min washes: an ethanol series (100%, 70%, 40%, v/v) and a final distilled-water wash. Finally, dry the glass slides at room temperature.
5. Stain the sections¹⁸.
   1. Prepare I₂KI stain: dissolve 2 g of potassium iodide (KI) and 0.2 g of iodine (I₂) in 100 mL of distilled water. Apply a drop of fresh I₂KI over the section(s) for 5 min and, then, discard the excess of stain by absorbing it with a blotting paper. Quickly proceed to the next step.
   2. Apply a small drop of a synthetic mounting media, place a small cover glass on top, and press hard. Once the mounting media dries, observe under a bright-field microscope for a preliminary evaluation of the ovary starch.
      Note: This step is not mandatory, although a better contrast between the starch and the background is obtained. If the section has to be reused with other stains after starch quantification, place the cover glass over the drop of stain and discard the excess by absorbing it with a blotting paper (see 2.5.1). Then, after starch quantification, wash out the I₂KI stain with distilled water and place the preparations over a heat surface at 35 - 40 °C until dry.

3. Quantification of the Starch Content

1. Calibrate the optical conditions.
   Note: The detection levels used by the image analyzer to detect the stained starch are directly dependent on light conditions and magnification of the microscope; thus, fix these conditions for all the preparations evaluated. Adapt the adjustment proposed here to the available microscope and light conditions.
   1. Adjust the aperture diaphragm at the 20X magnification and the brightness control or light intensity.
   2. Make sure that there are no filters on the filter holder, and select a bright-field condition in the microscope. Select a suitable magnification (e.g., 40X for sweet cherry ovary primordium).
2. Control the image acquisition conditions. Adjust the camera settings with a stained preparation without tissue via Image | Acquisition | Pre-view.
   1. Fix the brightness at 50%, the gain at 1.0x, and the histogram indicators the gamma value at 1.00 and the contrast at 0 - 100, lining up with the limits of the brightness distribution histogram.
   2. Activate the overexposure/underexposure function and adjust the exposure time at the limit of overexposure.
   3. Apply the white balance function to the complete image to display all neutral-colored components of the image without any color tone and the shading correction to the complete image to create a corrected and homogeneous image.
3. Calibrate the Image Analysis System to obtain the control values of the grey level (0, black; 255, white) of different optical densities (OD) that are obtained by the transmittance (T) values.
   1. Acquire an image of a stained preparation without tissue, considered control white, and measure the grey level of the black and white image via Measure | Grey measure | Calibrate grey | Reference value = 0 | Measure | Calibrate | OK. This corresponds with a 100% transmittance; thus, an optical density of 0, according to OD = 2 - log T.
   2. Acquire an image of the same preparation with a 4N filter, which reduces the amount of light 4x, and measure the grey level of the black and white image via Measure | Grey measure | Calibrate grey | Reference value = 0.6 | Measure | Calibrate | OK. This corresponds with a 25% transmittance; thus, an optical density of 0.6, according to OD = 2 - log T.
   3. Acquire an image of the same preparation without light, considered black, and measure the grey level of the black and white image via Measure | Grey measure | Calibrate grey | Reference value = 1 | Measure | Calibrate | OK. This corresponds with a 0% transmittance; thus, an optical density of 1, according to OD = 2 - log T.
4. Detect starch.
   1. Acquire a color image of the field to measure in TIFF format with a resolution of at least 300 dots per inch (dpi).
   2. Create a binary image corresponding to the area stained. Set the three color thresholds (values between 0 - 255 for each) until the binary image exactly reflects the stained starch granules observed, via Image | Detect | Select the thresholds of red, blue and green | OK. Make repeatedly visual comparisons in various preparations and tissues to tune up the final detection levels. Store and use these levels for all preparations.
   3. Quantify the starch. Convert the original color image into a black and white image with the image analysis system. Use the binary image as a superimposed mask on the black and white image via Image | Binary Edit. Measure the sum of the optical density of every pixel under the mask via Measure | Grey level | OK and consider this value as the starch content in the measured field.
   4. Repeat steps 3.4.1 - 3.4.3 in four places of the ovary primordia to obtain a representative value of the starch content in the ovary of flower primordia.
   5. Repeat steps 3.4.1 - 3.4.3 and step 3.4.5 in different flowers of each collecting date.

Wyniki

Dormancy studies require the determination of the moment when the chilling requirements are fulfilled. Despite the lack of phenological changes during winter under field conditions (Figure 1A), cherry trees do not recover the capacity of growth in suitable conditions until they pass a certain period under low temperatures. The regular transference of shoots to a controlled conditions chamber (Figure 1B) during winter time allowed...

Dyskusje

Dormancy in woody perennials presents clear implications in fruit production and forestry in a changing climate, although the biological process behind dormancy remains unclear. Dormancy studies can be approached from different points of view, but the research looking for a biological marker for winter dormancy has intensified over the last years. However, most attempts to find an unequivocal indicator showing when a bud has broken dormancy have been unsuccessful³. The methodology described herein...

Materiały

Name	Company	Catalog Number	Comments
Precision scale	Sartorius	CP225D
Stereoscopic microscope	Leica Microsystems	MZ-16
Drying-stove	Memmert	U15
Paraffin Embedding station	Leica Microsystems	EG1140H
Rotatory microtome	Reichert-Jung	1130/Biocut
Microtome blade	Feather	S35	Stainless steel
Bright field microscope	Leica Microsystems	DM2500
Digital Camera	Leica Microsystems	DC-300
Image Analysis System	Leica Microsystems	Quantiment Q550