Histology Basics and Cell Death Detection in Honeybee Tissue

Summary

Immunohistochemical methods are useful in honeybee research to detect and assess the level of apoptosis and necrosis in the midgut and hypopharyngeal glands of adult bees.

Abstract

Honeybees (Apis mellifera L.) inside the hive (nurse workers and other hive bees) and outside the hive (foragers) are exposed to climate and weather changes, various pesticides, pathogens, and malnutrition, mainly entering through the mouth and primarily affecting the digestive tracts of adult bees. To understand and prevent the effects of such external and internal stressors on honeybees, one useful research method is the immunohistochemical method. A basic protocol is described to prepare the midgut (ventriculus) and hypopharyngeal glands (HPGs) of adult bees for histological analysis. A detailed methodology is described to assess the level of cell damage and distinguish necrosis from programmed cell death (apoptosis) as a natural process of tissue regeneration. The results of adult honeybee treatment with oxalic acid and pesticides (insecticide and acaricide) and the determination of cell death in the ventriculus and HPGs are presented. The pros and cons of the methodology are also discussed.

Introduction

Honeybees (Apis mellifera L.) are, among other wild pollinators, the most important pollinators of agricultural plants. Over thousands of years, the changing environment has influenced bees to adapt their morphology, physiology, behavior, and tolerance to several pathogens and parasites. Therefore, honeybees have developed a highly diverse range of species and subspecies around the globe¹. These results are consistent with previous findings, that there is genetic variation in the honeybee's digestive tract structure, but also suggest that alterations of the midgut are due to environmental factors^2,3.

The digestive tract of the honeybee has three main parts: foregut, midgut (ventriculus), and hindgut⁴. The ventriculus is an essential organ for the digestion of pollen and nectar/honey; in the hindgut, osmotic control takes place through absorption of water and ions². The hypopharyngeal glands (HPGs) of honeybee workers are located in the head and synthesize and secrete royal jelly components to feed the brood, the queen, and members of the colony. Their size changes with age and tasks and depends on proper nutrition (quality pollen). Nurse workers aged 6 to 18 days perform brood rearing, and the size of HPGs increases^5,6. In forager bees, the HPGs degenerate and only secrete enzymes that are important to convert the complex sugars into simple ones (α-glucosidases, leucine arylamidase, invertase) in honey⁷.

Honeybees are exposed to several biotic and abiotic stressors⁸, and the digestive tract can be affected by several negative stimulants. The first barrier that protects the organism from pathogens is the peritrophic membrane in the midgut, which consists of intestinal mucosa to protect against pathogens⁴. The development and function of HPGs depend on diet, age, and colony condition⁹, and are affected by insecticides, acaricides¹⁰, and pathogens^11,12,13. Acaricide residues in the hive due to varroa control treatment and pesticides from the environment affect forager bees and nurse bees^14,15. The greatest threat to honeybee colonies is the mite Varroa destructor, both as a vector of viruses contributing to colony losses¹⁶ and as a consumer of the host's fat body (an important vital organ in honeybees), which consequently affects the individual's body and colony functions¹⁷.

However, intensive farmland habitats can provide a short-term food supply for honeybees. Therefore, agri-environmental schemes should enhance the availability of honey flowers in agricultural landscapes¹⁸. To assess the morphology of different subspecies^6,19,20,21 or sublethal effects of these factors at the cell or tissue levels, especially midgut and HPGs, histological and immunohistochemical methods are practical and sufficiently accurate to be used in histology research in honeybees.

Protocol

1. Basic histology for honeybee research

1. Dissection of honeybee tissue
   NOTE: For the dissection of worker bees, use a dissecting microscope with an LED light source. The most useful magnification is ~20x.
   1. Manipulation and dissection
      1. Carefully take a worker bee with forceps and put it on ice (or into the freezer at -20 °C) for 2 min to immobilize it²². Pin the bee on the Petri dish diagonally through the uppermost back portion of the thorax twice, from left to right and from right to left.
      2. Pour insect saline to cover the body. Place the Petri dish under the microscope, focus, and adjust.
      3. Prepare the instruments (see the Table of Materials).
   2. Dissection of midgut
      1. Start with the abdomen by inserting one point of the scissors under the tergite A5 (Figure 1) in the center of the right side of the bee body. Cut to the tergite A2.
      2. Keep the inner blade of the scissors parallel with the side of the body to avoid damaging the internal organs. Turn the scissors left and make one cut; turn right and make another cut. Gently open the left part of the abdomen and pin it. Repeat on the other side.
      3. Using forceps with one hand, gently pull the honeybee stomach upward, and with scissors in the other hand, cut at the very end of the esophagus. Pull the stomach and midgut away from the abdomen and cut at the rectum. Use a pipette with insect saline solution and remove any feces or parts of the tissue.
   3. Dissection of HPGs
      1. Immobilize a worker bee on ice as described in step 1.1.1. Cut the head off and place it on the smaller plate with the antennae facing up. Secure the head with two pins: one through the left compound eye and the second through the right compound eye.
      2. Make a cut across the first compound eye on the inner side of the pins, continue to the labrum, and then make another cut on the other side across the second compound eye (Figure 2).
      3. Cut off the antennae. Lift off the mask and cut where still attached. Take the forceps and carefully remove the glands together with the brain and part of the compound eyes.
2. Fixation, dehydration, and paraffin embedding
   NOTE: Wear protective gloves.
   1. Place the tissue in penicillin bottles, filled 3/4 with 10% formalin. Keep in a refrigerator at 4 °C.
   2. After 24 h, dehydrate the tissue in a series of alcohols: 70%, 80%, 90%, 100%, for 1 h each, 100% 2-propanol for 1 h, 100% 2-propanol for 12 h, and finally 100% 2-propanol for 1 h.
   3. Place the tissue in histocassettes; mark and place them in the glass chambers with 2-propanol and paraffin (1:1) in an incubator at 60 °C for 24 h.
   4. Move the histocassettes to another chamber with paraffin (I.) for another 24 h. Repeat the procedure with fresh paraffin twice more (II. and III.), both for 24 h.
   5. Finally, prepare the mounting station and start embedding the tissue into wax.
      1. Open each histocassette and remove the cover. Fill the mold with wax and carefully put the tissue with warm forceps in the middle of the mold.
      2. Place the histocassette on the mold and slightly cover it with wax. Immediately place the mold on the cold surface of the mounting station for a few seconds, then place it on the cold plate for a few minutes until the wax hardens and separates from the mold together and the histocassette.
   6. Store the finished samples in a box, away from dust and heat.
   7. Cut 4 µm thin sections on a microtome: first, two sections attached to each other and then one separately. Transfer the sections with forceps and let them float on distilled water (42 °C), then collect them on clean slides by placing two sections together on the left side of the objective glass and the third one on the right side, remaining distinctly separate. Leave the marked slides overnight on the heating device and finally store them in a box dedicated for histology samples.
3. Dewaxing and rehydration
   NOTE: Wear protective gloves.
   1. Prepare nine Coplin jars and put the sections into a series of clearing agents (I., II., III.) for 5 min each.
   2. Put into 2-propanol, ethanol 96% (I., II.), alcohol 90% and 80%, and distilled water for 3 min each.
4. Dyeing with hematoxylin and eosin
   NOTE: Wear protective gloves.
   1. Prepare six Coplin jars.
   2. For hematoxylin and eosin (H&E) staining, put the dewaxed, rehydrated sections in hematoxylin for 5 min, then carefully place them under the running tap water for 2 min. Then put them into distilled water for 1 min and eosin for 4 min (for eosin, the Coplin jar is not necessary).
   3. Place the slides in ethanol 96% for 1 min, then 2-propanol for 2 min, and finally into the clearing agent for 2 min.
   4. Add mounting medium and a cover glass and let them dry. Observe under a light microscope.

Figure 1: Dorsal view of honeybee body. A1-A7 tergites. The detailed instructions on honeybee dissection can be found in Carreck et al.²⁴. Please click here to view a larger version of this figure.

Figure 2: Dorsal view of HPGs, parts of compound eyes attached to the brain (not visible). A young worker bee aged 5 to 6 days has plump and creamy white HPGs. The acini are located on the brain and fill the head area with branches reaching the back of the brain. In foraging bees, these glands are greatly shrunken and leave only thin thread-like remains. For this reason, it is better to remove glands together with the brain to make it easier in further procedures to avoid losing the tissue. Scale bar = 500 µm. Please click here to view a larger version of this figure.

2. Cell death detection in tissue sections

1. Apoptosis detection kit (Assay A)
   NOTE: Follow the manufacturer's protocol (see the Table of Materials).
   1. Prepare the Coplin jars.
   2. After dewaxing and rehydration (see step 1.3), immerse the slides in 0.85% NaCl solution, and then in phosphate-buffered saline (PBS) (5 min).
   3. Put the slides in 4% paraformaldehyde 2 x 15 min.
   4. Place the slides flat in the container and add 100 µL of a Proteinase K (20 µg/mL) solution, then leave them for 10-30 min.
   5. Place the slides in PBS (5 min).
   6. Place the slides in 4% paraformaldehyde in PBS (5 min).
   7. Immerse the slides in PBS (2 x 5 min).
   8. Place the slides flat in the container, add 100 µL of equilibration buffer, and leave them for 5-10 min.
   9. Add 100 µL of TdT reaction mix. Put paper towels inside the container, around the slides, moisten the towels with water, and then cover with plastic wrap. Incubate slides for 60 min at 37 °C.
   10. Place the slides back in the staining rack and immerse in 2x saline-sodium citrate (SSC) for 15 min.
   11. Immerse the slides 3 x 5 min in PBS, then in 0.3% hydrogen peroxide for 3-5 min, and then in PBS again, 3 x 5 min.
   12. Again, place the slides flat in the container, add 100 µL of Streptavidin HRP (horseradish peroxidase), and leave for 30 min (cover with plastic wrap).
   13. Immerse the slides 3 x 5 min in PBS.
   14. Place the slides flat in the container and add 100 µL of 3,3'-diaminobenzidine (DAB) solution. Look for a light brown background.
   15. Return the slides to the rack and wash them several times in water (double-distilled).
   16. Mount the slides under glass coverslips in mounting medium and leave flat to dry.
   17. Observe under a light microscope.
2. Apoptosis detection kit (Assay B)
   NOTE: Follow the manufacturer's protocol (see the Table of Materials).
   1. Prepare Coplin jars.
   2. Prepare Proteinase K (20 µg/mL diluted in PBS).
   3. After dewaxing and rehydrating the sections (step 1.3), place the slides in PBS for 5 min.
   4. Place the slides flat in the container and add Proteinase K (20 µg/mL, 60 µL per 5 cm² specimen).
   5. Wash the slides 2 x 2 min in distilled water.
   6. Quench in endogenous peroxidase (in 3% hydrogen peroxidase) at room temperature.
   7. Rinse the slides 2 x 5 min with PBS or water.
   8. Place the slides flat in the container and apply equilibration buffer (75 µL/5 cm²) for 10 s at room temperature.
   9. Carefully wipe around the tissue.
   10. Add the TdT enzyme (terminal deoxynucleotidyl transferase) to each section and incubate in a humidified chamber for 1 h at 37 °C. Put paper towels inside the tray, around the slides, moisten the towels with water, and cover them with plastic wrap.
   11. After incubation, put the specimens in the rack and leave them in stop/wash buffer (10 min).
   12. Warm the anti-digoxigenin conjugate to room temperature.
   13. Wash the slides in PBS (3 x 1 min).
   14. Carefully wipe off around the tissue.
   15. Add two drops of Anti-Digoxigenin-Peroxidase conjugate (65 µL/5 cm²) to the sections and incubate for 30 min in a humidified container.
   16. After washing in PBS 4 x 2 min, prepare working-strength peroxidase substrate, and gently tap off excess liquid and aspirate around the section.
   17. Cover the sections with peroxidase substrate (75 µL/5 cm²) and stain for 5 min. Place a slide under the microscope and determine the optimal staining time.
   18. Wash the slides in a staining rack in distilled water (3 x 1 min).
   19. Incubate the slides in distilled water for 5 min.
   20. Counterstain using hematoxylin for 2 min.
   21. Place the slide under running tap water for 3 min.
   22. Wash the slide in distilled water.
   23. Mount the slides under glass coverslips in mounting medium and leave flat to dry.
   24. Observe under a light microscope.
3. Apoptosis detection kit (Assay C)
   NOTE: Follow the manufacturer's protocol (see the Table of Materials).
   1. Prepare the Coplin jars.
   2. Dewax and rehydrate the tissue sections (see step 1.3).
   3. Incubate the tissue with Proteinase K (15-30 min at 37 °C).
   4. Place the slides back on the rack and rinse 2x in PBS.
   5. Cover with 50 µL of 'TUNEL reaction mixture'. Place wet paper towels inside the container, cover them with plastic wrap, and leave them for 60 min at 37 °C.
   6. Rinse 3x with PBS.
   7. Place the slides in the container and dry the area around the tissue sample.
   8. Add 50 µL of Converter-AP to the sample and incubate in a humidified container for 30 min at 37 °C.
   9. Rinse 3x in PBS.
   10. Add 50-100 µL of substrate solution and leave for 10 min in the dark.
       NOTE: Observe the staining under a light microscope.
   11. Rinse the slides 3x with PBS.
   12. Counterstain by transferring sections into hematoxylin for 2 min and then carefully rinse in running tap water for 5 min.
   13. Mount the slides under glass coverslips in an aqueous mounting medium and leave them flat to dry.
   14. Observe under a light microscope. Assess the affected (positive) cells by counting 70 to 100 cells in each sample of the midgut or HPGs under a light microscope.

Representative Results

Cell death detection in the midgut
Newly emerged worker bees (Apis mellifera carnica) from the experimental apiary at the Agricultural Institute of Slovenia in Ljubljana were individually treated with 3% oxalic acid (OA)²³. OA is frequently used in beekeeping for Varroa destructor control. After the treatment, the worker bees (three from each group) were immobilized on ice. The midgut was dissected and fixed it in 10% formalin. The tissue was then dehydrated in a series of alcohol solutions and finally embedded in paraffin wax. After being cut with a microtome into 7 µm thin sections, the tissue samples were prepared for analysis. Using a light microscope, the percentage of affected cells (70-100 cells from each of three midgut samples) was calculated. The results with Assay B indicated that treatment with OA significantly affected the cells in the midgut (Figure 3). Assay A showed no difference between treated and control bees; rate of cell death was under 10%. In control bees, fed sugar syrup only, the morphology of the midgut was unaffected and well preserved.

Figure 3: Midgut. (A) Hematoxylin and eosin staining; (B) immunostaining (Assay C) of the midgut. Intense red staining is localized in the nuclei of the midgut cells. Scale bars = 100 µm. Please click here to view a larger version of this figure.

Cell death detection in HPGs
In the next trial, the experiment was conducted, selecting three disease-free colonies (Apis mellifera L.). Combs with covered brood were placed in an incubator (34.5 °C), and the newly emerged worker bees were marked with a spot on the thorax to define their age. This procedure was repeated three times to obtain differently aged bees. The bees were marked and returned to their colony. The bees were sampled after 30 days from the beginning of the trial. Finally, they were put into a 7.5 cm x 4 cm x 4 cm hoarding cage, with wire mesh on one side and kept in an incubator at 28 °C.

Workers were treated with insecticide (imidacloprid) or acaricide (coumaphos), both solutions in sublethal doses, or sugar syrup as a control group¹⁰. The bees of different groups were immobilized and the HPGs dissected. A sample consisted of three to five workers from the same group to obtain as many cells as possible. The affected cells were evaluated using immunohistology methods. Red (Assay C) and brown (Assay B) reaction products were detected in the apoptotic nuclei of HPGs. Positive red nuclei after imidacloprid or coumaphos treatment were determined in the majority of glandular cells (Figure 4), and only sporadic cell nuclei showed brown reaction product from the same treated groups. The control group had no damaged HPG cells.

Figure 4: Hypopharyngeal glands. (A) Hematoxylin and eosin staining; (B) immunostaining (Assay C). Red staining is localized in the nuclei of the cells. (C) Immunostaining (Assay B). Brown reaction product indicates the positive cell nuclei. Scale bars = 50 mm. Please click here to view a larger version of this figure.

Discussion

In living organisms, cell death is defined as apoptosis or necrosis²⁵ and can be accompanied by autophagy²⁶. The difference between apoptotic and necrotic cells is that apoptosis is a form of programmed cell death and appears in normal cells, whereas necrosis occurs due to lethal conditions (e.g., accident, disease)^27,28. Apoptosis can be detected using assay kits based on the TUNEL technique (detection ofDNA fragmentation by labeling the 3′-hydroxyl termini in the double-strand DNA breaks generated during apoptosis). Different kits provide several levels of sensitivity in detecting cell deletion.

One of the assays (Assay C) is highly sensitive and detects both apoptosis and necrosis²⁹; the other assay (B) shows higher sensitivity for detecting apoptotic cell death³⁰. The principle of Assay C is to detect DNA breaks in the early stages of apoptosis. After fixing and permeabilizing the apoptotic cells, the tissue is incubated with a TUNEL reaction mixture. Meanwhile, the role of TdT is to catalyze the addition of fluorescein-dUTP at free 3′-OH groups in DNA. After the tissue is washed, the anti-fluorescein antibody marks the label in the damaged parts of the DNA. The principle of the antibody is to attach to the enzyme alkaline phosphatase that works as a reporter. Lastly, the AP can be seen as a result of this specific reaction³¹.

Haematoxylin and eosin staining of organs is a straightforward and useful method for morphological analysis using light microscopy. Including this step first to observe any morphological changes of cells is recommended. For the detection of early stages of apoptosis in the thin sections of honeybee tissue, at least two kits are available for immunohistochemical analysis (see the Table of Materials). Both turn the apoptotic cell nuclei dark brown and are visualized using light microscopy. Using Assay A (TUNEL technique), the Streptavidin HRP (horseradish peroxidase) conjugates to biotinylated nucleotides, and apoptotic nuclei turn brown after the reaction of DAB (diaminobenzidine, a stable chromogen). Assay B distinguishes cell damage via the detection of DNA cleavage and condensed chromatin, which is a sign of early apoptosis.

In a healthy organism, the level of cell renewal can usually be assessed in small percentages^32,33. Cell death in the midgut increased after the OA treatment, which indicates that the use of OA has a detrimental effect on worker bees' midguts in lab experiments. The group of bees treated with imidacloprid and coumaphos revealed an increased cell death (red nuclei) in the food glands¹⁰, indicating cell damage or necrosis; programmed cell death was found at a low level (brown nuclei)¹⁰. However, necrotic and apoptotic cell death was found at high levels, especially after imidacloprid treatment. In the group of untreated bees, the level of programmed cell death in HPGs was not more than 10%, which is in accordance with normal tissue turnover³².

Cell death, both due to damage or programmed cell death, was detected by both assays (B and C) and resulted in different sensitivity; the first one detects both necrotic and programmed cell death¹¹. As confirmed in the healthy workers (control group), both assays detected sporadic positive cells only¹⁰. The apoptosis and necrosis detection assays used in immunohistochemical analysis of honeybee tissue turned out to be a powerful method to explore the sublethal effects of different substances on honeybees.

Critical steps in the protocol:
After being cut with a microtome, tissue sections must be placed onto the objective glass on a warm plate (flattening table, see Table of Materials) overnight. It is essential for the samples to be well dried for future steps in the protocols. When tissue is not well attached to the glass, it can detach from the surface in the procedure for cell death detection. It is advisable to use the light microscope to verify the presence of the desired tissue. Next, it is useful to dye the first slide with H&E to check for the correct section with many cells (especially the glandular tissue) and prepare new ones in case the midgut section is not appropriate. HPGs can be quite challenging to find, so care must be taken not to cut too many sections; otherwise, the glands will be lost.

Adding positive control to detect DNA fragmentation is useful but optional. It is important to treat the slides separately to avoid high background staining in the experimental slides. In Assay B, the positive controls are included in some of the kits (see Table of Materials); others should be purchased separately.

The method has a limitation in its length and precision. Preservation of tissue in an aqueous mounting medium is only short-term (under 3 months). If longer preservation is desired (not recommended due to possible changes of color), there are other mediums, but the results are not as reliable.

Using these two methods (apoptosis and necrosis detection) simultaneously is very useful to compare the different effects of pesticides on honeybee tissue, especially for sublethal effects. The alternative method would be the observation of foraging activity and its impact on the cognitive perception of worker bees affected by pesticides. Such a method would be faster in detecting sublethal effects on adult bees' activities, but would not answer any questions regarding the extent of the internal damage that can alter behavior in the early stage, as in young (nurse) bees.

Histological analysis of the simple morphology of honeybee tissue is a solid basis for approaching different research perspectives in cell damage, apoptosis, or malformations. The causes of pesticide use in the environment or colony treatment due to parasites and pests can be detrimental and significantly affect honeybee lifespan and colony survival. The midgut and HPGs are essential organs in honeybees and have the ability and purpose to quickly respond to any kind of negative external factors that affect the age-related activities of bees. The HPGs decrease in size and secretion abilities, and epithelial cells in the midgut respond by increased cell death. Immunohistochemistry methods, such as in situ studies, are useful tools for apoptosis detection in bee tissue. They also show the potential to be implemented in studies of possible adverse effects on honeybees and other beneficial insects.

Materials

2-Propanol
ApopTag Peroxidase kit (ApopTag Peroxidase In Situ Apoptosis Detection)	Sigma-Aldrich	S7100	Assay B, https://www.sigmaaldrich.com/SI/en/product/mm/s7100?gclid=CjwKCA jw7vuUBhBUEiwAEdu2pPanI9SE j81ZTl-nLHEoxXAv7ViKwPA_QRx H7fciMRNcYwR7lbPQbhoCqcQQA vD_BwE; Positive controls included in S7101
Covers
DeadEnd Colorimetric TUNEL system	Promega	G7360	Assay A, https://worldwide.promega.com/products/cell-health-assays/apoptosis-assays/deadend-colorimetric-tunel-system/?catNum=G7360
Dissecting microscope  (for bee dissection)	Zeiss
Distilled water
Embedding cassette
EnVision System alkaline phosphatase kit	Dako
Eosin Y Solution	Sigma-Aldrich		alcoholic
Ethanol			95% (or less pure), 90%, 80%
Faramount mounting medium, aqueous	Dako		mounting medium
Flattening table	Leica	HI1220
Forceps  (for bee dissection)	Fine science tools	11294-00	Standard #4
Formalin 10%			Formaldehyde
Hematoxylin	Sigma-Aldrich
HistoChoice Clearing Agent	Sigma-Aldrich		clearing agent
Hydrogen peroxidase 3%
Incubator	BioRad
Insect pins  (for bee dissection)	Entosphinx	44594	Insect pins stainless steel – white, size 2
ISCDDK, AP (In Situ Cell Death Detecteion Kit, Alkaline Phosphatase)	Roche	11684809910	Assay C, https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/362/737/11684809910b ul.pdf
KH2PO4
Lab clock
Light microscope	Leica
Microscope slides			Box with the slides must be preserved in a plastic wrap to prevent dust
Microtome	Leica
Modular tissue embedding station	Leica
Na2HPO4
NaCl
Paraformaldehyde 4%
Paraplast	Leica
Pasteur pipettes			1.5 mL; 3 mL
PBS
Petri dish  (for bee dissection)			Filled with condensation silicon  (Xantoprene L blue and Universal liquid plus activator)
Proteinase K	Merck	21627
Ringers' solution  (for bee dissection)			7.5 g NaCL, 2.38 g Na2HPO4, 2.72 g KH2PO4, 1 L distilled water
Scissors  (for bee dissection)	Fine science tools	1406-09, 14061-09	Straight and curved, 9 cm
Universal liquid plus activator  (for bee dissection)	Kulzer
Watchmaker’s forceps (for bee dissection)	Fine science tools	91100-12
Water bath	Leica
Watercolor brush			2x
Xantoprene L blue  (for bee dissection)	Kulzer